Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 90362 |
|---|---|
| ensemblid | ENSG00000169122.12 |
| hgncid | 28587 |
| symbol | FAM110B |
| name | family with sequence similarity 110 member B |
| refseq_nuc | NM_001377989.1 |
| refseq_prot | NP_001364918.1 |
| ensembl_nuc | ENST00000519262.6 |
| ensembl_prot | ENSP00000509301.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 57994523 |
| end | 58148784 |
| strand | + |
| ver | v1.2 |
| region | chr8:57994523-58148784 |
| region5000 | chr8:57989523-58153784 |
| regionname0 | FAM110B_chr8_57994523_58148784 |
| regionname5000 | FAM110B_chr8_57989523_58153784 |
| 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 | 370 | 298 | 88 | 54 | 118 | 12 | 24 | 90 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0002 | 0/0 | 370 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0003 | 0/0 | 370 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| 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 | 1113 | 298 | 88 | 54 | 118 | 12 | 24 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| c0002 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| c0003 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2237 | 72 | 11 | 13 | 35 | 5 | 7 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0002 | 1/0 | 2237 | 64 | 18 | 12 | 25 | 3 | 5 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0003 | 0/0 | 2237 | 60 | 27 | 4 | 25 | 1 | 3 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0004 | 0/0 | 2238 | 17 | 1 | 5 | 9 | 0 | 2 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0005 | 0/0 | 2238 | 15 | 3 | 2 | 9 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0006 | 0/0 | 2237 | 12 | 0 | 9 | 0 | 2 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0007 | 0/0 | 2236 | 9 | 8 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0008 | 0/0 | 2237 | 7 | 6 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0009 | 0/0 | 2238 | 7 | 2 | 1 | 3 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0010 | 0/0 | 2237 | 5 | 5 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0011 | 0/0 | 2237 | 3 | 0 | 2 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0012 | 0/0 | 2237 | 2 | 2 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0013 | 0/0 | 2237 | 2 | 0 | 0 | 2 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0014 | 0/0 | 2237 | 2 | 0 | 0 | 2 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0015 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0016 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0017 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0018 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0019 | 0/0 | 2236 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0020 | 0/0 | 2238 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0021 | 0/0 | 2237 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0022 | 0/0 | 2226 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0023 | 0/0 | 2237 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0024 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0025 | 0/0 | 2238 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0026 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0027 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0028 | 0/0 | 2238 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0029 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0030 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0031 | 0/0 | 2236 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0032 | 0/0 | 2237 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0033 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0034 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0035 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0036 | 0/0 | 2237 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| t0037 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0256 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| 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 | 1113 | 298 | 88 | 54 | 118 | 12 | 24 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0002c0002 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0003c0003 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3349 | 72 | 11 | 13 | 35 | 5 | 7 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0002 | 1/0 | 3349 | 64 | 18 | 12 | 25 | 3 | 5 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0003 | 0/0 | 3349 | 59 | 26 | 4 | 25 | 1 | 3 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0004 | 0/0 | 3350 | 17 | 1 | 5 | 9 | 0 | 2 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0005 | 0/0 | 3350 | 15 | 3 | 2 | 9 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0006 | 0/0 | 3349 | 12 | 0 | 9 | 0 | 2 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0007 | 0/0 | 3348 | 9 | 8 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0008 | 0/0 | 3349 | 7 | 6 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0009 | 0/0 | 3350 | 7 | 2 | 1 | 3 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0010 | 0/0 | 3349 | 5 | 5 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0011 | 0/0 | 3349 | 3 | 0 | 2 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0012 | 0/0 | 3349 | 2 | 2 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0013 | 0/0 | 3349 | 2 | 0 | 0 | 2 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0014 | 0/0 | 3349 | 2 | 0 | 0 | 2 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0015 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0017 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0018 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0019 | 0/0 | 3348 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0020 | 0/0 | 3350 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0021 | 0/0 | 3349 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0022 | 0/0 | 3338 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0023 | 0/0 | 3349 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0024 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0025 | 0/0 | 3350 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0026 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0027 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0028 | 0/0 | 3350 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0029 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0030 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0031 | 0/0 | 3348 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0032 | 0/0 | 3349 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0033 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0034 | 0/0 | 3349 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0035 | 0/0 | 3349 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0036 | 0/0 | 3349 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0001c0001t0037 | 0/0 | 3349 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0002c0002t0016 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| a0003c0003t0003 | 0/0 | 3349 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | copy fasta | chr8 | 57989523 | 58153784 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0256 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0010g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0011g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0011g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0011g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0012g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0013g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0013g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0014g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0014g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0017g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0018g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0019g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0020g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0021g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0022g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0023g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0024g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0025g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0026g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0027g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0028g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0029g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0030g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0031g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0032g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0033g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0034g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0035g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0036g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0001c0001t0037g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0002c0002t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| a0003c0003t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0021 | g0248 | EUR | GBR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0109 | EUR | GBR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0126 | EUR | FIN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0246 | EUR | FIN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0156 | EUR | FIN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00544 | hp2 | a0001 | c0001 | t0029 | g0276 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0188 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00609 | hp2 | a0001 | c0001 | t0014 | g0242 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | CHS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00741 | hp1 | a0001 | c0001 | t0022 | g0174 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01069 | hp1 | a0001 | c0001 | t0036 | g0132 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0219 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0025 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01081 | hp2 | a0001 | c0001 | t0020 | g0033 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0245 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01175 | hp1 | a0001 | c0001 | t0011 | g0212 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0113 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01192 | hp1 | a0001 | c0001 | t0031 | g0159 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0238 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0169 | AMR | PUR | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0155 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01261 | hp1 | a0001 | c0001 | t0011 | g0195 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0077 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0194 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | CLM | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01884 | hp2 | a0001 | c0001 | t0024 | g0176 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0160 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0131 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0116 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0101 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0053 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0202 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0168 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0197 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02080 | hp2 | a0001 | c0001 | t0033 | g0081 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | KHV | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | CDX | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CDX | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | CDX | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CDX | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02257 | hp1 | a0001 | c0001 | t0027 | g0137 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02258 | hp1 | a0002 | c0002 | t0016 | g0166 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0007 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0148 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0175 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0173 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02630 | hp2 | a0001 | c0001 | t0034 | g0244 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0051 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0300 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0247 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0296 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0140 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02897 | hp1 | a0001 | c0001 | t0030 | g0035 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0127 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0294 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0161 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0145 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0150 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0170 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0265 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0072 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0295 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0157 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03453 | hp2 | a0003 | c0003 | t0003 | g0264 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0090 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03669 | hp1 | a0001 | c0001 | t0009 | g0064 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0125 | SAS | PJL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | STU | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03688 | hp2 | a0001 | c0001 | t0025 | g0009 | SAS | STU | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0026 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03831 | hp2 | a0001 | c0001 | t0032 | g0114 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0275 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03834 | hp2 | a0001 | c0001 | t0011 | g0228 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03942 | hp1 | a0001 | c0001 | t0023 | g0085 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | STU | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | STU | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18942 | hp1 | a0001 | c0001 | t0018 | g0215 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18948 | hp1 | a0001 | c0001 | t0019 | g0222 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18959 | hp2 | a0001 | c0001 | t0037 | g0180 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18972 | hp2 | a0001 | c0001 | t0013 | g0177 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18989 | hp1 | a0001 | c0001 | t0013 | g0183 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18992 | hp1 | a0001 | c0001 | t0028 | g0182 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19006 | hp2 | a0001 | c0001 | t0026 | g0021 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19060 | hp1 | a0001 | c0001 | t0014 | g0243 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19064 | hp2 | a0001 | c0001 | t0009 | g0179 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19079 | hp2 | a0001 | c0001 | t0009 | g0199 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19087 | hp1 | a0001 | c0001 | t0009 | g0205 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19091 | hp1 | a0001 | c0001 | t0017 | g0119 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | YRI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | ASW | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0220 | EUR | TSI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0078 | EUR | TSI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02559 | hp1 | a0001 | c0001 | t0035 | g0290 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0135 | AFR | ACB | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0144 | AFR | MSL | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | USA | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | USA | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | USA | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | USA | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0079 | AFR | LWK | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0256 | REF | REF | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0052 | REF | REF | FAM110B_chr8_57989523_58153784 | FAM110B | chr8 | 57989523 | 58153784 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:58146669
|
C | T | 1 | a0003 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.439C>T | p.His147Tyr | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1234/3349 | 439/1113 | 147/370 | chr8 | 58146669 | ||
| chr8:58146870
|
G | A | 1 | a0002 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.640G>A | p.Ala214Thr | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1435/3349 | 640/1113 | 214/370 | chr8 | 58146870 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:57994553
|
C | T | 1 | a0001c0001t0037 | 1 | NA18959.hp2 | 5_prime_UTR_variant | MODIFIER | c.-765C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | 151678 | chr8 | 57994553 | |||||
| chr8:57994567
|
C | T | 1 | a0001c0001t0036 | 1 | HG01069.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-751C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | chr8 | 57994567 | ||||||
| chr8:57994585
|
G | T | 1 | a0001c0001t0035 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-733G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | 151646 | chr8 | 57994585 | |||||
| chr8:57994677
|
A | C | 1 | a0001c0001t0014 | 2 | HG00609.hp2 NA19060.hp1 |
5_prime_UTR_variant | MODIFIER | c.-641A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | 151554 | chr8 | 57994677 | |||||
| chr8:57994757
|
C | T | 1 | a0001c0001t0034 | 1 | HG02630.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-561C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | chr8 | 57994757 | ||||||
| chr8:57994766
|
G | T | 1 | a0001c0001t0033 | 1 | HG02080.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-552G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/4 | chr8 | 57994766 | ||||||
| chr8:58031651
|
C | T | 1 | a0001c0001t0032 | 1 | HG03831.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-466C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/4 | chr8 | 58031651 | ||||||
| chr8:58075619
|
C | G | 1 | a0001c0001t0031 | 1 | HG01192.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-329C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/4 | chr8 | 58075619 | ||||||
| chr8:58146023
|
G | A | 1 | a0001c0001t0015 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-208G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 208 | chr8 | 58146023 | |||||
| chr8:58146086
|
A | T | 1 | a0001c0001t0030 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-145A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 145 | chr8 | 58146086 | |||||
| chr8:58146090
|
G | T | 1 | a0001c0001t0029 | 1 | HG00544.hp2 | 5_prime_UTR_variant | MODIFIER | c.-141G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 141 | chr8 | 58146090 | |||||
| chr8:58147538
|
C | A | 1 | a0001c0001t0034 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*195C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 195 | chr8 | 58147538 | |||||
| chr8:58147541
|
G | A | 1 | a0002c0002t0016 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*198G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 198 | chr8 | 58147541 | |||||
| chr8:58147665
|
G | A | 1 | a0001c0001t0017 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 322 | chr8 | 58147665 | |||||
| chr8:58147716
|
A | G | 12 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(9): Show | 100 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*373A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 373 | chr8 | 58147716 | |||||
| chr8:58147813
|
G | A | 1 | a0001c0001t0012 | 2 | HG02451.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*470G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 470 | chr8 | 58147813 | |||||
| chr8:58147853
|
T | A | 1 | a0001c0001t0014 | 2 | HG00609.hp2 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*510T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 510 | chr8 | 58147853 | |||||
| chr8:58148090
|
T | C | 2 | a0001c0001t0018a0001c0001t0019 | 2 | NA18942.hp1 NA18948.hp1 |
3_prime_UTR_variant | MODIFIER | c.*747T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 747 | chr8 | 58148090 | |||||
| chr8:58148139
|
TA | T | 30 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(27): Show | 213 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*809delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 809 | INFO_REALIGN_3_PRIME | chr8 | 58148139 | ||||
| chr8:58148147
|
A | T | 1 | a0001c0001t0025 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*804A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 804 | chr8 | 58148147 | |||||
| chr8:58148166
|
G | GT | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(13): Show | 174 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*843dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 844 | INFO_REALIGN_3_PRIME | chr8 | 58148166 | ||||
| chr8:58148166
|
G | GTT | 3 | a0001c0001t0005a0001c0001t0009a0001c0001t0028 | 23 | HG00609.hp1 HG01243.hp1 HG01433.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*842_*843dupTT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 844 | INFO_REALIGN_3_PRIME | chr8 | 58148166 | ||||
| chr8:58148166
|
G | T | 2 | a0001c0001t0021a0001c0001t0030 | 2 | HG00099.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*823G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 823 | chr8 | 58148166 | |||||
| chr8:58148166
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0022 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*834_*843delTTTTTT others(4): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 834 | INFO_REALIGN_3_PRIME | chr8 | 58148166 | ||||
| chr8:58148171
|
T | TG | 1 | a0001c0001t0011 | 3 | HG01175.hp1 HG01261.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*828_*829insG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 829 | chr8 | 58148171 | |||||
| chr8:58148177
|
T | TG | 4 | a0001c0001t0006a0001c0001t0020a0001c0001t0023others(1): Show | 15 | HG00323.hp1 HG01070.hp1 HG01081.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*834_*835insG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 835 | chr8 | 58148177 | |||||
| chr8:58148242
|
G | C | 1 | a0001c0001t0025 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 899 | chr8 | 58148242 | |||||
| chr8:58148421
|
A | G | 2 | a0001c0001t0008a0001c0001t0030 | 8 | HG01243.hp2 HG02630.hp1 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1078A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1078 | chr8 | 58148421 | |||||
| chr8:58148513
|
T | C | 5 | a0001c0001t0006a0001c0001t0010a0001c0001t0020others(2): Show | 20 | HG00323.hp1 HG01070.hp1 HG01081.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1170T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1170 | chr8 | 58148513 | |||||
| chr8:58148524
|
T | A | 1 | a0001c0001t0024 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1181T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1181 | chr8 | 58148524 | |||||
| chr8:58148542
|
G | T | 2 | a0001c0001t0013a0001c0001t0028 | 3 | NA18972.hp2 NA18989.hp1 NA18992.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1199G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1199 | chr8 | 58148542 | |||||
| chr8:58148671
|
T | C | 1 | a0001c0001t0023 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1328T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 4/4 | 1328 | chr8 | 58148671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:57994887
|
G | A | 1 | a0001c0001t0002g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-512+81G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57994887 | ||||||
| chr8:57994902
|
G | T | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-512+96G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57994902 | ||||||
| chr8:57994906
|
G | T | 1 | a0001c0001t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-512+100G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57994906 | ||||||
| chr8:57995061
|
C | T | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-512+255C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995061 | ||||||
| chr8:57995131
|
C | CTGGAGCC others(5): Show |
1 | a0001c0001t0002g0298 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-512+333_-512+344d others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 57995131 | |||||
| chr8:57995141
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-512+335G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995141 | ||||||
| chr8:57995258
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-512+452C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995258 | ||||||
| chr8:57995313
|
A | T | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-512+507A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995313 | ||||||
| chr8:57995411
|
C | T | 2 | a0001c0001t0003g0295a0001c0001t0010g0294 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-512+605C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995411 | ||||||
| chr8:57995630
|
G | A | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-512+824G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995630 | ||||||
| chr8:57995871
|
T | C | 1 | a0001c0001t0007g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-512+1065T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995871 | ||||||
| chr8:57995903
|
A | G | 2 | a0001c0001t0002g0293a0001c0001t0003g0292 | 2 | NA18944.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-512+1097A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995903 | ||||||
| chr8:57995967
|
G | A | 1 | a0001c0001t0003g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-512+1161G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57995967 | ||||||
| chr8:57996114
|
A | T | 6 | a0001c0001t0002g0291a0001c0001t0003g0286a0001c0001t0003g0287others(3): Show | 6 | HG02559.hp1 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-512+1308A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57996114 | ||||||
| chr8:57996188
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0172a0001c0001t0001g0184others(127): Show | 130 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-512+1382C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57996188 | ||||||
| chr8:57996770
|
A | C | 14 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281others(11): Show | 14 | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.-512+1964A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57996770 | ||||||
| chr8:57996868
|
A | C | 7 | a0001c0001t0001g0267a0001c0001t0002g0266a0001c0001t0002g0268others(4): Show | 7 | HG00733.hp1 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-512+2062A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57996868 | ||||||
| chr8:57997818
|
A | G | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-512+3012A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57997818 | ||||||
| chr8:57998123
|
T | G | 1 | a0001c0001t0001g0006 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-512+3317T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998123 | ||||||
| chr8:57998211
|
A | G | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-512+3405A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998211 | ||||||
| chr8:57998217
|
A | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0073a0001c0001t0001g0084others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-512+3411A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998217 | ||||||
| chr8:57998320
|
G | C | 6 | a0001c0001t0001g0073a0001c0001t0003g0071a0001c0001t0003g0074others(3): Show | 6 | HG01109.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-512+3514G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998320 | ||||||
| chr8:57998400
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-512+3594G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998400 | ||||||
| chr8:57998514
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0158a0001c0001t0003g0071others(7): Show | 10 | HG01109.hp1 HG01192.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-512+3708C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998514 | ||||||
| chr8:57998548
|
G | T | 1 | a0001c0001t0002g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-512+3742G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998548 | ||||||
| chr8:57998762
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-512+3956A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998762 | ||||||
| chr8:57998903
|
A | T | 1 | a0001c0001t0002g0263 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-512+4097A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57998903 | ||||||
| chr8:57999047
|
G | T | 1 | a0001c0001t0006g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-512+4241G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999047 | ||||||
| chr8:57999089
|
G | A | 1 | a0001c0001t0010g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-512+4283G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999089 | ||||||
| chr8:57999150
|
A | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0067a0001c0001t0001g0068others(168): Show | 171 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.-512+4344A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999150 | ||||||
| chr8:57999153
|
A | G | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0004g0260 | 3 | HG01070.hp2 HG01071.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-512+4347A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999153 | ||||||
| chr8:57999261
|
G | A | 2 | a0001c0001t0002g0078a0001c0001t0009g0077 | 2 | HG01433.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-512+4455G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999261 | ||||||
| chr8:57999333
|
T | C | 1 | a0001c0001t0008g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-512+4527T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999333 | ||||||
| chr8:57999374
|
A | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0073others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-512+4568A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999374 | ||||||
| chr8:57999403
|
T | A | 1 | a0001c0001t0015g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-512+4597T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999403 | ||||||
| chr8:57999518
|
A | AT | 7 | a0001c0001t0001g0154a0001c0001t0002g0291a0001c0001t0003g0286others(4): Show | 7 | HG02559.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-512+4722dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 57999518 | |||||
| chr8:57999518
|
AT | A | 6 | a0001c0001t0001g0158a0001c0001t0007g0004a0001c0001t0007g0157others(3): Show | 6 | HG01109.hp1 HG01192.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-512+4722delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 57999518 | |||||
| chr8:57999554
|
A | G | 3 | a0001c0001t0007g0004a0001c0001t0008g0079a0001c0001t0031g0159 | 3 | HG01109.hp1 HG01192.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-512+4748A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999554 | ||||||
| chr8:57999673
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-512+4867C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999673 | ||||||
| chr8:57999802
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-512+4996C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 57999802 | ||||||
| chr8:58000229
|
C | A | 2 | a0001c0001t0002g0128a0001c0001t0005g0161 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-512+5423C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000229 | ||||||
| chr8:58000236
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0002g0178a0001c0001t0002g0181others(7): Show | 10 | HG02080.hp2 NA18959.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.-512+5430G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000236 | ||||||
| chr8:58000289
|
A | G | 9 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0258others(6): Show | 9 | HG00438.hp2 NA18948.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.-512+5483A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000289 | ||||||
| chr8:58000376
|
A | G | 3 | a0001c0001t0001g0124a0001c0001t0002g0126a0001c0001t0004g0125 | 3 | HG00280.hp1 HG02738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-512+5570A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000376 | ||||||
| chr8:58000393
|
C | T | 2 | a0001c0001t0002g0123a0001c0001t0003g0257 | 2 | HG01943.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-512+5587C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000393 | ||||||
| chr8:58000603
|
T | C | 8 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0002g0082others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-512+5797T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000603 | ||||||
| chr8:58000731
|
G | A | 52 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(49): Show | 52 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.-512+5925G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000731 | ||||||
| chr8:58000745
|
C | T | 4 | a0001c0001t0004g0260a0001c0001t0007g0090a0001c0001t0024g0176others(1): Show | 4 | HG01192.hp1 HG01884.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-512+5939C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58000745 | ||||||
| chr8:58001029
|
C | A | 1 | a0001c0001t0027g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-512+6223C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001029 | ||||||
| chr8:58001375
|
GGT | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(167): Show | 170 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.-512+6585_-512+658 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58001375 | |||||
| chr8:58001422
|
T | C | 5 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+6616T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001422 | ||||||
| chr8:58001563
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-512+6757C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001563 | ||||||
| chr8:58001564
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-512+6758G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001564 | ||||||
| chr8:58001665
|
A | T | 1 | a0001c0001t0003g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-512+6859A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001665 | ||||||
| chr8:58001792
|
G | T | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-512+6986G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001792 | ||||||
| chr8:58001804
|
C | T | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-512+6998C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58001804 | ||||||
| chr8:58002044
|
C | CAG | 3 | a0001c0001t0002g0152a0001c0001t0003g0151a0001c0001t0027g0137 | 3 | HG02257.hp1 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-512+7248_-512+724 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58002044 | |||||
| chr8:58002553
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-512+7747A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002553 | ||||||
| chr8:58002562
|
A | G | 5 | a0001c0001t0001g0158a0001c0001t0004g0260a0001c0001t0007g0090others(2): Show | 5 | HG01192.hp1 HG01884.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+7756A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002562 | ||||||
| chr8:58002580
|
C | T | 1 | a0001c0001t0005g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-512+7774C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002580 | ||||||
| chr8:58002812
|
A | C | 53 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(50): Show | 53 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-512+8006A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002812 | ||||||
| chr8:58002901
|
G | A | 2 | a0001c0001t0001g0267a0001c0001t0002g0266 | 2 | HG00733.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-512+8095G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002901 | ||||||
| chr8:58002970
|
T | A | 1 | a0001c0001t0002g0095 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-512+8164T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58002970 | ||||||
| chr8:58003244
|
C | T | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-512+8438C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003244 | ||||||
| chr8:58003258
|
G | A | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-512+8452G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003258 | ||||||
| chr8:58003321
|
G | A | 1 | a0001c0001t0012g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-512+8515G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003321 | ||||||
| chr8:58003381
|
C | T | 3 | a0001c0001t0002g0152a0001c0001t0003g0151a0001c0001t0027g0137 | 3 | HG02257.hp1 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-512+8575C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003381 | ||||||
| chr8:58003858
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(77): Show | 80 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-512+9052C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003858 | ||||||
| chr8:58003887
|
C | A | 1 | a0001c0001t0001g0060 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-512+9081C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003887 | ||||||
| chr8:58003920
|
C | T | 2 | a0001c0001t0013g0183a0001c0001t0028g0182 | 2 | NA18989.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-512+9114C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003920 | ||||||
| chr8:58003980
|
A | G | 3 | a0001c0001t0002g0167a0001c0001t0007g0135a0002c0002t0016g0166 | 3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-512+9174A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003980 | ||||||
| chr8:58003981
|
C | T | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+9175C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58003981 | ||||||
| chr8:58004001
|
A | G | 8 | a0001c0001t0001g0158a0001c0001t0002g0167a0001c0001t0004g0260others(5): Show | 8 | HG01192.hp1 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-512+9195A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004001 | ||||||
| chr8:58004017
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-512+9211G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004017 | ||||||
| chr8:58004059
|
T | C | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-512+9253T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004059 | ||||||
| chr8:58004154
|
G | A | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+9348G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004154 | ||||||
| chr8:58004291
|
A | C | 1 | a0001c0001t0001g0089 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-512+9485A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004291 | ||||||
| chr8:58004436
|
T | C | 1 | a0001c0001t0011g0228 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-512+9630T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004436 | ||||||
| chr8:58004566
|
G | A | 1 | a0001c0001t0004g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-512+9760G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004566 | ||||||
| chr8:58004774
|
G | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(172): Show | 175 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.-512+9968G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004774 | ||||||
| chr8:58004930
|
G | T | 1 | a0001c0001t0001g0256 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-512+10124G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58004930 | ||||||
| chr8:58005126
|
G | A | 5 | a0001c0001t0001g0158a0001c0001t0004g0260a0001c0001t0007g0090others(2): Show | 5 | HG01192.hp1 HG01884.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+10320G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005126 | ||||||
| chr8:58005146
|
A | G | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-512+10340A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005146 | ||||||
| chr8:58005255
|
G | A | 7 | a0001c0001t0001g0267a0001c0001t0002g0136a0001c0001t0002g0266others(4): Show | 7 | HG00733.hp1 HG02257.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-512+10449G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005255 | ||||||
| chr8:58005263
|
G | A | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+10457G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005263 | ||||||
| chr8:58005311
|
C | T | 1 | a0001c0001t0011g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-512+10505C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005311 | ||||||
| chr8:58005470
|
T | C | 3 | a0001c0001t0002g0032a0001c0001t0003g0034a0001c0001t0020g0033 | 3 | HG00642.hp1 HG01074.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-512+10664T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005470 | ||||||
| chr8:58005505
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-512+10699C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005505 | ||||||
| chr8:58005617
|
A | T | 1 | a0001c0001t0002g0120 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-512+10811A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005617 | ||||||
| chr8:58005637
|
C | T | 5 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+10831C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005637 | ||||||
| chr8:58005936
|
T | C | 3 | a0001c0001t0002g0152a0001c0001t0003g0151a0001c0001t0027g0137 | 3 | HG02257.hp1 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-512+11130T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005936 | ||||||
| chr8:58005976
|
A | G | 1 | a0001c0001t0003g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-512+11170A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58005976 | ||||||
| chr8:58006212
|
T | C | 10 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(7): Show | 10 | HG01192.hp1 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-512+11406T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006212 | ||||||
| chr8:58006525
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-512+11719G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006525 | ||||||
| chr8:58006532
|
C | G | 45 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(42): Show | 45 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.-512+11726C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006532 | ||||||
| chr8:58006558
|
C | T | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-512+11752C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006558 | ||||||
| chr8:58006604
|
A | AT | 9 | a0001c0001t0001g0029a0001c0001t0001g0259a0001c0001t0002g0162others(6): Show | 9 | HG00408.hp2 HG01891.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-512+11813dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006604 | |||||
| chr8:58006604
|
AT | A | 18 | a0001c0001t0002g0186a0001c0001t0002g0297a0001c0001t0003g0129others(15): Show | 18 | HG01069.hp1 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-512+11813delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006604 | |||||
| chr8:58006786
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-512+11980A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006786 | ||||||
| chr8:58006810
|
C | T | 1 | a0001c0001t0004g0194 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-512+12004C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006810 | ||||||
| chr8:58006830
|
C | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0258a0001c0001t0002g0121others(1): Show | 4 | HG00438.hp2 HG00621.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-512+12024C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006830 | ||||||
| chr8:58006901
|
G | GTA | 8 | a0001c0001t0002g0082a0001c0001t0002g0147a0001c0001t0002g0162others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+12117_-512+12 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATA | 8 | a0001c0001t0001g0172a0001c0001t0001g0261a0001c0001t0001g0262others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+12115_-512+12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-512+12109_-512+12 others(16): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(7): Show |
2 | a0001c0001t0002g0031a0001c0001t0002g0128 | 2 | HG02004.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-512+12105_-512+12 others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(41): Show |
1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-512+12109_-512+12 others(54): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(9): Show |
15 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0253others(12): Show | 15 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.-512+12103_-512+12 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(11): Show |
25 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0110others(22): Show | 25 | HG00099.hp2 HG00408.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-512+12101_-512+12 others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(13): Show |
13 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0042others(10): Show | 13 | HG00673.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-512+12099_-512+12 others(26): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(15): Show |
12 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0282others(9): Show | 12 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-512+12097_-512+12 others(28): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(17): Show |
9 | a0001c0001t0001g0098a0001c0001t0001g0281a0001c0001t0002g0099others(6): Show | 9 | HG01952.hp2 HG02155.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(30): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(19): Show |
2 | a0001c0001t0003g0151a0001c0001t0007g0300 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(32): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(23): Show |
2 | a0001c0001t0001g0230a0001c0001t0006g0155 | 2 | HG01255.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(36): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(27): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0185 | 2 | HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(40): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
G | GTATATAT others(33): Show |
1 | a0001c0001t0001g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(46): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
GTATA | G | 3 | a0001c0001t0001g0252a0001c0001t0003g0251a0001c0001t0017g0119 | 3 | NA18949.hp2 NA18997.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-512+12115_-512+12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006901
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-512+12107_-512+12 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006901 | |||||
| chr8:58006919
|
A | ATTTT | 38 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(35): Show | 38 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.-512+12114_-512+12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006919 | |||||
| chr8:58006919
|
A | T | 3 | a0001c0001t0001g0065a0001c0001t0005g0028a0001c0001t0005g0061 | 3 | NA18989.hp2 NA19079.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-512+12113A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006919 | ||||||
| chr8:58006921
|
A | ATTTT | 23 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0091others(20): Show | 23 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-512+12116_-512+12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006921 | |||||
| chr8:58006921
|
A | ATTTTT | 13 | a0001c0001t0001g0203a0001c0001t0001g0207a0001c0001t0001g0208others(10): Show | 13 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(10): Show |
intron_variant | MODIFIER | c.-512+12116_-512+12 others(11): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006921 | |||||
| chr8:58006921
|
A | T | 42 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(39): Show | 42 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-512+12115A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006921 | ||||||
| chr8:58006923
|
A | ATATATAT others(49): Show |
1 | a0001c0001t0003g0096 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(62): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(43): Show |
1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(56): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(40): Show |
2 | a0001c0001t0013g0183a0001c0001t0028g0182 | 2 | NA18989.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(53): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0003g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(40): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0002g0181 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(46): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(34): Show |
2 | a0001c0001t0002g0178a0001c0001t0013g0177 | 2 | NA18972.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(47): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(35): Show |
1 | a0001c0001t0003g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(48): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0002g0012 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(35): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0010g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(36): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0009g0179 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(43): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0008 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(44): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0006a0001c0001t0005g0139 | 2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(34): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0009g0140 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(40): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(29): Show |
3 | a0001c0001t0009g0199a0001c0001t0033g0081a0001c0001t0037g0180 | 3 | HG02080.hp2 NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(42): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0003g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(32): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0003g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(38): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(39): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0004g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(40): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(30): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075 | 3 | HG02486.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0088a0001c0001t0002g0266 | 2 | HG06807.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0267a0001c0001t0004g0194a0001c0001t0010g0160 | 3 | HG00733.hp1 HG01496.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(25): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(21): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0002g0066a0001c0001t0003g0187a0001c0001t0005g0058others(1): Show | 4 | HG01978.hp2 NA18975.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATAT others(11): Show |
8 | a0001c0001t0002g0136a0001c0001t0002g0263a0001c0001t0002g0268others(5): Show | 8 | HG00609.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATTT others(5): Show |
1 | a0001c0001t0007g0090 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATTT others(7): Show |
1 | a0001c0001t0001g0158 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATTT others(8): Show |
8 | a0001c0001t0001g0084a0001c0001t0003g0171a0001c0001t0003g0299others(5): Show | 8 | HG02129.hp2 HG02145.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(21): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATATTT others(9): Show |
17 | a0001c0001t0001g0226a0001c0001t0002g0011a0001c0001t0002g0059others(14): Show | 17 | HG00597.hp1 HG01928.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATTTTT others(9): Show |
1 | a0001c0001t0001g0089 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | ATATTTTT others(10): Show |
1 | a0001c0001t0011g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(23): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58006923 | |||||
| chr8:58006923
|
A | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(77): Show | 80 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-512+12117A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006923 | ||||||
| chr8:58006924
|
T | TATATATA others(10): Show |
1 | a0001c0001t0003g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(23): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006924 | ||||||
| chr8:58006924
|
T | TATATATA others(14): Show |
1 | a0001c0001t0004g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-512+12118_-512+12 others(27): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006924 | ||||||
| chr8:58006924
|
T | TATATATA others(22): Show |
2 | a0001c0001t0002g0036a0001c0001t0003g0198 | 2 | HG01433.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-512+12118_-512+12 others(35): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006924 | ||||||
| chr8:58006925
|
T | G | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-512+12119T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006925 | ||||||
| chr8:58006995
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-512+12189C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58006995 | ||||||
| chr8:58007039
|
G | C | 1 | a0001c0001t0001g0046 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-512+12233G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007039 | ||||||
| chr8:58007142
|
T | C | 2 | a0001c0001t0004g0260a0001c0001t0031g0159 | 2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-512+12336T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007142 | ||||||
| chr8:58007173
|
G | A | 2 | a0001c0001t0004g0260a0001c0001t0031g0159 | 2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-512+12367G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007173 | ||||||
| chr8:58007237
|
G | T | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-512+12431G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007237 | ||||||
| chr8:58007469
|
A | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-512+12663A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007469 | ||||||
| chr8:58007642
|
G | A | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-512+12836G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007642 | ||||||
| chr8:58007797
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-512+12991T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007797 | ||||||
| chr8:58007809
|
TTTTGTTA others(32): Show |
T | 1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-512+13006_-512+13 others(45): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58007809 | |||||
| chr8:58007828
|
A | G | 1 | a0001c0001t0005g0271 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-512+13022A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007828 | ||||||
| chr8:58007849
|
T | A | 1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-512+13043T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007849 | ||||||
| chr8:58007884
|
T | C | 4 | a0001c0001t0002g0030a0001c0001t0002g0050a0001c0001t0002g0070others(1): Show | 4 | HG01074.hp2 HG01168.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-512+13078T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58007884 | ||||||
| chr8:58008126
|
A | AT | 134 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0017others(131): Show | 134 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-512+13343dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58008126 | |||||
| chr8:58008126
|
A | ATT | 21 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0029others(18): Show | 21 | HG00738.hp2 HG02080.hp2 HG02647.hp1 others(18): Show |
intron_variant | MODIFIER | c.-512+13342_-512+13 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58008126 | |||||
| chr8:58008126
|
AT | A | 10 | a0001c0001t0001g0172a0001c0001t0001g0261a0001c0001t0001g0281others(7): Show | 10 | HG01070.hp2 HG01074.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-512+13343delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58008126 | |||||
| chr8:58008189
|
G | A | 9 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(6): Show | 9 | HG00323.hp1 HG01069.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-512+13383G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008189 | ||||||
| chr8:58008198
|
G | T | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-512+13392G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008198 | ||||||
| chr8:58008320
|
G | A | 5 | a0001c0001t0002g0167a0001c0001t0004g0260a0001c0001t0007g0135others(2): Show | 5 | HG01192.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+13514G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008320 | ||||||
| chr8:58008384
|
C | T | 5 | a0001c0001t0001g0172a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-512+13578C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008384 | ||||||
| chr8:58008385
|
G | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0178others(10): Show | 13 | HG00738.hp2 HG02080.hp2 NA18959.hp2 others(10): Show |
intron_variant | MODIFIER | c.-512+13579G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008385 | ||||||
| chr8:58008548
|
G | T | 5 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+13742G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008548 | ||||||
| chr8:58008658
|
T | C | 2 | a0001c0001t0007g0090a0001c0001t0024g0176 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-512+13852T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008658 | ||||||
| chr8:58008735
|
G | A | 1 | a0001c0001t0004g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-512+13929G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008735 | ||||||
| chr8:58008774
|
T | C | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-512+13968T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008774 | ||||||
| chr8:58008796
|
T | C | 45 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(42): Show | 45 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.-512+13990T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008796 | ||||||
| chr8:58008822
|
G | A | 4 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0005g0139others(1): Show | 4 | HG02622.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-512+14016G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008822 | ||||||
| chr8:58008974
|
C | G | 1 | a0001c0001t0002g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-512+14168C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58008974 | ||||||
| chr8:58009133
|
G | A | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-512+14327G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009133 | ||||||
| chr8:58009153
|
C | T | 2 | a0001c0001t0004g0260a0001c0001t0031g0159 | 2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-512+14347C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009153 | ||||||
| chr8:58009271
|
G | A | 5 | a0001c0001t0002g0167a0001c0001t0004g0260a0001c0001t0007g0135others(2): Show | 5 | HG01192.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-512+14465G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009271 | ||||||
| chr8:58009275
|
T | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0178others(10): Show | 13 | HG00738.hp2 HG02080.hp2 NA18959.hp2 others(10): Show |
intron_variant | MODIFIER | c.-512+14469T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009275 | ||||||
| chr8:58009516
|
T | C | 1 | a0001c0001t0008g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-512+14710T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009516 | ||||||
| chr8:58009521
|
C | T | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+14715C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009521 | ||||||
| chr8:58009679
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-512+14873A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009679 | ||||||
| chr8:58009724
|
T | C | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-512+14918T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009724 | ||||||
| chr8:58009738
|
C | T | 1 | a0001c0001t0005g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-512+14932C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009738 | ||||||
| chr8:58009929
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-512+15123C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009929 | ||||||
| chr8:58009958
|
C | T | 1 | a0001c0001t0030g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-512+15152C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58009958 | ||||||
| chr8:58010183
|
G | GT | 12 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0259others(9): Show | 12 | HG00738.hp2 HG02080.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.-512+15394dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58010183 | |||||
| chr8:58010300
|
G | A | 1 | a0001c0001t0003g0255 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-512+15494G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58010300 | ||||||
| chr8:58010318
|
G | A | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+15512G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58010318 | ||||||
| chr8:58010668
|
G | A | 13 | a0001c0001t0002g0167a0001c0001t0002g0186a0001c0001t0003g0129others(10): Show | 13 | HG01069.hp1 HG01192.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-512+15862G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58010668 | ||||||
| chr8:58010673
|
A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-512+15867A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58010673 | ||||||
| chr8:58010855
|
T | TTATGTGA others(316): Show |
1 | a0001c0001t0003g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-512+16065_-512+16 others(329): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58010855 | |||||
| chr8:58011096
|
G | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0154 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-512+16290G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011096 | ||||||
| chr8:58011382
|
T | A | 6 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-512+16576T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011382 | ||||||
| chr8:58011429
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0003g0289 | 2 | HG01993.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-512+16623C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011429 | ||||||
| chr8:58011506
|
A | G | 19 | a0001c0001t0001g0073a0001c0001t0002g0167a0001c0001t0002g0186others(16): Show | 19 | HG01069.hp1 HG01192.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-512+16700A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011506 | ||||||
| chr8:58011635
|
G | C | 103 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(100): Show | 103 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(100): Show |
intron_variant | MODIFIER | c.-512+16829G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011635 | ||||||
| chr8:58011660
|
A | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0002g0012others(7): Show | 10 | HG02622.hp1 HG02818.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-512+16854A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011660 | ||||||
| chr8:58011700
|
C | T | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+16894C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58011700 | ||||||
| chr8:58012231
|
A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-512+17425A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58012231 | ||||||
| chr8:58012259
|
A | AT | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0029others(12): Show | 15 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-512+17462dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58012259 | |||||
| chr8:58012390
|
G | A | 6 | a0001c0001t0001g0267a0001c0001t0002g0136a0001c0001t0002g0266others(3): Show | 6 | HG00733.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-512+17584G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58012390 | ||||||
| chr8:58012466
|
T | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0178others(11): Show | 14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-512+17660T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58012466 | ||||||
| chr8:58012999
|
C | T | 1 | a0001c0001t0008g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-512+18193C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58012999 | ||||||
| chr8:58013028
|
G | A | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-512+18222G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013028 | ||||||
| chr8:58013184
|
T | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0029 | 2 | NA18993.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-512+18378T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013184 | ||||||
| chr8:58013216
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0002g0012others(9): Show | 12 | HG01884.hp2 HG02622.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-511-18390T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013216 | ||||||
| chr8:58013271
|
G | A | 1 | a0001c0001t0030g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-511-18335G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013271 | ||||||
| chr8:58013568
|
A | G | 3 | a0001c0001t0002g0152a0001c0001t0003g0151a0001c0001t0027g0137 | 3 | HG02257.hp1 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-511-18038A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013568 | ||||||
| chr8:58013586
|
A | T | 83 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0001g0084others(80): Show | 83 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-511-18020A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013586 | ||||||
| chr8:58013641
|
C | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(159): Show | 162 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-511-17965C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013641 | ||||||
| chr8:58013860
|
T | A | 64 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0088others(61): Show | 64 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.-511-17746T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013860 | ||||||
| chr8:58013927
|
T | A | 5 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0004g0260others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-511-17679T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58013927 | ||||||
| chr8:58014028
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0031g0159 | 2 | HG01192.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-511-17578T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014028 | ||||||
| chr8:58014048
|
G | A | 1 | a0001c0001t0003g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-511-17558G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014048 | ||||||
| chr8:58014106
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-511-17500G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014106 | ||||||
| chr8:58014223
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-511-17383G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014223 | ||||||
| chr8:58014241
|
G | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0178others(11): Show | 14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-17365G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014241 | ||||||
| chr8:58014407
|
C | T | 258 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(255): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.-511-17199C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014407 | ||||||
| chr8:58014416
|
C | T | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-511-17190C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014416 | ||||||
| chr8:58014545
|
G | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-17061G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014545 | ||||||
| chr8:58014630
|
A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-16976A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014630 | ||||||
| chr8:58014674
|
A | T | 1 | a0001c0001t0003g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-511-16932A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014674 | ||||||
| chr8:58014784
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-511-16822C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014784 | ||||||
| chr8:58014812
|
T | TATG | 90 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(87): Show | 90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-16792_-511-16 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58014812 | |||||
| chr8:58014968
|
C | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0178others(11): Show | 14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-16638C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58014968 | ||||||
| chr8:58015109
|
A | T | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-511-16497A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58015109 | ||||||
| chr8:58015158
|
C | G | 9 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0003g0138others(6): Show | 9 | HG02622.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-511-16448C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58015158 | ||||||
| chr8:58015720
|
C | T | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0178others(11): Show | 14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-15886C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58015720 | ||||||
| chr8:58015844
|
C | CA | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0002g0241others(3): Show | 6 | HG02129.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-15746dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58015844 | |||||
| chr8:58015844
|
CA | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(96): Show | 99 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-511-15746delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58015844 | |||||
| chr8:58015875
|
G | A | 4 | a0001c0001t0002g0167a0001c0001t0004g0260a0001c0001t0007g0135others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-511-15731G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58015875 | ||||||
| chr8:58016048
|
C | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0088others(58): Show | 61 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.-511-15558C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016048 | ||||||
| chr8:58016049
|
G | A | 1 | a0001c0001t0005g0271 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-511-15557G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016049 | ||||||
| chr8:58016090
|
A | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0178others(11): Show | 14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-15516A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016090 | ||||||
| chr8:58016182
|
A | G | 4 | a0001c0001t0001g0045a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | NA18950.hp2 NA18975.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.-511-15424A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016182 | ||||||
| chr8:58016243
|
A | G | 1 | a0001c0001t0008g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-511-15363A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016243 | ||||||
| chr8:58016313
|
C | G | 90 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(87): Show | 90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-15293C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016313 | ||||||
| chr8:58016335
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0003g0138others(6): Show | 9 | HG02622.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-511-15271C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016335 | ||||||
| chr8:58016369
|
C | T | 62 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0088others(59): Show | 62 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.-511-15237C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016369 | ||||||
| chr8:58016389
|
G | C | 1 | a0001c0001t0003g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-511-15217G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016389 | ||||||
| chr8:58016448
|
A | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0178others(11): Show | 14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-15158A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016448 | ||||||
| chr8:58016478
|
A | C | 5 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-511-15128A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016478 | ||||||
| chr8:58016491
|
T | A | 1 | a0001c0001t0004g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-511-15115T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016491 | ||||||
| chr8:58016867
|
G | T | 1 | a0001c0001t0001g0088 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-511-14739G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016867 | ||||||
| chr8:58016897
|
G | T | 3 | a0001c0001t0003g0250a0001c0001t0012g0148a0001c0001t0012g0150 | 3 | HG01884.hp1 HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-511-14709G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58016897 | ||||||
| chr8:58017074
|
G | A | 90 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(87): Show | 90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-14532G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017074 | ||||||
| chr8:58017129
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(170): Show | 173 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.-511-14477G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017129 | ||||||
| chr8:58017166
|
T | C | 14 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(11): Show | 14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-14440T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017166 | ||||||
| chr8:58017230
|
C | T | 4 | a0001c0001t0001g0201a0001c0001t0003g0295a0001c0001t0007g0004others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-511-14376C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017230 | ||||||
| chr8:58017231
|
G | A | 13 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(10): Show | 13 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-511-14375G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017231 | ||||||
| chr8:58017244
|
C | G | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-511-14362C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017244 | ||||||
| chr8:58017341
|
A | G | 90 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(87): Show | 90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-14265A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017341 | ||||||
| chr8:58017366
|
G | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-14240G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017366 | ||||||
| chr8:58017391
|
A | C | 6 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0003g0138others(3): Show | 6 | HG02622.hp1 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-14215A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017391 | ||||||
| chr8:58017444
|
A | G | 1 | a0001c0001t0003g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-511-14162A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017444 | ||||||
| chr8:58017624
|
T | C | 1 | a0001c0001t0003g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-511-13982T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017624 | ||||||
| chr8:58017646
|
C | G | 8 | a0001c0001t0001g0073a0001c0001t0001g0158a0001c0001t0003g0074others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-13960C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017646 | ||||||
| chr8:58017945
|
G | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG01070.hp2 HG01071.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-511-13661G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58017945 | ||||||
| chr8:58018114
|
TCAAA | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0073others(14): Show | 17 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.-511-13487_-511-13 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58018114 | |||||
| chr8:58018284
|
C | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-511-13322C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58018284 | ||||||
| chr8:58018288
|
C | T | 76 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(73): Show | 76 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.-511-13318C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58018288 | ||||||
| chr8:58018809
|
A | AATAG | 78 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0029others(75): Show | 78 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.-511-12751_-511-12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58018809 | |||||
| chr8:58018809
|
A | AATAGATA others(1): Show |
14 | a0001c0001t0001g0103a0001c0001t0002g0001a0001c0001t0002g0078others(11): Show | 14 | HG00544.hp1 HG00741.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-12755_-511-12 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58018809 | |||||
| chr8:58018809
|
AATAG | A | 71 | a0001c0001t0001g0006a0001c0001t0001g0065a0001c0001t0001g0067others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.-511-12751_-511-12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58018809 | |||||
| chr8:58018809
|
AATAGATA others(1): Show |
A | 6 | a0001c0001t0002g0167a0001c0001t0003g0141a0001c0001t0003g0250others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-511-12755_-511-12 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58018809 | |||||
| chr8:58019160
|
C | CCCCATCT others(1): Show |
20 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0267others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-511-12444_-511-12 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019160 | |||||
| chr8:58019264
|
G | A | 6 | a0001c0001t0001g0267a0001c0001t0002g0136a0001c0001t0002g0266others(3): Show | 6 | HG00733.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-12342G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019264 | ||||||
| chr8:58019315
|
C | T | 55 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(52): Show | 55 | HG00438.hp1 HG00733.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-511-12291C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019315 | ||||||
| chr8:58019316
|
G | A | 4 | a0001c0001t0002g0167a0001c0001t0004g0010a0001c0001t0007g0135others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-511-12290G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019316 | ||||||
| chr8:58019336
|
CA | C | 14 | a0001c0001t0001g0098a0001c0001t0001g0158a0001c0001t0001g0172others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-12246delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019336 | |||||
| chr8:58019336
|
CAA | C | 100 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-511-12247_-511-12 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019336 | |||||
| chr8:58019336
|
CAAA | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(62): Show | 65 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-511-12248_-511-12 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019336 | |||||
| chr8:58019349
|
AAAAAAAA others(6): Show |
A | 7 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(4): Show | 7 | HG02896.hp1 HG02897.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-511-12253_-511-12 others(19): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019349 | |||||
| chr8:58019354
|
AAAAAAAG others(1): Show |
A | 8 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0003g0138others(5): Show | 8 | HG02622.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-511-12248_-511-12 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019354 | |||||
| chr8:58019355
|
AAAAAAGG | A | 48 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(45): Show | 48 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.-511-12247_-511-12 others(13): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019355 | |||||
| chr8:58019356
|
AAAAAGG | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0082others(12): Show | 15 | HG00738.hp2 HG02129.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-511-12246_-511-12 others(12): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58019356 | |||||
| chr8:58019361
|
G | A | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-511-12245G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019361 | ||||||
| chr8:58019362
|
G | A | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-511-12244G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019362 | ||||||
| chr8:58019365
|
A | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(83): Show | 86 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.-511-12241A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019365 | ||||||
| chr8:58019366
|
G | A | 2 | a0001c0001t0007g0135a0002c0002t0016g0166 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-511-12240G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019366 | ||||||
| chr8:58019369
|
A | G | 2 | a0001c0001t0007g0135a0002c0002t0016g0166 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-511-12237A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019369 | ||||||
| chr8:58019502
|
T | C | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-12104T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019502 | ||||||
| chr8:58019566
|
A | C | 6 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-12040A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019566 | ||||||
| chr8:58019602
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075 | 3 | HG02486.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-511-12004G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019602 | ||||||
| chr8:58019619
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0004g0026 | 3 | HG01192.hp2 HG01993.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-511-11987A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019619 | ||||||
| chr8:58019728
|
A | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(268): Show | 271 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.-511-11878A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019728 | ||||||
| chr8:58019987
|
C | A | 3 | a0001c0001t0002g0167a0001c0001t0007g0135a0002c0002t0016g0166 | 3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-511-11619C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58019987 | ||||||
| chr8:58020065
|
A | G | 1 | a0001c0001t0003g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-511-11541A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020065 | ||||||
| chr8:58020183
|
C | T | 1 | a0001c0001t0005g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-511-11423C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020183 | ||||||
| chr8:58020213
|
C | T | 3 | a0001c0001t0002g0167a0001c0001t0007g0135a0002c0002t0016g0166 | 3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-511-11393C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020213 | ||||||
| chr8:58020394
|
A | C | 2 | a0001c0001t0007g0090a0001c0001t0024g0176 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-511-11212A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020394 | ||||||
| chr8:58020606
|
A | G | 1 | a0001c0001t0007g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-511-11000A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020606 | ||||||
| chr8:58020677
|
A | T | 2 | a0001c0001t0007g0090a0001c0001t0024g0176 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-511-10929A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020677 | ||||||
| chr8:58020817
|
A | T | 1 | a0001c0001t0003g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-511-10789A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020817 | ||||||
| chr8:58020866
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0003g0206 | 2 | HG00408.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-511-10740G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020866 | ||||||
| chr8:58020908
|
C | CA | 101 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(98): Show | 101 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.-511-10698_-511-10 others(7): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020908 | ||||||
| chr8:58020960
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-511-10646C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58020960 | ||||||
| chr8:58021040
|
G | C | 1 | a0001c0001t0002g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-511-10566G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021040 | ||||||
| chr8:58021061
|
G | T | 2 | a0001c0001t0001g0054a0001c0001t0021g0248 | 2 | HG00099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-511-10545G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021061 | ||||||
| chr8:58021164
|
C | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-511-10442C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021164 | ||||||
| chr8:58021292
|
T | C | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-10314T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021292 | ||||||
| chr8:58021331
|
A | T | 299 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-511-10275A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021331 | ||||||
| chr8:58021469
|
G | A | 6 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-10137G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021469 | ||||||
| chr8:58021488
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0003g0156 | 2 | HG00323.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-511-10118T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021488 | ||||||
| chr8:58021902
|
A | G | 78 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(75): Show | 78 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-511-9704A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021902 | ||||||
| chr8:58021959
|
T | C | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-511-9647T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58021959 | ||||||
| chr8:58022004
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0002g0016a0001c0001t0002g0153 | 3 | HG00741.hp2 HG01168.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-511-9602G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022004 | ||||||
| chr8:58022143
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-511-9463A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022143 | ||||||
| chr8:58022406
|
G | A | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-511-9200G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022406 | ||||||
| chr8:58022499
|
T | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-511-9107T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022499 | ||||||
| chr8:58022511
|
A | G | 2 | a0001c0001t0007g0090a0001c0001t0024g0176 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-511-9095A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022511 | ||||||
| chr8:58022743
|
G | C | 1 | a0001c0001t0003g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-511-8863G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58022743 | ||||||
| chr8:58023171
|
AATTTTT | A | 90 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(87): Show | 90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-8416_-511-841 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58023171 | |||||
| chr8:58023383
|
C | T | 6 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-511-8223C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58023383 | ||||||
| chr8:58023512
|
C | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-8094C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58023512 | ||||||
| chr8:58023542
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-511-8064C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58023542 | ||||||
| chr8:58023620
|
A | C | 77 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-7986A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58023620 | ||||||
| chr8:58024158
|
A | C | 8 | a0001c0001t0002g0011a0001c0001t0002g0087a0001c0001t0002g0273others(5): Show | 8 | HG01928.hp2 HG01978.hp2 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.-511-7448A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024158 | ||||||
| chr8:58024172
|
C | CTTTTT | 64 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0084others(61): Show | 64 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.-511-7423_-511-741 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58024172 | |||||
| chr8:58024172
|
C | CTTTTTT | 25 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0002g0082others(22): Show | 25 | HG01069.hp1 HG01261.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-511-7424_-511-741 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58024172 | |||||
| chr8:58024209
|
G | A | 14 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(11): Show | 14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-7397G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024209 | ||||||
| chr8:58024700
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0002g0012others(7): Show | 10 | HG02622.hp1 HG02818.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-511-6906T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024700 | ||||||
| chr8:58024830
|
G | T | 1 | a0001c0001t0002g0240 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-511-6776G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024830 | ||||||
| chr8:58024882
|
T | C | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-511-6724T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024882 | ||||||
| chr8:58024910
|
A | G | 1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-511-6696A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024910 | ||||||
| chr8:58024966
|
G | T | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-6640G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024966 | ||||||
| chr8:58024979
|
C | G | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0003g0005others(1): Show | 4 | HG02145.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-511-6627C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58024979 | ||||||
| chr8:58025191
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(268): Show | 271 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.-511-6415T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025191 | ||||||
| chr8:58025205
|
A | G | 5 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-511-6401A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025205 | ||||||
| chr8:58025329
|
GAC | G | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(6): Show | 9 | HG00438.hp2 HG00621.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-511-6275_-511-627 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58025329 | |||||
| chr8:58025331
|
CAG | C | 3 | a0001c0001t0014g0242a0001c0001t0014g0243a0001c0001t0017g0119 | 3 | HG00609.hp2 NA19060.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-511-6274_-511-627 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025331 | ||||||
| chr8:58025333
|
G | T | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(6): Show | 9 | HG00438.hp2 HG00621.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-511-6273G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025333 | ||||||
| chr8:58025366
|
A | C | 1 | a0001c0001t0008g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-511-6240A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025366 | ||||||
| chr8:58025492
|
C | A | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-6114C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025492 | ||||||
| chr8:58025583
|
C | G | 14 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(11): Show | 14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-6023C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025583 | ||||||
| chr8:58025615
|
G | A | 13 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(10): Show | 13 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-511-5991G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025615 | ||||||
| chr8:58025710
|
C | T | 2 | a0001c0001t0013g0183a0001c0001t0028g0182 | 2 | NA18989.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-511-5896C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025710 | ||||||
| chr8:58025757
|
T | G | 1 | a0001c0001t0010g0175 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-511-5849T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025757 | ||||||
| chr8:58025782
|
C | T | 13 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(10): Show | 13 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-511-5824C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025782 | ||||||
| chr8:58025832
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-511-5774T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58025832 | ||||||
| chr8:58026112
|
G | A | 9 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0003g0138others(6): Show | 9 | HG02622.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-511-5494G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58026112 | ||||||
| chr8:58026223
|
G | A | 76 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(73): Show | 76 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.-511-5383G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58026223 | ||||||
| chr8:58026286
|
C | T | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-511-5320C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58026286 | ||||||
| chr8:58026705
|
C | T | 8 | a0001c0001t0002g0001a0001c0001t0002g0018a0001c0001t0002g0293others(5): Show | 8 | HG01496.hp2 HG02027.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-4901C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58026705 | ||||||
| chr8:58026894
|
T | C | 1 | a0001c0001t0006g0246 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-511-4712T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58026894 | ||||||
| chr8:58026984
|
T | TCTTGGAA | 91 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(88): Show | 91 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.-511-4619_-511-461 others(11): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58026984 | |||||
| chr8:58027102
|
C | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-4504C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027102 | ||||||
| chr8:58027240
|
T | C | 20 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0082others(17): Show | 20 | HG00738.hp2 HG01891.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.-511-4366T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027240 | ||||||
| chr8:58027423
|
GT | G | 90 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(87): Show | 90 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-511-4171delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58027423 | |||||
| chr8:58027509
|
C | T | 1 | a0001c0001t0004g0232 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-511-4097C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027509 | ||||||
| chr8:58027525
|
A | T | 1 | a0001c0001t0003g0074 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-511-4081A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027525 | ||||||
| chr8:58027739
|
C | T | 1 | a0001c0001t0003g0106 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-511-3867C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027739 | ||||||
| chr8:58027755
|
G | A | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-511-3851G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027755 | ||||||
| chr8:58027831
|
G | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(88): Show | 91 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.-511-3775G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027831 | ||||||
| chr8:58027993
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(88): Show | 91 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.-511-3613C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58027993 | ||||||
| chr8:58028104
|
C | T | 14 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(11): Show | 14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-3502C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028104 | ||||||
| chr8:58028244
|
C | G | 8 | a0001c0001t0001g0073a0001c0001t0003g0005a0001c0001t0003g0074others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-3362C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028244 | ||||||
| chr8:58028260
|
C | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-3346C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028260 | ||||||
| chr8:58028303
|
C | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-3303C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028303 | ||||||
| chr8:58028385
|
C | T | 7 | a0001c0001t0001g0073a0001c0001t0003g0005a0001c0001t0003g0074others(4): Show | 7 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-511-3221C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028385 | ||||||
| chr8:58028571
|
A | G | 1 | a0001c0001t0034g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-511-3035A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028571 | ||||||
| chr8:58028582
|
T | C | 77 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-3024T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028582 | ||||||
| chr8:58028583
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-511-3023T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028583 | ||||||
| chr8:58028644
|
G | T | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-511-2962G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028644 | ||||||
| chr8:58028661
|
T | C | 3 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075 | 3 | HG02486.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-511-2945T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028661 | ||||||
| chr8:58028737
|
G | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0004g0014 | 3 | HG00738.hp2 NA20129.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-511-2869G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028737 | ||||||
| chr8:58028755
|
G | A | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-511-2851G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028755 | ||||||
| chr8:58028904
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(69): Show | 72 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.-511-2702C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58028904 | ||||||
| chr8:58029243
|
G | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 77 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-511-2363G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029243 | ||||||
| chr8:58029259
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-511-2347A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029259 | ||||||
| chr8:58029328
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-511-2278A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029328 | ||||||
| chr8:58029451
|
G | A | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-511-2155G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029451 | ||||||
| chr8:58029538
|
A | AT | 7 | a0001c0001t0001g0158a0001c0001t0001g0256a0001c0001t0002g0293others(4): Show | 7 | HG00733.hp2 HG01243.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-511-2058dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58029538 | |||||
| chr8:58029538
|
ATT | A | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-511-2059_-511-205 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58029538 | |||||
| chr8:58029562
|
A | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0178others(11): Show | 14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-511-2044A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029562 | ||||||
| chr8:58029588
|
G | C | 2 | a0001c0001t0014g0242a0001c0001t0014g0243 | 2 | HG00609.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-511-2018G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029588 | ||||||
| chr8:58029673
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-511-1933A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029673 | ||||||
| chr8:58029750
|
A | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(69): Show | 72 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.-511-1856A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029750 | ||||||
| chr8:58029910
|
A | C | 13 | a0001c0001t0002g0167a0001c0001t0002g0186a0001c0001t0003g0129others(10): Show | 13 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-511-1696A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58029910 | ||||||
| chr8:58030034
|
A | G | 14 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(11): Show | 14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-1572A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030034 | ||||||
| chr8:58030180
|
G | T | 270 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(267): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-511-1426G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030180 | ||||||
| chr8:58030194
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-511-1412A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030194 | ||||||
| chr8:58030261
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(88): Show | 91 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.-511-1345G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030261 | ||||||
| chr8:58030266
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0002g0012 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-511-1340G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030266 | ||||||
| chr8:58030431
|
A | G | 13 | a0001c0001t0002g0167a0001c0001t0002g0186a0001c0001t0003g0129others(10): Show | 13 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-511-1175A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030431 | ||||||
| chr8:58030479
|
A | C | 1 | a0001c0001t0003g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-511-1127A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030479 | ||||||
| chr8:58030546
|
GGCATAGA others(7): Show |
G | 78 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(75): Show | 78 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-511-1058_-511-104 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 58030546 | |||||
| chr8:58030675
|
A | C | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-511-931A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030675 | ||||||
| chr8:58030791
|
C | T | 14 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(11): Show | 14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-511-815C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58030791 | ||||||
| chr8:58031045
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0005g0188 | 2 | HG00609.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-511-561T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58031045 | ||||||
| chr8:58031353
|
A | C | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-511-253A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58031353 | ||||||
| chr8:58031451
|
T | C | 1 | a0001c0001t0003g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-511-155T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58031451 | ||||||
| chr8:58031484
|
T | C | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-511-122T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | chr8 | 58031484 | ||||||
| chr8:58031741
|
G | A | 93 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(90): Show | 93 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.-414+38G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58031741 | ||||||
| chr8:58031831
|
C | G | 14 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(11): Show | 14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-414+128C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58031831 | ||||||
| chr8:58032112
|
C | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+409C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032112 | ||||||
| chr8:58032118
|
C | T | 5 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+415C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032118 | ||||||
| chr8:58032130
|
T | G | 5 | a0001c0001t0003g0129a0001c0001t0003g0134a0001c0001t0003g0164others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+427T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032130 | ||||||
| chr8:58032132
|
C | T | 7 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+429C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032132 | ||||||
| chr8:58032133
|
G | A | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-414+430G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032133 | ||||||
| chr8:58032305
|
A | G | 8 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0133others(5): Show | 8 | HG01069.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-414+602A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032305 | ||||||
| chr8:58032374
|
G | T | 6 | a0001c0001t0001g0267a0001c0001t0002g0136a0001c0001t0002g0266others(3): Show | 6 | HG00733.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-414+671G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032374 | ||||||
| chr8:58032436
|
T | G | 3 | a0001c0001t0002g0167a0001c0001t0007g0135a0002c0002t0016g0166 | 3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-414+733T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032436 | ||||||
| chr8:58032472
|
C | T | 14 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(11): Show | 14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-414+769C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032472 | ||||||
| chr8:58032487
|
C | G | 14 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(11): Show | 14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-414+784C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032487 | ||||||
| chr8:58032508
|
C | G | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+805C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032508 | ||||||
| chr8:58032533
|
C | A | 6 | a0001c0001t0001g0267a0001c0001t0002g0136a0001c0001t0002g0266others(3): Show | 6 | HG00733.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-414+830C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032533 | ||||||
| chr8:58032615
|
G | A | 14 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(11): Show | 14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-414+912G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032615 | ||||||
| chr8:58032664
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+961C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032664 | ||||||
| chr8:58032841
|
A | C | 5 | a0001c0001t0003g0080a0001c0001t0009g0179a0001c0001t0009g0199others(2): Show | 5 | HG02080.hp2 NA18959.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-414+1138A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032841 | ||||||
| chr8:58032878
|
G | T | 7 | a0001c0001t0001g0073a0001c0001t0003g0005a0001c0001t0003g0074others(4): Show | 7 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+1175G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032878 | ||||||
| chr8:58032937
|
A | G | 75 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.-414+1234A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58032937 | ||||||
| chr8:58033148
|
G | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+1445G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033148 | ||||||
| chr8:58033193
|
G | A | 3 | a0001c0001t0002g0167a0001c0001t0007g0135a0002c0002t0016g0166 | 3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-414+1490G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033193 | ||||||
| chr8:58033225
|
C | T | 14 | a0001c0001t0002g0147a0001c0001t0002g0167a0001c0001t0002g0186others(11): Show | 14 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-414+1522C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033225 | ||||||
| chr8:58033291
|
C | T | 71 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(68): Show | 71 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.-414+1588C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033291 | ||||||
| chr8:58033418
|
A | G | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-414+1715A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033418 | ||||||
| chr8:58033586
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0002g0012others(9): Show | 12 | HG01884.hp2 HG02622.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-414+1883C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033586 | ||||||
| chr8:58033587
|
G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+1884G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033587 | ||||||
| chr8:58033666
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+1963C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033666 | ||||||
| chr8:58033688
|
A | G | 100 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(97): Show | 100 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(97): Show |
intron_variant | MODIFIER | c.-414+1985A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033688 | ||||||
| chr8:58033755
|
TA | T | 10 | a0001c0001t0001g0253a0001c0001t0001g0258a0001c0001t0001g0267others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.-414+2061delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58033755 | |||||
| chr8:58033833
|
C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+2130C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033833 | ||||||
| chr8:58033851
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(71): Show | 74 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-414+2148C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033851 | ||||||
| chr8:58033911
|
A | C | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+2208A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58033911 | ||||||
| chr8:58034091
|
G | A | 44 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(41): Show | 44 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.-414+2388G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034091 | ||||||
| chr8:58034125
|
T | C | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+2422T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034125 | ||||||
| chr8:58034132
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+2429C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034132 | ||||||
| chr8:58034143
|
G | A | 3 | a0001c0001t0002g0167a0001c0001t0007g0135a0002c0002t0016g0166 | 3 | HG02258.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-414+2440G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034143 | ||||||
| chr8:58034249
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-414+2546G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034249 | ||||||
| chr8:58034507
|
A | T | 1 | a0001c0001t0002g0192 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-414+2804A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034507 | ||||||
| chr8:58034584
|
A | G | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-414+2881A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034584 | ||||||
| chr8:58034651
|
G | T | 2 | a0001c0001t0002g0126a0001c0001t0004g0125 | 2 | HG00280.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-414+2948G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034651 | ||||||
| chr8:58034804
|
G | C | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-414+3101G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034804 | ||||||
| chr8:58034930
|
T | C | 99 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(96): Show | 99 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.-414+3227T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034930 | ||||||
| chr8:58034959
|
A | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0001g0158others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-414+3256A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034959 | ||||||
| chr8:58034970
|
C | T | 84 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(81): Show | 84 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-414+3267C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58034970 | ||||||
| chr8:58035191
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-414+3488T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035191 | ||||||
| chr8:58035293
|
G | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0230a0001c0001t0003g0096others(2): Show | 5 | HG00544.hp1 HG02027.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-414+3590G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035293 | ||||||
| chr8:58035344
|
G | A | 7 | a0001c0001t0001g0073a0001c0001t0003g0005a0001c0001t0003g0074others(4): Show | 7 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+3641G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035344 | ||||||
| chr8:58035363
|
A | G | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-414+3660A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035363 | ||||||
| chr8:58035394
|
C | T | 1 | a0001c0001t0005g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-414+3691C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035394 | ||||||
| chr8:58035461
|
T | C | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+3758T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035461 | ||||||
| chr8:58035606
|
G | A | 1 | a0001c0001t0030g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-414+3903G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035606 | ||||||
| chr8:58035624
|
A | T | 90 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-414+3921A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035624 | ||||||
| chr8:58035771
|
T | C | 45 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(42): Show | 45 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.-414+4068T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035771 | ||||||
| chr8:58035996
|
G | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+4293G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58035996 | ||||||
| chr8:58036063
|
G | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+4360G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58036063 | ||||||
| chr8:58036395
|
C | T | 4 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0209others(1): Show | 4 | NA18960.hp2 NA18979.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+4692C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58036395 | ||||||
| chr8:58036680
|
C | T | 1 | a0001c0001t0009g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-414+4977C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58036680 | ||||||
| chr8:58036707
|
A | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+5004A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58036707 | ||||||
| chr8:58036954
|
C | T | 7 | a0001c0001t0001g0038a0001c0001t0002g0030a0001c0001t0002g0032others(4): Show | 7 | HG00642.hp1 HG01074.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+5251C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58036954 | ||||||
| chr8:58037079
|
A | G | 44 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0226others(41): Show | 44 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.-414+5376A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037079 | ||||||
| chr8:58037132
|
A | AT | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+5438dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58037132 | |||||
| chr8:58037288
|
C | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+5585C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037288 | ||||||
| chr8:58037306
|
G | GGTTT | 91 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(88): Show | 91 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.-414+5624_-414+562 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58037306 | |||||
| chr8:58037306
|
GGTTT | G | 7 | a0001c0001t0002g0146a0001c0001t0002g0152a0001c0001t0003g0151others(4): Show | 7 | HG02257.hp1 HG02615.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+5624_-414+562 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58037306 | |||||
| chr8:58037331
|
T | G | 96 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-414+5628T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037331 | ||||||
| chr8:58037344
|
G | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+5641G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037344 | ||||||
| chr8:58037372
|
G | A | 2 | a0001c0001t0002g0024a0001c0001t0003g0280 | 2 | HG00621.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.-414+5669G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037372 | ||||||
| chr8:58037471
|
C | CA | 46 | a0001c0001t0001g0022a0001c0001t0001g0084a0001c0001t0001g0088others(43): Show | 46 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-414+5779dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58037471 | |||||
| chr8:58037473
|
A | C | 1 | a0001c0001t0003g0288 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-414+5770A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037473 | ||||||
| chr8:58037479
|
A | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+5776A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037479 | ||||||
| chr8:58037483
|
T | A | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+5780T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037483 | ||||||
| chr8:58037510
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(71): Show | 74 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-414+5807C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037510 | ||||||
| chr8:58037519
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-414+5816C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037519 | ||||||
| chr8:58037711
|
T | G | 4 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0007g0130others(1): Show | 4 | HG01891.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+6008T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037711 | ||||||
| chr8:58037821
|
C | A | 1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-414+6118C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037821 | ||||||
| chr8:58037821
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-414+6118C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037821 | ||||||
| chr8:58037858
|
G | A | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-414+6155G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037858 | ||||||
| chr8:58037871
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0029 | 2 | NA18993.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-414+6168A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037871 | ||||||
| chr8:58037902
|
A | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+6199A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58037902 | ||||||
| chr8:58038151
|
T | C | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-414+6448T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038151 | ||||||
| chr8:58038162
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0003g0206 | 2 | HG00408.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-414+6459A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038162 | ||||||
| chr8:58038212
|
T | C | 3 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075 | 3 | HG02486.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-414+6509T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038212 | ||||||
| chr8:58038305
|
A | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+6602A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038305 | ||||||
| chr8:58038596
|
G | A | 6 | a0001c0001t0001g0084a0001c0001t0002g0167a0001c0001t0003g0198others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-414+6893G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038596 | ||||||
| chr8:58038606
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-414+6903G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038606 | ||||||
| chr8:58038706
|
C | T | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-414+7003C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038706 | ||||||
| chr8:58038755
|
C | CA | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(44): Show | 47 | HG00642.hp2 HG00738.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.-414+7065dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58038755 | |||||
| chr8:58038782
|
A | G | 1 | a0001c0001t0008g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-414+7079A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038782 | ||||||
| chr8:58038970
|
C | T | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-414+7267C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58038970 | ||||||
| chr8:58039174
|
G | A | 1 | a0001c0001t0005g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-414+7471G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039174 | ||||||
| chr8:58039182
|
T | A | 2 | a0001c0001t0002g0112a0001c0001t0017g0119 | 2 | NA18952.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-414+7479T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039182 | ||||||
| chr8:58039185
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+7482C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039185 | ||||||
| chr8:58039188
|
G | T | 5 | a0001c0001t0002g0167a0001c0001t0003g0198a0001c0001t0007g0135others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+7485G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039188 | ||||||
| chr8:58039359
|
C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-414+7656C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039359 | ||||||
| chr8:58039532
|
A | T | 50 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(47): Show | 50 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.-414+7829A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039532 | ||||||
| chr8:58039670
|
T | C | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+7967T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039670 | ||||||
| chr8:58039833
|
A | G | 1 | a0001c0001t0005g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-414+8130A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039833 | ||||||
| chr8:58039973
|
T | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+8270T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039973 | ||||||
| chr8:58039975
|
A | G | 1 | a0001c0001t0005g0274 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-414+8272A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58039975 | ||||||
| chr8:58040009
|
T | TA | 75 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(72): Show | 75 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-414+8313dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040009 | |||||
| chr8:58040089
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-414+8386C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040089 | ||||||
| chr8:58040164
|
A | C | 48 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(45): Show | 48 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.-414+8461A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040164 | ||||||
| chr8:58040232
|
C | T | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0178others(11): Show | 14 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-414+8529C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040232 | ||||||
| chr8:58040366
|
T | C | 51 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(48): Show | 51 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.-414+8663T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040366 | ||||||
| chr8:58040367
|
A | G | 264 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(261): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.-414+8664A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040367 | ||||||
| chr8:58040549
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-414+8846C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040549 | ||||||
| chr8:58040569
|
A | G | 70 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(67): Show | 70 | HG00733.hp1 HG00738.hp2 HG01099.hp1 others(67): Show |
intron_variant | MODIFIER | c.-414+8866A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040569 | ||||||
| chr8:58040748
|
A | G | 44 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0226others(41): Show | 44 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.-414+9045A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040748 | ||||||
| chr8:58040766
|
T | TA | 7 | a0001c0001t0001g0073a0001c0001t0003g0005a0001c0001t0003g0074others(4): Show | 7 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+9071dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040766 | |||||
| chr8:58040767
|
A | T | 150 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0040others(147): Show | 150 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-414+9064A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58040767 | ||||||
| chr8:58040935
|
C | CT | 90 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0042others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-414+9255dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040935 | |||||
| chr8:58040935
|
C | CTT | 7 | a0001c0001t0001g0104a0001c0001t0001g0252a0001c0001t0001g0258others(4): Show | 7 | HG00438.hp2 HG02004.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+9254_-414+925 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040935 | |||||
| chr8:58040935
|
CT | C | 33 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0001g0158others(30): Show | 33 | HG01069.hp1 HG01099.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.-414+9255delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040935 | |||||
| chr8:58040935
|
CTT | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0082others(18): Show | 21 | HG00738.hp2 HG01891.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.-414+9254_-414+925 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040935 | |||||
| chr8:58040935
|
CTTTT | C | 46 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(43): Show | 46 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-414+9252_-414+925 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58040935 | |||||
| chr8:58041184
|
C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+9481C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041184 | ||||||
| chr8:58041229
|
C | T | 5 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+9526C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041229 | ||||||
| chr8:58041320
|
C | T | 48 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(45): Show | 48 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.-414+9617C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041320 | ||||||
| chr8:58041365
|
G | A | 5 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+9662G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041365 | ||||||
| chr8:58041420
|
T | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(71): Show | 74 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-414+9717T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041420 | ||||||
| chr8:58041448
|
A | G | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-414+9745A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041448 | ||||||
| chr8:58041455
|
G | A | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+9752G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041455 | ||||||
| chr8:58041650
|
A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+9947A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041650 | ||||||
| chr8:58041662
|
T | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-414+9959T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041662 | ||||||
| chr8:58041782
|
T | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0002g0178others(12): Show | 15 | HG00738.hp2 HG02080.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-414+10079T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58041782 | ||||||
| chr8:58042054
|
T | C | 2 | a0001c0001t0003g0138a0001c0001t0003g0141 | 2 | HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-414+10351T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042054 | ||||||
| chr8:58042055
|
A | T | 51 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(48): Show | 51 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.-414+10352A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042055 | ||||||
| chr8:58042098
|
G | T | 3 | a0001c0001t0002g0128a0001c0001t0003g0143a0001c0001t0007g0144 | 3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-414+10395G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042098 | ||||||
| chr8:58042104
|
G | A | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.-414+10401G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042104 | ||||||
| chr8:58042354
|
G | A | 5 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+10651G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042354 | ||||||
| chr8:58042365
|
G | A | 2 | a0001c0001t0007g0090a0001c0001t0024g0176 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-414+10662G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042365 | ||||||
| chr8:58042544
|
A | G | 51 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(48): Show | 51 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.-414+10841A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042544 | ||||||
| chr8:58042652
|
A | G | 7 | a0001c0001t0001g0073a0001c0001t0003g0005a0001c0001t0003g0074others(4): Show | 7 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+10949A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042652 | ||||||
| chr8:58042903
|
C | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | NA18953.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-414+11200C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042903 | ||||||
| chr8:58042978
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0004g0014 | 2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-414+11275G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58042978 | ||||||
| chr8:58043090
|
G | T | 14 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(11): Show | 14 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.-414+11387G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043090 | ||||||
| chr8:58043100
|
C | T | 1 | a0001c0001t0004g0232 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-414+11397C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043100 | ||||||
| chr8:58043409
|
T | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(161): Show | 164 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.-414+11706T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043409 | ||||||
| chr8:58043512
|
A | G | 15 | a0001c0001t0001g0073a0001c0001t0002g0146a0001c0001t0002g0152others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-414+11809A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043512 | ||||||
| chr8:58043579
|
G | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(104): Show | 107 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-414+11876G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043579 | ||||||
| chr8:58043738
|
G | A | 26 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0060others(23): Show | 26 | HG00597.hp2 HG01081.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-414+12035G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043738 | ||||||
| chr8:58043746
|
T | G | 4 | a0001c0001t0003g0005a0001c0001t0003g0250a0001c0001t0012g0148others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+12043T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043746 | ||||||
| chr8:58043757
|
A | G | 4 | a0001c0001t0003g0005a0001c0001t0003g0250a0001c0001t0012g0148others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+12054A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043757 | ||||||
| chr8:58043774
|
T | G | 1 | a0001c0001t0007g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-414+12071T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58043774 | ||||||
| chr8:58044103
|
T | A | 1 | a0001c0001t0002g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-414+12400T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044103 | ||||||
| chr8:58044252
|
C | T | 4 | a0001c0001t0001g0103a0001c0001t0001g0230a0001c0001t0003g0100others(1): Show | 4 | HG00544.hp1 HG02027.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+12549C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044252 | ||||||
| chr8:58044470
|
A | G | 27 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0158others(24): Show | 27 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.-414+12767A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044470 | ||||||
| chr8:58044854
|
T | C | 1 | a0001c0001t0005g0061 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-414+13151T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044854 | ||||||
| chr8:58044914
|
A | G | 35 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0073others(32): Show | 35 | HG00738.hp2 HG01069.hp1 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.-414+13211A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044914 | ||||||
| chr8:58044927
|
C | T | 13 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(10): Show | 13 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-414+13224C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58044927 | ||||||
| chr8:58045021
|
T | G | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-414+13318T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045021 | ||||||
| chr8:58045028
|
C | T | 45 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0089others(42): Show | 45 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(42): Show |
intron_variant | MODIFIER | c.-414+13325C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045028 | ||||||
| chr8:58045130
|
A | C | 179 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(176): Show | 179 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.-414+13427A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045130 | ||||||
| chr8:58045163
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-414+13460G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045163 | ||||||
| chr8:58045297
|
C | G | 1 | a0001c0001t0027g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-414+13594C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045297 | ||||||
| chr8:58045336
|
A | G | 1 | a0001c0001t0010g0175 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-414+13633A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045336 | ||||||
| chr8:58045618
|
A | G | 31 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0158others(28): Show | 31 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.-414+13915A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045618 | ||||||
| chr8:58045673
|
G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+13970G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58045673 | ||||||
| chr8:58046177
|
A | G | 1 | a0001c0001t0005g0061 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-414+14474A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046177 | ||||||
| chr8:58046428
|
T | C | 31 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0158others(28): Show | 31 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.-414+14725T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046428 | ||||||
| chr8:58046551
|
T | C | 4 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157others(1): Show | 4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+14848T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046551 | ||||||
| chr8:58046626
|
C | G | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-414+14923C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046626 | ||||||
| chr8:58046748
|
A | G | 4 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157others(1): Show | 4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+15045A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046748 | ||||||
| chr8:58046774
|
G | A | 5 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0007g0090others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-414+15071G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58046774 | ||||||
| chr8:58047122
|
T | G | 4 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157others(1): Show | 4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+15419T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047122 | ||||||
| chr8:58047200
|
G | C | 5 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0007g0090others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-414+15497G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047200 | ||||||
| chr8:58047288
|
A | T | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-414+15585A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047288 | ||||||
| chr8:58047335
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-414+15632C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047335 | ||||||
| chr8:58047405
|
A | G | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-414+15702A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047405 | ||||||
| chr8:58047472
|
A | G | 1 | a0001c0001t0004g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-414+15769A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047472 | ||||||
| chr8:58047481
|
G | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+15778G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047481 | ||||||
| chr8:58047590
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0262 | 2 | HG01071.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-414+15887T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047590 | ||||||
| chr8:58047591
|
C | CCT | 49 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(46): Show | 49 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-414+15931_-414+15 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCT | 45 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0067others(42): Show | 45 | HG00597.hp1 HG00621.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.-414+15929_-414+15 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCT | 21 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0104others(18): Show | 21 | HG00408.hp1 HG00673.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.-414+15927_-414+15 others(12): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(1): Show |
6 | a0001c0001t0001g0259a0001c0001t0001g0261a0001c0001t0002g0095others(3): Show | 6 | HG01070.hp2 HG01934.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-414+15925_-414+15 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(3): Show |
4 | a0001c0001t0001g0097a0001c0001t0003g0133a0001c0001t0004g0026others(1): Show | 4 | HG02886.hp2 HG03195.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+15923_-414+15 others(16): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(5): Show |
10 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0154others(7): Show | 10 | HG00621.hp2 HG01243.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-414+15921_-414+15 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(7): Show |
9 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0149others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.-414+15919_-414+15 others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(9): Show |
5 | a0001c0001t0002g0082a0001c0001t0002g0109a0001c0001t0002g0297others(2): Show | 5 | HG00099.hp2 HG02155.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-414+15917_-414+15 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(11): Show |
12 | a0001c0001t0001g0102a0001c0001t0001g0184a0001c0001t0001g0252others(9): Show | 12 | HG00673.hp2 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-414+15915_-414+15 others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(13): Show |
8 | a0001c0001t0001g0185a0001c0001t0001g0236a0001c0001t0003g0076others(5): Show | 8 | HG01109.hp2 HG01934.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-414+15913_-414+15 others(26): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(15): Show |
7 | a0001c0001t0001g0111a0001c0001t0002g0120a0001c0001t0002g0123others(4): Show | 7 | HG01069.hp1 HG01175.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+15911_-414+15 others(28): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(17): Show |
15 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0110others(12): Show | 15 | HG01433.hp1 HG01943.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.-414+15909_-414+15 others(30): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(19): Show |
2 | a0001c0001t0001g0282a0001c0001t0002g0037 | 2 | HG00642.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-414+15907_-414+15 others(32): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(21): Show |
9 | a0001c0001t0001g0046a0001c0001t0001g0098a0001c0001t0001g0103others(6): Show | 9 | HG00280.hp1 HG00544.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.-414+15905_-414+15 others(34): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(23): Show |
3 | a0001c0001t0002g0240a0001c0001t0003g0255a0001c0001t0007g0300 | 3 | HG00408.hp2 HG02717.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-414+15903_-414+15 others(36): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(25): Show |
2 | a0001c0001t0003g0106a0001c0001t0007g0135 | 2 | HG02129.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-414+15901_-414+15 others(38): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CCTCTCTC others(29): Show |
2 | a0001c0001t0002g0186a0001c0001t0005g0271 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-414+15897_-414+15 others(42): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
C | CTCTCTCT others(6): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0262 | 2 | HG01071.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-414+15888_-414+15 others(19): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047591 | ||||||
| chr8:58047591
|
C | CTCTCTCT others(14): Show |
2 | a0001c0001t0001g0045a0001c0001t0002g0239 | 2 | NA18975.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-414+15888_-414+15 others(27): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047591 | ||||||
| chr8:58047591
|
C | CTCTCTCT others(22): Show |
1 | a0001c0001t0003g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-414+15888_-414+15 others(35): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047591 | ||||||
| chr8:58047591
|
CCT | C | 34 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0060others(31): Show | 34 | HG00280.hp2 HG00323.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.-414+15931_-414+15 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
CCTCT | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0031g0159 | 3 | HG01192.hp1 HG03017.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-414+15929_-414+15 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
CCTCTCTC others(5): Show |
C | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-414+15921_-414+15 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
CCTCTCTC others(7): Show |
C | 14 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0002g0146others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-414+15919_-414+15 others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047591
|
CCTCTCTC others(9): Show |
C | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-414+15917_-414+15 others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58047591 | |||||
| chr8:58047673
|
C | A | 1 | a0001c0001t0003g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-414+15970C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047673 | ||||||
| chr8:58047887
|
A | G | 7 | a0001c0001t0001g0158a0001c0001t0003g0138a0001c0001t0003g0141others(4): Show | 7 | HG02622.hp1 HG02886.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+16184A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047887 | ||||||
| chr8:58047893
|
T | A | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-414+16190T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58047893 | ||||||
| chr8:58048427
|
C | A | 1 | a0001c0001t0002g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-414+16724C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048427 | ||||||
| chr8:58048496
|
C | G | 35 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0073others(32): Show | 35 | HG00738.hp2 HG01069.hp1 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.-414+16793C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048496 | ||||||
| chr8:58048583
|
C | A | 1 | a0001c0001t0003g0288 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-414+16880C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048583 | ||||||
| chr8:58048586
|
T | C | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-414+16883T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048586 | ||||||
| chr8:58048617
|
A | T | 7 | a0001c0001t0001g0158a0001c0001t0003g0138a0001c0001t0003g0141others(4): Show | 7 | HG02622.hp1 HG02886.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+16914A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048617 | ||||||
| chr8:58048814
|
A | G | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-414+17111A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048814 | ||||||
| chr8:58048841
|
A | G | 35 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0073others(32): Show | 35 | HG00738.hp2 HG01069.hp1 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.-414+17138A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048841 | ||||||
| chr8:58048942
|
T | C | 1 | a0001c0001t0008g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-414+17239T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58048942 | ||||||
| chr8:58049162
|
A | G | 72 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(69): Show | 72 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.-414+17459A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049162 | ||||||
| chr8:58049186
|
G | A | 6 | a0001c0001t0002g0146a0001c0001t0008g0127a0001c0001t0010g0072others(3): Show | 6 | HG01891.hp1 HG02622.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-414+17483G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049186 | ||||||
| chr8:58049347
|
A | C | 1 | a0001c0001t0001g0029 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-414+17644A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049347 | ||||||
| chr8:58049453
|
G | A | 1 | a0001c0001t0013g0177 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-414+17750G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049453 | ||||||
| chr8:58049553
|
G | A | 2 | a0001c0001t0005g0139a0001c0001t0010g0294 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-414+17850G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049553 | ||||||
| chr8:58049573
|
G | T | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-414+17870G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049573 | ||||||
| chr8:58049664
|
C | T | 6 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075others(3): Show | 6 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-414+17961C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049664 | ||||||
| chr8:58049997
|
A | G | 1 | a0001c0001t0002g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-414+18294A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58049997 | ||||||
| chr8:58050054
|
G | A | 18 | a0001c0001t0001g0073a0001c0001t0002g0186a0001c0001t0002g0297others(15): Show | 18 | HG01069.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-414+18351G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050054 | ||||||
| chr8:58050162
|
T | C | 7 | a0001c0001t0002g0082a0001c0001t0002g0162a0001c0001t0002g0163others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-414+18459T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050162 | ||||||
| chr8:58050183
|
A | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0027others(8): Show | 11 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.-414+18480A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050183 | ||||||
| chr8:58050210
|
T | C | 4 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157others(1): Show | 4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+18507T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050210 | ||||||
| chr8:58050211
|
C | CT | 18 | a0001c0001t0001g0006a0001c0001t0001g0184a0001c0001t0001g0185others(15): Show | 18 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-414+18519dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58050211 | |||||
| chr8:58050235
|
T | C | 176 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(173): Show | 176 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.-414+18532T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050235 | ||||||
| chr8:58050289
|
A | G | 3 | a0001c0001t0002g0128a0001c0001t0003g0143a0001c0001t0007g0144 | 3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-414+18586A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050289 | ||||||
| chr8:58050343
|
A | C | 3 | a0001c0001t0001g0089a0001c0001t0004g0083a0001c0001t0004g0189 | 3 | HG02056.hp1 HG02129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-414+18640A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050343 | ||||||
| chr8:58050374
|
T | A | 12 | a0001c0001t0001g0158a0001c0001t0002g0082a0001c0001t0002g0162others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-414+18671T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050374 | ||||||
| chr8:58050414
|
T | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-414+18711T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050414 | ||||||
| chr8:58050434
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0002g0146others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-414+18731G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050434 | ||||||
| chr8:58050478
|
G | A | 77 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 77 | HG00733.hp1 HG00738.hp2 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.-414+18775G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050478 | ||||||
| chr8:58050521
|
G | A | 1 | a0001c0001t0007g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-414+18818G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050521 | ||||||
| chr8:58050525
|
G | A | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-414+18822G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050525 | ||||||
| chr8:58050601
|
C | T | 4 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0005g0139others(1): Show | 4 | HG02622.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+18898C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050601 | ||||||
| chr8:58050784
|
C | T | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-414+19081C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050784 | ||||||
| chr8:58050901
|
A | C | 86 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.-414+19198A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58050901 | ||||||
| chr8:58051024
|
A | G | 2 | a0001c0001t0001g0252a0001c0001t0003g0251 | 2 | NA18949.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-414+19321A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051024 | ||||||
| chr8:58051154
|
A | G | 1 | a0001c0001t0006g0246 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-414+19451A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051154 | ||||||
| chr8:58051333
|
C | A | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-414+19630C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051333 | ||||||
| chr8:58051365
|
AC | A | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0217others(2): Show | 5 | HG00597.hp2 NA18942.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.-414+19663delC | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051365 | ||||||
| chr8:58051450
|
C | G | 3 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157 | 3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-414+19747C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051450 | ||||||
| chr8:58051509
|
T | C | 4 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157others(1): Show | 4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-414+19806T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051509 | ||||||
| chr8:58051604
|
T | A | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-414+19901T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051604 | ||||||
| chr8:58051652
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-414+19949A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051652 | ||||||
| chr8:58051803
|
GA | G | 22 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-414+20102delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58051803 | |||||
| chr8:58051859
|
G | A | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-414+20156G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051859 | ||||||
| chr8:58051943
|
G | T | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-414+20240G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58051943 | ||||||
| chr8:58052008
|
A | G | 1 | a0001c0001t0007g0090 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-414+20305A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052008 | ||||||
| chr8:58052093
|
A | T | 3 | a0001c0001t0002g0128a0001c0001t0003g0143a0001c0001t0007g0144 | 3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-414+20390A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052093 | ||||||
| chr8:58052157
|
A | T | 22 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-414+20454A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052157 | ||||||
| chr8:58052186
|
C | G | 182 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(179): Show | 182 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.-414+20483C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052186 | ||||||
| chr8:58052204
|
G | A | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-414+20501G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052204 | ||||||
| chr8:58052217
|
A | G | 22 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-414+20514A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052217 | ||||||
| chr8:58052310
|
A | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0230a0001c0001t0003g0100others(1): Show | 4 | HG00544.hp1 HG02027.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-414+20607A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052310 | ||||||
| chr8:58052387
|
A | G | 2 | a0001c0001t0004g0041a0001c0001t0006g0101 | 2 | HG01109.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-414+20684A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052387 | ||||||
| chr8:58052493
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-414+20790C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052493 | ||||||
| chr8:58052494
|
G | A | 3 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157 | 3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-414+20791G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052494 | ||||||
| chr8:58052552
|
G | A | 22 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-414+20849G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052552 | ||||||
| chr8:58052661
|
G | T | 2 | a0001c0001t0003g0142a0001c0001t0009g0140 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-414+20958G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052661 | ||||||
| chr8:58052772
|
C | CT | 10 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0002g0032others(7): Show | 10 | HG00642.hp1 HG01081.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-414+21100dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | |||||
| chr8:58052772
|
CT | C | 25 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0118others(22): Show | 25 | HG00323.hp2 HG00597.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-414+21100delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | |||||
| chr8:58052772
|
CTT | C | 78 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0020others(75): Show | 78 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.-414+21099_-414+21 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | |||||
| chr8:58052772
|
CTTT | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-414+21098_-414+21 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | |||||
| chr8:58052772
|
CTTTT | C | 16 | a0001c0001t0002g0186a0001c0001t0002g0297a0001c0001t0003g0074others(13): Show | 16 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-414+21097_-414+21 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | |||||
| chr8:58052772
|
CTTTTTTT others(2): Show |
C | 22 | a0001c0001t0001g0089a0001c0001t0001g0201a0001c0001t0001g0267others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-414+21092_-414+21 others(15): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | |||||
| chr8:58052772
|
CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0002g0146a0001c0001t0002g0152a0001c0001t0002g0263others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-414+21091_-414+21 others(16): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | |||||
| chr8:58052772
|
CTTTTTTT others(4): Show |
C | 9 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0002g0153others(6): Show | 9 | HG01168.hp1 HG01192.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-414+21090_-414+21 others(17): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | |||||
| chr8:58052772
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0016a0001c0001t0003g0005 | 2 | HG00741.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-414+21089_-414+21 others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052772 | |||||
| chr8:58052911
|
G | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0154a0001c0001t0035g0290 | 3 | HG02559.hp1 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-414+21208G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052911 | ||||||
| chr8:58052934
|
C | T | 26 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-414+21231C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052934 | ||||||
| chr8:58052937
|
T | C | 26 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-414+21234T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052937 | ||||||
| chr8:58052947
|
G | A | 26 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-414+21244G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052947 | ||||||
| chr8:58052949
|
C | A | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-414+21246C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052949 | ||||||
| chr8:58052952
|
AT | A | 26 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-414+21255delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58052952 | |||||
| chr8:58052975
|
C | A | 26 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-414+21272C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58052975 | ||||||
| chr8:58053023
|
G | C | 1 | a0001c0001t0012g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-414+21320G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053023 | ||||||
| chr8:58053028
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0004g0083a0001c0001t0004g0189 | 3 | HG02056.hp1 HG02129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-414+21325G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053028 | ||||||
| chr8:58053162
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-414+21459T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053162 | ||||||
| chr8:58053169
|
C | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-414+21466C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053169 | ||||||
| chr8:58053266
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-414+21563G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053266 | ||||||
| chr8:58053436
|
GAAGA | G | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-414+21739_-414+21 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58053436 | |||||
| chr8:58053501
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-414+21798G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053501 | ||||||
| chr8:58053663
|
G | A | 5 | a0001c0001t0002g0059a0001c0001t0002g0190a0001c0001t0002g0191others(2): Show | 5 | HG00597.hp1 NA18948.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-413-21872G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58053663 | ||||||
| chr8:58054186
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-413-21349G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054186 | ||||||
| chr8:58054216
|
A | G | 22 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0221others(19): Show | 22 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-21319A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054216 | ||||||
| chr8:58054287
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-413-21248G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054287 | ||||||
| chr8:58054369
|
C | G | 3 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157 | 3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-21166C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054369 | ||||||
| chr8:58054783
|
A | G | 1 | a0001c0001t0002g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-413-20752A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054783 | ||||||
| chr8:58054792
|
T | A | 3 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157 | 3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-20743T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054792 | ||||||
| chr8:58054793
|
C | T | 3 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157 | 3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-20742C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054793 | ||||||
| chr8:58054881
|
T | A | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-413-20654T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58054881 | ||||||
| chr8:58054917
|
C | CT | 80 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(77): Show | 80 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.-413-20609dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58054917 | |||||
| chr8:58055012
|
C | G | 3 | a0001c0001t0002g0146a0001c0001t0008g0127a0001c0001t0010g0160 | 3 | HG01891.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-413-20523C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055012 | ||||||
| chr8:58055214
|
G | A | 1 | a0001c0001t0002g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-413-20321G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055214 | ||||||
| chr8:58055323
|
G | C | 3 | a0001c0001t0002g0128a0001c0001t0003g0143a0001c0001t0007g0144 | 3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-413-20212G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055323 | ||||||
| chr8:58055377
|
C | T | 3 | a0001c0001t0002g0128a0001c0001t0003g0143a0001c0001t0007g0144 | 3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-413-20158C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055377 | ||||||
| chr8:58055483
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-413-20052T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055483 | ||||||
| chr8:58055691
|
A | G | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-413-19844A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055691 | ||||||
| chr8:58055739
|
C | T | 4 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157others(1): Show | 4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-413-19796C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055739 | ||||||
| chr8:58055865
|
C | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-413-19670C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055865 | ||||||
| chr8:58055934
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-413-19601G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58055934 | ||||||
| chr8:58056008
|
G | T | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-413-19527G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58056008 | ||||||
| chr8:58056303
|
G | A | 1 | a0001c0001t0008g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-413-19232G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58056303 | ||||||
| chr8:58056369
|
T | A | 2 | a0001c0001t0006g0025a0001c0001t0006g0218 | 2 | HG01081.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-413-19166T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58056369 | ||||||
| chr8:58056374
|
T | A | 2 | a0001c0001t0003g0142a0001c0001t0009g0140 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-413-19161T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58056374 | ||||||
| chr8:58056845
|
TA | T | 12 | a0001c0001t0001g0158a0001c0001t0002g0082a0001c0001t0002g0162others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-413-18688delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58056845 | |||||
| chr8:58057133
|
C | T | 2 | a0001c0001t0003g0071a0001c0001t0007g0157 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-413-18402C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057133 | ||||||
| chr8:58057294
|
A | G | 1 | a0001c0001t0006g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-413-18241A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057294 | ||||||
| chr8:58057357
|
A | G | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-413-18178A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057357 | ||||||
| chr8:58057384
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0002g0146others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-413-18151G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057384 | ||||||
| chr8:58057389
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-413-18146C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057389 | ||||||
| chr8:58057550
|
C | G | 1 | a0001c0001t0005g0058 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-413-17985C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057550 | ||||||
| chr8:58057770
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-413-17765A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057770 | ||||||
| chr8:58057777
|
G | T | 2 | a0001c0001t0003g0142a0001c0001t0009g0140 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-413-17758G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057777 | ||||||
| chr8:58057779
|
T | C | 2 | a0001c0001t0024g0176a0001c0001t0031g0159 | 2 | HG01192.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.-413-17756T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057779 | ||||||
| chr8:58057870
|
G | A | 41 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0073others(38): Show | 41 | HG00735.hp1 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-413-17665G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58057870 | ||||||
| chr8:58058004
|
G | A | 26 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-17531G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058004 | ||||||
| chr8:58058132
|
C | G | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-413-17403C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058132 | ||||||
| chr8:58058302
|
T | C | 26 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-17233T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058302 | ||||||
| chr8:58058333
|
A | AG | 83 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0038others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-413-17200dupG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58058333 | |||||
| chr8:58058335
|
G | GA | 95 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(92): Show | 95 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.-413-17189dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58058335 | |||||
| chr8:58058336
|
A | G | 2 | a0001c0001t0001g0285a0001c0001t0003g0233 | 2 | NA18970.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-413-17199A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058336 | ||||||
| chr8:58058621
|
C | T | 22 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-16914C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058621 | ||||||
| chr8:58058680
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-413-16855A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058680 | ||||||
| chr8:58058807
|
T | C | 3 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157 | 3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-16728T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058807 | ||||||
| chr8:58058897
|
G | A | 1 | a0001c0001t0003g0234 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-413-16638G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58058897 | ||||||
| chr8:58059046
|
T | C | 26 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-16489T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059046 | ||||||
| chr8:58059052
|
T | G | 26 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-16483T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059052 | ||||||
| chr8:58059782
|
T | G | 1 | a0001c0001t0002g0120 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-413-15753T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059782 | ||||||
| chr8:58059926
|
G | T | 15 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0002g0146others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-413-15609G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059926 | ||||||
| chr8:58059934
|
G | A | 26 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-15601G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059934 | ||||||
| chr8:58059988
|
A | C | 26 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(23): Show | 26 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-15547A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58059988 | ||||||
| chr8:58060184
|
G | A | 4 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157others(1): Show | 4 | HG02055.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-413-15351G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060184 | ||||||
| chr8:58060203
|
A | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-15332A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060203 | ||||||
| chr8:58060446
|
T | A | 1 | a0001c0001t0002g0066 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-413-15089T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060446 | ||||||
| chr8:58060567
|
A | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-14968A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060567 | ||||||
| chr8:58060604
|
C | A | 1 | a0001c0001t0007g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-413-14931C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060604 | ||||||
| chr8:58060662
|
T | C | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-14873T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060662 | ||||||
| chr8:58060738
|
C | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0089others(38): Show | 41 | HG00733.hp1 HG01099.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.-413-14797C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060738 | ||||||
| chr8:58060773
|
C | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0027others(8): Show | 11 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.-413-14762C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58060773 | ||||||
| chr8:58061013
|
G | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-14522G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061013 | ||||||
| chr8:58061024
|
C | T | 3 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157 | 3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-14511C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061024 | ||||||
| chr8:58061102
|
T | C | 1 | a0001c0001t0002g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-413-14433T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061102 | ||||||
| chr8:58061383
|
A | G | 22 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-14152A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061383 | ||||||
| chr8:58061422
|
AC | A | 8 | a0001c0001t0002g0146a0001c0001t0002g0152a0001c0001t0008g0127others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-413-14112delC | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061422 | ||||||
| chr8:58061424
|
A | C | 22 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(19): Show | 22 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-14111A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061424 | ||||||
| chr8:58061668
|
C | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-13867C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061668 | ||||||
| chr8:58061702
|
A | G | 2 | a0001c0001t0003g0071a0001c0001t0007g0157 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-413-13833A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061702 | ||||||
| chr8:58061745
|
C | A | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-413-13790C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58061745 | ||||||
| chr8:58062038
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0002g0146others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-413-13497C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062038 | ||||||
| chr8:58062280
|
A | G | 1 | a0001c0001t0006g0245 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-413-13255A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062280 | ||||||
| chr8:58062497
|
T | C | 1 | a0001c0001t0021g0248 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-413-13038T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062497 | ||||||
| chr8:58062500
|
A | G | 61 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(58): Show | 61 | HG00735.hp1 HG00738.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.-413-13035A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062500 | ||||||
| chr8:58062704
|
C | T | 1 | a0001c0001t0012g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-413-12831C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062704 | ||||||
| chr8:58062790
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | NA18953.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-413-12745T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58062790 | ||||||
| chr8:58063178
|
G | A | 12 | a0001c0001t0001g0158a0001c0001t0002g0082a0001c0001t0002g0162others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-413-12357G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063178 | ||||||
| chr8:58063194
|
C | T | 20 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-12341C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063194 | ||||||
| chr8:58063214
|
C | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-12321C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063214 | ||||||
| chr8:58063469
|
C | CCATT | 92 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0073others(89): Show | 92 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(89): Show |
intron_variant | MODIFIER | c.-413-12066_-413-12 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063469 | ||||||
| chr8:58063536
|
G | A | 2 | a0001c0001t0003g0142a0001c0001t0009g0140 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-413-11999G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063536 | ||||||
| chr8:58063589
|
G | T | 94 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(91): Show | 94 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.-413-11946G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063589 | ||||||
| chr8:58063706
|
G | T | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-413-11829G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063706 | ||||||
| chr8:58063751
|
G | T | 3 | a0001c0001t0002g0147a0001c0001t0003g0071a0001c0001t0007g0157 | 3 | HG02717.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-11784G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063751 | ||||||
| chr8:58063790
|
A | G | 22 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0221others(19): Show | 22 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-11745A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063790 | ||||||
| chr8:58063855
|
A | T | 20 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-11680A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063855 | ||||||
| chr8:58063945
|
T | C | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-11590T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063945 | ||||||
| chr8:58063948
|
G | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(9): Show | 12 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-413-11587G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58063948 | ||||||
| chr8:58064085
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-413-11450C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58064085 | ||||||
| chr8:58064394
|
CT | C | 61 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(58): Show | 61 | HG00735.hp1 HG00738.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.-413-11130delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58064394 | |||||
| chr8:58064460
|
C | T | 98 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(95): Show | 98 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(95): Show |
intron_variant | MODIFIER | c.-413-11075C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58064460 | ||||||
| chr8:58064640
|
A | G | 2 | a0001c0001t0002g0293a0001c0001t0003g0223 | 2 | HG02027.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-413-10895A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58064640 | ||||||
| chr8:58064827
|
G | A | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-10708G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58064827 | ||||||
| chr8:58064927
|
G | A | 8 | a0001c0001t0002g0146a0001c0001t0002g0152a0001c0001t0008g0127others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-413-10608G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58064927 | ||||||
| chr8:58065110
|
T | A | 5 | a0001c0001t0003g0286a0001c0001t0003g0287a0001c0001t0003g0288others(2): Show | 5 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-413-10425T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065110 | ||||||
| chr8:58065269
|
T | C | 20 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-10266T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065269 | ||||||
| chr8:58065350
|
T | G | 1 | a0001c0001t0008g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-413-10185T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065350 | ||||||
| chr8:58065450
|
G | A | 1 | a0001c0001t0036g0132 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-413-10085G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065450 | ||||||
| chr8:58065763
|
A | G | 61 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(58): Show | 61 | HG00735.hp1 HG00738.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.-413-9772A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065763 | ||||||
| chr8:58065958
|
A | G | 1 | a0001c0001t0002g0178 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-413-9577A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58065958 | ||||||
| chr8:58066011
|
G | A | 20 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-9524G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066011 | ||||||
| chr8:58066246
|
T | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(127): Show | 130 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(127): Show |
intron_variant | MODIFIER | c.-413-9289T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066246 | ||||||
| chr8:58066436
|
G | C | 1 | a0001c0001t0003g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-413-9099G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066436 | ||||||
| chr8:58066591
|
A | G | 5 | a0001c0001t0002g0186a0001c0001t0003g0299a0001c0001t0007g0135others(2): Show | 5 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-413-8944A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066591 | ||||||
| chr8:58066594
|
GGCACAAG others(2): Show |
G | 5 | a0001c0001t0002g0186a0001c0001t0003g0299a0001c0001t0007g0135others(2): Show | 5 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-413-8940_-413-893 others(13): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066594 | ||||||
| chr8:58066633
|
C | A | 20 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-8902C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066633 | ||||||
| chr8:58066668
|
G | A | 15 | a0001c0001t0001g0158a0001c0001t0002g0082a0001c0001t0002g0162others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-413-8867G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066668 | ||||||
| chr8:58066710
|
C | T | 1 | a0001c0001t0002g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-413-8825C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066710 | ||||||
| chr8:58066734
|
A | G | 20 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-8801A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066734 | ||||||
| chr8:58066821
|
C | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-8714C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58066821 | ||||||
| chr8:58067014
|
A | C | 16 | a0001c0001t0001g0158a0001c0001t0002g0082a0001c0001t0002g0162others(13): Show | 16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-413-8521A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067014 | ||||||
| chr8:58067067
|
T | C | 36 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0158others(33): Show | 36 | HG00733.hp1 HG00741.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.-413-8468T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067067 | ||||||
| chr8:58067087
|
G | T | 1 | a0001c0001t0005g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-413-8448G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067087 | ||||||
| chr8:58067412
|
T | C | 20 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-8123T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067412 | ||||||
| chr8:58067448
|
T | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-8087T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067448 | ||||||
| chr8:58067529
|
G | A | 16 | a0001c0001t0001g0158a0001c0001t0002g0082a0001c0001t0002g0162others(13): Show | 16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-413-8006G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067529 | ||||||
| chr8:58067586
|
C | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-7949C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067586 | ||||||
| chr8:58067758
|
T | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-7777T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067758 | ||||||
| chr8:58067932
|
A | G | 7 | a0001c0001t0001g0060a0001c0001t0001g0088a0001c0001t0001g0252others(4): Show | 7 | NA18953.hp1 NA18975.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.-413-7603A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58067932 | ||||||
| chr8:58068312
|
T | A | 1 | a0001c0001t0015g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-413-7223T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068312 | ||||||
| chr8:58068376
|
T | G | 1 | a0001c0001t0003g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-413-7159T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068376 | ||||||
| chr8:58068391
|
T | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-7144T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068391 | ||||||
| chr8:58068422
|
A | G | 11 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0134others(8): Show | 11 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-413-7113A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068422 | ||||||
| chr8:58068598
|
TA | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(229): Show | 232 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.-413-6923delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58068598 | |||||
| chr8:58068622
|
A | T | 30 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0158others(27): Show | 30 | HG00733.hp1 HG00741.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.-413-6913A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068622 | ||||||
| chr8:58068705
|
C | A | 3 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0004g0260 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-413-6830C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068705 | ||||||
| chr8:58068721
|
G | A | 20 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-413-6814G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068721 | ||||||
| chr8:58068815
|
C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-6720C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58068815 | ||||||
| chr8:58069131
|
T | G | 10 | a0001c0001t0001g0158a0001c0001t0002g0162a0001c0001t0002g0163others(7): Show | 10 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-413-6404T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069131 | ||||||
| chr8:58069177
|
G | T | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-413-6358G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069177 | ||||||
| chr8:58069347
|
C | T | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-413-6188C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069347 | ||||||
| chr8:58069350
|
G | C | 14 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0002g0146others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-413-6185G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069350 | ||||||
| chr8:58069441
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-413-6094G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069441 | ||||||
| chr8:58069483
|
A | G | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-413-6052A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069483 | ||||||
| chr8:58069508
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-413-6027A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069508 | ||||||
| chr8:58069562
|
A | G | 13 | a0001c0001t0001g0065a0001c0001t0001g0226a0001c0001t0002g0011others(10): Show | 13 | HG00609.hp1 HG00621.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.-413-5973A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069562 | ||||||
| chr8:58069599
|
C | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-5936C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069599 | ||||||
| chr8:58069853
|
A | T | 5 | a0001c0001t0002g0059a0001c0001t0002g0190a0001c0001t0002g0191others(2): Show | 5 | HG00597.hp1 NA18948.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-413-5682A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069853 | ||||||
| chr8:58069909
|
G | A | 11 | a0001c0001t0001g0040a0001c0001t0001g0098a0001c0001t0001g0103others(8): Show | 11 | HG00544.hp1 HG02027.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.-413-5626G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58069909 | ||||||
| chr8:58070036
|
C | G | 1 | a0001c0001t0002g0016 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-413-5499C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070036 | ||||||
| chr8:58070175
|
C | T | 1 | a0001c0001t0002g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-413-5360C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070175 | ||||||
| chr8:58070309
|
C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-5226C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070309 | ||||||
| chr8:58070393
|
T | C | 8 | a0001c0001t0001g0158a0001c0001t0002g0162a0001c0001t0002g0163others(5): Show | 8 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-413-5142T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070393 | ||||||
| chr8:58070432
|
G | T | 17 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(14): Show | 17 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-413-5103G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070432 | ||||||
| chr8:58070765
|
TA | T | 3 | a0001c0001t0002g0167a0001c0001t0003g0133a0001c0001t0004g0260 | 3 | HG02922.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-413-4769delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070765 | ||||||
| chr8:58070968
|
T | G | 2 | a0001c0001t0001g0267a0001c0001t0002g0266 | 2 | HG00733.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-413-4567T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070968 | ||||||
| chr8:58070975
|
T | C | 15 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0002g0146others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-413-4560T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58070975 | ||||||
| chr8:58071009
|
C | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-4526C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071009 | ||||||
| chr8:58071059
|
G | A | 1 | a0001c0001t0003g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-413-4476G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071059 | ||||||
| chr8:58071298
|
G | A | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-413-4237G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071298 | ||||||
| chr8:58071417
|
C | T | 94 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(91): Show | 94 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.-413-4118C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071417 | ||||||
| chr8:58071529
|
T | C | 8 | a0001c0001t0001g0054a0001c0001t0002g0095a0001c0001t0002g0117others(5): Show | 8 | HG00099.hp1 HG00323.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-413-4006T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071529 | ||||||
| chr8:58071746
|
AT | A | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-3788delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071746 | ||||||
| chr8:58071748
|
C | T | 3 | a0001c0001t0002g0297a0001c0001t0003g0198a0001c0001t0007g0300 | 3 | HG02280.hp2 HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-413-3787C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071748 | ||||||
| chr8:58071879
|
C | T | 2 | a0001c0001t0003g0071a0001c0001t0007g0157 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-413-3656C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071879 | ||||||
| chr8:58071899
|
C | T | 25 | a0001c0001t0001g0073a0001c0001t0002g0082a0001c0001t0002g0147others(22): Show | 25 | HG01069.hp1 HG02055.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.-413-3636C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58071899 | ||||||
| chr8:58072099
|
G | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0200a0001c0001t0004g0202 | 3 | HG00280.hp2 HG01978.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-413-3436G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072099 | ||||||
| chr8:58072105
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(25): Show | 28 | HG00280.hp2 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-413-3430T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072105 | ||||||
| chr8:58072215
|
A | G | 65 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0040others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.-413-3320A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072215 | ||||||
| chr8:58072256
|
G | A | 1 | a0001c0001t0003g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-413-3279G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072256 | ||||||
| chr8:58072287
|
A | G | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(9): Show | 12 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-413-3248A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072287 | ||||||
| chr8:58072317
|
A | C | 8 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0185others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-413-3218A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072317 | ||||||
| chr8:58072411
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0002g0147 | 2 | HG00408.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-413-3124C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072411 | ||||||
| chr8:58072438
|
T | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-413-3097T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072438 | ||||||
| chr8:58072807
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-413-2728C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072807 | ||||||
| chr8:58072866
|
G | C | 1 | a0001c0001t0003g0292 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-413-2669G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072866 | ||||||
| chr8:58072882
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-413-2653A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072882 | ||||||
| chr8:58072902
|
G | A | 3 | a0001c0001t0002g0167a0001c0001t0003g0133a0001c0001t0004g0260 | 3 | HG02922.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-413-2633G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072902 | ||||||
| chr8:58072909
|
G | A | 1 | a0001c0001t0007g0090 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-413-2626G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072909 | ||||||
| chr8:58072941
|
T | C | 26 | a0001c0001t0001g0065a0001c0001t0001g0226a0001c0001t0002g0001others(23): Show | 26 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.-413-2594T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58072941 | ||||||
| chr8:58073008
|
A | G | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-2527A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073008 | ||||||
| chr8:58073212
|
T | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0026g0021 | 3 | NA18993.hp2 NA18994.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-413-2323T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073212 | ||||||
| chr8:58073601
|
C | G | 90 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(87): Show | 90 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.-413-1934C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073601 | ||||||
| chr8:58073608
|
G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-1927G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073608 | ||||||
| chr8:58073636
|
A | G | 21 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0060others(18): Show | 21 | HG00597.hp2 HG00642.hp2 HG02738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-413-1899A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073636 | ||||||
| chr8:58073644
|
C | G | 15 | a0001c0001t0001g0006a0001c0001t0002g0012a0001c0001t0002g0146others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-413-1891C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073644 | ||||||
| chr8:58073808
|
T | G | 119 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(116): Show | 119 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.-413-1727T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073808 | ||||||
| chr8:58073879
|
C | A | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-1656C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073879 | ||||||
| chr8:58073900
|
G | A | 88 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(85): Show | 88 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.-413-1635G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073900 | ||||||
| chr8:58073988
|
T | C | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-1547T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58073988 | ||||||
| chr8:58074044
|
T | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-1491T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074044 | ||||||
| chr8:58074082
|
G | C | 105 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(102): Show | 105 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(102): Show |
intron_variant | MODIFIER | c.-413-1453G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074082 | ||||||
| chr8:58074142
|
A | G | 1 | a0001c0001t0015g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-413-1393A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074142 | ||||||
| chr8:58074263
|
A | C | 28 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0172others(25): Show | 28 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-413-1272A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074263 | ||||||
| chr8:58074272
|
C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-1263C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074272 | ||||||
| chr8:58074319
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0008g0170 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-413-1216C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074319 | ||||||
| chr8:58074597
|
T | C | 1 | a0001c0001t0009g0140 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-413-938T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074597 | ||||||
| chr8:58074603
|
G | A | 9 | a0001c0001t0001g0158a0001c0001t0002g0162a0001c0001t0002g0163others(6): Show | 9 | HG00597.hp1 HG00741.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-413-932G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074603 | ||||||
| chr8:58074692
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0002g0012others(25): Show | 28 | HG00741.hp1 HG01192.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.-413-843C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074692 | ||||||
| chr8:58074957
|
A | G | 2 | a0001c0001t0002g0297a0001c0001t0024g0176 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-413-578A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074957 | ||||||
| chr8:58074979
|
T | C | 1 | a0001c0001t0005g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-413-556T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58074979 | ||||||
| chr8:58075265
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-413-269_-413-268i others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | |||||
| chr8:58075265
|
T | TTGTGTGT others(7): Show |
9 | a0001c0001t0001g0084a0001c0001t0001g0267a0001c0001t0002g0057others(6): Show | 9 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.-413-269_-413-268i others(16): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | |||||
| chr8:58075265
|
T | TTGTGTGT others(9): Show |
4 | a0001c0001t0001g0201a0001c0001t0002g0268a0001c0001t0008g0170others(1): Show | 4 | HG02886.hp1 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-413-269_-413-268i others(18): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | |||||
| chr8:58075265
|
T | TTGTGTGT others(11): Show |
1 | a0001c0001t0004g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-413-269_-413-268i others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | |||||
| chr8:58075265
|
T | TTGTGTGT others(13): Show |
1 | a0001c0001t0004g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-413-269_-413-268i others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | |||||
| chr8:58075265
|
T | TTGTGTGT others(15): Show |
1 | a0001c0001t0002g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-413-269_-413-268i others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075265 | |||||
| chr8:58075267
|
T | G | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-268T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075267 | ||||||
| chr8:58075267
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-413-267_-413-266i others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075267 | |||||
| chr8:58075267
|
T | TTGTGTGT others(11): Show |
1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-413-267_-413-266i others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075267 | |||||
| chr8:58075267
|
T | TTGTGTGT others(13): Show |
2 | a0001c0001t0001g0006a0001c0001t0002g0012 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-413-267_-413-266i others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075267 | |||||
| chr8:58075269
|
T | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0089others(19): Show | 22 | HG00733.hp1 HG00741.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-413-266T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075269 | ||||||
| chr8:58075269
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-413-265_-413-264i others(12): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075269 | |||||
| chr8:58075269
|
T | TTGTGTGT others(11): Show |
1 | a0001c0001t0002g0162 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-413-265_-413-264i others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075269 | |||||
| chr8:58075269
|
T | TTGTGTGT others(13): Show |
5 | a0001c0001t0001g0172a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-413-265_-413-264i others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075269 | |||||
| chr8:58075271
|
T | G | 44 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0015others(41): Show | 44 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-413-264T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075271 | ||||||
| chr8:58075271
|
T | TGTGTGTG others(16): Show |
1 | a0001c0001t0001g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-413-264_-413-263i others(25): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075271 | ||||||
| chr8:58075271
|
T | TTGGTGTG others(14): Show |
1 | a0001c0001t0010g0145 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-413-263_-413-262i others(23): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | |||||
| chr8:58075271
|
T | TTGGTGTG others(16): Show |
12 | a0001c0001t0002g0146a0001c0001t0002g0152a0001c0001t0003g0005others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-413-263_-413-262i others(25): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | |||||
| chr8:58075271
|
T | TTGGTGTG others(18): Show |
1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-413-263_-413-262i others(27): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | |||||
| chr8:58075271
|
T | TTGTGTGT others(11): Show |
3 | a0001c0001t0002g0163a0001c0001t0002g0291a0001c0001t0007g0090 | 3 | HG02647.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-413-263_-413-262i others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | |||||
| chr8:58075271
|
T | TTGTGTGT others(13): Show |
2 | a0001c0001t0005g0271a0001c0001t0007g0131 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-413-263_-413-262i others(22): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | |||||
| chr8:58075271
|
T | TTGTGTGT others(15): Show |
1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-413-263_-413-262i others(24): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | |||||
| chr8:58075271
|
T | TTGTGTGT others(21): Show |
1 | a0001c0001t0001g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-413-263_-413-262i others(30): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075271 | |||||
| chr8:58075273
|
T | G | 79 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(76): Show | 79 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.-413-262T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075273 | ||||||
| chr8:58075273
|
T | TTGTGTGT others(11): Show |
2 | a0001c0001t0001g0158a0001c0001t0007g0130 | 2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-413-261_-413-260i others(20): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075273 | |||||
| chr8:58075275
|
T | G | 89 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(86): Show | 89 | HG00621.hp2 HG00673.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.-413-260T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075275 | ||||||
| chr8:58075275
|
T | TTG | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(9): Show | 12 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-413-240_-413-239d others(4): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075275 | |||||
| chr8:58075275
|
T | TTGTGTGT others(19): Show |
1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-413-239_-413-238i others(28): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075275 | |||||
| chr8:58075275
|
T | TTTTTTGT others(17): Show |
1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-413-259_-413-258i others(26): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 58075275 | |||||
| chr8:58075277
|
G | T | 41 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0073others(38): Show | 41 | HG00408.hp2 HG01069.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.-413-258G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075277 | ||||||
| chr8:58075317
|
T | C | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-413-218T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075317 | ||||||
| chr8:58075479
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-413-56G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075479 | ||||||
| chr8:58075505
|
A | G | 8 | a0001c0001t0001g0158a0001c0001t0002g0162a0001c0001t0002g0163others(5): Show | 8 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-413-30A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | chr8 | 58075505 | ||||||
| chr8:58075661
|
G | A | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-325+38G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58075661 | ||||||
| chr8:58075751
|
A | G | 1 | a0001c0001t0002g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-325+128A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58075751 | ||||||
| chr8:58075825
|
C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-325+202C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58075825 | ||||||
| chr8:58075911
|
T | C | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-325+288T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58075911 | ||||||
| chr8:58076232
|
T | G | 1 | a0001c0001t0002g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-325+609T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076232 | ||||||
| chr8:58076345
|
C | T | 14 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-325+722C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076345 | ||||||
| chr8:58076474
|
G | A | 8 | a0001c0001t0001g0158a0001c0001t0002g0162a0001c0001t0002g0163others(5): Show | 8 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-325+851G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076474 | ||||||
| chr8:58076554
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-325+931C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076554 | ||||||
| chr8:58076829
|
A | G | 1 | a0001c0001t0003g0224 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-325+1206A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076829 | ||||||
| chr8:58076924
|
A | G | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-325+1301A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58076924 | ||||||
| chr8:58077062
|
C | T | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+1439C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077062 | ||||||
| chr8:58077067
|
C | T | 5 | a0001c0001t0002g0059a0001c0001t0002g0190a0001c0001t0002g0191others(2): Show | 5 | HG00597.hp1 NA18948.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+1444C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077067 | ||||||
| chr8:58077145
|
C | T | 1 | a0001c0001t0006g0051 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-325+1522C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077145 | ||||||
| chr8:58077441
|
G | C | 8 | a0001c0001t0001g0158a0001c0001t0002g0162a0001c0001t0002g0163others(5): Show | 8 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-325+1818G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077441 | ||||||
| chr8:58077462
|
G | A | 2 | a0001c0001t0003g0295a0001c0001t0030g0035 | 2 | HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-325+1839G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077462 | ||||||
| chr8:58077505
|
T | C | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-325+1882T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077505 | ||||||
| chr8:58077508
|
A | T | 6 | a0001c0001t0002g0146a0001c0001t0008g0127a0001c0001t0010g0072others(3): Show | 6 | HG01891.hp1 HG02622.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+1885A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077508 | ||||||
| chr8:58077553
|
GACTGGGA others(4): Show |
G | 3 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0026g0021 | 3 | NA18993.hp2 NA18994.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-325+1931_-325+194 others(15): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077553 | ||||||
| chr8:58077567
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0026g0021 | 3 | NA18993.hp2 NA18994.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-325+1944G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077567 | ||||||
| chr8:58077785
|
A | G | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-325+2162A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077785 | ||||||
| chr8:58077801
|
A | G | 8 | a0001c0001t0001g0158a0001c0001t0002g0162a0001c0001t0002g0163others(5): Show | 8 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-325+2178A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077801 | ||||||
| chr8:58077828
|
A | G | 3 | a0001c0001t0002g0167a0001c0001t0003g0133a0001c0001t0024g0176 | 3 | HG01884.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+2205A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077828 | ||||||
| chr8:58077845
|
A | G | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-325+2222A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077845 | ||||||
| chr8:58077929
|
G | A | 1 | a0001c0001t0009g0179 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-325+2306G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58077929 | ||||||
| chr8:58078099
|
T | A | 1 | a0001c0001t0001g0277 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-325+2476T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078099 | ||||||
| chr8:58078133
|
T | G | 1 | a0001c0001t0008g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-325+2510T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078133 | ||||||
| chr8:58078135
|
C | T | 18 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(15): Show | 18 | HG00733.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-325+2512C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078135 | ||||||
| chr8:58078169
|
A | G | 7 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0227others(4): Show | 7 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-325+2546A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078169 | ||||||
| chr8:58078547
|
C | CT | 41 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0073others(38): Show | 41 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-325+2945dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58078547 | |||||
| chr8:58078547
|
C | CTT | 32 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(29): Show | 32 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-325+2944_-325+294 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58078547 | |||||
| chr8:58078547
|
C | CTTT | 15 | a0001c0001t0001g0089a0001c0001t0001g0201a0001c0001t0001g0221others(12): Show | 15 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+2943_-325+294 others(7): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58078547 | |||||
| chr8:58078589
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-325+2966C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078589 | ||||||
| chr8:58078644
|
A | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(127): Show | 130 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.-325+3021A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078644 | ||||||
| chr8:58078750
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-325+3127C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078750 | ||||||
| chr8:58078752
|
A | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0001g0172others(16): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+3129A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078752 | ||||||
| chr8:58078774
|
T | C | 13 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+3151T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078774 | ||||||
| chr8:58078839
|
C | T | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+3216C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078839 | ||||||
| chr8:58078846
|
G | A | 15 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(12): Show | 15 | HG00438.hp2 HG00609.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+3223G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078846 | ||||||
| chr8:58078997
|
C | T | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+3374C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078997 | ||||||
| chr8:58078998
|
G | A | 13 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+3375G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58078998 | ||||||
| chr8:58079013
|
TGGTCCTC others(10): Show |
T | 5 | a0001c0001t0001g0172a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+3394_-325+341 others(21): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58079013 | |||||
| chr8:58079234
|
C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+3611C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079234 | ||||||
| chr8:58079285
|
G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0001g0172others(33): Show | 36 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-325+3662G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079285 | ||||||
| chr8:58079372
|
T | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-325+3749T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079372 | ||||||
| chr8:58079401
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-325+3778A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079401 | ||||||
| chr8:58079464
|
A | G | 1 | a0001c0001t0009g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-325+3841A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079464 | ||||||
| chr8:58079488
|
A | G | 7 | a0001c0001t0001g0158a0001c0001t0002g0162a0001c0001t0002g0163others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-325+3865A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079488 | ||||||
| chr8:58079515
|
G | A | 1 | a0001c0001t0004g0194 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-325+3892G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079515 | ||||||
| chr8:58079563
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-325+3940G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079563 | ||||||
| chr8:58079583
|
C | G | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-325+3960C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079583 | ||||||
| chr8:58079622
|
A | T | 4 | a0001c0001t0003g0005a0001c0001t0003g0250a0001c0001t0012g0148others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-325+3999A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079622 | ||||||
| chr8:58079629
|
A | T | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-325+4006A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079629 | ||||||
| chr8:58079673
|
C | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+4050C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079673 | ||||||
| chr8:58079782
|
TA | T | 13 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+4170delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58079782 | |||||
| chr8:58079816
|
T | G | 1 | a0001c0001t0001g0277 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-325+4193T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079816 | ||||||
| chr8:58079846
|
G | A | 42 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0089others(39): Show | 42 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.-325+4223G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079846 | ||||||
| chr8:58079922
|
C | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+4299C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58079922 | ||||||
| chr8:58080005
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-325+4382G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58080005 | ||||||
| chr8:58080137
|
G | C | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+4514G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58080137 | ||||||
| chr8:58080150
|
A | C | 1 | a0001c0001t0028g0182 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-325+4527A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58080150 | ||||||
| chr8:58080478
|
G | C | 115 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(112): Show | 115 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.-325+4855G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58080478 | ||||||
| chr8:58080731
|
G | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0001g0172others(16): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+5108G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58080731 | ||||||
| chr8:58081115
|
A | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0001g0172others(16): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+5492A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081115 | ||||||
| chr8:58081307
|
T | C | 5 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+5684T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081307 | ||||||
| chr8:58081381
|
A | G | 13 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+5758A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081381 | ||||||
| chr8:58081486
|
C | T | 6 | a0001c0001t0002g0146a0001c0001t0008g0127a0001c0001t0010g0072others(3): Show | 6 | HG01891.hp1 HG02622.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+5863C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081486 | ||||||
| chr8:58081529
|
A | C | 5 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+5906A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081529 | ||||||
| chr8:58081669
|
C | A | 1 | a0001c0001t0002g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-325+6046C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081669 | ||||||
| chr8:58081696
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-325+6073G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081696 | ||||||
| chr8:58081704
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(22): Show | 25 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-325+6081C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081704 | ||||||
| chr8:58081709
|
T | A | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+6086T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081709 | ||||||
| chr8:58081751
|
A | T | 1 | a0001c0001t0008g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-325+6128A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081751 | ||||||
| chr8:58081952
|
A | C | 1 | a0001c0001t0004g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-325+6329A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58081952 | ||||||
| chr8:58082072
|
A | G | 1 | a0001c0001t0004g0194 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-325+6449A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082072 | ||||||
| chr8:58082152
|
T | A | 2 | a0001c0001t0002g0123a0001c0001t0003g0257 | 2 | HG01943.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-325+6529T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082152 | ||||||
| chr8:58082226
|
A | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+6603A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082226 | ||||||
| chr8:58082280
|
G | A | 2 | a0001c0001t0003g0071a0001c0001t0007g0157 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-325+6657G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082280 | ||||||
| chr8:58082355
|
C | T | 32 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0094others(29): Show | 32 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-325+6732C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082355 | ||||||
| chr8:58082583
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-325+6960C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082583 | ||||||
| chr8:58082597
|
C | T | 1 | a0001c0001t0007g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-325+6974C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082597 | ||||||
| chr8:58082775
|
C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+7152C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082775 | ||||||
| chr8:58082818
|
G | A | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-325+7195G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082818 | ||||||
| chr8:58082824
|
C | T | 32 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0094others(29): Show | 32 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-325+7201C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082824 | ||||||
| chr8:58082842
|
T | TTG | 19 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0001g0172others(16): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+7220_-325+722 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58082842 | |||||
| chr8:58082847
|
G | GT | 34 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0094others(31): Show | 34 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.-325+7238dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58082847 | |||||
| chr8:58082847
|
G | GTT | 14 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-325+7237_-325+723 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58082847 | |||||
| chr8:58082847
|
G | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0001g0172others(16): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+7224G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082847 | ||||||
| chr8:58082847
|
GT | G | 28 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0201others(25): Show | 28 | HG00609.hp1 HG00733.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.-325+7238delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58082847 | |||||
| chr8:58082914
|
C | T | 2 | a0001c0001t0003g0164a0001c0001t0003g0165 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-325+7291C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082914 | ||||||
| chr8:58082915
|
G | A | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-325+7292G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58082915 | ||||||
| chr8:58083012
|
T | TA | 20 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0001g0172others(17): Show | 20 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-325+7406dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58083012 | |||||
| chr8:58083012
|
TA | T | 23 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0146others(20): Show | 23 | HG00323.hp2 HG01081.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.-325+7406delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58083012 | |||||
| chr8:58083108
|
A | G | 5 | a0001c0001t0003g0286a0001c0001t0003g0287a0001c0001t0003g0288others(2): Show | 5 | HG02055.hp1 HG03139.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+7485A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083108 | ||||||
| chr8:58083215
|
G | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0001g0172others(16): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+7592G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083215 | ||||||
| chr8:58083629
|
G | C | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-325+8006G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083629 | ||||||
| chr8:58083773
|
G | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+8150G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083773 | ||||||
| chr8:58083826
|
G | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+8203G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083826 | ||||||
| chr8:58083976
|
G | A | 1 | a0001c0001t0011g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-325+8353G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58083976 | ||||||
| chr8:58084393
|
C | CT | 6 | a0001c0001t0002g0039a0001c0001t0003g0142a0001c0001t0003g0280others(3): Show | 6 | HG00609.hp2 HG00673.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+8785dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58084393 | |||||
| chr8:58084393
|
CTT | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0089others(21): Show | 24 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-325+8784_-325+878 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58084393 | |||||
| chr8:58084475
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-325+8852C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084475 | ||||||
| chr8:58084543
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(22): Show | 25 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-325+8920C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084543 | ||||||
| chr8:58084590
|
A | G | 14 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-325+8967A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084590 | ||||||
| chr8:58084644
|
G | A | 5 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+9021G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084644 | ||||||
| chr8:58084724
|
G | A | 73 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0073others(70): Show | 73 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.-325+9101G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084724 | ||||||
| chr8:58084772
|
G | GT | 19 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0001g0172others(16): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-325+9151dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58084772 | |||||
| chr8:58084844
|
A | G | 2 | a0001c0001t0002g0297a0001c0001t0003g0076 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-325+9221A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084844 | ||||||
| chr8:58084926
|
G | A | 73 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0073others(70): Show | 73 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.-325+9303G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58084926 | ||||||
| chr8:58085063
|
G | A | 5 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+9440G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085063 | ||||||
| chr8:58085147
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-325+9524G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085147 | ||||||
| chr8:58085179
|
A | T | 1 | a0001c0001t0009g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-325+9556A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085179 | ||||||
| chr8:58085289
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-325+9666G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085289 | ||||||
| chr8:58085461
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+9838C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085461 | ||||||
| chr8:58085462
|
G | A | 6 | a0001c0001t0001g0267a0001c0001t0002g0136a0001c0001t0002g0266others(3): Show | 6 | HG00733.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+9839G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085462 | ||||||
| chr8:58085794
|
G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0001g0172others(33): Show | 36 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-325+10171G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085794 | ||||||
| chr8:58085811
|
A | T | 1 | a0001c0001t0004g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-325+10188A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085811 | ||||||
| chr8:58085838
|
C | T | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+10215C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58085838 | ||||||
| chr8:58086116
|
C | G | 5 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+10493C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086116 | ||||||
| chr8:58086281
|
A | T | 16 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-325+10658A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086281 | ||||||
| chr8:58086425
|
T | C | 5 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+10802T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086425 | ||||||
| chr8:58086550
|
G | T | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+10927G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086550 | ||||||
| chr8:58086563
|
A | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+10940A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086563 | ||||||
| chr8:58086595
|
A | G | 73 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0073others(70): Show | 73 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.-325+10972A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086595 | ||||||
| chr8:58086596
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-325+10973C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086596 | ||||||
| chr8:58086617
|
C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+10994C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086617 | ||||||
| chr8:58086772
|
C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+11149C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086772 | ||||||
| chr8:58086834
|
C | A | 2 | a0001c0001t0003g0142a0001c0001t0009g0140 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-325+11211C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086834 | ||||||
| chr8:58086882
|
G | A | 4 | a0001c0001t0003g0299a0001c0001t0007g0135a0001c0001t0007g0197others(1): Show | 4 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-325+11259G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086882 | ||||||
| chr8:58086966
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-325+11343T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086966 | ||||||
| chr8:58086981
|
G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-325+11358G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086981 | ||||||
| chr8:58086989
|
G | A | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+11366G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086989 | ||||||
| chr8:58086999
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+11376C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58086999 | ||||||
| chr8:58087099
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-325+11476G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087099 | ||||||
| chr8:58087115
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0025a0001c0001t0006g0218 | 3 | HG01081.hp1 HG01255.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-325+11492C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087115 | ||||||
| chr8:58087149
|
A | C | 1 | a0001c0001t0003g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-325+11526A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087149 | ||||||
| chr8:58087381
|
G | A | 32 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0094others(29): Show | 32 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-325+11758G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087381 | ||||||
| chr8:58087405
|
T | C | 5 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+11782T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087405 | ||||||
| chr8:58087556
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0089others(38): Show | 41 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.-325+11933A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087556 | ||||||
| chr8:58087630
|
T | C | 2 | a0001c0001t0006g0219a0001c0001t0006g0220 | 2 | HG01070.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-325+12007T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58087630 | ||||||
| chr8:58088119
|
T | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+12496T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088119 | ||||||
| chr8:58088147
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+12524C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088147 | ||||||
| chr8:58088617
|
T | C | 1 | a0001c0001t0011g0228 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-325+12994T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088617 | ||||||
| chr8:58088643
|
G | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0098a0001c0001t0001g0282others(3): Show | 6 | HG02155.hp2 HG02165.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+13020G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088643 | ||||||
| chr8:58088671
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | NA18944.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-325+13048A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088671 | ||||||
| chr8:58088690
|
G | T | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-325+13067G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088690 | ||||||
| chr8:58088926
|
A | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0154a0001c0001t0035g0290 | 3 | HG02559.hp1 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-325+13303A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088926 | ||||||
| chr8:58088936
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-325+13313C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088936 | ||||||
| chr8:58088938
|
T | C | 13 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(10): Show | 13 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-325+13315T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58088938 | ||||||
| chr8:58089053
|
G | A | 115 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(112): Show | 115 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.-325+13430G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089053 | ||||||
| chr8:58089061
|
T | C | 5 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+13438T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089061 | ||||||
| chr8:58089141
|
A | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+13518A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089141 | ||||||
| chr8:58089186
|
G | A | 5 | a0001c0001t0001g0172a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+13563G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089186 | ||||||
| chr8:58089262
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-325+13639A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089262 | ||||||
| chr8:58089384
|
G | A | 1 | a0001c0001t0004g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-325+13761G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089384 | ||||||
| chr8:58089493
|
C | T | 3 | a0001c0001t0002g0128a0001c0001t0003g0143a0001c0001t0007g0144 | 3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-325+13870C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089493 | ||||||
| chr8:58089816
|
A | G | 1 | a0001c0001t0002g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-325+14193A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089816 | ||||||
| chr8:58089870
|
T | A | 1 | a0001c0001t0008g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-325+14247T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089870 | ||||||
| chr8:58089914
|
A | G | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-325+14291A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089914 | ||||||
| chr8:58089999
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-325+14376T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58089999 | ||||||
| chr8:58090191
|
G | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(24): Show | 27 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-325+14568G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58090191 | ||||||
| chr8:58090497
|
A | G | 5 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-325+14874A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58090497 | ||||||
| chr8:58090560
|
A | T | 1 | a0001c0001t0002g0266 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-325+14937A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58090560 | ||||||
| chr8:58090620
|
A | G | 62 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(59): Show | 62 | HG00735.hp1 HG00738.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.-325+14997A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58090620 | ||||||
| chr8:58090976
|
A | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+15353A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58090976 | ||||||
| chr8:58091022
|
A | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+15399A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091022 | ||||||
| chr8:58091156
|
A | T | 1 | a0001c0001t0003g0224 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-325+15533A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091156 | ||||||
| chr8:58091164
|
A | C | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+15541A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091164 | ||||||
| chr8:58091191
|
C | G | 1 | a0001c0001t0006g0220 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-325+15568C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091191 | ||||||
| chr8:58091387
|
C | T | 21 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0158others(18): Show | 21 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-325+15764C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091387 | ||||||
| chr8:58091417
|
C | T | 3 | a0001c0001t0002g0128a0001c0001t0003g0143a0001c0001t0007g0144 | 3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-325+15794C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091417 | ||||||
| chr8:58091443
|
C | T | 9 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0286others(6): Show | 9 | HG02055.hp1 HG02622.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+15820C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091443 | ||||||
| chr8:58091444
|
G | A | 3 | a0001c0001t0009g0199a0001c0001t0033g0081a0001c0001t0037g0180 | 3 | HG02080.hp2 NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-325+15821G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091444 | ||||||
| chr8:58091514
|
C | A | 1 | a0001c0001t0003g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-325+15891C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091514 | ||||||
| chr8:58091646
|
A | G | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+16023A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091646 | ||||||
| chr8:58091675
|
C | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+16052C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091675 | ||||||
| chr8:58091710
|
G | A | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+16087G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091710 | ||||||
| chr8:58091819
|
T | C | 9 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0134others(6): Show | 9 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+16196T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091819 | ||||||
| chr8:58091853
|
C | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+16230C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58091853 | ||||||
| chr8:58092188
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-325+16565G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092188 | ||||||
| chr8:58092235
|
A | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+16612A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092235 | ||||||
| chr8:58092298
|
G | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+16675G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092298 | ||||||
| chr8:58092406
|
C | A | 39 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0158others(36): Show | 39 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-325+16783C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092406 | ||||||
| chr8:58092776
|
C | T | 1 | a0001c0001t0003g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-325+17153C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092776 | ||||||
| chr8:58092880
|
C | G | 1 | a0001c0001t0003g0234 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-325+17257C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58092880 | ||||||
| chr8:58093098
|
G | A | 1 | a0001c0001t0008g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-325+17475G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093098 | ||||||
| chr8:58093156
|
G | A | 1 | a0001c0001t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-325+17533G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093156 | ||||||
| chr8:58093301
|
G | A | 1 | a0001c0001t0004g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-325+17678G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093301 | ||||||
| chr8:58093309
|
C | A | 1 | a0001c0001t0004g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-325+17686C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093309 | ||||||
| chr8:58093348
|
G | A | 15 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+17725G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093348 | ||||||
| chr8:58093529
|
G | A | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-325+17906G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093529 | ||||||
| chr8:58093584
|
T | C | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+17961T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093584 | ||||||
| chr8:58093601
|
G | A | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-325+17978G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093601 | ||||||
| chr8:58093645
|
C | G | 1 | a0001c0001t0003g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-325+18022C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093645 | ||||||
| chr8:58093967
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-325+18344C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58093967 | ||||||
| chr8:58094027
|
T | A | 24 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(21): Show | 24 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.-325+18404T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094027 | ||||||
| chr8:58094068
|
G | A | 4 | a0001c0001t0002g0082a0001c0001t0004g0063a0001c0001t0004g0279others(1): Show | 4 | HG02735.hp2 HG03453.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-325+18445G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094068 | ||||||
| chr8:58094111
|
T | C | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+18488T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094111 | ||||||
| chr8:58094349
|
A | C | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+18726A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094349 | ||||||
| chr8:58094433
|
A | C | 1 | a0001c0001t0003g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-325+18810A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094433 | ||||||
| chr8:58094607
|
T | C | 1 | a0001c0001t0004g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-325+18984T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094607 | ||||||
| chr8:58094609
|
G | A | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-325+18986G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094609 | ||||||
| chr8:58094616
|
A | T | 3 | a0001c0001t0001g0253a0001c0001t0001g0258a0001c0001t0002g0121 | 3 | HG00438.hp2 HG03688.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-325+18993A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094616 | ||||||
| chr8:58094628
|
A | G | 1 | a0001c0001t0003g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-325+19005A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094628 | ||||||
| chr8:58094637
|
C | T | 24 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(21): Show | 24 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.-325+19014C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094637 | ||||||
| chr8:58094644
|
G | A | 1 | a0001c0001t0011g0228 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-325+19021G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094644 | ||||||
| chr8:58094652
|
A | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+19029A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094652 | ||||||
| chr8:58094728
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-325+19105C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094728 | ||||||
| chr8:58094729
|
G | A | 23 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0158others(20): Show | 23 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-325+19106G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094729 | ||||||
| chr8:58094757
|
T | G | 71 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0084others(68): Show | 71 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.-325+19134T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094757 | ||||||
| chr8:58094824
|
G | A | 1 | a0001c0001t0023g0085 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-325+19201G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094824 | ||||||
| chr8:58094839
|
T | C | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+19216T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094839 | ||||||
| chr8:58094882
|
T | C | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+19259T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094882 | ||||||
| chr8:58094954
|
G | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0201others(5): Show | 8 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-325+19331G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094954 | ||||||
| chr8:58094962
|
C | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+19339C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58094962 | ||||||
| chr8:58095035
|
G | A | 2 | a0001c0001t0006g0219a0001c0001t0006g0220 | 2 | HG01070.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-325+19412G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095035 | ||||||
| chr8:58095092
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-325+19469G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095092 | ||||||
| chr8:58095190
|
C | T | 21 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0158others(18): Show | 21 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-325+19567C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095190 | ||||||
| chr8:58095231
|
G | A | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+19608G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095231 | ||||||
| chr8:58095296
|
G | A | 1 | a0001c0001t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-325+19673G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095296 | ||||||
| chr8:58095704
|
G | T | 2 | a0001c0001t0001g0042a0001c0001t0002g0048 | 2 | HG01517.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-325+20081G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095704 | ||||||
| chr8:58095811
|
G | A | 1 | a0001c0001t0002g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-325+20188G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095811 | ||||||
| chr8:58095823
|
C | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+20200C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095823 | ||||||
| chr8:58095917
|
A | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+20294A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095917 | ||||||
| chr8:58095931
|
T | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+20308T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58095931 | ||||||
| chr8:58096040
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-325+20417T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096040 | ||||||
| chr8:58096236
|
C | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+20613C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096236 | ||||||
| chr8:58096300
|
C | T | 13 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(10): Show | 13 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-325+20677C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096300 | ||||||
| chr8:58096301
|
G | A | 15 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+20678G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096301 | ||||||
| chr8:58096466
|
G | A | 9 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0201others(6): Show | 9 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+20843G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096466 | ||||||
| chr8:58096475
|
C | T | 1 | a0001c0001t0008g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-325+20852C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096475 | ||||||
| chr8:58096501
|
C | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(9): Show | 12 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-325+20878C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096501 | ||||||
| chr8:58096519
|
T | C | 1 | a0001c0001t0003g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-325+20896T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096519 | ||||||
| chr8:58096684
|
T | C | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+21061T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096684 | ||||||
| chr8:58096787
|
T | G | 3 | a0001c0001t0003g0076a0001c0001t0007g0157a0001c0001t0031g0159 | 3 | HG01192.hp1 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-325+21164T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096787 | ||||||
| chr8:58096819
|
A | G | 15 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+21196A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096819 | ||||||
| chr8:58096937
|
G | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+21314G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096937 | ||||||
| chr8:58096948
|
G | A | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+21325G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58096948 | ||||||
| chr8:58097000
|
G | T | 1 | a0001c0001t0006g0246 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-325+21377G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097000 | ||||||
| chr8:58097143
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-325+21520A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097143 | ||||||
| chr8:58097190
|
A | G | 25 | a0001c0001t0001g0065a0001c0001t0001g0226a0001c0001t0002g0001others(22): Show | 25 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-325+21567A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097190 | ||||||
| chr8:58097303
|
C | G | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-325+21680C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097303 | ||||||
| chr8:58097307
|
G | T | 21 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0158others(18): Show | 21 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-325+21684G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097307 | ||||||
| chr8:58097441
|
A | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+21818A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097441 | ||||||
| chr8:58097592
|
T | G | 71 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0084others(68): Show | 71 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.-325+21969T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097592 | ||||||
| chr8:58097624
|
G | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0201others(5): Show | 8 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-325+22001G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097624 | ||||||
| chr8:58097686
|
C | T | 4 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0004g0083others(1): Show | 4 | HG02056.hp1 HG02129.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.-325+22063C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097686 | ||||||
| chr8:58097819
|
C | T | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-325+22196C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097819 | ||||||
| chr8:58097953
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-325+22330C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097953 | ||||||
| chr8:58097954
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0002g0016a0001c0001t0002g0153 | 3 | HG00741.hp2 HG01168.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-325+22331G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097954 | ||||||
| chr8:58097981
|
G | A | 45 | a0001c0001t0001g0027a0001c0001t0001g0084a0001c0001t0001g0089others(42): Show | 45 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-325+22358G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097981 | ||||||
| chr8:58097998
|
C | T | 115 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(112): Show | 115 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.-325+22375C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58097998 | ||||||
| chr8:58098126
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-325+22503G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098126 | ||||||
| chr8:58098172
|
C | G | 1 | a0001c0001t0001g0203 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-325+22549C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098172 | ||||||
| chr8:58098267
|
G | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0172a0001c0001t0001g0184others(23): Show | 26 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-325+22644G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098267 | ||||||
| chr8:58098284
|
T | C | 1 | a0001c0001t0003g0092 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-325+22661T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098284 | ||||||
| chr8:58098315
|
G | A | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+22692G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098315 | ||||||
| chr8:58098361
|
T | C | 71 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0084others(68): Show | 71 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.-325+22738T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098361 | ||||||
| chr8:58098602
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-325+22979C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098602 | ||||||
| chr8:58098760
|
A | G | 115 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(112): Show | 115 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.-325+23137A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098760 | ||||||
| chr8:58098808
|
G | A | 1 | a0001c0001t0005g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-325+23185G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098808 | ||||||
| chr8:58098816
|
C | T | 14 | a0001c0001t0002g0082a0001c0001t0002g0186a0001c0001t0003g0129others(11): Show | 14 | HG01069.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-325+23193C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098816 | ||||||
| chr8:58098846
|
C | T | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-325+23223C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58098846 | ||||||
| chr8:58099049
|
C | T | 5 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+23426C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099049 | ||||||
| chr8:58099142
|
A | G | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-325+23519A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099142 | ||||||
| chr8:58099727
|
CTG | C | 32 | a0001c0001t0001g0015a0001c0001t0001g0073a0001c0001t0001g0221others(29): Show | 32 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-325+24108_-325+24 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58099727 | |||||
| chr8:58099769
|
T | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0172a0001c0001t0001g0184others(23): Show | 26 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-325+24146T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099769 | ||||||
| chr8:58099804
|
A | G | 5 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+24181A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099804 | ||||||
| chr8:58099922
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-325+24299T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099922 | ||||||
| chr8:58099935
|
C | T | 3 | a0001c0001t0002g0167a0001c0001t0003g0071a0001c0001t0003g0133 | 3 | HG02717.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+24312C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58099935 | ||||||
| chr8:58100231
|
C | G | 15 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+24608C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100231 | ||||||
| chr8:58100252
|
GA | G | 95 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0068others(92): Show | 95 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-325+24643delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58100252 | |||||
| chr8:58100321
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-325+24698C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100321 | ||||||
| chr8:58100640
|
A | G | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-325+25017A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100640 | ||||||
| chr8:58100699
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-325+25076T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100699 | ||||||
| chr8:58100746
|
T | G | 1 | a0001c0001t0021g0248 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-325+25123T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100746 | ||||||
| chr8:58100942
|
A | G | 43 | a0001c0001t0001g0027a0001c0001t0001g0089a0001c0001t0001g0094others(40): Show | 43 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-325+25319A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58100942 | ||||||
| chr8:58101077
|
T | C | 1 | a0001c0001t0003g0092 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-325+25454T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101077 | ||||||
| chr8:58101093
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-325+25470C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101093 | ||||||
| chr8:58101099
|
C | A | 1 | a0001c0001t0003g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-325+25476C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101099 | ||||||
| chr8:58101134
|
G | A | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+25511G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101134 | ||||||
| chr8:58101301
|
T | C | 5 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+25678T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101301 | ||||||
| chr8:58101303
|
G | C | 1 | a0001c0001t0008g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-325+25680G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101303 | ||||||
| chr8:58101408
|
C | G | 8 | a0001c0001t0002g0146a0001c0001t0003g0164a0001c0001t0003g0165others(5): Show | 8 | HG01891.hp1 HG02622.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-325+25785C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101408 | ||||||
| chr8:58101461
|
C | G | 20 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0158others(17): Show | 20 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-325+25838C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101461 | ||||||
| chr8:58101545
|
C | T | 1 | a0001c0001t0027g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-325+25922C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101545 | ||||||
| chr8:58101550
|
A | G | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+25927A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101550 | ||||||
| chr8:58101781
|
A | G | 25 | a0001c0001t0001g0065a0001c0001t0001g0226a0001c0001t0002g0001others(22): Show | 25 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-325+26158A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101781 | ||||||
| chr8:58101881
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-325+26258G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58101881 | ||||||
| chr8:58102028
|
A | G | 1 | a0001c0001t0006g0220 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-325+26405A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102028 | ||||||
| chr8:58102032
|
G | A | 11 | a0001c0001t0001g0158a0001c0001t0002g0162a0001c0001t0002g0163others(8): Show | 11 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-325+26409G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102032 | ||||||
| chr8:58102184
|
C | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-325+26561C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102184 | ||||||
| chr8:58102318
|
G | T | 2 | a0001c0001t0005g0139a0001c0001t0010g0294 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-325+26695G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102318 | ||||||
| chr8:58102505
|
C | T | 1 | a0001c0001t0006g0025 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-325+26882C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102505 | ||||||
| chr8:58102512
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-325+26889C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102512 | ||||||
| chr8:58102534
|
C | T | 51 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0073others(48): Show | 51 | HG00621.hp2 HG00673.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.-325+26911C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102534 | ||||||
| chr8:58102587
|
C | T | 1 | a0001c0001t0003g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-325+26964C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102587 | ||||||
| chr8:58102638
|
C | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0172a0001c0001t0001g0184others(23): Show | 26 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-325+27015C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102638 | ||||||
| chr8:58102701
|
C | A | 1 | a0001c0001t0004g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-325+27078C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102701 | ||||||
| chr8:58102944
|
C | T | 46 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0172others(43): Show | 46 | HG00735.hp1 HG01069.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.-325+27321C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58102944 | ||||||
| chr8:58103002
|
G | GA | 58 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.-325+27401dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | |||||
| chr8:58103002
|
G | GAA | 6 | a0001c0001t0001g0089a0001c0001t0001g0201a0001c0001t0001g0252others(3): Show | 6 | HG02056.hp1 HG03942.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-325+27400_-325+27 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | |||||
| chr8:58103002
|
GA | G | 23 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0060others(20): Show | 23 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-325+27401delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | |||||
| chr8:58103002
|
GAA | G | 13 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+27400_-325+27 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | |||||
| chr8:58103002
|
GAAAAAAA others(1): Show |
G | 62 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0067others(59): Show | 62 | HG00438.hp2 HG00609.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.-325+27394_-325+27 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | |||||
| chr8:58103002
|
GAAAAAAA others(2): Show |
G | 9 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0134others(6): Show | 9 | HG01069.hp1 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+27393_-325+27 others(15): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103002 | |||||
| chr8:58103218
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-325+27595G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103218 | ||||||
| chr8:58103321
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-325+27698C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103321 | ||||||
| chr8:58103360
|
C | T | 15 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+27737C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103360 | ||||||
| chr8:58103375
|
A | G | 20 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0158others(17): Show | 20 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-325+27752A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103375 | ||||||
| chr8:58103580
|
G | A | 3 | a0001c0001t0002g0082a0001c0001t0004g0063a0001c0001t0004g0279 | 3 | HG02735.hp2 NA18990.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-325+27957G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103580 | ||||||
| chr8:58103755
|
C | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0201others(5): Show | 8 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-325+28132C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58103755 | ||||||
| chr8:58103819
|
C | CT | 14 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(11): Show | 14 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.-325+28203dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58103819 | |||||
| chr8:58104179
|
G | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+28556G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104179 | ||||||
| chr8:58104189
|
G | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-325+28566G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104189 | ||||||
| chr8:58104480
|
T | G | 5 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+28857T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104480 | ||||||
| chr8:58104512
|
A | G | 3 | a0001c0001t0003g0142a0001c0001t0009g0140a0001c0001t0022g0174 | 3 | HG00741.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-325+28889A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104512 | ||||||
| chr8:58104749
|
C | T | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+29126C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104749 | ||||||
| chr8:58104915
|
C | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(257): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.-325+29292C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104915 | ||||||
| chr8:58104958
|
A | G | 20 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0158others(17): Show | 20 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-325+29335A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58104958 | ||||||
| chr8:58104962
|
G | GA | 109 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(106): Show | 109 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.-325+29354dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58104962 | |||||
| chr8:58104962
|
G | GAA | 6 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0057others(3): Show | 6 | HG02056.hp1 HG02129.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-325+29353_-325+29 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58104962 | |||||
| chr8:58104999
|
C | CT | 9 | a0001c0001t0001g0073a0001c0001t0002g0152a0001c0001t0003g0074others(6): Show | 9 | HG01943.hp1 HG02145.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+29390dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58104999 | |||||
| chr8:58104999
|
CT | C | 8 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0057others(5): Show | 8 | HG01070.hp1 HG02056.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.-325+29390delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58104999 | |||||
| chr8:58105556
|
A | AT | 116 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(113): Show | 116 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-325+29963dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | |||||
| chr8:58105556
|
A | ATT | 13 | a0001c0001t0001g0043a0001c0001t0001g0230a0001c0001t0002g0152others(10): Show | 13 | HG01071.hp2 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-325+29962_-325+29 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | |||||
| chr8:58105556
|
ATT | A | 9 | a0001c0001t0002g0167a0001c0001t0002g0297a0001c0001t0003g0071others(6): Show | 9 | HG01433.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-325+29962_-325+29 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | |||||
| chr8:58105556
|
ATTT | A | 17 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0104others(14): Show | 17 | HG00438.hp2 HG00609.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-325+29961_-325+29 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | |||||
| chr8:58105556
|
ATTTT | A | 24 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0253others(21): Show | 24 | HG01070.hp1 HG01081.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.-325+29960_-325+29 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | |||||
| chr8:58105556
|
ATTTTTTT | A | 13 | a0001c0001t0002g0186a0001c0001t0003g0129a0001c0001t0003g0134others(10): Show | 13 | HG00741.hp1 HG01069.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-325+29957_-325+29 others(13): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | |||||
| chr8:58105556
|
ATTTTTTT others(1): Show |
A | 12 | a0001c0001t0001g0006a0001c0001t0001g0172a0001c0001t0001g0184others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-325+29956_-325+29 others(14): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58105556 | |||||
| chr8:58105816
|
C | T | 1 | a0001c0001t0025g0009 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-325+30193C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58105816 | ||||||
| chr8:58105850
|
A | G | 114 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(111): Show | 114 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.-325+30227A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58105850 | ||||||
| chr8:58105949
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-325+30326C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58105949 | ||||||
| chr8:58106015
|
A | T | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+30392A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106015 | ||||||
| chr8:58106078
|
C | T | 5 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+30455C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106078 | ||||||
| chr8:58106085
|
T | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0172a0001c0001t0001g0184others(23): Show | 26 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-325+30462T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106085 | ||||||
| chr8:58106093
|
A | G | 15 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-325+30470A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106093 | ||||||
| chr8:58106115
|
G | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+30492G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106115 | ||||||
| chr8:58106147
|
G | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+30524G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106147 | ||||||
| chr8:58106409
|
A | G | 1 | a0001c0001t0002g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-325+30786A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106409 | ||||||
| chr8:58106565
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-325+30942A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106565 | ||||||
| chr8:58106625
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-325+31002G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106625 | ||||||
| chr8:58106641
|
T | G | 5 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0057others(2): Show | 5 | HG02056.hp1 HG02129.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+31018T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106641 | ||||||
| chr8:58106650
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0003g0251 | 2 | HG02080.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.-325+31027A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106650 | ||||||
| chr8:58106674
|
AAGGAGTT others(3): Show |
A | 1 | a0001c0001t0001g0203 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-325+31054_-325+31 others(16): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58106674 | |||||
| chr8:58106832
|
A | C | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-325+31209A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106832 | ||||||
| chr8:58106991
|
G | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0149a0001c0001t0001g0154others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-325+31368G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58106991 | ||||||
| chr8:58107013
|
C | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0094others(44): Show | 47 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.-325+31390C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107013 | ||||||
| chr8:58107077
|
T | TA | 50 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0068others(47): Show | 50 | HG00438.hp2 HG00609.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.-325+31465dupA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58107077 | |||||
| chr8:58107077
|
TA | T | 18 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0152others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-325+31465delA | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58107077 | |||||
| chr8:58107111
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-325+31488C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107111 | ||||||
| chr8:58107221
|
A | G | 1 | a0001c0001t0004g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-325+31598A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107221 | ||||||
| chr8:58107340
|
G | T | 110 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(107): Show | 110 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.-325+31717G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107340 | ||||||
| chr8:58107409
|
C | G | 1 | a0001c0001t0002g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-325+31786C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107409 | ||||||
| chr8:58107535
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-325+31912G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107535 | ||||||
| chr8:58107610
|
G | A | 114 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(111): Show | 114 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.-325+31987G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107610 | ||||||
| chr8:58107709
|
G | T | 49 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0094others(46): Show | 49 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.-325+32086G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107709 | ||||||
| chr8:58107846
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-325+32223C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107846 | ||||||
| chr8:58107862
|
G | A | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+32239G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58107862 | ||||||
| chr8:58108003
|
G | A | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-325+32380G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108003 | ||||||
| chr8:58108009
|
A | G | 1 | a0001c0001t0003g0049 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-325+32386A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108009 | ||||||
| chr8:58108017
|
T | A | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-325+32394T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108017 | ||||||
| chr8:58108232
|
G | A | 1 | a0001c0001t0003g0234 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-325+32609G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108232 | ||||||
| chr8:58108542
|
C | T | 8 | a0001c0001t0001g0158a0001c0001t0002g0162a0001c0001t0002g0163others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-325+32919C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108542 | ||||||
| chr8:58108770
|
G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-325+33147G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108770 | ||||||
| chr8:58108847
|
C | T | 27 | a0001c0001t0001g0006a0001c0001t0001g0172a0001c0001t0001g0184others(24): Show | 27 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-325+33224C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108847 | ||||||
| chr8:58108889
|
G | T | 36 | a0001c0001t0001g0015a0001c0001t0001g0073a0001c0001t0001g0089others(33): Show | 36 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.-325+33266G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108889 | ||||||
| chr8:58108963
|
T | A | 2 | a0001c0001t0003g0198a0001c0001t0007g0300 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-325+33340T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58108963 | ||||||
| chr8:58109089
|
G | A | 98 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(95): Show | 98 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.-325+33466G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109089 | ||||||
| chr8:58109108
|
C | T | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-325+33485C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109108 | ||||||
| chr8:58109218
|
A | G | 11 | a0001c0001t0001g0040a0001c0001t0001g0098a0001c0001t0001g0103others(8): Show | 11 | HG00544.hp1 HG02027.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.-325+33595A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109218 | ||||||
| chr8:58109286
|
G | A | 21 | a0001c0001t0001g0015a0001c0001t0001g0221a0001c0001t0001g0285others(18): Show | 21 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.-325+33663G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109286 | ||||||
| chr8:58109763
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0002g0032a0001c0001t0003g0034others(2): Show | 5 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-325+34140G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109763 | ||||||
| chr8:58109957
|
G | A | 20 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0158others(17): Show | 20 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-325+34334G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58109957 | ||||||
| chr8:58110062
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-325+34439A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110062 | ||||||
| chr8:58110136
|
A | C | 1 | a0001c0001t0010g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-325+34513A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110136 | ||||||
| chr8:58110265
|
G | T | 2 | a0001c0001t0007g0135a0001c0001t0007g0197 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-325+34642G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110265 | ||||||
| chr8:58110453
|
C | G | 1 | a0001c0001t0003g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-325+34830C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110453 | ||||||
| chr8:58110679
|
A | G | 1 | a0001c0001t0006g0245 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-325+35056A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110679 | ||||||
| chr8:58110810
|
T | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-35097T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110810 | ||||||
| chr8:58110925
|
C | G | 21 | a0001c0001t0001g0015a0001c0001t0001g0221a0001c0001t0001g0285others(18): Show | 21 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.-324-34982C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58110925 | ||||||
| chr8:58111099
|
G | A | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-324-34808G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111099 | ||||||
| chr8:58111163
|
C | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-34744C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111163 | ||||||
| chr8:58111190
|
C | T | 1 | a0001c0001t0026g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-324-34717C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111190 | ||||||
| chr8:58111280
|
G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-34627G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111280 | ||||||
| chr8:58111369
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-324-34538G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111369 | ||||||
| chr8:58111410
|
G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-34497G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111410 | ||||||
| chr8:58111538
|
A | C | 1 | a0001c0001t0002g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-324-34369A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111538 | ||||||
| chr8:58111644
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-324-34263A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111644 | ||||||
| chr8:58111751
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-324-34156C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111751 | ||||||
| chr8:58111771
|
T | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-324-34136T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111771 | ||||||
| chr8:58111922
|
G | C | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-324-33985G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58111922 | ||||||
| chr8:58112027
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-324-33880T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112027 | ||||||
| chr8:58112154
|
T | C | 115 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(112): Show | 115 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.-324-33753T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112154 | ||||||
| chr8:58112213
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-324-33694C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112213 | ||||||
| chr8:58112244
|
G | A | 21 | a0001c0001t0001g0015a0001c0001t0001g0221a0001c0001t0001g0285others(18): Show | 21 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.-324-33663G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112244 | ||||||
| chr8:58112278
|
A | C | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-33629A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112278 | ||||||
| chr8:58112279
|
A | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-33628A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112279 | ||||||
| chr8:58112281
|
A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-33626A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112281 | ||||||
| chr8:58112282
|
T | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-33625T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112282 | ||||||
| chr8:58112299
|
A | G | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-33608A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112299 | ||||||
| chr8:58112433
|
G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-33474G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112433 | ||||||
| chr8:58112555
|
T | C | 22 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0158others(19): Show | 22 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.-324-33352T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112555 | ||||||
| chr8:58112756
|
G | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-33151G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112756 | ||||||
| chr8:58112837
|
G | A | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-324-33070G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112837 | ||||||
| chr8:58112885
|
C | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-33022C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58112885 | ||||||
| chr8:58113088
|
TG | T | 96 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(93): Show | 96 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.-324-32810delG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58113088 | |||||
| chr8:58113502
|
C | T | 1 | a0001c0001t0005g0274 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-324-32405C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113502 | ||||||
| chr8:58113636
|
A | G | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-324-32271A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113636 | ||||||
| chr8:58113759
|
C | T | 36 | a0001c0001t0001g0015a0001c0001t0001g0073a0001c0001t0001g0089others(33): Show | 36 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.-324-32148C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113759 | ||||||
| chr8:58113814
|
T | G | 299 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-324-32093T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113814 | ||||||
| chr8:58113880
|
A | G | 4 | a0001c0001t0002g0031a0001c0001t0002g0036a0001c0001t0002g0126others(1): Show | 4 | HG00280.hp1 HG01433.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-324-32027A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113880 | ||||||
| chr8:58113935
|
G | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0258a0001c0001t0002g0121 | 3 | HG00438.hp2 HG03688.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-324-31972G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113935 | ||||||
| chr8:58113961
|
A | T | 3 | a0001c0001t0002g0128a0001c0001t0003g0143a0001c0001t0007g0144 | 3 | HG03130.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-324-31946A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58113961 | ||||||
| chr8:58114283
|
C | T | 34 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0068others(31): Show | 34 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.-324-31624C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114283 | ||||||
| chr8:58114301
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0002g0012 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-324-31606A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114301 | ||||||
| chr8:58114383
|
G | A | 37 | a0001c0001t0001g0015a0001c0001t0001g0073a0001c0001t0001g0089others(34): Show | 37 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.-324-31524G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114383 | ||||||
| chr8:58114578
|
C | T | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-31329C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114578 | ||||||
| chr8:58114615
|
G | A | 5 | a0001c0001t0001g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-324-31292G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114615 | ||||||
| chr8:58114706
|
G | A | 3 | a0001c0001t0003g0142a0001c0001t0009g0140a0001c0001t0022g0174 | 3 | HG00741.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-324-31201G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114706 | ||||||
| chr8:58114709
|
A | G | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-324-31198A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114709 | ||||||
| chr8:58114797
|
G | T | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-324-31110G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114797 | ||||||
| chr8:58114919
|
G | A | 2 | a0001c0001t0002g0126a0001c0001t0004g0125 | 2 | HG00280.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-324-30988G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58114919 | ||||||
| chr8:58115007
|
GTT | G | 16 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0185others(13): Show | 16 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-324-30887_-324-30 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58115007 | |||||
| chr8:58115007
|
GTTT | G | 102 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(99): Show | 102 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.-324-30888_-324-30 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58115007 | |||||
| chr8:58115294
|
T | C | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-324-30613T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115294 | ||||||
| chr8:58115361
|
A | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-30546A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115361 | ||||||
| chr8:58115379
|
A | AT | 47 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0001g0158others(44): Show | 47 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.-324-30520dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58115379 | |||||
| chr8:58115493
|
AG | A | 6 | a0001c0001t0002g0291a0001c0001t0003g0142a0001c0001t0007g0090others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-324-30413delG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115493 | ||||||
| chr8:58115672
|
C | A | 42 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0046others(39): Show | 42 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-324-30235C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115672 | ||||||
| chr8:58115755
|
G | T | 1 | a0001c0001t0010g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-324-30152G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115755 | ||||||
| chr8:58115822
|
C | G | 1 | a0001c0001t0008g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-324-30085C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115822 | ||||||
| chr8:58115974
|
C | G | 4 | a0001c0001t0001g0038a0001c0001t0003g0034a0001c0001t0006g0051others(1): Show | 4 | HG01074.hp1 HG01081.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-324-29933C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58115974 | ||||||
| chr8:58116035
|
T | C | 3 | a0001c0001t0004g0260a0001c0001t0005g0139a0001c0001t0010g0294 | 3 | HG02965.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-324-29872T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116035 | ||||||
| chr8:58116092
|
G | A | 24 | a0001c0001t0001g0015a0001c0001t0001g0089a0001c0001t0001g0221others(21): Show | 24 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-324-29815G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116092 | ||||||
| chr8:58116104
|
A | G | 1 | a0001c0001t0004g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-324-29803A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116104 | ||||||
| chr8:58116112
|
A | G | 2 | a0001c0001t0002g0297a0001c0001t0031g0159 | 2 | HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-324-29795A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116112 | ||||||
| chr8:58116135
|
A | G | 5 | a0001c0001t0001g0285a0001c0001t0002g0059a0001c0001t0002g0190others(2): Show | 5 | NA18948.hp2 NA18970.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-324-29772A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116135 | ||||||
| chr8:58116179
|
A | G | 24 | a0001c0001t0001g0015a0001c0001t0001g0089a0001c0001t0001g0221others(21): Show | 24 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-324-29728A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116179 | ||||||
| chr8:58116257
|
T | C | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-324-29650T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116257 | ||||||
| chr8:58116301
|
G | A | 66 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0045others(63): Show | 66 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-324-29606G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116301 | ||||||
| chr8:58116627
|
G | A | 42 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0046others(39): Show | 42 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-324-29280G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116627 | ||||||
| chr8:58116840
|
G | A | 1 | a0001c0001t0004g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-324-29067G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116840 | ||||||
| chr8:58116939
|
A | G | 2 | a0001c0001t0007g0135a0001c0001t0007g0197 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-324-28968A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58116939 | ||||||
| chr8:58117035
|
G | A | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-324-28872G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117035 | ||||||
| chr8:58117047
|
G | A | 1 | a0001c0001t0007g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-324-28860G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117047 | ||||||
| chr8:58117076
|
T | A | 48 | a0001c0001t0001g0073a0001c0001t0001g0158a0001c0001t0001g0172others(45): Show | 48 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.-324-28831T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117076 | ||||||
| chr8:58117164
|
G | A | 118 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0045others(115): Show | 118 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.-324-28743G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117164 | ||||||
| chr8:58117310
|
T | G | 5 | a0001c0001t0001g0172a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-324-28597T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117310 | ||||||
| chr8:58117524
|
T | C | 3 | a0001c0001t0004g0260a0001c0001t0005g0139a0001c0001t0010g0294 | 3 | HG02965.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-324-28383T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117524 | ||||||
| chr8:58117566
|
G | A | 2 | a0001c0001t0002g0297a0001c0001t0031g0159 | 2 | HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-324-28341G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117566 | ||||||
| chr8:58117705
|
C | T | 42 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0046others(39): Show | 42 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-324-28202C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117705 | ||||||
| chr8:58117734
|
C | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0111a0001c0001t0001g0118others(2): Show | 5 | NA18942.hp2 NA18950.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-324-28173C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58117734 | ||||||
| chr8:58118011
|
C | A | 2 | a0001c0001t0002g0297a0001c0001t0031g0159 | 2 | HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-324-27896C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118011 | ||||||
| chr8:58118018
|
A | G | 24 | a0001c0001t0001g0073a0001c0001t0001g0158a0001c0001t0002g0128others(21): Show | 24 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.-324-27889A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118018 | ||||||
| chr8:58118204
|
T | C | 157 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(154): Show | 157 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.-324-27703T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118204 | ||||||
| chr8:58118339
|
T | A | 30 | a0001c0001t0001g0015a0001c0001t0001g0089a0001c0001t0001g0221others(27): Show | 30 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-324-27568T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118339 | ||||||
| chr8:58118443
|
G | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0094others(32): Show | 35 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-324-27464G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118443 | ||||||
| chr8:58118537
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0154 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-324-27370T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118537 | ||||||
| chr8:58118553
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-324-27354A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118553 | ||||||
| chr8:58118646
|
G | T | 8 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0003g0295others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-27261G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118646 | ||||||
| chr8:58118663
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-324-27244C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118663 | ||||||
| chr8:58118881
|
C | T | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-324-27026C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118881 | ||||||
| chr8:58118934
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0094others(26): Show | 29 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.-324-26973C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58118934 | ||||||
| chr8:58119148
|
C | A | 1 | a0001c0001t0004g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-324-26759C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119148 | ||||||
| chr8:58119163
|
T | C | 1 | a0001c0001t0008g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-324-26744T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119163 | ||||||
| chr8:58119336
|
G | A | 16 | a0001c0001t0001g0047a0001c0001t0001g0098a0001c0001t0001g0110others(13): Show | 16 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.-324-26571G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119336 | ||||||
| chr8:58119397
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-324-26510C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119397 | ||||||
| chr8:58119488
|
A | G | 3 | a0001c0001t0007g0090a0001c0001t0007g0130a0001c0001t0007g0131 | 3 | HG01891.hp2 HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-324-26419A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119488 | ||||||
| chr8:58119812
|
G | A | 30 | a0001c0001t0001g0015a0001c0001t0001g0089a0001c0001t0001g0221others(27): Show | 30 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-324-26095G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119812 | ||||||
| chr8:58119902
|
T | G | 2 | a0001c0001t0002g0024a0001c0001t0003g0280 | 2 | HG00621.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.-324-26005T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119902 | ||||||
| chr8:58119996
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-324-25911G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58119996 | ||||||
| chr8:58120013
|
C | T | 121 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0045others(118): Show | 121 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.-324-25894C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120013 | ||||||
| chr8:58120042
|
C | T | 42 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0046others(39): Show | 42 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-324-25865C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120042 | ||||||
| chr8:58120112
|
A | G | 1 | a0001c0001t0002g0059 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-324-25795A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120112 | ||||||
| chr8:58120324
|
A | G | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-324-25583A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120324 | ||||||
| chr8:58120390
|
TC | T | 6 | a0001c0001t0002g0291a0001c0001t0003g0142a0001c0001t0007g0090others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-324-25515delC | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58120390 | |||||
| chr8:58120444
|
G | A | 1 | a0001c0001t0006g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-324-25463G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120444 | ||||||
| chr8:58120457
|
A | G | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-25450A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120457 | ||||||
| chr8:58120621
|
G | C | 72 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0045others(69): Show | 72 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.-324-25286G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120621 | ||||||
| chr8:58120656
|
G | A | 2 | a0001c0001t0002g0167a0001c0001t0003g0133 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-324-25251G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120656 | ||||||
| chr8:58120662
|
G | T | 4 | a0001c0001t0003g0129a0001c0001t0003g0134a0001c0001t0005g0161others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-324-25245G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120662 | ||||||
| chr8:58120741
|
A | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0094others(26): Show | 29 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.-324-25166A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120741 | ||||||
| chr8:58120833
|
C | T | 121 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0045others(118): Show | 121 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.-324-25074C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120833 | ||||||
| chr8:58120914
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-324-24993G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58120914 | ||||||
| chr8:58121167
|
G | A | 1 | a0001c0001t0007g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-324-24740G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121167 | ||||||
| chr8:58121183
|
G | A | 44 | a0001c0001t0001g0073a0001c0001t0001g0158a0001c0001t0001g0172others(41): Show | 44 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-324-24724G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121183 | ||||||
| chr8:58121284
|
A | G | 30 | a0001c0001t0001g0015a0001c0001t0001g0089a0001c0001t0001g0221others(27): Show | 30 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-324-24623A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121284 | ||||||
| chr8:58121364
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-324-24543C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121364 | ||||||
| chr8:58121433
|
A | G | 2 | a0001c0001t0003g0295a0001c0001t0030g0035 | 2 | HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-324-24474A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121433 | ||||||
| chr8:58121629
|
A | G | 157 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(154): Show | 157 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.-324-24278A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121629 | ||||||
| chr8:58121704
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-324-24203G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121704 | ||||||
| chr8:58121706
|
C | T | 1 | a0001c0001t0021g0248 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-324-24201C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121706 | ||||||
| chr8:58121805
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0094others(25): Show | 28 | HG00621.hp2 HG00673.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-324-24102C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121805 | ||||||
| chr8:58121910
|
G | A | 3 | a0001c0001t0004g0260a0001c0001t0005g0139a0001c0001t0010g0294 | 3 | HG02965.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-324-23997G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58121910 | ||||||
| chr8:58122069
|
T | A | 3 | a0001c0001t0004g0260a0001c0001t0005g0139a0001c0001t0010g0294 | 3 | HG02965.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-324-23838T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58122069 | ||||||
| chr8:58122093
|
G | C | 1 | a0001c0001t0003g0049 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-324-23814G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58122093 | ||||||
| chr8:58122343
|
G | A | 1 | a0001c0001t0007g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-324-23564G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58122343 | ||||||
| chr8:58122446
|
T | C | 43 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0046others(40): Show | 43 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-324-23461T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58122446 | ||||||
| chr8:58123140
|
G | A | 8 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0003g0295others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-22767G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58123140 | ||||||
| chr8:58123300
|
G | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0256a0001c0001t0001g0267others(1): Show | 4 | HG00733.hp1 HG00735.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-324-22607G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58123300 | ||||||
| chr8:58123840
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-324-22067C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58123840 | ||||||
| chr8:58123918
|
G | A | 1 | a0001c0001t0002g0059 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-324-21989G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58123918 | ||||||
| chr8:58124011
|
C | A | 72 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0045others(69): Show | 72 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.-324-21896C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124011 | ||||||
| chr8:58124069
|
G | C | 1 | a0001c0001t0002g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-324-21838G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124069 | ||||||
| chr8:58124134
|
A | G | 2 | a0001c0001t0003g0142a0001c0001t0009g0140 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-324-21773A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124134 | ||||||
| chr8:58124309
|
C | T | 3 | a0001c0001t0004g0260a0001c0001t0005g0139a0001c0001t0010g0294 | 3 | HG02965.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-324-21598C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124309 | ||||||
| chr8:58124359
|
G | C | 104 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0045others(101): Show | 104 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.-324-21548G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124359 | ||||||
| chr8:58124476
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-324-21431C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124476 | ||||||
| chr8:58124588
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0118 | 2 | NA18942.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-324-21319A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124588 | ||||||
| chr8:58124629
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-324-21278T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124629 | ||||||
| chr8:58124658
|
T | A | 1 | a0001c0001t0001g0042 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-324-21249T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124658 | ||||||
| chr8:58124703
|
C | T | 299 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-324-21204C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124703 | ||||||
| chr8:58124728
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0025a0001c0001t0006g0218 | 3 | HG01081.hp1 HG01255.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-324-21179C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124728 | ||||||
| chr8:58124764
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(241): Show | 244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-324-21143A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124764 | ||||||
| chr8:58124824
|
G | A | 16 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0185others(13): Show | 16 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-324-21083G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124824 | ||||||
| chr8:58124891
|
G | A | 45 | a0001c0001t0001g0073a0001c0001t0001g0158a0001c0001t0001g0172others(42): Show | 45 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-324-21016G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124891 | ||||||
| chr8:58124952
|
A | T | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-324-20955A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58124952 | ||||||
| chr8:58125213
|
T | A | 1 | a0001c0001t0007g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-324-20694T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125213 | ||||||
| chr8:58125305
|
G | A | 1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-324-20602G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125305 | ||||||
| chr8:58125397
|
C | A | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-20510C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125397 | ||||||
| chr8:58125430
|
G | A | 1 | a0001c0001t0036g0132 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-324-20477G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125430 | ||||||
| chr8:58125460
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-324-20447G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125460 | ||||||
| chr8:58125574
|
T | C | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-324-20333T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125574 | ||||||
| chr8:58125712
|
C | T | 9 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0003g0295others(6): Show | 9 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.-324-20195C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125712 | ||||||
| chr8:58125743
|
T | G | 1 | a0001c0001t0003g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-324-20164T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125743 | ||||||
| chr8:58125808
|
G | C | 154 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(151): Show | 154 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.-324-20099G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125808 | ||||||
| chr8:58125902
|
G | A | 1 | a0001c0001t0003g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-324-20005G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58125902 | ||||||
| chr8:58125917
|
CTA | C | 149 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(146): Show | 149 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.-324-19986_-324-19 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58125917 | |||||
| chr8:58126236
|
CT | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0221a0001c0001t0002g0078others(18): Show | 21 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.-324-19667delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58126236 | |||||
| chr8:58126438
|
G | C | 1 | a0001c0001t0003g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-324-19469G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58126438 | ||||||
| chr8:58126738
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-324-19169A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58126738 | ||||||
| chr8:58126793
|
G | A | 1 | a0001c0001t0004g0232 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-324-19114G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58126793 | ||||||
| chr8:58126888
|
A | C | 1 | a0001c0001t0005g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-324-19019A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58126888 | ||||||
| chr8:58127496
|
GCTT | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0073others(72): Show | 75 | HG00621.hp2 HG00673.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-324-18404_-324-18 others(9): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58127496 | |||||
| chr8:58128035
|
G | A | 6 | a0001c0001t0002g0291a0001c0001t0003g0142a0001c0001t0007g0090others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-324-17872G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58128035 | ||||||
| chr8:58128464
|
C | T | 7 | a0001c0001t0001g0201a0001c0001t0002g0291a0001c0001t0003g0142others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-324-17443C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58128464 | ||||||
| chr8:58128777
|
A | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0094others(26): Show | 29 | HG00621.hp2 HG00673.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.-324-17130A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58128777 | ||||||
| chr8:58128915
|
C | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0073others(72): Show | 75 | HG00621.hp2 HG00673.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-324-16992C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58128915 | ||||||
| chr8:58129017
|
C | T | 19 | a0001c0001t0001g0015a0001c0001t0001g0221a0001c0001t0002g0078others(16): Show | 19 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-324-16890C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129017 | ||||||
| chr8:58129025
|
G | C | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-16882G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129025 | ||||||
| chr8:58129463
|
C | T | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-324-16444C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129463 | ||||||
| chr8:58129464
|
G | A | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-16443G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129464 | ||||||
| chr8:58129499
|
T | C | 1 | a0001c0001t0005g0028 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-324-16408T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129499 | ||||||
| chr8:58129559
|
G | C | 1 | a0001c0001t0008g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-324-16348G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129559 | ||||||
| chr8:58129720
|
T | C | 1 | a0001c0001t0003g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-324-16187T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129720 | ||||||
| chr8:58129803
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-324-16104G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129803 | ||||||
| chr8:58129893
|
C | G | 1 | a0001c0001t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-324-16014C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129893 | ||||||
| chr8:58129976
|
G | A | 1 | a0001c0001t0007g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-324-15931G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58129976 | ||||||
| chr8:58130011
|
A | G | 1 | a0001c0001t0002g0240 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-324-15896A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130011 | ||||||
| chr8:58130096
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-324-15811C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130096 | ||||||
| chr8:58130197
|
A | G | 48 | a0001c0001t0001g0089a0001c0001t0001g0158a0001c0001t0001g0172others(45): Show | 48 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-324-15710A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130197 | ||||||
| chr8:58130504
|
T | C | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-15403T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130504 | ||||||
| chr8:58130571
|
A | G | 21 | a0001c0001t0001g0158a0001c0001t0001g0201a0001c0001t0002g0128others(18): Show | 21 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-324-15336A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130571 | ||||||
| chr8:58130639
|
C | T | 1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-324-15268C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130639 | ||||||
| chr8:58130741
|
A | ATC | 141 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0045others(138): Show | 141 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.-324-15164_-324-15 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58130741 | |||||
| chr8:58130784
|
C | T | 15 | a0001c0001t0001g0172a0001c0001t0001g0261a0001c0001t0001g0262others(12): Show | 15 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-324-15123C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130784 | ||||||
| chr8:58130818
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-324-15089C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130818 | ||||||
| chr8:58130870
|
G | A | 12 | a0001c0001t0003g0076a0001c0001t0003g0138a0001c0001t0003g0141others(9): Show | 12 | HG01261.hp1 HG01496.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-324-15037G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130870 | ||||||
| chr8:58130928
|
G | A | 7 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0227others(4): Show | 7 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-324-14979G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130928 | ||||||
| chr8:58130930
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0056others(3): Show | 6 | HG00738.hp1 HG02056.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.-324-14977G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58130930 | ||||||
| chr8:58131361
|
T | C | 1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-324-14546T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131361 | ||||||
| chr8:58131433
|
G | C | 1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-324-14474G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131433 | ||||||
| chr8:58131443
|
T | G | 27 | a0001c0001t0001g0089a0001c0001t0001g0172a0001c0001t0001g0252others(24): Show | 27 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-324-14464T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131443 | ||||||
| chr8:58131480
|
G | A | 69 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0067others(66): Show | 69 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.-324-14427G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131480 | ||||||
| chr8:58131531
|
A | G | 1 | a0001c0001t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-324-14376A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131531 | ||||||
| chr8:58131533
|
C | A | 7 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0227others(4): Show | 7 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-324-14374C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131533 | ||||||
| chr8:58131608
|
A | C | 8 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0136others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-14299A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131608 | ||||||
| chr8:58131878
|
C | G | 5 | a0001c0001t0001g0038a0001c0001t0003g0034a0001c0001t0006g0051others(2): Show | 5 | HG00323.hp1 HG01074.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-324-14029C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131878 | ||||||
| chr8:58131932
|
A | C | 1 | a0001c0001t0003g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-324-13975A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131932 | ||||||
| chr8:58131951
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0007g0300 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-324-13956G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58131951 | ||||||
| chr8:58132121
|
C | CCAAA | 161 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(158): Show | 161 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(158): Show |
intron_variant | MODIFIER | c.-324-13785_-324-13 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58132121 | |||||
| chr8:58132151
|
T | C | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-13756T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132151 | ||||||
| chr8:58132159
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-324-13748A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132159 | ||||||
| chr8:58132278
|
G | A | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-13629G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132278 | ||||||
| chr8:58132312
|
C | T | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-324-13595C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132312 | ||||||
| chr8:58132397
|
A | AT | 67 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0067others(64): Show | 67 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-324-13499dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58132397 | |||||
| chr8:58132642
|
A | G | 3 | a0001c0001t0007g0090a0001c0001t0007g0130a0001c0001t0007g0131 | 3 | HG01891.hp2 HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-324-13265A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132642 | ||||||
| chr8:58132780
|
C | T | 3 | a0001c0001t0002g0030a0001c0001t0002g0032a0001c0001t0002g0087 | 3 | HG00642.hp1 HG01074.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.-324-13127C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132780 | ||||||
| chr8:58132950
|
A | G | 69 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0067others(66): Show | 69 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.-324-12957A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132950 | ||||||
| chr8:58132988
|
G | A | 8 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0136others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-12919G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58132988 | ||||||
| chr8:58133132
|
T | TGATCAGA others(313): Show |
1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-12760_-324-12 others(326): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58133132 | |||||
| chr8:58133205
|
G | GT | 117 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(114): Show | 117 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.-324-12688dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58133205 | |||||
| chr8:58133205
|
G | GTT | 6 | a0001c0001t0002g0297a0001c0001t0003g0129a0001c0001t0003g0134others(3): Show | 6 | HG01192.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-324-12689_-324-12 others(8): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58133205 | |||||
| chr8:58133391
|
C | T | 39 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0067others(36): Show | 39 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-324-12516C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133391 | ||||||
| chr8:58133392
|
G | A | 1 | a0001c0001t0010g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-324-12515G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133392 | ||||||
| chr8:58133440
|
G | A | 1 | a0001c0001t0003g0187 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-324-12467G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133440 | ||||||
| chr8:58133469
|
G | T | 27 | a0001c0001t0001g0073a0001c0001t0001g0172a0001c0001t0001g0201others(24): Show | 27 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-324-12438G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133469 | ||||||
| chr8:58133487
|
C | T | 1 | a0001c0001t0007g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-324-12420C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133487 | ||||||
| chr8:58133492
|
A | G | 1 | a0001c0001t0003g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-324-12415A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133492 | ||||||
| chr8:58133504
|
AG | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0258a0001c0001t0002g0121 | 3 | HG00438.hp2 HG03688.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-324-12401delG | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58133504 | |||||
| chr8:58133630
|
C | T | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-12277C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133630 | ||||||
| chr8:58133657
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-324-12250C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133657 | ||||||
| chr8:58133710
|
GCCTGT | G | 72 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0067others(69): Show | 72 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.-324-12196_-324-12 others(11): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133710 | ||||||
| chr8:58133718
|
T | A | 72 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0067others(69): Show | 72 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.-324-12189T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133718 | ||||||
| chr8:58133733
|
C | T | 1 | a0001c0001t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-324-12174C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133733 | ||||||
| chr8:58133758
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-324-12149C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133758 | ||||||
| chr8:58133932
|
A | G | 8 | a0001c0001t0001g0089a0001c0001t0001g0252a0001c0001t0002g0136others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-11975A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58133932 | ||||||
| chr8:58134082
|
ATTAT | A | 20 | a0001c0001t0001g0015a0001c0001t0001g0221a0001c0001t0002g0078others(17): Show | 20 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-324-11820_-324-11 others(10): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58134082 | |||||
| chr8:58134234
|
A | G | 1 | a0001c0001t0002g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-324-11673A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134234 | ||||||
| chr8:58134307
|
C | A | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-11600C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134307 | ||||||
| chr8:58134313
|
C | T | 2 | a0001c0001t0003g0235a0001c0001t0017g0119 | 2 | NA18952.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-324-11594C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134313 | ||||||
| chr8:58134503
|
G | C | 4 | a0001c0001t0002g0117a0001c0001t0002g0266a0001c0001t0002g0268others(1): Show | 4 | HG02257.hp2 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-324-11404G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134503 | ||||||
| chr8:58134617
|
C | T | 1 | a0001c0001t0008g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-324-11290C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134617 | ||||||
| chr8:58134753
|
C | T | 119 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0045others(116): Show | 119 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.-324-11154C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134753 | ||||||
| chr8:58134896
|
T | C | 3 | a0001c0001t0001g0115a0001c0001t0002g0016a0001c0001t0002g0153 | 3 | HG00741.hp2 HG01168.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-324-11011T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58134896 | ||||||
| chr8:58135137
|
T | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-10770T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135137 | ||||||
| chr8:58135143
|
G | T | 1 | a0001c0001t0009g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-324-10764G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135143 | ||||||
| chr8:58135720
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0003g0034a0001c0001t0006g0051others(2): Show | 5 | HG00323.hp1 HG01074.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-324-10187C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135720 | ||||||
| chr8:58135811
|
G | A | 1 | a0001c0001t0003g0257 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-324-10096G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135811 | ||||||
| chr8:58135815
|
G | A | 1 | a0001c0001t0024g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-324-10092G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135815 | ||||||
| chr8:58135858
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-324-10049G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58135858 | ||||||
| chr8:58136003
|
CT | C | 8 | a0001c0001t0001g0282a0001c0001t0002g0018a0001c0001t0002g0120others(5): Show | 8 | HG00741.hp1 HG01175.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-9878delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58136003 | |||||
| chr8:58136003
|
CTT | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0017others(124): Show | 127 | HG00280.hp1 HG00280.hp2 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.-324-9879_-324-987 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58136003 | |||||
| chr8:58136003
|
CTTT | C | 124 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-324-9880_-324-987 others(7): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58136003 | |||||
| chr8:58136003
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-324-9892_-324-987 others(19): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58136003 | |||||
| chr8:58136159
|
G | A | 2 | a0001c0001t0004g0189a0001c0001t0017g0119 | 2 | HG02129.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-324-9748G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58136159 | ||||||
| chr8:58136529
|
C | A | 1 | a0001c0001t0002g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-324-9378C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58136529 | ||||||
| chr8:58136595
|
T | C | 1 | a0001c0001t0003g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-324-9312T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58136595 | ||||||
| chr8:58136642
|
G | C | 18 | a0001c0001t0002g0012a0001c0001t0002g0146a0001c0001t0002g0186others(15): Show | 18 | HG00733.hp2 HG01069.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-324-9265G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58136642 | ||||||
| chr8:58136781
|
G | A | 268 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-324-9126G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58136781 | ||||||
| chr8:58137073
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-324-8834T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137073 | ||||||
| chr8:58137102
|
A | C | 6 | a0001c0001t0002g0057a0001c0001t0007g0135a0001c0001t0007g0157others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-324-8805A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137102 | ||||||
| chr8:58137116
|
A | G | 1 | a0003c0003t0003g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-324-8791A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137116 | ||||||
| chr8:58137144
|
G | A | 2 | a0001c0001t0005g0161a0001c0001t0035g0290 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-324-8763G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137144 | ||||||
| chr8:58137247
|
C | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-8660C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137247 | ||||||
| chr8:58137334
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-324-8573C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137334 | ||||||
| chr8:58137504
|
G | T | 1 | a0001c0001t0005g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-324-8403G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137504 | ||||||
| chr8:58137517
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-324-8390G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137517 | ||||||
| chr8:58137803
|
T | A | 1 | a0001c0001t0003g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-324-8104T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137803 | ||||||
| chr8:58137962
|
G | C | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-324-7945G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58137962 | ||||||
| chr8:58138044
|
G | A | 4 | a0001c0001t0002g0117a0001c0001t0002g0266a0001c0001t0002g0268others(1): Show | 4 | HG02257.hp2 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-324-7863G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58138044 | ||||||
| chr8:58138350
|
G | A | 42 | a0001c0001t0001g0038a0001c0001t0001g0149a0001c0001t0001g0154others(39): Show | 42 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.-324-7557G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58138350 | ||||||
| chr8:58138366
|
G | A | 41 | a0001c0001t0001g0038a0001c0001t0001g0149a0001c0001t0001g0154others(38): Show | 41 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.-324-7541G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58138366 | ||||||
| chr8:58138684
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-324-7223T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58138684 | ||||||
| chr8:58139053
|
T | G | 2 | a0001c0001t0001g0207a0001c0001t0006g0245 | 2 | HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-324-6854T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58139053 | ||||||
| chr8:58139150
|
C | T | 20 | a0001c0001t0001g0073a0001c0001t0001g0201a0001c0001t0002g0152others(17): Show | 20 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-324-6757C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58139150 | ||||||
| chr8:58139708
|
A | C | 73 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.-324-6199A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58139708 | ||||||
| chr8:58139755
|
C | T | 10 | a0001c0001t0006g0025a0001c0001t0006g0051a0001c0001t0006g0155others(7): Show | 10 | HG00323.hp1 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-324-6152C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58139755 | ||||||
| chr8:58139930
|
A | AAAT | 5 | a0001c0001t0002g0121a0001c0001t0008g0127a0001c0001t0011g0195others(2): Show | 5 | HG01175.hp1 HG01261.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-324-5959_-324-595 others(7): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58139930 | |||||
| chr8:58140038
|
A | C | 1 | a0001c0001t0003g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-324-5869A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58140038 | ||||||
| chr8:58140410
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-324-5497G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58140410 | ||||||
| chr8:58140733
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(156): Show | 159 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.-324-5174C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58140733 | ||||||
| chr8:58140745
|
G | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-5162G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58140745 | ||||||
| chr8:58141019
|
T | C | 15 | a0001c0001t0001g0282a0001c0001t0003g0034a0001c0001t0003g0055others(12): Show | 15 | HG00323.hp2 HG01074.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-324-4888T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141019 | ||||||
| chr8:58141141
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(111): Show | 114 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-324-4766T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141141 | ||||||
| chr8:58141349
|
C | A | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-4558C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141349 | ||||||
| chr8:58141515
|
A | G | 1 | a0001c0001t0004g0010 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-324-4392A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141515 | ||||||
| chr8:58141584
|
C | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(4): Show | 7 | HG00738.hp1 HG01993.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-324-4323C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141584 | ||||||
| chr8:58141778
|
G | A | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-324-4129G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141778 | ||||||
| chr8:58141816
|
G | A | 7 | a0001c0001t0007g0090a0001c0001t0007g0130a0001c0001t0007g0131others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-324-4091G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141816 | ||||||
| chr8:58141935
|
G | A | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-324-3972G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58141935 | ||||||
| chr8:58142001
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-324-3906A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142001 | ||||||
| chr8:58142308
|
G | A | 1 | a0001c0001t0003g0080 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-324-3599G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142308 | ||||||
| chr8:58142309
|
A | T | 1 | a0001c0001t0007g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-324-3598A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142309 | ||||||
| chr8:58142325
|
G | A | 1 | a0001c0001t0007g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-324-3582G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142325 | ||||||
| chr8:58142492
|
T | G | 8 | a0001c0001t0001g0073a0001c0001t0001g0172a0001c0001t0001g0201others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-3415T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142492 | ||||||
| chr8:58142557
|
C | T | 1 | a0001c0001t0004g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-324-3350C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142557 | ||||||
| chr8:58142559
|
T | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(165): Show | 168 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.-324-3348T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142559 | ||||||
| chr8:58142646
|
C | T | 1 | a0001c0001t0005g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-324-3261C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142646 | ||||||
| chr8:58142661
|
T | G | 1 | a0001c0001t0001g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-324-3246T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142661 | ||||||
| chr8:58142662
|
T | A | 1 | a0001c0001t0001g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-324-3245T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142662 | ||||||
| chr8:58142744
|
C | T | 11 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(8): Show | 11 | HG00408.hp2 HG00673.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.-324-3163C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142744 | ||||||
| chr8:58142787
|
A | G | 1 | a0001c0001t0019g0222 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-324-3120A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142787 | ||||||
| chr8:58142898
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-324-3009G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58142898 | ||||||
| chr8:58143038
|
A | AGT | 115 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(112): Show | 115 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-324-2868_-324-286 others(6): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58143038 | |||||
| chr8:58143041
|
C | T | 1 | a0001c0001t0003g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-324-2866C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143041 | ||||||
| chr8:58143358
|
C | A | 1 | a0001c0001t0002g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-324-2549C>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143358 | ||||||
| chr8:58143378
|
C | G | 1 | a0001c0001t0022g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-324-2529C>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143378 | ||||||
| chr8:58143381
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-324-2526C>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143381 | ||||||
| chr8:58143543
|
A | T | 8 | a0001c0001t0001g0073a0001c0001t0001g0172a0001c0001t0001g0201others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-2364A>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143543 | ||||||
| chr8:58143611
|
A | G | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-2296A>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143611 | ||||||
| chr8:58143883
|
T | G | 1 | a0001c0001t0002g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-324-2024T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143883 | ||||||
| chr8:58143908
|
T | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-324-1999T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58143908 | ||||||
| chr8:58144106
|
G | C | 4 | a0001c0001t0007g0090a0001c0001t0007g0130a0001c0001t0007g0131others(1): Show | 4 | HG01891.hp2 HG02280.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-324-1801G>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144106 | ||||||
| chr8:58144169
|
T | A | 6 | a0001c0001t0002g0057a0001c0001t0008g0079a0001c0001t0008g0127others(3): Show | 6 | HG01243.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-324-1738T>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144169 | ||||||
| chr8:58144224
|
G | T | 1 | a0001c0001t0007g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-324-1683G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144224 | ||||||
| chr8:58144239
|
G | A | 1 | a0001c0001t0002g0298 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-324-1668G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144239 | ||||||
| chr8:58144275
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-324-1632T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144275 | ||||||
| chr8:58144400
|
G | A | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-324-1507G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144400 | ||||||
| chr8:58144567
|
G | A | 1 | a0001c0001t0002g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-324-1340G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144567 | ||||||
| chr8:58144607
|
T | G | 1 | a0001c0001t0030g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-324-1300T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144607 | ||||||
| chr8:58144670
|
T | C | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-1237T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144670 | ||||||
| chr8:58144682
|
G | T | 16 | a0001c0001t0002g0037a0001c0001t0002g0117a0001c0001t0002g0128others(13): Show | 16 | HG00642.hp2 HG01099.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.-324-1225G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144682 | ||||||
| chr8:58144824
|
G | T | 1 | a0001c0001t0011g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-324-1083G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144824 | ||||||
| chr8:58144854
|
T | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(96): Show | 99 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-324-1053T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58144854 | ||||||
| chr8:58145018
|
G | A | 1 | a0002c0002t0016g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-324-889G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145018 | ||||||
| chr8:58145023
|
G | T | 2 | a0001c0001t0006g0025a0001c0001t0006g0218 | 2 | HG01081.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-324-884G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145023 | ||||||
| chr8:58145063
|
G | T | 2 | a0001c0001t0003g0164a0001c0001t0003g0165 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-324-844G>T | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145063 | ||||||
| chr8:58145070
|
G | A | 5 | a0001c0001t0007g0004a0001c0001t0007g0300a0001c0001t0022g0174others(2): Show | 5 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-324-837G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145070 | ||||||
| chr8:58145144
|
T | G | 1 | a0001c0001t0031g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-324-763T>G | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145144 | ||||||
| chr8:58145315
|
G | GT | 8 | a0001c0001t0003g0005a0001c0001t0003g0284a0001c0001t0004g0062others(5): Show | 8 | HG01978.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-324-576dupT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58145315 | |||||
| chr8:58145315
|
GT | G | 40 | a0001c0001t0001g0282a0001c0001t0003g0034a0001c0001t0003g0055others(37): Show | 40 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.-324-576delT | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 58145315 | |||||
| chr8:58145328
|
T | C | 1 | a0001c0001t0003g0237 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-324-579T>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145328 | ||||||
| chr8:58145459
|
A | C | 35 | a0001c0001t0001g0282a0001c0001t0003g0034a0001c0001t0003g0055others(32): Show | 35 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.-324-448A>C | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145459 | ||||||
| chr8:58145489
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-324-418G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145489 | ||||||
| chr8:58145885
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-324-22G>A | FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 3/3 | chr8 | 58145885 |