Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23196 |
|---|---|
| ensemblid | ENSG00000048828.18 |
| hgncid | 13247 |
| symbol | FAM120A |
| name | family with sequence similarity 120A |
| refseq_nuc | NM_014612.5 |
| refseq_prot | NP_055427.2 |
| ensembl_nuc | ENST00000277165.11 |
| ensembl_prot | ENSP00000277165.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 93451685 |
| end | 93566112 |
| strand | + |
| ver | v1.2 |
| region | chr9:93451685-93566112 |
| region5000 | chr9:93446685-93571112 |
| regionname0 | FAM120A_chr9_93451685_93566112 |
| regionname5000 | FAM120A_chr9_93446685_93571112 |
| 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 | 1118 | 317 | 88 | 58 | 135 | 16 | 18 | 103 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0002 | 0/0 | 1118 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3357 | 131 | 18 | 30 | 70 | 6 | 6 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| c0002 | 1/0 | 3357 | 109 | 27 | 16 | 47 | 8 | 10 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| c0003 | 0/0 | 3357 | 60 | 34 | 11 | 12 | 2 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| c0004 | 0/0 | 3357 | 5 | 0 | 0 | 5 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| c0005 | 0/0 | 3357 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| c0006 | 0/0 | 3357 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| c0007 | 0/0 | 3357 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| c0008 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| c0009 | 0/0 | 3357 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| c0010 | 0/0 | 3357 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| c0011 | 0/0 | 3357 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| c0012 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| 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 | 0/0 | 1804 | 99 | 20 | 11 | 54 | 6 | 8 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0002 | 0/1 | 1804 | 99 | 43 | 23 | 25 | 4 | 3 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0003 | 0/0 | 1804 | 64 | 3 | 15 | 39 | 4 | 3 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0004 | 0/0 | 1805 | 10 | 0 | 2 | 7 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0005 | 0/0 | 1805 | 10 | 3 | 0 | 7 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0006 | 0/0 | 1803 | 7 | 7 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0007 | 0/0 | 1805 | 7 | 4 | 3 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0008 | 1/0 | 1804 | 7 | 1 | 1 | 0 | 2 | 2 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0009 | 0/0 | 1803 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0010 | 0/0 | 1803 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0011 | 0/0 | 1805 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0012 | 0/0 | 1805 | 2 | 0 | 1 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0013 | 0/0 | 1804 | 2 | 0 | 0 | 2 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0014 | 0/0 | 1806 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0015 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| t0016 | 0/0 | 1804 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3357 | 131 | 18 | 30 | 70 | 6 | 6 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0002 | 1/0 | 3357 | 109 | 27 | 16 | 47 | 8 | 10 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0003 | 0/0 | 3357 | 60 | 34 | 11 | 12 | 2 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0004 | 0/0 | 3357 | 5 | 0 | 0 | 5 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0005 | 0/0 | 3357 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0006 | 0/0 | 3357 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0007 | 0/0 | 3357 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0008 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0010 | 0/0 | 3357 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0011 | 0/0 | 3357 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0012 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0002c0009 | 0/0 | 3357 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5160 | 12 | 2 | 0 | 10 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0001t0002 | 0/1 | 5160 | 37 | 9 | 11 | 12 | 2 | 2 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0001t0003 | 0/0 | 5160 | 62 | 3 | 15 | 37 | 4 | 3 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0001t0004 | 0/0 | 5161 | 9 | 0 | 2 | 6 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0001t0005 | 0/0 | 5161 | 3 | 2 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0001t0006 | 0/0 | 5159 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0001t0011 | 0/0 | 5161 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0001t0013 | 0/0 | 5160 | 2 | 0 | 0 | 2 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0001t0014 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0001t0015 | 0/0 | 5159 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0001t0016 | 0/0 | 5160 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0002t0001 | 0/0 | 5160 | 86 | 17 | 11 | 44 | 6 | 8 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0002t0002 | 0/0 | 5160 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0002t0003 | 0/0 | 5160 | 2 | 0 | 0 | 2 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0002t0004 | 0/0 | 5161 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0002t0005 | 0/0 | 5161 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0002t0007 | 0/0 | 5161 | 7 | 4 | 3 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0002t0008 | 1/0 | 5160 | 7 | 1 | 1 | 0 | 2 | 2 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0002t0012 | 0/0 | 5161 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0003t0002 | 0/0 | 5160 | 52 | 26 | 11 | 12 | 2 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0003t0006 | 0/0 | 5159 | 6 | 6 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0003t0010 | 0/0 | 5159 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0004t0005 | 0/0 | 5161 | 5 | 0 | 0 | 5 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0005t0009 | 0/0 | 5159 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0006t0002 | 0/0 | 5160 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0007t0012 | 0/0 | 5161 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0008t0001 | 0/0 | 5160 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0010t0005 | 0/0 | 5161 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0011t0002 | 0/0 | 5160 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0001c0012t0002 | 0/0 | 5160 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| a0002c0009t0002 | 0/0 | 5160 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | copy fasta | chr9 | 93446685 | 93571112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0006g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0011g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0013g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0013g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0014g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0015g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0001t0016g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0007g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0007g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0007g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0008g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0008g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0008g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0008g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0008g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0002t0012g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0003t0010g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0004t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0004t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0004t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0004t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0004t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0005t0009g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0005t0009g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0005t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0005t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0006t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0006t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0006t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0007t0012g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0008t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0010t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0011t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0001c0012t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| a0002c0009t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0198 | EUR | GBR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0161 | EUR | GBR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0086 | EUR | FIN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0147 | EUR | FIN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0204 | EUR | FIN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0085 | EUR | FIN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | CHS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | CHS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00438 | hp2 | a0001 | c0004 | t0005 | g0295 | EAS | CHS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | CHS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | CHS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | CHS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00639 | hp1 | a0001 | c0002 | t0008 | g0252 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00642 | hp2 | a0001 | c0002 | t0007 | g0236 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00673 | hp1 | a0001 | c0003 | t0002 | g0154 | EAS | CHS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | CHS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0220 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG00741 | hp2 | a0001 | c0002 | t0012 | g0194 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01109 | hp1 | a0001 | c0002 | t0007 | g0256 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0101 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01168 | hp2 | a0001 | c0003 | t0002 | g0153 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01175 | hp2 | a0001 | c0002 | t0007 | g0237 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01261 | hp1 | a0001 | c0001 | t0011 | g0038 | AMR | CLM | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0168 | AMR | CLM | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0170 | AMR | CLM | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | CLM | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | CLM | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0172 | AMR | CLM | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | CLM | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0039 | EUR | IBS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0121 | EUR | IBS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01516 | hp2 | a0001 | c0002 | t0008 | g0253 | EUR | IBS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0129 | EUR | IBS | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01884 | hp1 | a0001 | c0005 | t0009 | g0113 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0244 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0022 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01928 | hp1 | a0001 | c0003 | t0002 | g0171 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0175 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01952 | hp1 | a0001 | c0011 | t0002 | g0009 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01975 | hp2 | a0001 | c0003 | t0002 | g0166 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01978 | hp1 | a0001 | c0001 | t0011 | g0073 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0173 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02015 | hp1 | a0001 | c0004 | t0005 | g0290 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02129 | hp1 | a0001 | c0004 | t0005 | g0296 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0308 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02148 | hp1 | a0001 | c0003 | t0002 | g0169 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CDX | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | CDX | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CDX | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0018 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0157 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02273 | hp2 | a0001 | c0003 | t0002 | g0174 | AMR | PEL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02280 | hp1 | a0001 | c0001 | t0016 | g0312 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02280 | hp2 | a0001 | c0002 | t0008 | g0238 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0303 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | KHV | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02572 | hp2 | a0001 | c0008 | t0001 | g0251 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02615 | hp1 | a0001 | c0002 | t0007 | g0176 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02622 | hp1 | a0001 | c0002 | t0007 | g0178 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02622 | hp2 | a0001 | c0003 | t0006 | g0025 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0274 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02630 | hp2 | a0001 | c0003 | t0006 | g0017 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02647 | hp1 | a0001 | c0003 | t0002 | g0156 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0029 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0240 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02723 | hp2 | a0001 | c0003 | t0006 | g0110 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02735 | hp1 | a0001 | c0002 | t0008 | g0248 | SAS | PJL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0019 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02809 | hp2 | a0001 | c0005 | t0009 | g0114 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0008 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02886 | hp1 | a0001 | c0006 | t0002 | g0279 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0007 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02895 | hp1 | a0001 | c0003 | t0002 | g0003 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0028 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0302 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02897 | hp1 | a0001 | c0003 | t0002 | g0003 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02922 | hp1 | a0001 | c0006 | t0002 | g0280 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02965 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02970 | hp2 | a0001 | c0006 | t0002 | g0281 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02976 | hp1 | a0001 | c0003 | t0002 | g0305 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02976 | hp2 | a0001 | c0003 | t0002 | g0005 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0182 | SAS | PJL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0186 | SAS | PJL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03098 | hp1 | a0001 | c0002 | t0007 | g0239 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03098 | hp2 | a0001 | c0003 | t0010 | g0023 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03130 | hp1 | a0001 | c0003 | t0002 | g0011 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03130 | hp2 | a0001 | c0005 | t0009 | g0116 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03139 | hp1 | a0001 | c0002 | t0007 | g0246 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03139 | hp2 | a0001 | c0003 | t0002 | g0016 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0010 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0262 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0255 | SAS | PJL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0263 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0027 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0314 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03486 | hp2 | a0001 | c0003 | t0010 | g0024 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03516 | hp1 | a0001 | c0012 | t0002 | g0112 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0155 | AFR | ESN | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03540 | hp1 | a0001 | c0005 | t0009 | g0115 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | GWD | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0165 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | MSL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03688 | hp1 | a0001 | c0003 | t0002 | g0162 | SAS | STU | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03688 | hp2 | a0001 | c0007 | t0012 | g0232 | SAS | STU | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0180 | SAS | PJL | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03927 | hp1 | a0001 | c0002 | t0008 | g0247 | SAS | BEB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0184 | SAS | BEB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | STU | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0193 | SAS | STU | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0048 | SAS | STU | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0190 | SAS | STU | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | YRI | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | YRI | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18747 | hp1 | a0001 | c0003 | t0002 | g0152 | EAS | CHB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | CHB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | YRI | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | YRI | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18939 | hp1 | a0001 | c0002 | t0004 | g0212 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18939 | hp2 | a0001 | c0004 | t0005 | g0291 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0164 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18961 | hp1 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18962 | hp2 | a0001 | c0003 | t0002 | g0118 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18968 | hp1 | a0001 | c0003 | t0002 | g0160 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18970 | hp1 | a0001 | c0003 | t0002 | g0163 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18974 | hp1 | a0001 | c0001 | t0014 | g0035 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18975 | hp2 | a0001 | c0003 | t0002 | g0159 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18977 | hp1 | a0001 | c0001 | t0013 | g0120 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18980 | hp1 | a0001 | c0004 | t0005 | g0293 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18984 | hp2 | a0001 | c0003 | t0002 | g0149 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18999 | hp1 | a0002 | c0009 | t0002 | g0135 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19001 | hp2 | a0001 | c0003 | t0002 | g0158 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19010 | hp2 | a0001 | c0003 | t0002 | g0148 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0304 | AFR | LWK | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0306 | AFR | LWK | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19063 | hp1 | a0001 | c0003 | t0002 | g0150 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19065 | hp1 | a0001 | c0001 | t0013 | g0133 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19077 | hp1 | a0001 | c0010 | t0005 | g0288 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19081 | hp2 | a0001 | c0001 | t0015 | g0105 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19083 | hp1 | a0001 | c0003 | t0002 | g0151 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0213 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA20129 | hp1 | a0001 | c0003 | t0006 | g0026 | AFR | ASW | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0307 | AFR | ASW | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | TSI | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0205 | EUR | TSI | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0179 | EUR | TSI | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA20805 | hp2 | a0001 | c0002 | t0008 | g0250 | EUR | TSI | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01123 | hp1 | a0001 | c0003 | t0002 | g0167 | AMR | CLM | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0218 | AMR | CLM | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02109 | hp1 | a0001 | c0003 | t0006 | g0021 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0315 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0020 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | ACB | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG06807 | hp1 | a0001 | c0003 | t0006 | g0014 | AFR | USA | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | USA | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA20300 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | USA | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | USA | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0275 | AFR | LWK | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | LWK | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0127 | REF | REF | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0008 | g0249 | REF | REF | FAM120A_chr9_93446685_93571112 | FAM120A | chr9 | 93446685 | 93571112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:93516193
|
G | A | 1 | a0002 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.1342G>A | p.Val448Met | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/18 | 1573/5160 | 1342/3357 | 448/1118 | chr9 | 93516193 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:93476296
|
C | T | 9 | a0001c0001a0001c0003a0001c0004others(6): Show | 207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
synonymous_variant | LOW | c.762C>T | p.His254His | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/18 | 993/5160 | 762/3357 | 254/1118 | chr9 | 93476296 | ||
| chr9:93497503
|
C | T | 1 | a0001c0008 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.837C>T | p.Cys279Cys | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 4/18 | 1068/5160 | 837/3357 | 279/1118 | chr9 | 93497503 | ||
| chr9:93515764
|
C | G | 1 | a0001c0012 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.1128C>G | p.Pro376Pro | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 6/18 | 1359/5160 | 1128/3357 | 376/1118 | chr9 | 93515764 | ||
| chr9:93516009
|
C | T | 4 | a0001c0003a0001c0005a0001c0006others(1): Show | 68 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(65): Show |
synonymous_variant | LOW | c.1158C>T | p.Gly386Gly | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/18 | 1389/5160 | 1158/3357 | 386/1118 | chr9 | 93516009 | ||
| chr9:93516015
|
G | A | 1 | a0001c0004 | 5 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(2): Show |
synonymous_variant | LOW | c.1164G>A | p.Pro388Pro | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/18 | 1395/5160 | 1164/3357 | 388/1118 | chr9 | 93516015 | ||
| chr9:93516192
|
C | T | 4 | a0001c0003a0001c0005a0001c0006others(1): Show | 68 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(65): Show |
synonymous_variant | LOW | c.1341C>T | p.His447His | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/18 | 1572/5160 | 1341/3357 | 447/1118 | chr9 | 93516192 | ||
| chr9:93532256
|
C | G | 1 | a0001c0007 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.1836C>G | p.Val612Val | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/18 | 2067/5160 | 1836/3357 | 612/1118 | chr9 | 93532256 | ||
| chr9:93543463
|
C | T | 1 | a0001c0006 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
synonymous_variant | LOW | c.2151C>T | p.Cys717Cys | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/18 | 2382/5160 | 2151/3357 | 717/1118 | chr9 | 93543463 | ||
| chr9:93557898
|
C | T | 1 | a0001c0005 | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
synonymous_variant | LOW | c.2556C>T | p.Ser852Ser | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 14/18 | 2787/5160 | 2556/3357 | 852/1118 | chr9 | 93557898 | ||
| chr9:93564363
|
G | A | 1 | a0001c0011 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.3180G>A | p.Pro1060Pro | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 18/18 | 3411/5160 | 3180/3357 | 1060/1118 | chr9 | 93564363 | ||
| chr9:93564537
|
G | A | 1 | a0001c0010 | 1 | NA19077.hp1 | synonymous_variant | LOW | c.3354G>A | p.Glu1118Glu | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 18/18 | 3585/5160 | 3354/3357 | 1118/1118 | chr9 | 93564537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:93451796
|
G | T | 1 | a0001c0001t0016 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-120G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/18 | 120 | chr9 | 93451796 | |||||
| chr9:93451815
|
G | A | 1 | a0001c0003t0010 | 2 | HG03098.hp2 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-101G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/18 | 101 | chr9 | 93451815 | |||||
| chr9:93451901
|
G | GC | 4 | a0001c0001t0011a0001c0001t0014a0001c0002t0012others(1): Show | 5 | HG00741.hp2 HG01261.hp1 HG01978.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-10dupC | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/18 | 9 | INFO_REALIGN_3_PRIME | chr9 | 93451901 | ||||
| chr9:93564583
|
A | G | 1 | a0001c0001t0013 | 2 | NA18977.hp1 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*43A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 18/18 | 43 | chr9 | 93564583 | |||||
| chr9:93564836
|
T | A | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*296T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 18/18 | 296 | chr9 | 93564836 | |||||
| chr9:93565409
|
A | C | 12 | a0001c0001t0002a0001c0001t0006a0001c0001t0013others(9): Show | 111 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*869A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 18/18 | 869 | chr9 | 93565409 | |||||
| chr9:93565694
|
T | TA | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0014others(5): Show | 28 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1167dupA | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 18/18 | 1168 | INFO_REALIGN_3_PRIME | chr9 | 93565694 | ||||
| chr9:93565694
|
TA | T | 5 | a0001c0001t0006a0001c0001t0015a0001c0003t0006others(2): Show | 14 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1167delA | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 18/18 | 1167 | INFO_REALIGN_3_PRIME | chr9 | 93565694 | ||||
| chr9:93566021
|
T | C | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(4): Show | 78 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1481T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 18/18 | 1481 | chr9 | 93566021 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:93452531
|
G | C | 1 | a0001c0001t0001g0004 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.474+142G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93452531 | ||||||
| chr9:93452581
|
A | G | 6 | a0001c0001t0002g0310a0001c0001t0002g0311a0001c0001t0002g0313others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.474+192A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93452581 | ||||||
| chr9:93452646
|
G | A | 108 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(105): Show | 109 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.474+257G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93452646 | ||||||
| chr9:93452745
|
A | G | 1 | a0001c0002t0001g0309 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.474+356A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93452745 | ||||||
| chr9:93452817
|
A | G | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.474+428A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93452817 | ||||||
| chr9:93452898
|
T | C | 2 | a0001c0002t0001g0111a0001c0012t0002g0112 | 2 | HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.474+509T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93452898 | ||||||
| chr9:93452902
|
G | A | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+513G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93452902 | ||||||
| chr9:93452930
|
A | C | 2 | a0001c0003t0002g0003a0001c0003t0002g0305 | 3 | HG02895.hp1 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.474+541A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93452930 | ||||||
| chr9:93452961
|
C | T | 1 | a0001c0002t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.474+572C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93452961 | ||||||
| chr9:93453135
|
T | A | 1 | a0001c0002t0003g0117 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.474+746T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453135 | ||||||
| chr9:93453137
|
C | G | 1 | a0001c0003t0006g0110 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.474+748C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453137 | ||||||
| chr9:93453238
|
C | G | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.474+849C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453238 | ||||||
| chr9:93453536
|
C | G | 2 | a0001c0002t0001g0300a0001c0002t0001g0301 | 2 | NA19063.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.474+1147C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453536 | ||||||
| chr9:93453678
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.474+1289C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453678 | ||||||
| chr9:93453682
|
C | T | 2 | a0001c0001t0002g0298a0001c0001t0002g0299 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.474+1293C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453682 | ||||||
| chr9:93453693
|
C | T | 1 | a0001c0001t0002g0297 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.474+1304C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453693 | ||||||
| chr9:93453708
|
C | T | 9 | a0001c0001t0005g0289a0001c0001t0005g0292a0001c0001t0005g0294others(6): Show | 9 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+1319C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453708 | ||||||
| chr9:93453780
|
A | C | 2 | a0001c0002t0001g0286a0001c0002t0001g0287 | 2 | NA19064.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.474+1391A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453780 | ||||||
| chr9:93453795
|
T | C | 1 | a0001c0003t0002g0118 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.474+1406T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453795 | ||||||
| chr9:93453807
|
G | A | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.474+1418G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453807 | ||||||
| chr9:93453834
|
G | A | 60 | a0001c0001t0002g0013a0001c0003t0002g0005a0001c0003t0002g0006others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.474+1445G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453834 | ||||||
| chr9:93453905
|
C | G | 11 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(8): Show | 11 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.474+1516C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93453905 | ||||||
| chr9:93454127
|
A | T | 192 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(189): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.474+1738A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93454127 | ||||||
| chr9:93454198
|
A | G | 1 | a0001c0002t0001g0276 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.474+1809A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93454198 | ||||||
| chr9:93454256
|
T | C | 1 | a0001c0002t0007g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.474+1867T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93454256 | ||||||
| chr9:93454288
|
A | G | 209 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(206): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.474+1899A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93454288 | ||||||
| chr9:93454328
|
T | G | 1 | a0001c0001t0002g0119 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.474+1939T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93454328 | ||||||
| chr9:93454452
|
C | T | 8 | a0001c0002t0001g0264a0001c0002t0001g0265a0001c0002t0001g0266others(5): Show | 8 | NA18944.hp2 NA18962.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+2063C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93454452 | ||||||
| chr9:93454464
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.474+2075C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93454464 | ||||||
| chr9:93454558
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.474+2169G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93454558 | ||||||
| chr9:93455165
|
A | G | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.474+2776A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93455165 | ||||||
| chr9:93455365
|
A | G | 7 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(4): Show | 7 | HG01081.hp2 HG02922.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+2976A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93455365 | ||||||
| chr9:93455519
|
T | G | 1 | a0001c0002t0001g0177 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.474+3130T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93455519 | ||||||
| chr9:93455912
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.474+3523C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93455912 | ||||||
| chr9:93455995
|
T | C | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+3606T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93455995 | ||||||
| chr9:93456031
|
T | C | 1 | a0001c0002t0007g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.474+3642T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93456031 | ||||||
| chr9:93456388
|
A | G | 2 | a0001c0002t0007g0176a0001c0002t0007g0256 | 2 | HG01109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.474+3999A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93456388 | ||||||
| chr9:93456408
|
C | T | 1 | a0001c0002t0001g0255 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.474+4019C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93456408 | ||||||
| chr9:93456492
|
T | A | 1 | a0001c0001t0013g0120 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.474+4103T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93456492 | ||||||
| chr9:93456498
|
A | G | 1 | a0001c0003t0002g0175 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.474+4109A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93456498 | ||||||
| chr9:93456580
|
C | G | 1 | a0001c0002t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.474+4191C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93456580 | ||||||
| chr9:93456677
|
A | C | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.474+4288A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93456677 | ||||||
| chr9:93456765
|
TTC | T | 205 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.474+4379_474+4380d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93456765 | |||||
| chr9:93456804
|
G | A | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.474+4415G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93456804 | ||||||
| chr9:93456814
|
C | G | 1 | a0001c0002t0002g0303 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.474+4425C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93456814 | ||||||
| chr9:93456969
|
C | T | 205 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.474+4580C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93456969 | ||||||
| chr9:93457346
|
A | G | 5 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(2): Show | 5 | NA19003.hp2 NA19007.hp1 NA19077.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+4957A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93457346 | ||||||
| chr9:93457802
|
C | CT | 17 | a0001c0001t0001g0142a0001c0001t0002g0134a0001c0001t0002g0136others(14): Show | 17 | HG00423.hp1 HG01175.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.474+5427dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93457802 | |||||
| chr9:93457802
|
CT | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.474+5427delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93457802 | |||||
| chr9:93457803
|
T | C | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.474+5414T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93457803 | ||||||
| chr9:93457832
|
C | T | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+5443C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93457832 | ||||||
| chr9:93457882
|
A | G | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.474+5493A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93457882 | ||||||
| chr9:93458033
|
T | C | 292 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(289): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.474+5644T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93458033 | ||||||
| chr9:93458058
|
A | G | 2 | a0001c0002t0008g0252a0001c0002t0008g0253 | 2 | HG00639.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.474+5669A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93458058 | ||||||
| chr9:93458064
|
A | T | 10 | a0001c0003t0002g0166a0001c0003t0002g0167a0001c0003t0002g0168others(7): Show | 10 | HG01123.hp1 HG01261.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+5675A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93458064 | ||||||
| chr9:93458077
|
A | G | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.474+5688A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93458077 | ||||||
| chr9:93458160
|
C | T | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.474+5771C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93458160 | ||||||
| chr9:93458227
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.474+5838G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93458227 | ||||||
| chr9:93458312
|
C | T | 34 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.474+5923C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93458312 | ||||||
| chr9:93458327
|
G | A | 63 | a0001c0001t0002g0013a0001c0003t0002g0005a0001c0003t0002g0006others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.474+5938G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93458327 | ||||||
| chr9:93458424
|
A | G | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.474+6035A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93458424 | ||||||
| chr9:93458564
|
A | G | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.474+6175A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93458564 | ||||||
| chr9:93458770
|
C | G | 4 | a0001c0002t0001g0235a0001c0002t0001g0255a0001c0002t0002g0302others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+6381C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93458770 | ||||||
| chr9:93459059
|
C | G | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+6670C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93459059 | ||||||
| chr9:93459119
|
A | G | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.474+6730A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93459119 | ||||||
| chr9:93459437
|
C | G | 1 | a0001c0008t0001g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.474+7048C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93459437 | ||||||
| chr9:93459452
|
G | A | 3 | a0001c0002t0007g0236a0001c0002t0007g0237a0001c0002t0008g0238 | 3 | HG00642.hp2 HG01175.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.474+7063G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93459452 | ||||||
| chr9:93459559
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.474+7170G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93459559 | ||||||
| chr9:93459732
|
AT | A | 110 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(107): Show | 110 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.474+7348delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93459732 | |||||
| chr9:93459834
|
A | G | 2 | a0001c0001t0013g0120a0001c0001t0013g0133 | 2 | NA18977.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.474+7445A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93459834 | ||||||
| chr9:93459844
|
A | G | 2 | a0001c0001t0003g0103a0001c0001t0003g0104 | 2 | HG02040.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.474+7455A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93459844 | ||||||
| chr9:93460335
|
G | A | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.474+7946G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93460335 | ||||||
| chr9:93460384
|
CAA | C | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.474+7996_474+7997d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93460384 | ||||||
| chr9:93460446
|
A | T | 2 | a0001c0002t0001g0233a0001c0002t0001g0234 | 2 | HG02135.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.474+8057A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93460446 | ||||||
| chr9:93460489
|
G | A | 1 | a0001c0002t0001g0179 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.474+8100G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93460489 | ||||||
| chr9:93460582
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.474+8193G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93460582 | ||||||
| chr9:93460700
|
G | A | 1 | a0001c0003t0002g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.474+8311G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93460700 | ||||||
| chr9:93460723
|
G | T | 2 | a0001c0003t0002g0028a0001c0003t0002g0029 | 2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.474+8334G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93460723 | ||||||
| chr9:93460786
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.474+8397G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93460786 | ||||||
| chr9:93460789
|
A | G | 1 | a0001c0002t0002g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.474+8400A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93460789 | ||||||
| chr9:93460920
|
G | A | 30 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.474+8531G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93460920 | ||||||
| chr9:93460924
|
A | G | 5 | a0001c0001t0002g0143a0001c0001t0002g0144a0001c0001t0002g0145others(2): Show | 5 | HG00423.hp1 HG02056.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.474+8535A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93460924 | ||||||
| chr9:93461056
|
T | C | 16 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0277others(13): Show | 16 | HG00438.hp2 HG00558.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.474+8667T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461056 | ||||||
| chr9:93461290
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.474+8901C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461290 | ||||||
| chr9:93461389
|
T | G | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.474+9000T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461389 | ||||||
| chr9:93461396
|
C | G | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.474+9007C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461396 | ||||||
| chr9:93461425
|
C | A | 1 | a0001c0002t0001g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.474+9036C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461425 | ||||||
| chr9:93461489
|
A | G | 1 | a0001c0001t0004g0102 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.474+9100A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461489 | ||||||
| chr9:93461661
|
T | C | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG00558.hp2 HG02135.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.474+9272T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461661 | ||||||
| chr9:93461731
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.474+9342C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461731 | ||||||
| chr9:93461732
|
G | A | 1 | a0001c0002t0001g0181 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.474+9343G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461732 | ||||||
| chr9:93461754
|
T | C | 83 | a0001c0002t0001g0002a0001c0002t0001g0177a0001c0002t0001g0179others(80): Show | 84 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.474+9365T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461754 | ||||||
| chr9:93461819
|
G | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.475-9322G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461819 | ||||||
| chr9:93461922
|
G | A | 1 | a0001c0002t0007g0256 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.475-9219G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93461922 | ||||||
| chr9:93462019
|
C | A | 308 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(305): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.475-9122C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93462019 | ||||||
| chr9:93462210
|
AT | A | 5 | a0001c0001t0004g0033a0001c0001t0004g0034a0001c0001t0004g0036others(2): Show | 5 | HG00423.hp2 HG02080.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.475-8929delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93462210 | |||||
| chr9:93462293
|
T | A | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.475-8848T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93462293 | ||||||
| chr9:93462311
|
C | T | 1 | a0001c0003t0002g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.475-8830C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93462311 | ||||||
| chr9:93462312
|
G | A | 18 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.475-8829G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93462312 | ||||||
| chr9:93462341
|
C | A | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.475-8800C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93462341 | ||||||
| chr9:93462387
|
T | TCTC | 209 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(206): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.475-8752_475-8751i others(5): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93462387 | |||||
| chr9:93462426
|
C | T | 11 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(8): Show | 11 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-8715C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93462426 | ||||||
| chr9:93462583
|
C | T | 1 | a0001c0003t0002g0027 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.475-8558C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93462583 | ||||||
| chr9:93462801
|
G | A | 1 | a0001c0003t0002g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.475-8340G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93462801 | ||||||
| chr9:93462805
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.475-8336C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93462805 | ||||||
| chr9:93462966
|
A | C | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.475-8175A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93462966 | ||||||
| chr9:93462966
|
A | G | 1 | a0001c0001t0004g0101 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.475-8175A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93462966 | ||||||
| chr9:93463196
|
A | T | 122 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(119): Show | 123 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.475-7945A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93463196 | ||||||
| chr9:93463328
|
T | C | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.475-7813T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93463328 | ||||||
| chr9:93463679
|
A | G | 34 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.475-7462A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93463679 | ||||||
| chr9:93463719
|
G | C | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.475-7422G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93463719 | ||||||
| chr9:93463882
|
A | G | 11 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(8): Show | 11 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-7259A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93463882 | ||||||
| chr9:93464229
|
A | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.475-6912A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93464229 | ||||||
| chr9:93464361
|
G | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.475-6780G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93464361 | ||||||
| chr9:93464399
|
C | T | 1 | a0001c0002t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.475-6742C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93464399 | ||||||
| chr9:93464422
|
A | G | 1 | a0001c0007t0012g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.475-6719A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93464422 | ||||||
| chr9:93464445
|
A | G | 1 | a0001c0003t0006g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.475-6696A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93464445 | ||||||
| chr9:93464533
|
G | A | 2 | a0001c0001t0003g0039a0001c0001t0011g0038 | 2 | HG01261.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.475-6608G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93464533 | ||||||
| chr9:93464741
|
T | C | 1 | a0001c0001t0004g0033 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.475-6400T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93464741 | ||||||
| chr9:93464785
|
G | C | 1 | a0001c0001t0003g0040 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.475-6356G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93464785 | ||||||
| chr9:93464818
|
G | A | 83 | a0001c0002t0001g0002a0001c0002t0001g0177a0001c0002t0001g0179others(80): Show | 84 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.475-6323G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93464818 | ||||||
| chr9:93465033
|
GTAGCT | G | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.475-6104_475-6100d others(7): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93465033 | |||||
| chr9:93465208
|
A | G | 6 | a0001c0002t0001g0228a0001c0002t0001g0229a0001c0002t0001g0230others(3): Show | 6 | HG00673.hp2 HG02015.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-5933A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93465208 | ||||||
| chr9:93465559
|
C | A | 1 | a0001c0001t0002g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.475-5582C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93465559 | ||||||
| chr9:93465571
|
C | G | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.475-5570C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93465571 | ||||||
| chr9:93465571
|
C | T | 26 | a0001c0001t0002g0013a0001c0003t0002g0005a0001c0003t0002g0006others(23): Show | 26 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.475-5570C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93465571 | ||||||
| chr9:93465818
|
C | T | 1 | a0001c0002t0001g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.475-5323C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93465818 | ||||||
| chr9:93466016
|
C | T | 63 | a0001c0001t0002g0013a0001c0003t0002g0005a0001c0003t0002g0006others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.475-5125C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93466016 | ||||||
| chr9:93466126
|
G | A | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.475-5015G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93466126 | ||||||
| chr9:93466248
|
T | C | 3 | a0001c0003t0002g0008a0001c0003t0002g0028a0001c0003t0002g0029 | 3 | HG02717.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.475-4893T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93466248 | ||||||
| chr9:93466475
|
C | T | 2 | a0001c0002t0001g0111a0001c0002t0001g0304 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.475-4666C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93466475 | ||||||
| chr9:93466540
|
C | T | 181 | a0001c0001t0001g0004a0001c0001t0001g0056a0001c0001t0001g0057others(178): Show | 182 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.475-4601C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93466540 | ||||||
| chr9:93466615
|
T | A | 31 | a0001c0001t0001g0142a0001c0001t0002g0121a0001c0001t0002g0122others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.475-4526T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93466615 | ||||||
| chr9:93466670
|
G | A | 70 | a0001c0001t0001g0004a0001c0001t0001g0056a0001c0001t0001g0057others(67): Show | 71 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.475-4471G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93466670 | ||||||
| chr9:93466725
|
G | A | 1 | a0001c0011t0002g0009 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.475-4416G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93466725 | ||||||
| chr9:93467068
|
CT | C | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.475-4072delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467068 | ||||||
| chr9:93467158
|
G | T | 62 | a0001c0001t0002g0013a0001c0001t0003g0030a0001c0001t0003g0032others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.475-3983G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467158 | ||||||
| chr9:93467246
|
A | AC | 35 | a0001c0001t0002g0311a0001c0002t0002g0302a0001c0002t0008g0247others(32): Show | 36 | HG00639.hp1 HG00673.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.475-3883dupC | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93467246 | |||||
| chr9:93467246
|
A | ACC | 32 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0272others(29): Show | 32 | HG00140.hp2 HG00642.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.475-3884_475-3883d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93467246 | |||||
| chr9:93467246
|
AC | A | 32 | a0001c0001t0003g0030a0001c0001t0004g0034a0001c0001t0014g0035others(29): Show | 32 | HG00140.hp1 HG00558.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.475-3883delC | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93467246 | |||||
| chr9:93467246
|
ACC | A | 67 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(64): Show | 68 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.475-3884_475-3883d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93467246 | |||||
| chr9:93467257
|
C | A | 2 | a0001c0003t0002g0306a0001c0003t0002g0307 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.475-3884C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467257 | ||||||
| chr9:93467258
|
C | CCCCCCCC others(9): Show |
1 | a0001c0001t0003g0107 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.475-3883_475-3882i others(18): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467258 | ||||||
| chr9:93467258
|
C | CCCCCCCC others(4): Show |
2 | a0001c0001t0002g0277a0001c0001t0003g0108 | 2 | HG02055.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.475-3883_475-3882i others(13): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467258 | ||||||
| chr9:93467258
|
C | CCCCCCCG | 18 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0003g0058others(15): Show | 18 | HG01261.hp1 HG02132.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.475-3883_475-3882i others(9): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467258 | ||||||
| chr9:93467258
|
C | CCCCCCG | 21 | a0001c0001t0002g0098a0001c0001t0002g0136a0001c0001t0002g0145others(18): Show | 22 | HG00423.hp1 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.475-3883_475-3882i others(8): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467258 | ||||||
| chr9:93467258
|
C | CCCCCG | 19 | a0001c0001t0002g0137a0001c0001t0003g0041a0001c0001t0003g0079others(16): Show | 19 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.475-3883_475-3882i others(7): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467258 | ||||||
| chr9:93467258
|
C | CCCCG | 17 | a0001c0001t0002g0119a0001c0001t0002g0123a0001c0001t0002g0124others(14): Show | 17 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.475-3883_475-3882i others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467258 | ||||||
| chr9:93467258
|
C | CCCG | 18 | a0001c0001t0001g0142a0001c0001t0002g0125a0001c0001t0002g0126others(15): Show | 18 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.475-3883_475-3882i others(5): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467258 | ||||||
| chr9:93467259
|
T | A | 198 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0060others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.475-3882T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467259 | ||||||
| chr9:93467280
|
T | C | 190 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0060others(187): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.475-3861T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467280 | ||||||
| chr9:93467333
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.475-3808C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467333 | ||||||
| chr9:93467390
|
C | T | 66 | a0001c0001t0002g0013a0001c0001t0002g0272a0001c0001t0002g0273others(63): Show | 67 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.475-3751C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467390 | ||||||
| chr9:93467780
|
AAAGTC | A | 3 | a0001c0003t0006g0025a0001c0003t0010g0023a0001c0003t0010g0024 | 3 | HG02622.hp2 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.475-3356_475-3352d others(7): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 93467780 | |||||
| chr9:93467912
|
G | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(48): Show | 52 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.475-3229G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467912 | ||||||
| chr9:93467920
|
C | T | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.475-3221C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93467920 | ||||||
| chr9:93468049
|
T | A | 1 | a0001c0001t0003g0078 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.475-3092T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93468049 | ||||||
| chr9:93468152
|
G | A | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG00558.hp2 HG02135.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.475-2989G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93468152 | ||||||
| chr9:93468206
|
C | G | 1 | a0001c0001t0002g0013 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.475-2935C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93468206 | ||||||
| chr9:93468721
|
C | T | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-2420C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93468721 | ||||||
| chr9:93468880
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.475-2261G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93468880 | ||||||
| chr9:93468889
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.475-2252T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93468889 | ||||||
| chr9:93468959
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.475-2182C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93468959 | ||||||
| chr9:93469088
|
C | T | 1 | a0001c0002t0001g0177 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.475-2053C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93469088 | ||||||
| chr9:93469157
|
C | A | 1 | a0001c0001t0003g0062 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.475-1984C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93469157 | ||||||
| chr9:93469717
|
C | G | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.475-1424C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93469717 | ||||||
| chr9:93469778
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.475-1363C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93469778 | ||||||
| chr9:93469805
|
T | C | 1 | a0001c0002t0002g0303 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.475-1336T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93469805 | ||||||
| chr9:93469830
|
G | A | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.475-1311G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93469830 | ||||||
| chr9:93469847
|
G | C | 1 | a0001c0003t0002g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.475-1294G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93469847 | ||||||
| chr9:93469999
|
G | C | 1 | a0001c0001t0005g0292 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.475-1142G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93469999 | ||||||
| chr9:93470120
|
A | G | 31 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0002g0098others(28): Show | 31 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.475-1021A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93470120 | ||||||
| chr9:93470237
|
G | A | 1 | a0001c0001t0003g0108 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.475-904G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93470237 | ||||||
| chr9:93470288
|
G | A | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.475-853G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93470288 | ||||||
| chr9:93470334
|
T | C | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.475-807T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93470334 | ||||||
| chr9:93470358
|
G | T | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.475-783G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93470358 | ||||||
| chr9:93470359
|
A | T | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.475-782A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93470359 | ||||||
| chr9:93470460
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.475-681T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93470460 | ||||||
| chr9:93470592
|
G | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.475-549G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 1/17 | chr9 | 93470592 | ||||||
| chr9:93471469
|
G | T | 2 | a0001c0003t0002g0173a0001c0003t0002g0174 | 2 | HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.721+82G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93471469 | ||||||
| chr9:93471814
|
A | G | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.721+427A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93471814 | ||||||
| chr9:93471826
|
A | T | 2 | a0001c0002t0001g0286a0001c0002t0001g0287 | 2 | NA19064.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.721+439A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93471826 | ||||||
| chr9:93472146
|
G | C | 40 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(37): Show | 41 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.721+759G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93472146 | ||||||
| chr9:93472186
|
G | T | 80 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(77): Show | 80 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.721+799G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93472186 | ||||||
| chr9:93472215
|
G | A | 1 | a0001c0002t0008g0250 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.721+828G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93472215 | ||||||
| chr9:93472223
|
G | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.721+836G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93472223 | ||||||
| chr9:93472410
|
A | G | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.721+1023A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93472410 | ||||||
| chr9:93472729
|
A | G | 2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.721+1342A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93472729 | ||||||
| chr9:93472785
|
A | G | 1 | a0001c0001t0003g0052 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.721+1398A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93472785 | ||||||
| chr9:93472802
|
G | T | 1 | a0001c0002t0001g0226 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.721+1415G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93472802 | ||||||
| chr9:93472821
|
A | G | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.721+1434A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93472821 | ||||||
| chr9:93472835
|
G | A | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.721+1448G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93472835 | ||||||
| chr9:93472870
|
G | A | 1 | a0001c0001t0015g0105 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.721+1483G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93472870 | ||||||
| chr9:93473003
|
G | A | 1 | a0001c0003t0002g0147 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.721+1616G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473003 | ||||||
| chr9:93473016
|
T | C | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.721+1629T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473016 | ||||||
| chr9:93473022
|
A | AT | 77 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(74): Show | 77 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.721+1649dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 93473022 | |||||
| chr9:93473022
|
AT | A | 7 | a0001c0001t0003g0063a0001c0001t0003g0077a0001c0002t0001g0202others(4): Show | 7 | HG02145.hp1 HG02523.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.721+1649delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 93473022 | |||||
| chr9:93473303
|
G | A | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.721+1916G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473303 | ||||||
| chr9:93473377
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.721+1990C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473377 | ||||||
| chr9:93473441
|
G | A | 62 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.721+2054G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473441 | ||||||
| chr9:93473549
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.721+2162C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473549 | ||||||
| chr9:93473603
|
C | T | 77 | a0001c0001t0001g0142a0001c0001t0002g0136a0001c0001t0002g0137others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.721+2216C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473603 | ||||||
| chr9:93473648
|
C | T | 7 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(4): Show | 7 | HG01081.hp2 HG02922.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.721+2261C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473648 | ||||||
| chr9:93473696
|
G | T | 1 | a0001c0003t0002g0164 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.721+2309G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473696 | ||||||
| chr9:93473751
|
T | A | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.721+2364T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473751 | ||||||
| chr9:93473846
|
G | A | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.722-2410G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473846 | ||||||
| chr9:93473960
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.722-2296A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93473960 | ||||||
| chr9:93474086
|
A | AAAAC | 205 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.722-2167_722-2166i others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 93474086 | |||||
| chr9:93474133
|
T | C | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.722-2123T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93474133 | ||||||
| chr9:93474202
|
T | G | 2 | a0001c0002t0001g0181a0001c0002t0001g0185 | 2 | NA19012.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.722-2054T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93474202 | ||||||
| chr9:93474394
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.722-1862C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93474394 | ||||||
| chr9:93474429
|
G | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.722-1827G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93474429 | ||||||
| chr9:93474468
|
G | A | 1 | a0001c0001t0016g0312 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.722-1788G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93474468 | ||||||
| chr9:93474577
|
G | A | 1 | a0001c0003t0002g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.722-1679G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93474577 | ||||||
| chr9:93474742
|
C | T | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.722-1514C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93474742 | ||||||
| chr9:93474835
|
C | T | 3 | a0001c0002t0008g0252a0001c0002t0008g0253a0001c0004t0005g0296 | 3 | HG00639.hp1 HG01516.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.722-1421C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93474835 | ||||||
| chr9:93474911
|
C | T | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.722-1345C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93474911 | ||||||
| chr9:93474927
|
A | G | 2 | a0001c0003t0002g0006a0001c0012t0002g0112 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.722-1329A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93474927 | ||||||
| chr9:93475066
|
CTGAAATG others(41): Show |
C | 2 | a0001c0001t0003g0282a0001c0001t0003g0283 | 2 | NA19054.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.722-1185_722-1138d others(50): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 93475066 | |||||
| chr9:93475091
|
T | G | 110 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(107): Show | 110 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.722-1165T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475091 | ||||||
| chr9:93475094
|
A | G | 80 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(77): Show | 81 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.722-1162A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475094 | ||||||
| chr9:93475109
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.722-1147G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475109 | ||||||
| chr9:93475122
|
T | C | 2 | a0001c0001t0003g0071a0001c0001t0003g0079 | 2 | HG01070.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.722-1134T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475122 | ||||||
| chr9:93475276
|
C | T | 2 | a0001c0001t0003g0030a0001c0001t0003g0031 | 2 | HG00558.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.722-980C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475276 | ||||||
| chr9:93475494
|
A | T | 17 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(14): Show | 17 | HG00438.hp2 HG00558.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.722-762A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475494 | ||||||
| chr9:93475576
|
C | T | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG00558.hp2 HG02135.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.722-680C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475576 | ||||||
| chr9:93475805
|
T | G | 1 | a0001c0001t0004g0102 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.722-451T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475805 | ||||||
| chr9:93475813
|
G | A | 192 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(189): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.722-443G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475813 | ||||||
| chr9:93475905
|
A | C | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.722-351A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475905 | ||||||
| chr9:93475936
|
T | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.722-320T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475936 | ||||||
| chr9:93475963
|
G | C | 1 | a0001c0002t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.722-293G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93475963 | ||||||
| chr9:93476072
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.722-184G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93476072 | ||||||
| chr9:93476114
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.722-142C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 2/17 | chr9 | 93476114 | ||||||
| chr9:93476449
|
C | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.804+111C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93476449 | ||||||
| chr9:93476672
|
A | G | 1 | a0001c0001t0003g0109 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.804+334A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93476672 | ||||||
| chr9:93476698
|
A | G | 1 | a0001c0003t0002g0175 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.804+360A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93476698 | ||||||
| chr9:93476808
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.804+470C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93476808 | ||||||
| chr9:93476876
|
C | T | 30 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.804+538C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93476876 | ||||||
| chr9:93477118
|
G | C | 2 | a0001c0002t0007g0236a0001c0002t0007g0237 | 2 | HG00642.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.804+780G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93477118 | ||||||
| chr9:93477129
|
C | T | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.804+791C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93477129 | ||||||
| chr9:93477232
|
G | A | 1 | a0001c0002t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.804+894G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93477232 | ||||||
| chr9:93477387
|
C | G | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(9): Show | 12 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.804+1049C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93477387 | ||||||
| chr9:93477476
|
T | C | 17 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(14): Show | 17 | HG00438.hp2 HG00558.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.804+1138T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93477476 | ||||||
| chr9:93477677
|
C | T | 1 | a0001c0003t0002g0167 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.804+1339C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93477677 | ||||||
| chr9:93477917
|
T | G | 1 | a0001c0001t0003g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.804+1579T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93477917 | ||||||
| chr9:93477942
|
C | A | 189 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(186): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.804+1604C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93477942 | ||||||
| chr9:93477968
|
A | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+1630A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93477968 | ||||||
| chr9:93478039
|
T | C | 2 | a0001c0003t0002g0149a0001c0003t0002g0150 | 2 | NA18984.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.804+1701T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478039 | ||||||
| chr9:93478052
|
A | G | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.804+1714A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478052 | ||||||
| chr9:93478122
|
C | T | 1 | a0001c0002t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.804+1784C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478122 | ||||||
| chr9:93478154
|
AT | A | 13 | a0001c0001t0001g0142a0001c0001t0002g0136a0001c0001t0002g0137others(10): Show | 13 | HG00423.hp1 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.804+1818delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93478154 | |||||
| chr9:93478277
|
A | T | 25 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.804+1939A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478277 | ||||||
| chr9:93478278
|
G | GT | 25 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.804+1940_804+1941i others(3): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478278 | ||||||
| chr9:93478279
|
G | GT | 13 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(10): Show | 14 | HG01243.hp2 HG01346.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.804+1954dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93478279 | |||||
| chr9:93478279
|
G | T | 25 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.804+1941G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478279 | ||||||
| chr9:93478297
|
G | A | 29 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0003g0041others(26): Show | 29 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.804+1959G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478297 | ||||||
| chr9:93478432
|
G | A | 1 | a0001c0002t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.804+2094G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478432 | ||||||
| chr9:93478655
|
T | C | 2 | a0001c0002t0008g0252a0001c0002t0008g0253 | 2 | HG00639.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.804+2317T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478655 | ||||||
| chr9:93478691
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+2353G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478691 | ||||||
| chr9:93478751
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.804+2413T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478751 | ||||||
| chr9:93478758
|
G | T | 1 | a0001c0002t0001g0226 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.804+2420G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478758 | ||||||
| chr9:93478767
|
C | T | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.804+2429C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478767 | ||||||
| chr9:93478949
|
G | T | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.804+2611G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478949 | ||||||
| chr9:93478961
|
A | G | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.804+2623A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478961 | ||||||
| chr9:93478981
|
G | A | 17 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(14): Show | 17 | HG00438.hp2 HG00558.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.804+2643G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93478981 | ||||||
| chr9:93479031
|
T | C | 3 | a0001c0002t0001g0187a0001c0002t0001g0204a0001c0002t0001g0205 | 3 | HG00323.hp1 HG01243.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.804+2693T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479031 | ||||||
| chr9:93479047
|
G | A | 1 | a0001c0003t0002g0306 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.804+2709G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479047 | ||||||
| chr9:93479078
|
T | A | 13 | a0001c0001t0001g0142a0001c0001t0002g0136a0001c0001t0002g0137others(10): Show | 13 | HG00423.hp1 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.804+2740T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479078 | ||||||
| chr9:93479090
|
A | ATT | 6 | a0001c0002t0002g0302a0001c0002t0002g0303a0001c0002t0007g0237others(3): Show | 6 | HG01175.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+2777_804+2778d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93479090 | |||||
| chr9:93479090
|
AT | A | 175 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(172): Show | 177 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.804+2778delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93479090 | |||||
| chr9:93479090
|
ATT | A | 69 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0131others(66): Show | 70 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.804+2777_804+2778d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93479090 | |||||
| chr9:93479090
|
ATTT | A | 29 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(26): Show | 29 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.804+2776_804+2778d others(5): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93479090 | |||||
| chr9:93479111
|
T | C | 83 | a0001c0002t0001g0002a0001c0002t0001g0177a0001c0002t0001g0179others(80): Show | 84 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.804+2773T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479111 | ||||||
| chr9:93479159
|
C | T | 2 | a0001c0001t0002g0298a0001c0001t0002g0299 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.804+2821C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479159 | ||||||
| chr9:93479184
|
C | T | 2 | a0001c0002t0007g0178a0001c0002t0007g0246 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.804+2846C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479184 | ||||||
| chr9:93479192
|
G | A | 1 | a0001c0002t0001g0188 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.804+2854G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479192 | ||||||
| chr9:93479289
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+2951G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479289 | ||||||
| chr9:93479450
|
C | G | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.804+3112C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479450 | ||||||
| chr9:93479516
|
T | C | 17 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(14): Show | 17 | HG00438.hp2 HG00558.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.804+3178T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479516 | ||||||
| chr9:93479526
|
C | T | 5 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0243others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+3188C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479526 | ||||||
| chr9:93479809
|
TCTGA | T | 10 | a0001c0001t0001g0142a0001c0001t0002g0139a0001c0001t0002g0140others(7): Show | 10 | HG00423.hp1 HG01192.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.804+3475_804+3478d others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93479809 | |||||
| chr9:93479859
|
C | G | 1 | a0001c0002t0001g0205 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.804+3521C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479859 | ||||||
| chr9:93479898
|
C | T | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.804+3560C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479898 | ||||||
| chr9:93479899
|
G | A | 1 | a0001c0002t0007g0239 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.804+3561G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93479899 | ||||||
| chr9:93480173
|
T | C | 306 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(303): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.804+3835T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93480173 | ||||||
| chr9:93480245
|
G | A | 62 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.804+3907G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93480245 | ||||||
| chr9:93480372
|
T | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(189): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.804+4034T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93480372 | ||||||
| chr9:93480399
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.804+4061C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93480399 | ||||||
| chr9:93480481
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+4143G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93480481 | ||||||
| chr9:93480854
|
C | T | 1 | a0001c0001t0002g0130 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.804+4516C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93480854 | ||||||
| chr9:93480949
|
G | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+4611G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93480949 | ||||||
| chr9:93480964
|
A | G | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+4626A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93480964 | ||||||
| chr9:93481019
|
T | G | 312 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(309): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.804+4681T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93481019 | ||||||
| chr9:93481072
|
T | C | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+4734T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93481072 | ||||||
| chr9:93481238
|
C | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.804+4900C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93481238 | ||||||
| chr9:93481284
|
C | T | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.804+4946C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93481284 | ||||||
| chr9:93481384
|
G | A | 59 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(56): Show | 59 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.804+5046G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93481384 | ||||||
| chr9:93481463
|
A | G | 93 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(90): Show | 93 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.804+5125A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93481463 | ||||||
| chr9:93481566
|
A | T | 2 | a0001c0003t0002g0003a0001c0003t0002g0305 | 3 | HG02895.hp1 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.804+5228A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93481566 | ||||||
| chr9:93481709
|
G | C | 2 | a0001c0001t0003g0081a0001c0001t0003g0082 | 2 | NA18984.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.804+5371G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93481709 | ||||||
| chr9:93482071
|
A | G | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+5733A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93482071 | ||||||
| chr9:93482128
|
C | T | 59 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(56): Show | 59 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.804+5790C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93482128 | ||||||
| chr9:93482184
|
A | ATTTTT | 78 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0045others(75): Show | 79 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.804+5861_804+5865d others(7): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93482184 | |||||
| chr9:93482184
|
AT | A | 12 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(9): Show | 12 | HG00423.hp1 HG01175.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.804+5865delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93482184 | |||||
| chr9:93482280
|
C | T | 25 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.804+5942C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93482280 | ||||||
| chr9:93482440
|
C | G | 2 | a0001c0002t0001g0286a0001c0002t0001g0287 | 2 | NA19064.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.804+6102C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93482440 | ||||||
| chr9:93482459
|
A | G | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.804+6121A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93482459 | ||||||
| chr9:93482574
|
CT | C | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.804+6240delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93482574 | |||||
| chr9:93482709
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+6371C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93482709 | ||||||
| chr9:93483005
|
C | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.804+6667C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93483005 | ||||||
| chr9:93483080
|
G | C | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+6742G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93483080 | ||||||
| chr9:93483133
|
C | T | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.804+6795C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93483133 | ||||||
| chr9:93483288
|
A | C | 1 | a0001c0002t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.804+6950A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93483288 | ||||||
| chr9:93483386
|
T | G | 16 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0277others(13): Show | 16 | HG00438.hp2 HG00558.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.804+7048T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93483386 | ||||||
| chr9:93483405
|
T | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.804+7067T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93483405 | ||||||
| chr9:93483430
|
A | G | 63 | a0001c0001t0002g0013a0001c0003t0002g0005a0001c0003t0002g0006others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.804+7092A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93483430 | ||||||
| chr9:93483564
|
GAAAC | G | 4 | a0001c0002t0002g0274a0001c0002t0002g0275a0001c0002t0002g0302others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+7229_804+7232d others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93483564 | |||||
| chr9:93483831
|
G | T | 34 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.804+7493G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93483831 | ||||||
| chr9:93483898
|
C | T | 21 | a0001c0002t0001g0002a0001c0002t0001g0179a0001c0002t0001g0181others(18): Show | 22 | HG00558.hp1 HG00735.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.804+7560C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93483898 | ||||||
| chr9:93484038
|
C | CT | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.804+7713dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93484038 | |||||
| chr9:93484038
|
CT | C | 8 | a0001c0001t0002g0013a0001c0001t0002g0143a0001c0001t0003g0090others(5): Show | 8 | HG01081.hp1 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+7713delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93484038 | |||||
| chr9:93484204
|
C | T | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.804+7866C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484204 | ||||||
| chr9:93484276
|
A | G | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.804+7938A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484276 | ||||||
| chr9:93484286
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+7948G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484286 | ||||||
| chr9:93484394
|
T | G | 1 | a0001c0001t0001g0056 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.804+8056T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484394 | ||||||
| chr9:93484451
|
A | G | 2 | a0001c0003t0002g0149a0001c0003t0002g0150 | 2 | NA18984.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.804+8113A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484451 | ||||||
| chr9:93484505
|
C | T | 1 | a0001c0001t0016g0312 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.804+8167C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484505 | ||||||
| chr9:93484534
|
A | G | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+8196A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484534 | ||||||
| chr9:93484606
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+8268C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484606 | ||||||
| chr9:93484687
|
C | T | 1 | a0001c0001t0003g0077 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.804+8349C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484687 | ||||||
| chr9:93484825
|
C | T | 1 | a0001c0001t0004g0101 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.804+8487C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484825 | ||||||
| chr9:93484832
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+8494C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484832 | ||||||
| chr9:93484836
|
A | G | 16 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0277others(13): Show | 16 | HG00438.hp2 HG00558.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.804+8498A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484836 | ||||||
| chr9:93484995
|
C | G | 1 | a0001c0001t0004g0037 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.804+8657C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93484995 | ||||||
| chr9:93485015
|
A | G | 1 | a0001c0003t0002g0308 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.804+8677A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93485015 | ||||||
| chr9:93485251
|
G | A | 2 | a0001c0001t0003g0001a0001c0001t0003g0059 | 3 | HG01099.hp1 HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.804+8913G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93485251 | ||||||
| chr9:93485263
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+8925G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93485263 | ||||||
| chr9:93485429
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+9091C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93485429 | ||||||
| chr9:93485432
|
T | C | 1 | a0001c0001t0003g0107 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.804+9094T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93485432 | ||||||
| chr9:93485470
|
C | T | 1 | a0001c0002t0001g0224 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.804+9132C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93485470 | ||||||
| chr9:93485479
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.804+9141C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93485479 | ||||||
| chr9:93485602
|
A | G | 10 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(7): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.804+9264A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93485602 | ||||||
| chr9:93485763
|
A | G | 2 | a0001c0001t0003g0282a0001c0001t0003g0283 | 2 | NA19054.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.804+9425A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93485763 | ||||||
| chr9:93485773
|
G | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | NA18952.hp1 NA18975.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+9435G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93485773 | ||||||
| chr9:93485959
|
A | G | 1 | a0001c0002t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.804+9621A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93485959 | ||||||
| chr9:93486036
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+9698G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93486036 | ||||||
| chr9:93486200
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.804+9862C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93486200 | ||||||
| chr9:93486351
|
T | A | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.804+10013T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93486351 | ||||||
| chr9:93486495
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.804+10157A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93486495 | ||||||
| chr9:93486535
|
CT | C | 6 | a0001c0001t0003g0049a0001c0001t0004g0102a0001c0002t0001g0181others(3): Show | 6 | HG01884.hp1 HG02965.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+10211delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93486535 | |||||
| chr9:93486565
|
A | G | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG00558.hp2 HG02135.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.804+10227A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93486565 | ||||||
| chr9:93486661
|
G | A | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.804+10323G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93486661 | ||||||
| chr9:93486737
|
T | C | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+10399T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93486737 | ||||||
| chr9:93486851
|
G | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.804+10513G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93486851 | ||||||
| chr9:93486906
|
C | T | 1 | a0001c0001t0003g0070 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.805-10565C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93486906 | ||||||
| chr9:93486957
|
A | G | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.805-10514A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93486957 | ||||||
| chr9:93487188
|
G | T | 1 | a0001c0001t0003g0061 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.805-10283G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93487188 | ||||||
| chr9:93487189
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.805-10282C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93487189 | ||||||
| chr9:93487310
|
C | T | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.805-10161C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93487310 | ||||||
| chr9:93487542
|
G | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.805-9929G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93487542 | ||||||
| chr9:93487566
|
T | C | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.805-9905T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93487566 | ||||||
| chr9:93487631
|
A | C | 1 | a0001c0002t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.805-9840A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93487631 | ||||||
| chr9:93487695
|
C | T | 1 | a0001c0003t0002g0307 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.805-9776C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93487695 | ||||||
| chr9:93487783
|
G | A | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.805-9688G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93487783 | ||||||
| chr9:93487805
|
G | A | 18 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.805-9666G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93487805 | ||||||
| chr9:93487928
|
A | C | 1 | a0001c0001t0003g0032 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.805-9543A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93487928 | ||||||
| chr9:93487952
|
C | G | 1 | a0001c0001t0002g0132 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.805-9519C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93487952 | ||||||
| chr9:93488017
|
C | G | 1 | a0001c0008t0001g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805-9454C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93488017 | ||||||
| chr9:93488115
|
G | A | 1 | a0001c0001t0003g0064 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.805-9356G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93488115 | ||||||
| chr9:93488232
|
G | T | 1 | a0001c0008t0001g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805-9239G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93488232 | ||||||
| chr9:93488292
|
A | G | 1 | a0001c0008t0001g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805-9179A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93488292 | ||||||
| chr9:93488322
|
T | C | 306 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(303): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.805-9149T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93488322 | ||||||
| chr9:93488779
|
T | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(78): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.805-8692T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93488779 | ||||||
| chr9:93489008
|
T | TA | 107 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(104): Show | 108 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.805-8447dupA | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93489008 | |||||
| chr9:93489008
|
T | TAA | 16 | a0001c0001t0001g0284a0001c0001t0002g0013a0001c0001t0002g0277others(13): Show | 16 | HG00438.hp2 HG00558.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.805-8448_805-8447d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93489008 | |||||
| chr9:93489008
|
TA | T | 8 | a0001c0002t0001g0222a0001c0002t0001g0223a0001c0002t0002g0274others(5): Show | 8 | HG00140.hp2 HG00558.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.805-8447delA | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93489008 | |||||
| chr9:93489036
|
A | C | 80 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(77): Show | 81 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.805-8435A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93489036 | ||||||
| chr9:93489098
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | NA18952.hp1 NA18959.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-8373C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93489098 | ||||||
| chr9:93489201
|
C | A | 292 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(289): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.805-8270C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93489201 | ||||||
| chr9:93489286
|
A | G | 25 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.805-8185A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93489286 | ||||||
| chr9:93489287
|
T | C | 1 | a0001c0001t0002g0143 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.805-8184T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93489287 | ||||||
| chr9:93489371
|
G | GGTATTCC others(2): Show |
35 | a0001c0002t0001g0227a0001c0003t0002g0118a0001c0003t0002g0147others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.805-8092_805-8091i others(11): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93489371 | |||||
| chr9:93489416
|
C | G | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.805-8055C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93489416 | ||||||
| chr9:93489464
|
C | T | 2 | a0001c0003t0002g0153a0001c0003t0002g0161 | 2 | HG00140.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.805-8007C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93489464 | ||||||
| chr9:93489468
|
G | A | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.805-8003G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93489468 | ||||||
| chr9:93489642
|
A | T | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-7829A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93489642 | ||||||
| chr9:93490001
|
A | G | 6 | a0001c0002t0007g0236a0001c0002t0007g0237a0001c0002t0008g0238others(3): Show | 6 | HG00642.hp2 HG01175.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-7470A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93490001 | ||||||
| chr9:93490093
|
T | C | 1 | a0001c0001t0003g0099 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.805-7378T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93490093 | ||||||
| chr9:93490101
|
A | G | 1 | a0001c0001t0003g0001 | 2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.805-7370A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93490101 | ||||||
| chr9:93490772
|
A | G | 1 | a0001c0003t0002g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.805-6699A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93490772 | ||||||
| chr9:93490807
|
C | T | 1 | a0002c0009t0002g0135 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.805-6664C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93490807 | ||||||
| chr9:93490856
|
A | G | 1 | a0001c0002t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.805-6615A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93490856 | ||||||
| chr9:93490887
|
C | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.805-6584C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93490887 | ||||||
| chr9:93490896
|
T | G | 111 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(108): Show | 112 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.805-6575T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93490896 | ||||||
| chr9:93491112
|
G | T | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.805-6359G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93491112 | ||||||
| chr9:93491157
|
T | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.805-6314T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93491157 | ||||||
| chr9:93491169
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.805-6302C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93491169 | ||||||
| chr9:93491188
|
G | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.805-6283G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93491188 | ||||||
| chr9:93491390
|
A | T | 2 | a0001c0002t0001g0188a0001c0002t0001g0200 | 2 | NA19010.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.805-6081A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93491390 | ||||||
| chr9:93491415
|
A | G | 1 | a0001c0003t0002g0174 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.805-6056A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93491415 | ||||||
| chr9:93491810
|
CT | C | 117 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(114): Show | 118 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.805-5650delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93491810 | |||||
| chr9:93491988
|
T | G | 25 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.805-5483T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93491988 | ||||||
| chr9:93492000
|
G | A | 1 | a0001c0003t0002g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.805-5471G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492000 | ||||||
| chr9:93492164
|
T | TTG | 5 | a0001c0001t0002g0277a0001c0001t0002g0278a0001c0001t0003g0001others(2): Show | 6 | HG01099.hp1 HG01192.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-5291_805-5290d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93492164 | |||||
| chr9:93492178
|
G | GTA | 24 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(21): Show | 24 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.805-5292_805-5291i others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93492178 | |||||
| chr9:93492180
|
G | A | 64 | a0001c0002t0001g0177a0001c0002t0001g0276a0001c0003t0002g0003others(61): Show | 65 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.805-5291G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492180 | ||||||
| chr9:93492180
|
GTA | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 9 | HG01109.hp1 HG01516.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.805-5277_805-5276d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93492180 | |||||
| chr9:93492182
|
A | G | 85 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0060others(82): Show | 86 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.805-5289A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492182 | ||||||
| chr9:93492184
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(4): Show | 7 | HG02451.hp2 HG02896.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.805-5287A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492184 | ||||||
| chr9:93492243
|
T | A | 1 | a0001c0002t0001g0206 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.805-5228T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492243 | ||||||
| chr9:93492276
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.805-5195A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492276 | ||||||
| chr9:93492329
|
T | C | 1 | a0001c0001t0005g0289 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.805-5142T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492329 | ||||||
| chr9:93492466
|
G | C | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.805-5005G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492466 | ||||||
| chr9:93492478
|
G | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.805-4993G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492478 | ||||||
| chr9:93492583
|
C | T | 295 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.805-4888C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492583 | ||||||
| chr9:93492632
|
G | A | 1 | a0001c0001t0003g0072 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.805-4839G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492632 | ||||||
| chr9:93492661
|
C | T | 2 | a0001c0002t0001g0300a0001c0002t0001g0301 | 2 | NA19063.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.805-4810C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492661 | ||||||
| chr9:93492940
|
G | C | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.805-4531G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492940 | ||||||
| chr9:93492982
|
C | T | 18 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.805-4489C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93492982 | ||||||
| chr9:93493111
|
G | A | 1 | a0001c0003t0002g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.805-4360G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93493111 | ||||||
| chr9:93493322
|
T | C | 13 | a0001c0001t0001g0142a0001c0001t0002g0136a0001c0001t0002g0137others(10): Show | 13 | HG00423.hp1 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.805-4149T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93493322 | ||||||
| chr9:93493523
|
C | G | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.805-3948C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93493523 | ||||||
| chr9:93493562
|
C | T | 1 | a0001c0001t0002g0277 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.805-3909C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93493562 | ||||||
| chr9:93493663
|
G | A | 5 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(2): Show | 5 | HG00558.hp2 HG02135.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-3808G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93493663 | ||||||
| chr9:93493752
|
G | C | 1 | a0001c0001t0003g0095 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.805-3719G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93493752 | ||||||
| chr9:93493835
|
GC | G | 4 | a0001c0003t0002g0155a0001c0003t0002g0156a0001c0003t0002g0157others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-3634delC | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93493835 | |||||
| chr9:93493884
|
G | A | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.805-3587G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93493884 | ||||||
| chr9:93494046
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.805-3425C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494046 | ||||||
| chr9:93494100
|
C | T | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.805-3371C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494100 | ||||||
| chr9:93494176
|
T | C | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.805-3295T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494176 | ||||||
| chr9:93494205
|
C | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.805-3266C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494205 | ||||||
| chr9:93494228
|
G | A | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-3243G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494228 | ||||||
| chr9:93494278
|
A | G | 1 | a0001c0002t0001g0271 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.805-3193A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494278 | ||||||
| chr9:93494301
|
G | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.805-3170G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494301 | ||||||
| chr9:93494319
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.805-3152G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494319 | ||||||
| chr9:93494406
|
G | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.805-3065G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494406 | ||||||
| chr9:93494410
|
C | T | 30 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0002g0098others(27): Show | 30 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.805-3061C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494410 | ||||||
| chr9:93494494
|
C | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.805-2977C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494494 | ||||||
| chr9:93494565
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(84): Show | 88 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.805-2906G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494565 | ||||||
| chr9:93494595
|
C | T | 1 | a0001c0001t0003g0055 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.805-2876C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494595 | ||||||
| chr9:93494600
|
A | C | 1 | a0001c0002t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.805-2871A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494600 | ||||||
| chr9:93494767
|
C | G | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.805-2704C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494767 | ||||||
| chr9:93494807
|
G | A | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.805-2664G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494807 | ||||||
| chr9:93494906
|
A | G | 1 | a0001c0006t0002g0280 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.805-2565A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494906 | ||||||
| chr9:93494940
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.805-2531G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93494940 | ||||||
| chr9:93495110
|
G | T | 1 | a0001c0001t0002g0277 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.805-2361G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93495110 | ||||||
| chr9:93495149
|
G | A | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-2322G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93495149 | ||||||
| chr9:93495344
|
A | G | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.805-2127A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93495344 | ||||||
| chr9:93495368
|
A | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.805-2103A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93495368 | ||||||
| chr9:93495646
|
A | T | 1 | a0001c0002t0001g0223 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.805-1825A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93495646 | ||||||
| chr9:93495914
|
A | G | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-1557A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93495914 | ||||||
| chr9:93496048
|
T | C | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.805-1423T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93496048 | ||||||
| chr9:93496264
|
G | A | 2 | a0001c0002t0008g0252a0001c0002t0008g0253 | 2 | HG00639.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.805-1207G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93496264 | ||||||
| chr9:93496556
|
C | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.805-915C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93496556 | ||||||
| chr9:93496557
|
G | A | 23 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.805-914G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93496557 | ||||||
| chr9:93496749
|
A | G | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.805-722A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93496749 | ||||||
| chr9:93497044
|
C | CT | 17 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.805-425dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93497044 | |||||
| chr9:93497160
|
C | A | 1 | a0001c0001t0005g0292 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.805-311C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93497160 | ||||||
| chr9:93497300
|
C | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.805-171C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 3/17 | chr9 | 93497300 | ||||||
| chr9:93497601
|
T | TA | 114 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(111): Show | 115 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.933+13dupA | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr9 | 93497601 | |||||
| chr9:93497613
|
C | A | 1 | a0001c0003t0002g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.933+14C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 4/17 | chr9 | 93497613 | ||||||
| chr9:93497662
|
G | A | 3 | a0001c0002t0001g0183a0001c0002t0001g0207a0001c0002t0001g0208 | 3 | HG00609.hp2 NA18747.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.933+63G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 4/17 | chr9 | 93497662 | ||||||
| chr9:93498292
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.934-498C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 4/17 | chr9 | 93498292 | ||||||
| chr9:93498318
|
G | A | 1 | a0001c0003t0002g0151 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.934-472G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 4/17 | chr9 | 93498318 | ||||||
| chr9:93498356
|
G | A | 1 | a0001c0011t0002g0009 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.934-434G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 4/17 | chr9 | 93498356 | ||||||
| chr9:93498398
|
A | T | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.934-392A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 4/17 | chr9 | 93498398 | ||||||
| chr9:93498522
|
A | G | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.934-268A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 4/17 | chr9 | 93498522 | ||||||
| chr9:93498636
|
A | G | 1 | a0001c0007t0012g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.934-154A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 4/17 | chr9 | 93498636 | ||||||
| chr9:93498762
|
T | C | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.934-28T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 4/17 | chr9 | 93498762 | ||||||
| chr9:93498956
|
A | G | 2 | a0001c0003t0002g0156a0001c0003t0002g0157 | 2 | HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1030+70A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93498956 | ||||||
| chr9:93499402
|
C | T | 2 | a0001c0001t0004g0047a0001c0001t0004g0048 | 2 | HG00642.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1030+516C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93499402 | ||||||
| chr9:93499600
|
A | G | 2 | a0001c0001t0005g0289a0001c0001t0005g0294 | 2 | HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1030+714A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93499600 | ||||||
| chr9:93499678
|
G | A | 79 | a0001c0002t0001g0002a0001c0002t0001g0177a0001c0002t0001g0179others(76): Show | 80 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1030+792G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93499678 | ||||||
| chr9:93499788
|
T | C | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030+902T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93499788 | ||||||
| chr9:93499824
|
G | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1030+938G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93499824 | ||||||
| chr9:93499972
|
G | A | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030+1086G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93499972 | ||||||
| chr9:93499988
|
G | A | 7 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0125others(4): Show | 7 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1030+1102G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93499988 | ||||||
| chr9:93500150
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1030+1264C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93500150 | ||||||
| chr9:93500155
|
C | T | 22 | a0001c0003t0002g0118a0001c0003t0002g0148a0001c0003t0002g0149others(19): Show | 22 | HG00673.hp1 HG01123.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1030+1269C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93500155 | ||||||
| chr9:93500156
|
A | G | 18 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1030+1270A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93500156 | ||||||
| chr9:93500443
|
C | T | 26 | a0001c0001t0001g0142a0001c0001t0002g0121a0001c0001t0002g0122others(23): Show | 26 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1030+1557C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93500443 | ||||||
| chr9:93500444
|
G | A | 8 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(5): Show | 9 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1030+1558G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93500444 | ||||||
| chr9:93500510
|
C | T | 2 | a0001c0003t0002g0155a0001c0003t0002g0165 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1030+1624C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93500510 | ||||||
| chr9:93500619
|
G | T | 3 | a0001c0003t0006g0014a0001c0003t0006g0021a0001c0003t0006g0025 | 3 | HG02109.hp1 HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1030+1733G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93500619 | ||||||
| chr9:93500657
|
A | G | 1 | a0001c0002t0007g0239 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1030+1771A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93500657 | ||||||
| chr9:93500824
|
T | C | 2 | a0001c0002t0001g0219a0001c0002t0001g0222 | 2 | NA18972.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1030+1938T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93500824 | ||||||
| chr9:93500911
|
T | C | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1030+2025T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93500911 | ||||||
| chr9:93500979
|
G | A | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1030+2093G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93500979 | ||||||
| chr9:93501361
|
A | G | 2 | a0001c0003t0002g0149a0001c0003t0002g0150 | 2 | NA18984.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1030+2475A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93501361 | ||||||
| chr9:93501374
|
T | C | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1030+2488T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93501374 | ||||||
| chr9:93501531
|
G | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1030+2645G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93501531 | ||||||
| chr9:93501827
|
A | C | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1030+2941A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93501827 | ||||||
| chr9:93502031
|
C | T | 292 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(289): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1030+3145C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93502031 | ||||||
| chr9:93502245
|
AATC | A | 8 | a0001c0003t0006g0014a0001c0003t0006g0017a0001c0003t0006g0021others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030+3362_1030+336 others(7): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93502245 | |||||
| chr9:93502374
|
T | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1030+3488T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93502374 | ||||||
| chr9:93502491
|
A | G | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1030+3605A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93502491 | ||||||
| chr9:93502565
|
T | TAC | 13 | a0001c0001t0002g0278a0001c0001t0002g0310a0001c0001t0002g0311others(10): Show | 14 | HG00642.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1030+3712_1030+371 others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93502565 | |||||
| chr9:93502565
|
T | TACAC | 7 | a0001c0001t0002g0277a0001c0002t0001g0218a0001c0002t0001g0221others(4): Show | 7 | HG01123.hp2 HG01884.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1030+3710_1030+371 others(8): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93502565 | |||||
| chr9:93502565
|
T | TACACAC | 5 | a0001c0002t0001g0181a0001c0002t0001g0198a0001c0002t0001g0199others(2): Show | 5 | HG00140.hp1 HG00673.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.1030+3708_1030+371 others(10): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93502565 | |||||
| chr9:93502565
|
T | TACACACA others(1): Show |
60 | a0001c0002t0001g0002a0001c0002t0001g0180a0001c0002t0001g0182others(57): Show | 61 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.1030+3706_1030+371 others(12): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93502565 | |||||
| chr9:93502565
|
T | TACACACA others(3): Show |
7 | a0001c0002t0001g0179a0001c0002t0001g0191a0001c0002t0001g0192others(4): Show | 7 | HG01361.hp1 HG02056.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1030+3704_1030+371 others(14): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93502565 | |||||
| chr9:93502565
|
T | TACACACA others(5): Show |
5 | a0001c0002t0001g0177a0001c0002t0001g0189a0001c0002t0001g0204others(2): Show | 5 | HG00323.hp1 HG01993.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1030+3702_1030+371 others(16): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93502565 | |||||
| chr9:93502565
|
T | TACACACA others(7): Show |
1 | a0001c0002t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1030+3700_1030+371 others(18): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93502565 | |||||
| chr9:93502565
|
TAC | T | 147 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(144): Show | 148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1030+3712_1030+371 others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93502565 | |||||
| chr9:93502565
|
TACAC | T | 33 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(30): Show | 33 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1030+3710_1030+371 others(8): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93502565 | |||||
| chr9:93502594
|
A | G | 1 | a0001c0003t0002g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1030+3708A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93502594 | ||||||
| chr9:93502629
|
T | C | 197 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(194): Show | 199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1030+3743T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93502629 | ||||||
| chr9:93502681
|
T | C | 1 | a0001c0001t0003g0053 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1030+3795T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93502681 | ||||||
| chr9:93502966
|
G | A | 2 | a0001c0001t0005g0289a0001c0001t0005g0294 | 2 | HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1030+4080G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93502966 | ||||||
| chr9:93502976
|
C | T | 205 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1030+4090C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93502976 | ||||||
| chr9:93503318
|
C | T | 98 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(95): Show | 99 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1030+4432C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93503318 | ||||||
| chr9:93503413
|
G | A | 4 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0083others(1): Show | 4 | HG01928.hp2 HG01978.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1030+4527G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93503413 | ||||||
| chr9:93503828
|
CA | C | 37 | a0001c0001t0001g0004a0001c0001t0001g0056a0001c0001t0001g0067others(34): Show | 37 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.1030+4952delA | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93503828 | |||||
| chr9:93503865
|
A | G | 67 | a0001c0003t0002g0003a0001c0003t0002g0005a0001c0003t0002g0006others(64): Show | 68 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.1030+4979A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93503865 | ||||||
| chr9:93504445
|
T | C | 1 | a0001c0002t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1030+5559T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93504445 | ||||||
| chr9:93504701
|
A | G | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1030+5815A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93504701 | ||||||
| chr9:93504989
|
T | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1030+6103T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93504989 | ||||||
| chr9:93505044
|
C | T | 1 | a0001c0002t0001g0255 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1030+6158C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93505044 | ||||||
| chr9:93505051
|
G | GT | 57 | a0001c0001t0002g0127a0001c0001t0002g0132a0001c0001t0002g0134others(54): Show | 57 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1030+6192dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93505051 | |||||
| chr9:93505051
|
G | GTT | 32 | a0001c0001t0002g0310a0001c0002t0001g0002a0001c0002t0001g0179others(29): Show | 33 | HG00558.hp1 HG00735.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1030+6191_1030+619 others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93505051 | |||||
| chr9:93505051
|
GT | G | 53 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(50): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1030+6192delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93505051 | |||||
| chr9:93505051
|
GTT | G | 13 | a0001c0003t0002g0003a0001c0003t0002g0028a0001c0003t0002g0029others(10): Show | 14 | HG02717.hp2 HG02723.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.1030+6191_1030+619 others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93505051 | |||||
| chr9:93505051
|
GTTTTTTT others(3): Show |
G | 3 | a0001c0001t0003g0097a0001c0001t0003g0282a0001c0001t0003g0283 | 3 | NA19054.hp2 NA19088.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1030+6183_1030+619 others(14): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93505051 | |||||
| chr9:93505051
|
GTTTTTTT others(4): Show |
G | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1030+6182_1030+619 others(15): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93505051 | |||||
| chr9:93505051
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0003g0095 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1030+6181_1030+619 others(16): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93505051 | |||||
| chr9:93505092
|
G | A | 1 | a0001c0002t0001g0195 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1030+6206G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93505092 | ||||||
| chr9:93505107
|
C | G | 1 | a0001c0003t0002g0171 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1030+6221C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93505107 | ||||||
| chr9:93505154
|
A | G | 111 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(108): Show | 112 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1030+6268A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93505154 | ||||||
| chr9:93505303
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1030+6417G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93505303 | ||||||
| chr9:93505306
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1030+6420C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93505306 | ||||||
| chr9:93505319
|
C | T | 1 | a0001c0002t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1030+6433C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93505319 | ||||||
| chr9:93505336
|
A | G | 2 | a0001c0002t0001g0111a0001c0002t0001g0304 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1030+6450A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93505336 | ||||||
| chr9:93505364
|
C | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1030+6478C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93505364 | ||||||
| chr9:93505555
|
T | G | 12 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0003g0049others(9): Show | 12 | HG00438.hp1 HG02155.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.1030+6669T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93505555 | ||||||
| chr9:93505725
|
T | C | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1030+6839T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93505725 | ||||||
| chr9:93505896
|
GTT | G | 195 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(192): Show | 197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1030+7014_1030+701 others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93505896 | |||||
| chr9:93506026
|
A | G | 59 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(56): Show | 59 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1030+7140A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93506026 | ||||||
| chr9:93506055
|
G | A | 3 | a0001c0003t0002g0148a0001c0003t0002g0151a0001c0003t0002g0154 | 3 | HG00673.hp1 NA19010.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1030+7169G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93506055 | ||||||
| chr9:93506111
|
A | G | 1 | a0001c0002t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1030+7225A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93506111 | ||||||
| chr9:93506196
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1030+7310C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93506196 | ||||||
| chr9:93506223
|
C | A | 1 | a0001c0002t0001g0264 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1030+7337C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93506223 | ||||||
| chr9:93506564
|
C | A | 1 | a0001c0001t0002g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1030+7678C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93506564 | ||||||
| chr9:93506584
|
AT | A | 59 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(56): Show | 59 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1030+7709delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93506584 | |||||
| chr9:93506619
|
A | G | 2 | a0001c0003t0002g0153a0001c0003t0002g0161 | 2 | HG00140.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1030+7733A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93506619 | ||||||
| chr9:93506637
|
G | A | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1030+7751G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93506637 | ||||||
| chr9:93506718
|
C | T | 1 | a0001c0003t0002g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1030+7832C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93506718 | ||||||
| chr9:93506733
|
G | T | 1 | a0001c0002t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1030+7847G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93506733 | ||||||
| chr9:93506902
|
G | A | 290 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(287): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1030+8016G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93506902 | ||||||
| chr9:93507133
|
G | T | 2 | a0001c0001t0003g0103a0001c0001t0003g0104 | 2 | HG02040.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1030+8247G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93507133 | ||||||
| chr9:93507314
|
C | T | 1 | a0001c0001t0003g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1031-8353C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93507314 | ||||||
| chr9:93507516
|
A | G | 8 | a0001c0003t0006g0014a0001c0003t0006g0017a0001c0003t0006g0021others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-8151A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93507516 | ||||||
| chr9:93507520
|
G | T | 3 | a0001c0002t0001g0195a0001c0002t0001g0216a0001c0002t0001g0217 | 3 | NA19067.hp1 NA19079.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1031-8147G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93507520 | ||||||
| chr9:93507677
|
C | T | 1 | a0001c0002t0001g0245 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1031-7990C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93507677 | ||||||
| chr9:93507694
|
T | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | NA18952.hp1 NA18975.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1031-7973T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93507694 | ||||||
| chr9:93507728
|
G | A | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1031-7939G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93507728 | ||||||
| chr9:93507778
|
A | G | 1 | a0001c0002t0001g0231 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1031-7889A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93507778 | ||||||
| chr9:93507955
|
G | C | 111 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(108): Show | 112 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1031-7712G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93507955 | ||||||
| chr9:93508017
|
G | C | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1031-7650G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93508017 | ||||||
| chr9:93508174
|
A | G | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-7493A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93508174 | ||||||
| chr9:93508412
|
G | A | 4 | a0001c0003t0002g0155a0001c0003t0002g0156a0001c0003t0002g0157others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1031-7255G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93508412 | ||||||
| chr9:93508474
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1031-7193C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93508474 | ||||||
| chr9:93508500
|
C | T | 3 | a0001c0006t0002g0279a0001c0006t0002g0280a0001c0006t0002g0281 | 3 | HG02886.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1031-7167C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93508500 | ||||||
| chr9:93508672
|
C | A | 4 | a0001c0002t0001g0002a0001c0002t0001g0201a0001c0002t0001g0221others(1): Show | 5 | HG01099.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1031-6995C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93508672 | ||||||
| chr9:93508764
|
A | G | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1031-6903A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93508764 | ||||||
| chr9:93508784
|
T | G | 1 | a0001c0002t0001g0190 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1031-6883T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93508784 | ||||||
| chr9:93509012
|
A | G | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1031-6655A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509012 | ||||||
| chr9:93509085
|
T | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1031-6582T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509085 | ||||||
| chr9:93509230
|
GCTGGACC others(3): Show |
G | 1 | a0001c0003t0010g0023 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1031-6425_1031-641 others(14): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93509230 | |||||
| chr9:93509470
|
G | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1031-6197G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509470 | ||||||
| chr9:93509539
|
A | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1031-6128A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509539 | ||||||
| chr9:93509648
|
G | A | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1031-6019G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509648 | ||||||
| chr9:93509765
|
G | A | 30 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0002g0098others(27): Show | 30 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1031-5902G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509765 | ||||||
| chr9:93509772
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1031-5895C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509772 | ||||||
| chr9:93509776
|
A | G | 7 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(4): Show | 7 | HG01081.hp2 HG02922.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1031-5891A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509776 | ||||||
| chr9:93509846
|
A | G | 1 | a0001c0002t0001g0230 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1031-5821A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509846 | ||||||
| chr9:93509872
|
A | G | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1031-5795A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509872 | ||||||
| chr9:93509979
|
G | A | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-5688G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509979 | ||||||
| chr9:93509989
|
A | T | 8 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(5): Show | 9 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1031-5678A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509989 | ||||||
| chr9:93509999
|
G | A | 5 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0243others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1031-5668G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93509999 | ||||||
| chr9:93510044
|
C | T | 1 | a0001c0005t0009g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1031-5623C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510044 | ||||||
| chr9:93510106
|
C | T | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1031-5561C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510106 | ||||||
| chr9:93510282
|
A | G | 300 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(297): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1031-5385A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510282 | ||||||
| chr9:93510342
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1031-5325C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510342 | ||||||
| chr9:93510343
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1031-5324C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510343 | ||||||
| chr9:93510364
|
C | T | 203 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(200): Show | 205 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1031-5303C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510364 | ||||||
| chr9:93510379
|
T | C | 1 | a0001c0003t0002g0165 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1031-5288T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510379 | ||||||
| chr9:93510380
|
G | A | 1 | a0001c0003t0002g0165 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1031-5287G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510380 | ||||||
| chr9:93510390
|
C | T | 1 | a0001c0011t0002g0009 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1031-5277C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510390 | ||||||
| chr9:93510418
|
T | C | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-5249T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510418 | ||||||
| chr9:93510478
|
T | C | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1031-5189T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510478 | ||||||
| chr9:93510528
|
C | G | 18 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1031-5139C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510528 | ||||||
| chr9:93510710
|
C | CT | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1031-4957_1031-495 others(5): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510710 | ||||||
| chr9:93510721
|
G | T | 1 | a0001c0001t0003g0070 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1031-4946G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510721 | ||||||
| chr9:93510879
|
G | C | 25 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1031-4788G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510879 | ||||||
| chr9:93510886
|
T | C | 25 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1031-4781T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510886 | ||||||
| chr9:93510891
|
A | G | 25 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1031-4776A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93510891 | ||||||
| chr9:93511073
|
A | G | 295 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1031-4594A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511073 | ||||||
| chr9:93511154
|
G | A | 23 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(20): Show | 24 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1031-4513G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511154 | ||||||
| chr9:93511203
|
T | C | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1031-4464T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511203 | ||||||
| chr9:93511264
|
C | A | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-4403C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511264 | ||||||
| chr9:93511283
|
C | T | 8 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(5): Show | 9 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1031-4384C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511283 | ||||||
| chr9:93511485
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1031-4182C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511485 | ||||||
| chr9:93511488
|
C | T | 13 | a0001c0001t0001g0142a0001c0001t0002g0136a0001c0001t0002g0137others(10): Show | 13 | HG00423.hp1 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1031-4179C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511488 | ||||||
| chr9:93511489
|
G | A | 1 | a0001c0002t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1031-4178G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511489 | ||||||
| chr9:93511553
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1031-4114G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511553 | ||||||
| chr9:93511628
|
C | T | 25 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1031-4039C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511628 | ||||||
| chr9:93511733
|
C | T | 1 | a0001c0002t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1031-3934C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511733 | ||||||
| chr9:93511885
|
A | G | 26 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1031-3782A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511885 | ||||||
| chr9:93511895
|
C | T | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-3772C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511895 | ||||||
| chr9:93511902
|
C | G | 2 | a0001c0002t0001g0197a0001c0002t0001g0202 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1031-3765C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511902 | ||||||
| chr9:93511905
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(9): Show | 12 | HG00423.hp2 HG02080.hp1 NA18941.hp1 others(9): Show |
intron_variant | MODIFIER | c.1031-3762C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511905 | ||||||
| chr9:93511980
|
C | T | 1 | a0001c0002t0001g0201 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1031-3687C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511980 | ||||||
| chr9:93511998
|
G | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18952.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1031-3669G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93511998 | ||||||
| chr9:93512223
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1031-3444G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93512223 | ||||||
| chr9:93512356
|
G | A | 8 | a0001c0003t0006g0014a0001c0003t0006g0017a0001c0003t0006g0021others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-3311G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93512356 | ||||||
| chr9:93512464
|
C | T | 1 | a0001c0001t0003g0053 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1031-3203C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93512464 | ||||||
| chr9:93512536
|
A | AT | 83 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0002t0001g0002others(80): Show | 84 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1031-3120dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93512536 | |||||
| chr9:93512548
|
A | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1031-3119A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93512548 | ||||||
| chr9:93512586
|
G | T | 2 | a0001c0002t0007g0236a0001c0002t0007g0237 | 2 | HG00642.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1031-3081G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93512586 | ||||||
| chr9:93512626
|
G | A | 1 | a0001c0003t0002g0308 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1031-3041G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93512626 | ||||||
| chr9:93512636
|
T | C | 1 | a0001c0002t0008g0248 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1031-3031T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93512636 | ||||||
| chr9:93513150
|
G | A | 2 | a0001c0003t0002g0003a0001c0003t0002g0305 | 3 | HG02895.hp1 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1031-2517G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513150 | ||||||
| chr9:93513337
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1031-2330G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513337 | ||||||
| chr9:93513384
|
G | A | 1 | a0001c0003t0002g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1031-2283G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513384 | ||||||
| chr9:93513623
|
C | T | 17 | a0001c0003t0002g0005a0001c0003t0002g0006a0001c0003t0002g0007others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.1031-2044C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513623 | ||||||
| chr9:93513624
|
G | A | 8 | a0001c0003t0006g0014a0001c0003t0006g0017a0001c0003t0006g0021others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-2043G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513624 | ||||||
| chr9:93513684
|
T | C | 203 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(200): Show | 205 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1031-1983T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513684 | ||||||
| chr9:93513694
|
T | C | 1 | a0001c0002t0001g0198 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1031-1973T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513694 | ||||||
| chr9:93513747
|
A | G | 8 | a0001c0003t0006g0014a0001c0003t0006g0017a0001c0003t0006g0021others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-1920A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513747 | ||||||
| chr9:93513801
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1031-1866C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513801 | ||||||
| chr9:93513825
|
G | C | 3 | a0001c0001t0003g0001a0001c0001t0003g0058a0001c0001t0003g0059 | 4 | HG01099.hp1 HG01192.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1031-1842G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513825 | ||||||
| chr9:93513843
|
G | A | 1 | a0001c0001t0003g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1031-1824G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513843 | ||||||
| chr9:93513853
|
T | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1031-1814T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513853 | ||||||
| chr9:93513946
|
AG | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1031-1720delG | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93513946 | ||||||
| chr9:93514132
|
G | A | 1 | a0001c0002t0001g0199 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1031-1535G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93514132 | ||||||
| chr9:93514179
|
A | G | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1031-1488A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93514179 | ||||||
| chr9:93514269
|
C | T | 1 | a0001c0002t0001g0177 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1031-1398C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93514269 | ||||||
| chr9:93514334
|
G | A | 2 | a0001c0001t0005g0294a0001c0003t0006g0025 | 2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1031-1333G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93514334 | ||||||
| chr9:93514628
|
C | G | 47 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(44): Show | 48 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.1031-1039C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93514628 | ||||||
| chr9:93514736
|
C | G | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1031-931C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93514736 | ||||||
| chr9:93514794
|
C | T | 1 | a0001c0001t0003g0069 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1031-873C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93514794 | ||||||
| chr9:93514808
|
C | T | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-859C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93514808 | ||||||
| chr9:93514846
|
G | A | 1 | a0001c0002t0001g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1031-821G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93514846 | ||||||
| chr9:93515083
|
A | T | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1031-584A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93515083 | ||||||
| chr9:93515115
|
C | CTAATTGC others(126): Show |
13 | a0001c0001t0001g0142a0001c0001t0002g0136a0001c0001t0002g0137others(10): Show | 13 | HG00423.hp1 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1031-488_1031-487i others(135): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93515115 | |||||
| chr9:93515163
|
C | G | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1031-504C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93515163 | ||||||
| chr9:93515180
|
T | G | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1031-487T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93515180 | ||||||
| chr9:93515210
|
A | G | 1 | a0001c0001t0003g0108 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1031-457A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93515210 | ||||||
| chr9:93515286
|
G | C | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1031-381G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93515286 | ||||||
| chr9:93515293
|
C | A | 2 | a0001c0002t0001g0111a0001c0002t0001g0304 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1031-374C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93515293 | ||||||
| chr9:93515293
|
C | T | 1 | a0001c0002t0001g0225 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1031-374C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93515293 | ||||||
| chr9:93515469
|
G | C | 200 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0060others(197): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1031-198G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93515469 | ||||||
| chr9:93515469
|
G | T | 1 | a0001c0002t0002g0274 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1031-198G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93515469 | ||||||
| chr9:93515610
|
C | T | 1 | a0001c0003t0002g0161 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1031-57C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 5/17 | chr9 | 93515610 | ||||||
| chr9:93515811
|
G | C | 117 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(114): Show | 118 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1131+44G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 6/17 | chr9 | 93515811 | ||||||
| chr9:93515816
|
C | T | 117 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(114): Show | 118 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1131+49C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 6/17 | chr9 | 93515816 | ||||||
| chr9:93515817
|
G | A | 117 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(114): Show | 118 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1131+50G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 6/17 | chr9 | 93515817 | ||||||
| chr9:93515962
|
G | C | 8 | a0001c0003t0006g0014a0001c0003t0006g0017a0001c0003t0006g0021others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1132-21G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 6/17 | chr9 | 93515962 | ||||||
| chr9:93516293
|
G | A | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1418+24G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93516293 | ||||||
| chr9:93516334
|
G | A | 2 | a0001c0001t0003g0095a0001c0002t0001g0184 | 2 | HG03927.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1418+65G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93516334 | ||||||
| chr9:93516379
|
C | T | 1 | a0001c0008t0001g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1418+110C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93516379 | ||||||
| chr9:93516390
|
T | C | 34 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1418+121T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93516390 | ||||||
| chr9:93516502
|
T | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1418+233T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93516502 | ||||||
| chr9:93516517
|
C | G | 4 | a0001c0002t0001g0195a0001c0002t0001g0216a0001c0002t0001g0217others(1): Show | 4 | NA18961.hp1 NA19067.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1418+248C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93516517 | ||||||
| chr9:93516643
|
C | T | 8 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(5): Show | 9 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1418+374C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93516643 | ||||||
| chr9:93516746
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1418+477A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93516746 | ||||||
| chr9:93516801
|
CTG | C | 67 | a0001c0003t0002g0003a0001c0003t0002g0005a0001c0003t0002g0006others(64): Show | 68 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.1418+538_1418+539d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93516801 | |||||
| chr9:93516813
|
G | A | 1 | a0001c0002t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1418+544G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93516813 | ||||||
| chr9:93517052
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1418+783G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93517052 | ||||||
| chr9:93517153
|
T | G | 3 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138 | 3 | HG01175.hp1 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1418+884T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93517153 | ||||||
| chr9:93517165
|
A | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1418+896A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93517165 | ||||||
| chr9:93517370
|
C | G | 5 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(2): Show | 6 | HG02145.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1418+1101C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93517370 | ||||||
| chr9:93517389
|
C | A | 2 | a0001c0001t0002g0298a0001c0001t0002g0299 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1418+1120C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93517389 | ||||||
| chr9:93517541
|
G | A | 13 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(10): Show | 13 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1418+1272G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93517541 | ||||||
| chr9:93517821
|
A | G | 1 | a0001c0001t0003g0088 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1418+1552A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93517821 | ||||||
| chr9:93518111
|
A | G | 2 | a0001c0003t0002g0156a0001c0003t0002g0157 | 2 | HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1418+1842A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93518111 | ||||||
| chr9:93518181
|
G | C | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1418+1912G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93518181 | ||||||
| chr9:93518229
|
G | A | 5 | a0001c0002t0002g0274a0001c0002t0002g0275a0001c0002t0002g0302others(2): Show | 5 | HG02451.hp2 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1418+1960G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93518229 | ||||||
| chr9:93518274
|
AG | A | 18 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1418+2009delG | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93518274 | |||||
| chr9:93518320
|
A | G | 1 | a0001c0008t0001g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1418+2051A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93518320 | ||||||
| chr9:93518443
|
T | G | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1418+2174T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93518443 | ||||||
| chr9:93518482
|
G | T | 6 | a0001c0002t0001g0177a0001c0002t0001g0198a0001c0002t0001g0206others(3): Show | 6 | HG00140.hp1 HG02523.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1418+2213G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93518482 | ||||||
| chr9:93518491
|
G | C | 1 | a0001c0001t0003g0040 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1418+2222G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93518491 | ||||||
| chr9:93518650
|
C | T | 2 | a0001c0002t0001g0184a0001c0002t0001g0189 | 2 | HG01993.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1418+2381C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93518650 | ||||||
| chr9:93518705
|
A | G | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1418+2436A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93518705 | ||||||
| chr9:93518784
|
C | T | 9 | a0001c0001t0005g0289a0001c0001t0005g0292a0001c0001t0005g0294others(6): Show | 9 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1418+2515C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93518784 | ||||||
| chr9:93519131
|
C | T | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1418+2862C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519131 | ||||||
| chr9:93519132
|
G | A | 1 | a0001c0003t0002g0148 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1418+2863G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519132 | ||||||
| chr9:93519206
|
A | G | 1 | a0001c0003t0002g0154 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1418+2937A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519206 | ||||||
| chr9:93519366
|
T | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1418+3097T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519366 | ||||||
| chr9:93519392
|
C | T | 16 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0002t0001g0181others(13): Show | 16 | HG00741.hp2 HG01123.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.1418+3123C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519392 | ||||||
| chr9:93519457
|
G | T | 3 | a0001c0003t0006g0017a0001c0003t0006g0026a0001c0003t0006g0110 | 3 | HG02630.hp2 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1418+3188G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519457 | ||||||
| chr9:93519494
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1418+3225C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519494 | ||||||
| chr9:93519576
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1418+3307C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519576 | ||||||
| chr9:93519621
|
C | A | 1 | a0001c0001t0003g0055 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1418+3352C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519621 | ||||||
| chr9:93519664
|
T | A | 7 | a0001c0001t0005g0292a0001c0004t0005g0290a0001c0004t0005g0291others(4): Show | 7 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1418+3395T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519664 | ||||||
| chr9:93519841
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1418+3572C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519841 | ||||||
| chr9:93519954
|
T | C | 195 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(192): Show | 197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1418+3685T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519954 | ||||||
| chr9:93519987
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1418+3718C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93519987 | ||||||
| chr9:93520003
|
A | G | 203 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(200): Show | 205 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1418+3734A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93520003 | ||||||
| chr9:93520015
|
A | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1418+3746A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93520015 | ||||||
| chr9:93520236
|
C | T | 68 | a0001c0001t0002g0013a0001c0003t0002g0003a0001c0003t0002g0005others(65): Show | 69 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.1418+3967C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93520236 | ||||||
| chr9:93520365
|
C | T | 1 | a0001c0003t0006g0110 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1418+4096C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93520365 | ||||||
| chr9:93520533
|
G | A | 5 | a0001c0002t0007g0176a0001c0002t0007g0178a0001c0002t0007g0239others(2): Show | 5 | HG01109.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1418+4264G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93520533 | ||||||
| chr9:93520768
|
A | C | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1418+4499A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93520768 | ||||||
| chr9:93520770
|
A | G | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1418+4501A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93520770 | ||||||
| chr9:93521022
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1418+4753C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93521022 | ||||||
| chr9:93521089
|
G | A | 13 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0002t0001g0181others(10): Show | 13 | HG00741.hp2 HG01123.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1418+4820G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93521089 | ||||||
| chr9:93521104
|
A | G | 1 | a0001c0002t0001g0223 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1418+4835A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93521104 | ||||||
| chr9:93521159
|
A | T | 8 | a0001c0002t0001g0264a0001c0002t0001g0265a0001c0002t0001g0266others(5): Show | 8 | NA18944.hp2 NA18962.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1418+4890A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93521159 | ||||||
| chr9:93521487
|
C | T | 8 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(5): Show | 9 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1418+5218C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93521487 | ||||||
| chr9:93521519
|
C | T | 2 | a0001c0002t0001g0207a0001c0002t0001g0208 | 2 | HG00609.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1418+5250C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93521519 | ||||||
| chr9:93521817
|
A | G | 18 | a0001c0001t0002g0013a0001c0003t0002g0005a0001c0003t0002g0006others(15): Show | 18 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1419-5338A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93521817 | ||||||
| chr9:93522012
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1419-5143G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522012 | ||||||
| chr9:93522063
|
G | C | 1 | a0001c0001t0004g0101 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1419-5092G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522063 | ||||||
| chr9:93522114
|
C | G | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1419-5041C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522114 | ||||||
| chr9:93522208
|
T | A | 1 | a0001c0002t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1419-4947T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522208 | ||||||
| chr9:93522232
|
A | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1419-4923A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522232 | ||||||
| chr9:93522259
|
A | G | 1 | a0001c0001t0003g0078 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1419-4896A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522259 | ||||||
| chr9:93522424
|
C | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1419-4731C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522424 | ||||||
| chr9:93522470
|
C | T | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1419-4685C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522470 | ||||||
| chr9:93522568
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1419-4587T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522568 | ||||||
| chr9:93522624
|
T | C | 1 | a0001c0001t0003g0032 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1419-4531T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522624 | ||||||
| chr9:93522700
|
T | C | 1 | a0001c0007t0012g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1419-4455T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522700 | ||||||
| chr9:93522730
|
G | A | 1 | a0001c0003t0002g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1419-4425G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93522730 | ||||||
| chr9:93523081
|
T | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1419-4074T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93523081 | ||||||
| chr9:93523090
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1419-4065G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93523090 | ||||||
| chr9:93523163
|
G | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0042 | 2 | NA18945.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1419-3992G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93523163 | ||||||
| chr9:93523189
|
G | T | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1419-3966G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93523189 | ||||||
| chr9:93523217
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1419-3938G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93523217 | ||||||
| chr9:93523454
|
CTTTATA | C | 111 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(108): Show | 112 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1419-3695_1419-369 others(10): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93523454 | |||||
| chr9:93523618
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1419-3537C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93523618 | ||||||
| chr9:93523818
|
C | T | 1 | a0001c0003t0002g0151 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1419-3337C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93523818 | ||||||
| chr9:93523881
|
A | G | 111 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(108): Show | 112 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1419-3274A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93523881 | ||||||
| chr9:93523956
|
T | C | 8 | a0001c0003t0006g0014a0001c0003t0006g0017a0001c0003t0006g0021others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1419-3199T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93523956 | ||||||
| chr9:93523986
|
G | C | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1419-3169G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93523986 | ||||||
| chr9:93524052
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1419-3103C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93524052 | ||||||
| chr9:93524066
|
A | C | 18 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1419-3089A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93524066 | ||||||
| chr9:93524251
|
T | G | 3 | a0001c0001t0003g0001a0001c0001t0003g0058a0001c0001t0003g0059 | 4 | HG01099.hp1 HG01192.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1419-2904T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93524251 | ||||||
| chr9:93524614
|
C | G | 1 | a0001c0001t0003g0090 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1419-2541C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93524614 | ||||||
| chr9:93524645
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1419-2510C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93524645 | ||||||
| chr9:93524889
|
G | T | 1 | a0001c0008t0001g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1419-2266G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93524889 | ||||||
| chr9:93524891
|
A | G | 1 | a0001c0001t0003g0055 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1419-2264A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93524891 | ||||||
| chr9:93525072
|
T | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1419-2083T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93525072 | ||||||
| chr9:93525351
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1419-1804C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93525351 | ||||||
| chr9:93525642
|
G | A | 34 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1419-1513G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93525642 | ||||||
| chr9:93525646
|
A | G | 1 | a0001c0002t0002g0302 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1419-1509A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93525646 | ||||||
| chr9:93525667
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1419-1488C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93525667 | ||||||
| chr9:93525735
|
C | T | 4 | a0001c0002t0001g0177a0001c0002t0001g0198a0001c0002t0001g0206others(1): Show | 4 | HG00140.hp1 HG02523.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.1419-1420C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93525735 | ||||||
| chr9:93525736
|
TG | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1419-1415delG | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93525736 | |||||
| chr9:93525861
|
A | G | 5 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(2): Show | 6 | HG02145.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1419-1294A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93525861 | ||||||
| chr9:93525881
|
C | G | 1 | a0001c0003t0002g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1419-1274C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93525881 | ||||||
| chr9:93526252
|
A | G | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1419-903A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93526252 | ||||||
| chr9:93526288
|
G | A | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1419-867G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93526288 | ||||||
| chr9:93526511
|
C | CT | 7 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1419-634dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93526511 | |||||
| chr9:93526704
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1419-451C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93526704 | ||||||
| chr9:93526949
|
G | A | 26 | a0001c0001t0002g0013a0001c0003t0002g0005a0001c0003t0002g0006others(23): Show | 26 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1419-206G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93526949 | ||||||
| chr9:93526969
|
A | T | 1 | a0001c0003t0002g0162 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1419-186A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93526969 | ||||||
| chr9:93526987
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1419-168C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93526987 | ||||||
| chr9:93527008
|
T | C | 1 | a0001c0003t0002g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1419-147T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 7/17 | chr9 | 93527008 | ||||||
| chr9:93527337
|
C | G | 1 | a0001c0001t0003g0100 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1506+95C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93527337 | ||||||
| chr9:93527461
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1506+219C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93527461 | ||||||
| chr9:93527557
|
A | T | 10 | a0001c0002t0001g0223a0001c0002t0001g0224a0001c0002t0001g0264others(7): Show | 10 | HG00558.hp1 NA18944.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.1506+315A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93527557 | ||||||
| chr9:93527594
|
T | A | 1 | a0001c0002t0001g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1506+352T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93527594 | ||||||
| chr9:93527602
|
T | A | 5 | a0001c0002t0007g0176a0001c0002t0007g0178a0001c0002t0007g0239others(2): Show | 5 | HG01109.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506+360T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93527602 | ||||||
| chr9:93527614
|
A | AT | 106 | a0001c0001t0001g0060a0001c0001t0001g0284a0001c0001t0001g0285others(103): Show | 107 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1506+398dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93527614 | |||||
| chr9:93527614
|
A | ATT | 83 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(80): Show | 84 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1506+397_1506+398d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93527614 | |||||
| chr9:93527614
|
A | ATTT | 24 | a0001c0001t0001g0046a0001c0001t0002g0136a0001c0001t0002g0140others(21): Show | 24 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.1506+396_1506+398d others(5): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93527614 | |||||
| chr9:93527614
|
AT | A | 7 | a0001c0002t0001g0111a0001c0002t0001g0241a0001c0002t0001g0242others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1506+398delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93527614 | |||||
| chr9:93527614
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1506+389_1506+398d others(12): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93527614 | |||||
| chr9:93527614
|
ATTTTTTT others(5): Show |
A | 34 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1506+387_1506+398d others(14): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93527614 | |||||
| chr9:93527654
|
G | A | 5 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(2): Show | 5 | HG00558.hp2 HG02135.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506+412G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93527654 | ||||||
| chr9:93527821
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1506+579C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93527821 | ||||||
| chr9:93528028
|
C | T | 4 | a0001c0003t0002g0155a0001c0003t0002g0156a0001c0003t0002g0157others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506+786C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93528028 | ||||||
| chr9:93528639
|
A | G | 203 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(200): Show | 205 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1507-714A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93528639 | ||||||
| chr9:93528814
|
TG | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1507-538delG | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93528814 | ||||||
| chr9:93528840
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1507-513G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93528840 | ||||||
| chr9:93528869
|
A | G | 2 | a0001c0002t0007g0236a0001c0002t0007g0237 | 2 | HG00642.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1507-484A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93528869 | ||||||
| chr9:93528873
|
CTA | C | 60 | a0001c0001t0002g0013a0001c0003t0002g0005a0001c0003t0002g0006others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1507-478_1507-477d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93528873 | |||||
| chr9:93528942
|
G | A | 195 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(192): Show | 197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1507-411G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93528942 | ||||||
| chr9:93528957
|
A | G | 1 | a0001c0003t0002g0170 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1507-396A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 8/17 | chr9 | 93528957 | ||||||
| chr9:93529653
|
T | C | 1 | a0001c0003t0002g0153 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1734+73T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93529653 | ||||||
| chr9:93529743
|
A | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1734+163A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93529743 | ||||||
| chr9:93529874
|
T | G | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1734+294T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93529874 | ||||||
| chr9:93529884
|
A | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1734+304A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93529884 | ||||||
| chr9:93530209
|
AT | A | 91 | a0001c0001t0001g0142a0001c0001t0002g0013a0001c0001t0002g0119others(88): Show | 91 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1734+635delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr9 | 93530209 | |||||
| chr9:93530418
|
A | G | 1 | a0001c0001t0003g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1734+838A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93530418 | ||||||
| chr9:93530419
|
T | G | 3 | a0001c0002t0001g0195a0001c0002t0001g0216a0001c0002t0001g0217 | 3 | NA19067.hp1 NA19079.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1734+839T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93530419 | ||||||
| chr9:93530550
|
T | G | 1 | a0001c0001t0003g0059 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1734+970T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93530550 | ||||||
| chr9:93530682
|
G | T | 1 | a0001c0002t0002g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1734+1102G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93530682 | ||||||
| chr9:93530841
|
C | T | 20 | a0001c0002t0001g0002a0001c0002t0001g0179a0001c0002t0001g0201others(17): Show | 21 | HG00558.hp1 HG00735.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1734+1261C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93530841 | ||||||
| chr9:93530923
|
A | G | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1735-1232A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93530923 | ||||||
| chr9:93531050
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1735-1105G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93531050 | ||||||
| chr9:93531428
|
G | A | 1 | a0001c0003t0002g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1735-727G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93531428 | ||||||
| chr9:93531512
|
C | T | 18 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1735-643C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93531512 | ||||||
| chr9:93531642
|
G | A | 3 | a0001c0003t0002g0008a0001c0003t0002g0028a0001c0003t0002g0029 | 3 | HG02717.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1735-513G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 9/17 | chr9 | 93531642 | ||||||
| chr9:93532462
|
C | T | 2 | a0001c0001t0002g0272a0001c0001t0002g0273 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1909+133C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93532462 | ||||||
| chr9:93532820
|
C | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1909+491C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93532820 | ||||||
| chr9:93533149
|
A | C | 26 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1909+820A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93533149 | ||||||
| chr9:93533239
|
G | T | 1 | a0001c0001t0003g0090 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1909+910G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93533239 | ||||||
| chr9:93533329
|
A | G | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1909+1000A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93533329 | ||||||
| chr9:93533454
|
G | A | 1 | a0001c0002t0001g0206 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1909+1125G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93533454 | ||||||
| chr9:93533455
|
C | A | 1 | a0001c0002t0001g0206 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1909+1126C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93533455 | ||||||
| chr9:93533821
|
C | A | 208 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(205): Show | 210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1909+1492C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93533821 | ||||||
| chr9:93533926
|
A | T | 1 | a0001c0001t0002g0132 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1909+1597A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93533926 | ||||||
| chr9:93533974
|
C | T | 26 | a0001c0001t0002g0013a0001c0003t0002g0005a0001c0003t0002g0006others(23): Show | 26 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1909+1645C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93533974 | ||||||
| chr9:93534000
|
A | G | 1 | a0001c0003t0002g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1909+1671A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93534000 | ||||||
| chr9:93534153
|
T | C | 8 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(5): Show | 9 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1909+1824T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93534153 | ||||||
| chr9:93534154
|
A | G | 1 | a0001c0001t0003g0100 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1909+1825A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93534154 | ||||||
| chr9:93534248
|
A | C | 1 | a0001c0002t0005g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1909+1919A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93534248 | ||||||
| chr9:93534438
|
G | C | 195 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(192): Show | 197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1909+2109G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93534438 | ||||||
| chr9:93534530
|
G | A | 1 | a0001c0003t0002g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1909+2201G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93534530 | ||||||
| chr9:93534830
|
CT | C | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1909+2504delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93534830 | |||||
| chr9:93535499
|
A | G | 1 | a0001c0003t0002g0306 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1909+3170A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93535499 | ||||||
| chr9:93535643
|
T | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1909+3314T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93535643 | ||||||
| chr9:93535818
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1909+3489T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93535818 | ||||||
| chr9:93536048
|
A | ACT | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1909+3720_1909+372 others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93536048 | |||||
| chr9:93536223
|
G | C | 2 | a0001c0002t0001g0211a0001c0002t0001g0225 | 2 | NA18974.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1909+3894G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93536223 | ||||||
| chr9:93536516
|
A | G | 1 | a0001c0001t0003g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1909+4187A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93536516 | ||||||
| chr9:93536529
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1909+4200C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93536529 | ||||||
| chr9:93536690
|
T | A | 191 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(188): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1909+4361T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93536690 | ||||||
| chr9:93536705
|
G | A | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1909+4376G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93536705 | ||||||
| chr9:93536884
|
C | A | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1909+4555C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93536884 | ||||||
| chr9:93537244
|
A | G | 2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1909+4915A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93537244 | ||||||
| chr9:93537617
|
A | G | 1 | a0001c0002t0001g0224 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1909+5288A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93537617 | ||||||
| chr9:93537775
|
T | C | 1 | a0001c0002t0001g0269 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1909+5446T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93537775 | ||||||
| chr9:93537837
|
T | C | 2 | a0001c0002t0001g0111a0001c0002t0001g0304 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1910-5385T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93537837 | ||||||
| chr9:93538013
|
A | T | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1910-5209A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538013 | ||||||
| chr9:93538039
|
C | CT | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1910-5171dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93538039 | |||||
| chr9:93538039
|
CT | C | 87 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(84): Show | 88 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1910-5171delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93538039 | |||||
| chr9:93538213
|
T | TG | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-5006dupG | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93538213 | |||||
| chr9:93538298
|
C | G | 1 | a0001c0002t0001g0198 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1910-4924C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538298 | ||||||
| chr9:93538315
|
A | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-4907A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538315 | ||||||
| chr9:93538400
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-4822G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538400 | ||||||
| chr9:93538489
|
G | A | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1910-4733G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538489 | ||||||
| chr9:93538522
|
C | T | 1 | a0001c0002t0002g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1910-4700C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538522 | ||||||
| chr9:93538571
|
C | T | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1910-4651C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538571 | ||||||
| chr9:93538572
|
G | A | 31 | a0001c0001t0001g0142a0001c0001t0002g0119a0001c0001t0002g0121others(28): Show | 31 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1910-4650G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538572 | ||||||
| chr9:93538603
|
A | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-4619A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538603 | ||||||
| chr9:93538839
|
C | T | 1 | a0001c0003t0002g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1910-4383C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538839 | ||||||
| chr9:93538877
|
GT | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-4338delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93538877 | |||||
| chr9:93538961
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-4261G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538961 | ||||||
| chr9:93538990
|
A | T | 204 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(201): Show | 206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1910-4232A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93538990 | ||||||
| chr9:93539002
|
G | GT | 98 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0284others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1910-4207dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93539002 | |||||
| chr9:93539054
|
G | C | 1 | a0001c0003t0002g0169 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1910-4168G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539054 | ||||||
| chr9:93539072
|
A | G | 5 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(2): Show | 6 | HG02145.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1910-4150A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539072 | ||||||
| chr9:93539083
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1910-4139C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539083 | ||||||
| chr9:93539188
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-4034G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539188 | ||||||
| chr9:93539239
|
C | T | 2 | a0001c0001t0013g0120a0001c0001t0013g0133 | 2 | NA18977.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1910-3983C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539239 | ||||||
| chr9:93539277
|
G | A | 1 | a0001c0002t0001g0179 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1910-3945G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539277 | ||||||
| chr9:93539288
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-3934C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539288 | ||||||
| chr9:93539437
|
G | C | 107 | a0001c0001t0001g0142a0001c0001t0001g0284a0001c0001t0001g0285others(104): Show | 108 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1910-3785G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539437 | ||||||
| chr9:93539518
|
T | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-3704T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539518 | ||||||
| chr9:93539881
|
T | G | 1 | a0001c0001t0003g0081 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1910-3341T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539881 | ||||||
| chr9:93539886
|
T | G | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1910-3336T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539886 | ||||||
| chr9:93539889
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1910-3333C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93539889 | ||||||
| chr9:93540224
|
A | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-2998A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93540224 | ||||||
| chr9:93540361
|
A | G | 5 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(2): Show | 6 | HG02145.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1910-2861A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93540361 | ||||||
| chr9:93540378
|
C | G | 3 | a0001c0003t0006g0017a0001c0003t0006g0026a0001c0003t0006g0110 | 3 | HG02630.hp2 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1910-2844C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93540378 | ||||||
| chr9:93540404
|
T | A | 26 | a0001c0001t0002g0013a0001c0003t0002g0005a0001c0003t0002g0006others(23): Show | 26 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1910-2818T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93540404 | ||||||
| chr9:93540428
|
A | G | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1910-2794A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93540428 | ||||||
| chr9:93540524
|
G | A | 1 | a0001c0003t0002g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1910-2698G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93540524 | ||||||
| chr9:93541012
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1910-2210A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93541012 | ||||||
| chr9:93541077
|
T | TG | 292 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(289): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1910-2139dupG | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93541077 | |||||
| chr9:93541131
|
T | C | 1 | a0001c0002t0001g0184 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1910-2091T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93541131 | ||||||
| chr9:93541311
|
C | T | 2 | a0001c0002t0001g0179a0001c0002t0001g0226 | 2 | HG01361.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1910-1911C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93541311 | ||||||
| chr9:93541696
|
A | G | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1910-1526A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93541696 | ||||||
| chr9:93541873
|
G | A | 1 | a0001c0003t0006g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1910-1349G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93541873 | ||||||
| chr9:93541996
|
C | T | 191 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(188): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1910-1226C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93541996 | ||||||
| chr9:93542025
|
C | T | 1 | a0001c0002t0001g0231 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1910-1197C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93542025 | ||||||
| chr9:93542315
|
T | C | 288 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(285): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1910-907T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93542315 | ||||||
| chr9:93542374
|
A | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-848A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93542374 | ||||||
| chr9:93542485
|
T | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1910-737T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93542485 | ||||||
| chr9:93542620
|
A | C | 2 | a0001c0003t0002g0005a0001c0003t0002g0020 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1910-602A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93542620 | ||||||
| chr9:93542785
|
G | C | 1 | a0001c0001t0002g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1910-437G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93542785 | ||||||
| chr9:93542865
|
C | T | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1910-357C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93542865 | ||||||
| chr9:93542882
|
T | A | 1 | a0001c0001t0003g0109 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1910-340T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93542882 | ||||||
| chr9:93542914
|
A | T | 1 | a0001c0002t0001g0190 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1910-308A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 10/17 | chr9 | 93542914 | ||||||
| chr9:93543700
|
T | C | 18 | a0001c0001t0002g0013a0001c0003t0002g0005a0001c0003t0002g0006others(15): Show | 18 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.2159+229T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93543700 | ||||||
| chr9:93543809
|
C | T | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2159+338C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93543809 | ||||||
| chr9:93543862
|
C | T | 1 | a0001c0002t0001g0245 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2159+391C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93543862 | ||||||
| chr9:93543909
|
A | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2159+438A>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93543909 | ||||||
| chr9:93544109
|
A | G | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2159+638A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93544109 | ||||||
| chr9:93544455
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2159+984C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93544455 | ||||||
| chr9:93544533
|
A | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(81): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2159+1062A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93544533 | ||||||
| chr9:93544628
|
T | C | 2 | a0001c0002t0007g0178a0001c0002t0007g0246 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2159+1157T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93544628 | ||||||
| chr9:93544785
|
G | A | 2 | a0001c0001t0003g0282a0001c0001t0003g0283 | 2 | NA19054.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2159+1314G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93544785 | ||||||
| chr9:93544906
|
C | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2159+1435C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93544906 | ||||||
| chr9:93545193
|
T | C | 1 | a0001c0008t0001g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2159+1722T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93545193 | ||||||
| chr9:93545230
|
T | C | 208 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(205): Show | 210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2159+1759T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93545230 | ||||||
| chr9:93545233
|
G | A | 13 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(10): Show | 14 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2159+1762G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93545233 | ||||||
| chr9:93545304
|
AT | A | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2159+1835delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545304 | |||||
| chr9:93545355
|
G | T | 7 | a0001c0002t0001g0183a0001c0002t0001g0207a0001c0002t0001g0208others(4): Show | 7 | HG00609.hp2 NA18747.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.2159+1884G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93545355 | ||||||
| chr9:93545576
|
T | C | 8 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(5): Show | 9 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.2159+2105T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93545576 | ||||||
| chr9:93545609
|
G | A | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0002t0001g0254 | 3 | HG02258.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2159+2138G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93545609 | ||||||
| chr9:93545779
|
C | CTTTTTTT others(17): Show |
1 | a0001c0003t0002g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2159+2308_2159+230 others(28): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93545779 | ||||||
| chr9:93545780
|
C | CT | 18 | a0001c0002t0001g0184a0001c0002t0001g0189a0001c0002t0001g0193others(15): Show | 18 | HG00741.hp2 HG01884.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.2159+2335dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTT | 9 | a0001c0001t0002g0272a0001c0001t0002g0310a0001c0001t0002g0311others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2159+2333_2159+233 others(7): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTT | 7 | a0001c0001t0002g0273a0001c0001t0002g0278a0001c0001t0002g0315others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2159+2332_2159+233 others(8): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(3): Show |
4 | a0001c0002t0001g0254a0001c0004t0005g0291a0001c0004t0005g0296others(1): Show | 4 | HG02129.hp1 HG03579.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.2159+2326_2159+233 others(14): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0005g0292a0001c0004t0005g0293 | 2 | NA18972.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.2159+2325_2159+233 others(15): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0003g0032a0001c0001t0003g0283a0001c0001t0005g0289others(2): Show | 5 | HG00438.hp2 HG02965.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.2159+2324_2159+233 others(16): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0054others(1): Show | 4 | HG00558.hp2 HG02135.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.2159+2323_2159+233 others(17): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(7): Show |
12 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0055others(9): Show | 12 | HG01069.hp1 HG01168.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.2159+2322_2159+233 others(18): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(8): Show |
12 | a0001c0001t0001g0044a0001c0001t0003g0052a0001c0001t0003g0053others(9): Show | 12 | HG00609.hp1 HG00642.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.2159+2321_2159+233 others(19): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(9): Show |
11 | a0001c0001t0001g0043a0001c0001t0003g0049a0001c0001t0003g0050others(8): Show | 11 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.2159+2320_2159+233 others(20): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(10): Show |
8 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0075others(5): Show | 8 | HG00735.hp1 HG00741.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.2159+2319_2159+233 others(21): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0003g0095 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2159+2318_2159+233 others(22): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0003g0084a0001c0001t0004g0037 | 2 | HG02155.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.2159+2317_2159+233 others(23): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(13): Show |
6 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0003g0069others(3): Show | 6 | HG01891.hp2 NA18952.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.2159+2316_2159+233 others(24): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0001g0046a0001c0001t0015g0105 | 2 | NA18952.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2159+2315_2159+233 others(25): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0003g0059 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2159+2312_2159+233 others(28): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(18): Show |
2 | a0001c0001t0003g0106a0001c0001t0003g0109 | 2 | NA19077.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2159+2311_2159+233 others(29): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(19): Show |
2 | a0001c0001t0003g0061a0001c0001t0004g0074 | 2 | HG02970.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2159+2310_2159+233 others(30): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(20): Show |
2 | a0001c0001t0003g0090a0001c0003t0002g0029 | 2 | HG02717.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2159+2335_2159+233 others(31): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(21): Show |
3 | a0001c0001t0004g0034a0001c0001t0014g0035a0001c0003t0002g0008 | 3 | HG02818.hp1 NA18974.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2159+2335_2159+233 others(32): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(22): Show |
4 | a0001c0001t0001g0067a0001c0001t0002g0013a0001c0001t0011g0038others(1): Show | 4 | HG01081.hp1 HG01261.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.2159+2335_2159+233 others(33): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(23): Show |
2 | a0001c0001t0002g0098a0001c0001t0003g0082 | 2 | HG02717.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2159+2335_2159+233 others(34): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0003g0081 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2159+2335_2159+233 others(35): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0003g0062 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2159+2335_2159+233 others(37): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(29): Show |
1 | a0001c0001t0003g0039 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2159+2335_2159+233 others(40): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | CTTTTTTT others(31): Show |
1 | a0001c0001t0003g0064 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2159+2335_2159+233 others(42): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
C | T | 1 | a0001c0003t0002g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2159+2309C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93545780 | ||||||
| chr9:93545780
|
CTT | C | 26 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(23): Show | 26 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.2159+2334_2159+233 others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
CTTT | C | 40 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0129others(37): Show | 41 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.2159+2333_2159+233 others(7): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93545780
|
CTTTT | C | 8 | a0001c0001t0001g0142a0001c0002t0001g0226a0001c0003t0002g0149others(5): Show | 8 | HG01361.hp1 HG02886.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2159+2332_2159+233 others(8): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93545780 | |||||
| chr9:93546037
|
C | T | 1 | a0001c0002t0002g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2159+2566C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93546037 | ||||||
| chr9:93546258
|
C | T | 1 | a0001c0002t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2159+2787C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93546258 | ||||||
| chr9:93546374
|
G | A | 22 | a0001c0003t0002g0118a0001c0003t0002g0148a0001c0003t0002g0149others(19): Show | 22 | HG00673.hp1 HG01123.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.2159+2903G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93546374 | ||||||
| chr9:93546384
|
C | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(79): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.2159+2913C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93546384 | ||||||
| chr9:93546419
|
G | C | 1 | a0001c0001t0003g0081 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2159+2948G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93546419 | ||||||
| chr9:93546733
|
A | G | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2159+3262A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93546733 | ||||||
| chr9:93546757
|
A | G | 295 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(292): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.2159+3286A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93546757 | ||||||
| chr9:93546881
|
TG | T | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2159+3414delG | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93546881 | |||||
| chr9:93547091
|
G | T | 1 | a0001c0002t0001g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2160-3486G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93547091 | ||||||
| chr9:93547367
|
A | G | 1 | a0001c0002t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2160-3210A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93547367 | ||||||
| chr9:93547651
|
A | G | 1 | a0001c0003t0002g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2160-2926A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93547651 | ||||||
| chr9:93547942
|
T | A | 285 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(282): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.2160-2635T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93547942 | ||||||
| chr9:93548114
|
A | T | 14 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0277others(11): Show | 14 | HG00438.hp2 HG02015.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2160-2463A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93548114 | ||||||
| chr9:93548295
|
A | G | 1 | a0001c0002t0001g0255 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2160-2282A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93548295 | ||||||
| chr9:93548784
|
T | C | 5 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(2): Show | 6 | HG02145.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2160-1793T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93548784 | ||||||
| chr9:93548830
|
A | G | 5 | a0001c0002t0002g0274a0001c0002t0002g0275a0001c0002t0002g0302others(2): Show | 5 | HG02451.hp2 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2160-1747A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93548830 | ||||||
| chr9:93548853
|
G | A | 4 | a0001c0002t0002g0274a0001c0002t0002g0275a0001c0002t0002g0302others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2160-1724G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93548853 | ||||||
| chr9:93548912
|
G | A | 199 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(196): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.2160-1665G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93548912 | ||||||
| chr9:93548925
|
C | G | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG00558.hp2 HG02135.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2160-1652C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93548925 | ||||||
| chr9:93548974
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(93): Show | 97 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.2160-1603C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93548974 | ||||||
| chr9:93549067
|
C | CA | 30 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(27): Show | 30 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.2160-1501dupA | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 93549067 | |||||
| chr9:93549114
|
G | A | 4 | a0001c0002t0001g0002a0001c0002t0001g0201a0001c0002t0001g0221others(1): Show | 5 | HG01099.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.2160-1463G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93549114 | ||||||
| chr9:93549440
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2160-1137C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93549440 | ||||||
| chr9:93549838
|
C | G | 3 | a0001c0003t0002g0306a0001c0003t0002g0307a0001c0003t0002g0308 | 3 | HG02145.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2160-739C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93549838 | ||||||
| chr9:93549852
|
C | T | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2160-725C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93549852 | ||||||
| chr9:93549893
|
A | G | 1 | a0001c0002t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2160-684A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93549893 | ||||||
| chr9:93549955
|
G | T | 3 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138 | 3 | HG01175.hp1 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2160-622G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93549955 | ||||||
| chr9:93550091
|
C | G | 1 | a0001c0001t0003g0030 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2160-486C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93550091 | ||||||
| chr9:93550299
|
G | A | 3 | a0001c0001t0002g0098a0001c0001t0002g0277a0001c0001t0002g0278 | 3 | HG02055.hp2 HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2160-278G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93550299 | ||||||
| chr9:93550316
|
A | G | 1 | a0001c0002t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2160-261A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93550316 | ||||||
| chr9:93550532
|
C | T | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2160-45C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | chr9 | 93550532 | ||||||
| chr9:93550730
|
C | T | 72 | a0001c0001t0002g0013a0001c0001t0002g0272a0001c0001t0002g0273others(69): Show | 73 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.2274+39C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93550730 | ||||||
| chr9:93550763
|
C | G | 1 | a0001c0001t0002g0013 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2274+72C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93550763 | ||||||
| chr9:93550847
|
C | T | 1 | a0001c0001t0004g0033 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2274+156C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93550847 | ||||||
| chr9:93550893
|
A | G | 1 | a0001c0001t0003g0100 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2274+202A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93550893 | ||||||
| chr9:93550962
|
T | G | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2274+271T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93550962 | ||||||
| chr9:93551232
|
A | G | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.2274+541A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93551232 | ||||||
| chr9:93551290
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2274+599T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93551290 | ||||||
| chr9:93551400
|
A | T | 1 | a0001c0002t0001g0179 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2274+709A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93551400 | ||||||
| chr9:93551467
|
A | G | 5 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0243others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2274+776A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93551467 | ||||||
| chr9:93551607
|
T | A | 2 | a0001c0001t0003g0282a0001c0001t0003g0283 | 2 | NA19054.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2274+916T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93551607 | ||||||
| chr9:93552115
|
A | T | 77 | a0001c0001t0003g0001a0001c0001t0003g0030a0001c0001t0003g0031others(74): Show | 78 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.2274+1424A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93552115 | ||||||
| chr9:93552150
|
G | A | 1 | a0001c0001t0003g0065 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2274+1459G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93552150 | ||||||
| chr9:93552212
|
A | G | 1 | a0001c0003t0002g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2274+1521A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93552212 | ||||||
| chr9:93552413
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2274+1722A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93552413 | ||||||
| chr9:93552550
|
G | C | 18 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.2274+1859G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93552550 | ||||||
| chr9:93552557
|
AAGGC | A | 8 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(5): Show | 9 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.2274+1869_2274+187 others(8): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93552557 | |||||
| chr9:93552958
|
G | C | 72 | a0001c0001t0002g0013a0001c0001t0002g0272a0001c0001t0002g0273others(69): Show | 73 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.2274+2267G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93552958 | ||||||
| chr9:93553157
|
T | G | 1 | a0001c0002t0008g0238 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2274+2466T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93553157 | ||||||
| chr9:93553164
|
T | G | 1 | a0001c0001t0002g0127 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2274+2473T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93553164 | ||||||
| chr9:93553404
|
C | T | 1 | a0001c0003t0002g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2274+2713C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93553404 | ||||||
| chr9:93553755
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2275-2627C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93553755 | ||||||
| chr9:93553756
|
G | A | 8 | a0001c0003t0006g0014a0001c0003t0006g0017a0001c0003t0006g0021others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2275-2626G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93553756 | ||||||
| chr9:93553802
|
T | A | 4 | a0001c0002t0002g0274a0001c0002t0002g0275a0001c0002t0002g0302others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2275-2580T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93553802 | ||||||
| chr9:93553840
|
T | G | 1 | a0001c0001t0002g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2275-2542T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93553840 | ||||||
| chr9:93554073
|
T | G | 1 | a0001c0007t0012g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2275-2309T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93554073 | ||||||
| chr9:93554120
|
T | TAC | 20 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0002g0143others(17): Show | 20 | HG00423.hp2 HG00738.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.2275-2203_2275-220 others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACAC | 32 | a0001c0001t0001g0045a0001c0001t0001g0057a0001c0001t0002g0121others(29): Show | 34 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.2275-2205_2275-220 others(8): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACAC | 27 | a0001c0001t0001g0046a0001c0001t0002g0123a0001c0001t0002g0129others(24): Show | 28 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.2275-2207_2275-220 others(10): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(1): Show |
30 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0002g0138others(27): Show | 30 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2275-2209_2275-220 others(12): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(3): Show |
21 | a0001c0001t0002g0128a0001c0001t0002g0145a0001c0001t0003g0054others(18): Show | 21 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.2275-2211_2275-220 others(14): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(5): Show |
21 | a0001c0001t0001g0060a0001c0001t0001g0285a0001c0001t0002g0132others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.2275-2213_2275-220 others(16): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(7): Show |
18 | a0001c0001t0001g0056a0001c0001t0002g0119a0001c0001t0003g0041others(15): Show | 18 | HG00558.hp1 HG01109.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.2275-2215_2275-220 others(18): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(9): Show |
13 | a0001c0001t0002g0141a0001c0001t0003g0050a0001c0001t0003g0062others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2275-2217_2275-220 others(20): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(11): Show |
5 | a0001c0001t0001g0284a0001c0001t0002g0140a0001c0001t0002g0298others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2275-2219_2275-220 others(22): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(13): Show |
6 | a0001c0001t0003g0068a0001c0001t0003g0075a0001c0002t0001g0199others(3): Show | 6 | HG01928.hp2 HG02572.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.2275-2221_2275-220 others(24): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(15): Show |
9 | a0001c0001t0002g0098a0001c0001t0003g0051a0001c0001t0003g0063others(6): Show | 9 | HG00323.hp2 HG02056.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2275-2223_2275-220 others(26): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(17): Show |
6 | a0001c0002t0001g0111a0001c0002t0001g0181a0001c0002t0001g0207others(3): Show | 6 | HG02451.hp1 NA18946.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.2275-2225_2275-220 others(28): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(19): Show |
5 | a0001c0001t0003g0066a0001c0002t0001g0197a0001c0002t0001g0202others(2): Show | 5 | HG00438.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2275-2227_2275-220 others(30): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(21): Show |
2 | a0001c0001t0002g0277a0001c0002t0001g0270 | 2 | HG02055.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.2275-2229_2275-220 others(32): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(27): Show |
1 | a0001c0002t0001g0269 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2275-2235_2275-220 others(38): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(31): Show |
2 | a0001c0001t0002g0130a0001c0002t0001g0266 | 2 | NA18994.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2275-2239_2275-220 others(42): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(37): Show |
1 | a0001c0002t0001g0210 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2275-2245_2275-220 others(48): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
T | TACACACA others(3): Show |
1 | a0001c0003t0002g0165 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2275-2255_2275-225 others(14): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TAC | T | 8 | a0001c0001t0002g0124a0001c0001t0003g0040a0001c0001t0011g0073others(5): Show | 8 | HG01069.hp2 HG01346.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.2275-2203_2275-220 others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TACAC | T | 10 | a0001c0001t0002g0125a0001c0001t0002g0146a0001c0001t0002g0297others(7): Show | 10 | HG01358.hp1 HG01361.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.2275-2205_2275-220 others(8): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TACACAC | T | 5 | a0001c0001t0003g0282a0001c0001t0014g0035a0001c0003t0002g0158others(2): Show | 5 | HG01261.hp2 HG01975.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.2275-2207_2275-220 others(10): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TACACACA others(1): Show |
T | 6 | a0001c0001t0002g0126a0001c0001t0004g0034a0001c0002t0001g0230others(3): Show | 6 | HG00639.hp2 HG02015.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2275-2209_2275-220 others(12): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TACACACA others(3): Show |
T | 6 | a0001c0001t0002g0131a0001c0002t0001g0258a0001c0002t0001g0262others(3): Show | 6 | HG01109.hp2 HG01928.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2275-2211_2275-220 others(14): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0067 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2275-2213_2275-220 others(16): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TACACACA others(7): Show |
T | 6 | a0001c0001t0002g0013a0001c0001t0002g0272a0001c0001t0002g0313others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.2275-2215_2275-220 others(18): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TACACACA others(9): Show |
T | 17 | a0001c0001t0002g0273a0001c0001t0002g0310a0001c0001t0002g0311others(14): Show | 17 | HG01123.hp1 HG01358.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2275-2217_2275-220 others(20): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TACACACA others(11): Show |
T | 11 | a0001c0002t0001g0206a0001c0003t0002g0005a0001c0003t0002g0006others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2275-2219_2275-220 others(22): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TACACACA others(13): Show |
T | 5 | a0001c0002t0001g0229a0001c0003t0002g0008a0001c0003t0002g0012others(2): Show | 5 | HG02129.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2275-2221_2275-220 others(24): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TACACACA others(19): Show |
T | 1 | a0001c0003t0002g0149 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2275-2227_2275-220 others(30): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554120
|
TACACACA others(21): Show |
T | 1 | a0001c0001t0002g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2275-2229_2275-220 others(32): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554120 | |||||
| chr9:93554250
|
G | A | 2 | a0001c0002t0007g0176a0001c0002t0007g0256 | 2 | HG01109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2275-2132G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93554250 | ||||||
| chr9:93554365
|
C | T | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2275-2017C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93554365 | ||||||
| chr9:93554366
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2275-2016G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93554366 | ||||||
| chr9:93554484
|
C | G | 12 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(9): Show | 12 | HG00423.hp1 HG01175.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.2275-1898C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93554484 | ||||||
| chr9:93554545
|
C | T | 1 | a0001c0001t0016g0312 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2275-1837C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93554545 | ||||||
| chr9:93554617
|
G | A | 2 | a0001c0001t0003g0053a0001c0001t0003g0070 | 2 | NA19012.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2275-1765G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93554617 | ||||||
| chr9:93554716
|
C | CTT | 4 | a0001c0003t0002g0155a0001c0003t0002g0156a0001c0003t0002g0157others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2275-1665_2275-166 others(6): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93554716 | |||||
| chr9:93554920
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2275-1462C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93554920 | ||||||
| chr9:93554951
|
T | G | 4 | a0001c0002t0002g0274a0001c0002t0002g0275a0001c0002t0002g0302others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2275-1431T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93554951 | ||||||
| chr9:93555184
|
A | AT | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.2275-1192dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93555184 | |||||
| chr9:93555557
|
A | G | 2 | a0001c0002t0001g0192a0001c0002t0001g0210 | 2 | HG02056.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2275-825A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93555557 | ||||||
| chr9:93556235
|
G | A | 4 | a0001c0002t0002g0274a0001c0002t0002g0275a0001c0002t0002g0302others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2275-147G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93556235 | ||||||
| chr9:93556327
|
G | T | 1 | a0001c0002t0001g0214 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2275-55G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | chr9 | 93556327 | ||||||
| chr9:93556601
|
G | A | 1 | a0001c0004t0005g0296 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2484+10G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93556601 | ||||||
| chr9:93556792
|
T | G | 1 | a0001c0002t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2484+201T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93556792 | ||||||
| chr9:93556825
|
G | A | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2484+234G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93556825 | ||||||
| chr9:93556861
|
C | A | 203 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0013others(200): Show | 205 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2484+270C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93556861 | ||||||
| chr9:93556975
|
T | A | 1 | a0001c0001t0002g0130 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2484+384T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93556975 | ||||||
| chr9:93557022
|
G | A | 1 | a0001c0002t0007g0239 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2484+431G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93557022 | ||||||
| chr9:93557026
|
AT | A | 4 | a0001c0002t0002g0274a0001c0002t0002g0275a0001c0002t0002g0302others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2484+437delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr9 | 93557026 | |||||
| chr9:93557102
|
C | A | 1 | a0001c0001t0003g0090 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2484+511C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93557102 | ||||||
| chr9:93557127
|
G | GT | 20 | a0001c0001t0003g0052a0001c0001t0003g0070a0001c0001t0003g0095others(17): Show | 21 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(18): Show |
intron_variant | MODIFIER | c.2484+555dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr9 | 93557127 | |||||
| chr9:93557127
|
G | GTT | 89 | a0001c0001t0002g0013a0001c0001t0002g0098a0001c0001t0002g0119others(86): Show | 89 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2484+554_2484+555d others(4): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr9 | 93557127 | |||||
| chr9:93557127
|
G | GTTT | 8 | a0001c0001t0002g0122a0001c0001t0002g0136a0001c0001t0002g0138others(5): Show | 8 | HG00738.hp2 HG01175.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.2484+553_2484+555d others(5): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr9 | 93557127 | |||||
| chr9:93557127
|
GT | G | 90 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(87): Show | 91 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.2484+555delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr9 | 93557127 | |||||
| chr9:93557128
|
T | G | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2484+537T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93557128 | ||||||
| chr9:93557129
|
T | G | 1 | a0001c0002t0001g0198 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2484+538T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93557129 | ||||||
| chr9:93557192
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0142a0001c0002t0001g0211others(1): Show | 4 | NA18954.hp2 NA18974.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.2484+601C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93557192 | ||||||
| chr9:93557320
|
G | A | 2 | a0001c0003t0002g0149a0001c0003t0002g0150 | 2 | NA18984.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2485-507G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93557320 | ||||||
| chr9:93557412
|
G | A | 64 | a0001c0001t0002g0013a0001c0001t0002g0272a0001c0001t0002g0273others(61): Show | 64 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.2485-415G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93557412 | ||||||
| chr9:93557462
|
A | T | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0310others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2485-365A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93557462 | ||||||
| chr9:93557787
|
C | T | 1 | a0001c0003t0002g0012 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2485-40C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 13/17 | chr9 | 93557787 | ||||||
| chr9:93558055
|
T | G | 1 | a0001c0003t0002g0166 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2668+45T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 14/17 | chr9 | 93558055 | ||||||
| chr9:93558062
|
A | G | 2 | a0001c0002t0002g0274a0001c0002t0002g0275 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2668+52A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 14/17 | chr9 | 93558062 | ||||||
| chr9:93558122
|
T | C | 2 | a0001c0002t0002g0302a0001c0002t0002g0303 | 2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2668+112T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 14/17 | chr9 | 93558122 | ||||||
| chr9:93558160
|
G | A | 1 | a0001c0002t0001g0181 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2668+150G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 14/17 | chr9 | 93558160 | ||||||
| chr9:93558423
|
AG | A | 88 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(85): Show | 89 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.2669-155delG | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93558423 | |||||
| chr9:93558898
|
C | G | 1 | a0002c0009t0002g0135 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2806+180C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93558898 | ||||||
| chr9:93559204
|
T | G | 1 | a0001c0003t0002g0005 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2806+486T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93559204 | ||||||
| chr9:93559535
|
C | T | 1 | a0001c0002t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2806+817C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93559535 | ||||||
| chr9:93559684
|
C | CT | 26 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.2806+967dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr9 | 93559684 | |||||
| chr9:93560040
|
T | C | 2 | a0001c0002t0008g0252a0001c0002t0008g0253 | 2 | HG00639.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2807-1069T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93560040 | ||||||
| chr9:93560072
|
T | C | 5 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(2): Show | 5 | HG00558.hp2 HG02135.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.2807-1037T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93560072 | ||||||
| chr9:93560090
|
C | G | 2 | a0001c0002t0007g0178a0001c0002t0007g0246 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2807-1019C>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93560090 | ||||||
| chr9:93560198
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2807-911G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93560198 | ||||||
| chr9:93560309
|
T | A | 1 | a0001c0002t0002g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2807-800T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93560309 | ||||||
| chr9:93560376
|
T | C | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2807-733T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93560376 | ||||||
| chr9:93560437
|
T | C | 30 | a0001c0003t0002g0118a0001c0003t0002g0147a0001c0003t0002g0148others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.2807-672T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93560437 | ||||||
| chr9:93560679
|
T | C | 5 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(2): Show | 6 | HG02145.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2807-430T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93560679 | ||||||
| chr9:93560709
|
G | C | 1 | a0001c0003t0002g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2807-400G>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93560709 | ||||||
| chr9:93560739
|
T | G | 34 | a0001c0001t0002g0013a0001c0001t0002g0272a0001c0001t0002g0273others(31): Show | 34 | HG01081.hp1 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.2807-370T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93560739 | ||||||
| chr9:93560764
|
G | A | 4 | a0001c0002t0002g0274a0001c0002t0002g0275a0001c0002t0002g0302others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2807-345G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 15/17 | chr9 | 93560764 | ||||||
| chr9:93561412
|
C | T | 1 | a0001c0003t0002g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2948+162C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 16/17 | chr9 | 93561412 | ||||||
| chr9:93561591
|
C | T | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.2948+341C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 16/17 | chr9 | 93561591 | ||||||
| chr9:93561613
|
T | C | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2948+363T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 16/17 | chr9 | 93561613 | ||||||
| chr9:93561646
|
C | T | 5 | a0001c0003t0002g0003a0001c0003t0002g0305a0001c0003t0002g0306others(2): Show | 6 | HG02145.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2948+396C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 16/17 | chr9 | 93561646 | ||||||
| chr9:93561713
|
G | A | 1 | a0001c0002t0008g0248 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2948+463G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 16/17 | chr9 | 93561713 | ||||||
| chr9:93561760
|
CATTAAAT others(11): Show |
C | 2 | a0001c0002t0001g0197a0001c0002t0001g0202 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2949-433_2949-416d others(20): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr9 | 93561760 | |||||
| chr9:93561870
|
G | A | 30 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(27): Show | 30 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.2949-338G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 16/17 | chr9 | 93561870 | ||||||
| chr9:93561962
|
A | G | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0002t0001g0254 | 3 | HG02258.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2949-246A>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 16/17 | chr9 | 93561962 | ||||||
| chr9:93561984
|
C | A | 1 | a0001c0001t0011g0038 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2949-224C>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 16/17 | chr9 | 93561984 | ||||||
| chr9:93562561
|
C | T | 1 | a0001c0001t0002g0132 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3045+257C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93562561 | ||||||
| chr9:93562664
|
T | C | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3045+360T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93562664 | ||||||
| chr9:93562665
|
C | CT | 17 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0098others(14): Show | 17 | HG00438.hp2 HG01069.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.3045+378dupT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr9 | 93562665 | |||||
| chr9:93562665
|
C | T | 1 | a0001c0012t0002g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3045+361C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93562665 | ||||||
| chr9:93562665
|
CT | C | 7 | a0001c0001t0003g0082a0001c0002t0001g0188a0001c0002t0001g0264others(4): Show | 7 | HG02257.hp2 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3045+378delT | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr9 | 93562665 | |||||
| chr9:93562840
|
G | T | 1 | a0001c0001t0002g0145 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3045+536G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93562840 | ||||||
| chr9:93562879
|
G | T | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.3045+575G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93562879 | ||||||
| chr9:93563032
|
T | A | 2 | a0001c0001t0003g0282a0001c0001t0003g0283 | 2 | NA19054.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3045+728T>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93563032 | ||||||
| chr9:93563075
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3045+771G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93563075 | ||||||
| chr9:93563295
|
G | A | 14 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0119others(11): Show | 14 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.3046-934G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93563295 | ||||||
| chr9:93563347
|
C | T | 5 | a0001c0002t0002g0274a0001c0002t0002g0275a0001c0002t0002g0302others(2): Show | 5 | HG02451.hp2 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3046-882C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93563347 | ||||||
| chr9:93563348
|
G | A | 4 | a0001c0005t0009g0113a0001c0005t0009g0114a0001c0005t0009g0115others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-881G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93563348 | ||||||
| chr9:93563380
|
G | A | 1 | a0001c0002t0001g0243 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3046-849G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93563380 | ||||||
| chr9:93563438
|
T | G | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.3046-791T>G | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93563438 | ||||||
| chr9:93563474
|
G | T | 30 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(27): Show | 30 | HG00423.hp1 HG00639.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.3046-755G>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93563474 | ||||||
| chr9:93563512
|
C | T | 2 | a0001c0001t0002g0136a0001c0001t0002g0137 | 2 | HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.3046-717C>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93563512 | ||||||
| chr9:93563804
|
G | A | 3 | a0001c0001t0002g0098a0001c0001t0002g0277a0001c0001t0002g0278 | 3 | HG02055.hp2 HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3046-425G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93563804 | ||||||
| chr9:93563845
|
T | C | 77 | a0001c0001t0003g0001a0001c0001t0003g0030a0001c0001t0003g0031others(74): Show | 78 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3046-384T>C | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93563845 | ||||||
| chr9:93564020
|
A | T | 1 | a0001c0001t0002g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3046-209A>T | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93564020 | ||||||
| chr9:93564058
|
AGGTAGAG others(8): Show |
A | 4 | a0001c0003t0002g0155a0001c0003t0002g0156a0001c0003t0002g0157others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046-169_3046-155d others(17): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr9 | 93564058 | |||||
| chr9:93564074
|
G | A | 12 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0005g0289others(9): Show | 12 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.3046-155G>A | FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 17/17 | chr9 | 93564074 |