Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10086 |
|---|---|
| ensemblid | ENSG00000132297.13 |
| hgncid | 4904 |
| symbol | HHLA1 |
| name | HHLA1 neighbor of OC90 |
| refseq_nuc | NM_001145095.3 |
| refseq_prot | NP_001138567.1 |
| ensembl_nuc | ENST00000414222.2 |
| ensembl_prot | ENSP00000388322.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 132061480 |
| end | 132111157 |
| strand | - |
| ver | v1.2 |
| region | chr8:132061480-132111157 |
| region5000 | chr8:132056480-132116157 |
| regionname0 | HHLA1_chr8_132061480_132111157 |
| regionname5000 | HHLA1_chr8_132056480_132116157 |
| 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 | 0/1 | 531 | 191 | 51 | 36 | 75 | 5 | 23 | 55 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002 | 1/0 | 531 | 85 | 12 | 10 | 49 | 4 | 9 | 37 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0003 | 0/0 | 531 | 61 | 13 | 23 | 17 | 2 | 6 | 15 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0004 | 0/0 | 531 | 21 | 7 | 8 | 2 | 1 | 3 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0005 | 0/0 | 531 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0006 | 0/0 | 531 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0007 | 0/0 | 531 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0008 | 0/0 | 531 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0009 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0010 | 0/0 | 531 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0011 | 0/0 | 531 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0012 | 0/0 | 531 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0013 | 0/0 | 531 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| 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 | 1596 | 132 | 23 | 22 | 62 | 4 | 20 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0002 | 0/0 | 1596 | 61 | 13 | 23 | 17 | 2 | 6 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0003 | 0/0 | 1596 | 42 | 11 | 4 | 21 | 1 | 5 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0004 | 1/0 | 1596 | 36 | 0 | 5 | 26 | 1 | 3 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0005 | 0/0 | 1596 | 32 | 13 | 8 | 10 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0006 | 0/0 | 1596 | 21 | 7 | 8 | 2 | 1 | 3 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0007 | 0/0 | 1596 | 12 | 6 | 2 | 2 | 0 | 2 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0008 | 0/0 | 1596 | 7 | 7 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0009 | 0/0 | 1596 | 6 | 6 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0010 | 0/0 | 1596 | 3 | 0 | 0 | 3 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0011 | 0/0 | 1596 | 3 | 3 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0012 | 0/0 | 1596 | 3 | 0 | 2 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0013 | 0/0 | 1596 | 3 | 0 | 0 | 0 | 2 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0014 | 0/0 | 1596 | 3 | 1 | 0 | 2 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0015 | 0/0 | 1596 | 2 | 0 | 0 | 2 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0016 | 0/0 | 1596 | 2 | 2 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0017 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0018 | 0/0 | 1596 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0019 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0020 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0021 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0022 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0023 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0024 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0025 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0026 | 0/0 | 1596 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0027 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| c0028 | 0/0 | 1596 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2593 | 204 | 31 | 54 | 84 | 11 | 22 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0002 | 0/0 | 2593 | 105 | 16 | 13 | 56 | 1 | 19 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0003 | 0/0 | 2593 | 11 | 10 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0004 | 0/0 | 2593 | 10 | 0 | 3 | 6 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0005 | 0/0 | 2593 | 10 | 8 | 2 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0006 | 0/0 | 2593 | 8 | 8 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0007 | 0/0 | 2593 | 5 | 4 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0008 | 0/0 | 2593 | 5 | 5 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0009 | 0/0 | 2593 | 5 | 4 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0010 | 0/0 | 2593 | 3 | 3 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0011 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0012 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0013 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0014 | 0/0 | 2593 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0015 | 0/0 | 2593 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0016 | 0/0 | 2593 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0017 | 0/0 | 2593 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0018 | 0/0 | 2593 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0019 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0020 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0021 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0022 | 0/0 | 2593 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0023 | 0/0 | 2593 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| t0024 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| 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 | 7 | 0 | 0 | 7 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0002 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| 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 | 1596 | 132 | 23 | 22 | 62 | 4 | 20 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0005 | 0/0 | 1596 | 32 | 13 | 8 | 10 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0007 | 0/0 | 1596 | 12 | 6 | 2 | 2 | 0 | 2 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0009 | 0/0 | 1596 | 6 | 6 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0012 | 0/0 | 1596 | 3 | 0 | 2 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0016 | 0/0 | 1596 | 2 | 2 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0020 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0023 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0024 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0027 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0003 | 0/0 | 1596 | 42 | 11 | 4 | 21 | 1 | 5 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0004 | 1/0 | 1596 | 36 | 0 | 5 | 26 | 1 | 3 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0013 | 0/0 | 1596 | 3 | 0 | 0 | 0 | 2 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0014 | 0/0 | 1596 | 3 | 1 | 0 | 2 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0017 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0003c0002 | 0/0 | 1596 | 61 | 13 | 23 | 17 | 2 | 6 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0004c0006 | 0/0 | 1596 | 21 | 7 | 8 | 2 | 1 | 3 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0005c0008 | 0/0 | 1596 | 7 | 7 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0006c0010 | 0/0 | 1596 | 3 | 0 | 0 | 3 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0006c0015 | 0/0 | 1596 | 2 | 0 | 0 | 2 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0007c0011 | 0/0 | 1596 | 3 | 3 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0008c0021 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0008c0022 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0009c0019 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0010c0028 | 0/0 | 1596 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0011c0026 | 0/0 | 1596 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0012c0025 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0013c0018 | 0/0 | 1596 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4188 | 69 | 2 | 13 | 37 | 4 | 12 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0002 | 0/0 | 4188 | 30 | 2 | 3 | 18 | 0 | 7 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0003 | 0/0 | 4188 | 10 | 9 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0004 | 0/0 | 4188 | 9 | 0 | 2 | 6 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0005 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0006 | 0/0 | 4188 | 2 | 2 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0009 | 0/0 | 4188 | 3 | 2 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0011 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0013 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0014 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0018 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0019 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0020 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0022 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0001t0024 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0005t0001 | 0/0 | 4188 | 14 | 2 | 6 | 5 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0005t0002 | 0/0 | 4188 | 6 | 1 | 0 | 5 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0005t0005 | 0/0 | 4188 | 9 | 7 | 2 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0005t0006 | 0/0 | 4188 | 2 | 2 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0005t0009 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0007t0001 | 0/0 | 4188 | 7 | 3 | 2 | 2 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0007t0002 | 0/0 | 4188 | 3 | 1 | 0 | 0 | 0 | 2 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0007t0006 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0007t0021 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0009t0002 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0009t0007 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0009t0008 | 0/0 | 4188 | 4 | 4 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0012t0001 | 0/0 | 4188 | 3 | 0 | 2 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0016t0002 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0016t0006 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0020t0001 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0023t0001 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0024t0001 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0001c0027t0001 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0003t0001 | 0/0 | 4188 | 28 | 9 | 3 | 14 | 1 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0003t0002 | 0/0 | 4188 | 13 | 2 | 1 | 7 | 0 | 3 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0003t0023 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0004t0001 | 1/0 | 4188 | 10 | 0 | 2 | 7 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0004t0002 | 0/0 | 4188 | 25 | 0 | 3 | 19 | 1 | 2 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0004t0015 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0013t0001 | 0/0 | 4188 | 3 | 0 | 0 | 0 | 2 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0014t0001 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0014t0002 | 0/0 | 4188 | 2 | 1 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0002c0017t0002 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0003c0002t0001 | 0/0 | 4188 | 39 | 2 | 17 | 14 | 2 | 4 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0003c0002t0002 | 0/0 | 4188 | 13 | 4 | 5 | 2 | 0 | 2 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0003c0002t0004 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0003c0002t0006 | 0/0 | 4188 | 2 | 2 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0003c0002t0008 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0003c0002t0010 | 0/0 | 4188 | 3 | 3 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0003c0002t0012 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0003c0002t0017 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0004c0006t0001 | 0/0 | 4188 | 16 | 6 | 7 | 1 | 1 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0004c0006t0002 | 0/0 | 4188 | 4 | 1 | 0 | 1 | 0 | 2 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0004c0006t0016 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0005c0008t0001 | 0/0 | 4188 | 4 | 4 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0005c0008t0002 | 0/0 | 4188 | 2 | 2 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0005c0008t0009 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0006c0010t0001 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0006c0010t0002 | 0/0 | 4188 | 2 | 0 | 0 | 2 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0006c0015t0001 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0006c0015t0002 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0007c0011t0007 | 0/0 | 4188 | 3 | 3 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0008c0021t0003 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0008c0022t0001 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0009c0019t0001 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0010c0028t0002 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0011c0026t0001 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0012c0025t0007 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| a0013c0018t0001 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | copy fasta | chr8 | 132056480 | 132116157 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0003g0002 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0009g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0009g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0011g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0013g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0014g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0018g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0019g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0020g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0022g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0001t0024g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0005g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0005g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0005t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0007t0021g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0009t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0009t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0009t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0009t0008g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0009t0008g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0009t0008g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0012t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0012t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0012t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0016t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0016t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0020t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0023t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0024t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0001c0027t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0003t0023g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0001g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0004t0015g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0013t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0013t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0013t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0014t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0014t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0014t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0002c0017t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0010g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0010g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0003c0002t0017g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0004c0006t0016g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0005c0008t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0005c0008t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0005c0008t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0005c0008t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0005c0008t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0005c0008t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0005c0008t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0006c0010t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0006c0010t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0006c0010t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0006c0015t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0006c0015t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0007c0011t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0007c0011t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0007c0011t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0008c0021t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0008c0022t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0009c0019t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0010c0028t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0011c0026t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0012c0025t0007g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| a0013c0018t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00280 | hp2 | a0001 | c0005 | t0001 | g0060 | EUR | FIN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00323 | hp1 | a0002 | c0003 | t0001 | g0074 | EUR | FIN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0327 | EUR | FIN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00408 | hp1 | a0001 | c0005 | t0001 | g0086 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00408 | hp2 | a0004 | c0006 | t0001 | g0035 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00423 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00438 | hp1 | a0002 | c0004 | t0002 | g0083 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00438 | hp2 | a0001 | c0005 | t0002 | g0066 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00558 | hp1 | a0002 | c0004 | t0002 | g0072 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00597 | hp1 | a0002 | c0003 | t0002 | g0349 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0334 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00639 | hp1 | a0003 | c0002 | t0001 | g0243 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00642 | hp1 | a0003 | c0002 | t0001 | g0221 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00642 | hp2 | a0004 | c0006 | t0001 | g0203 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00673 | hp1 | a0003 | c0002 | t0017 | g0229 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00673 | hp2 | a0002 | c0003 | t0002 | g0134 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00733 | hp1 | a0001 | c0005 | t0005 | g0003 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00733 | hp2 | a0004 | c0006 | t0001 | g0094 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00735 | hp1 | a0001 | c0024 | t0001 | g0195 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00735 | hp2 | a0003 | c0002 | t0001 | g0032 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00738 | hp1 | a0003 | c0002 | t0001 | g0222 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00738 | hp2 | a0002 | c0004 | t0002 | g0048 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00741 | hp1 | a0003 | c0002 | t0001 | g0200 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01069 | hp2 | a0004 | c0006 | t0001 | g0198 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01071 | hp1 | a0004 | c0006 | t0001 | g0197 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01074 | hp2 | a0003 | c0002 | t0002 | g0024 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01081 | hp1 | a0001 | c0001 | t0022 | g0328 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01081 | hp2 | a0004 | c0006 | t0016 | g0162 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01099 | hp1 | a0002 | c0004 | t0001 | g0053 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01099 | hp2 | a0001 | c0005 | t0005 | g0008 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01106 | hp1 | a0001 | c0001 | t0009 | g0303 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01106 | hp2 | a0003 | c0002 | t0004 | g0246 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01109 | hp1 | a0002 | c0017 | t0002 | g0352 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01167 | hp1 | a0012 | c0025 | t0007 | g0283 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01168 | hp1 | a0001 | c0005 | t0001 | g0068 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01169 | hp2 | a0001 | c0005 | t0001 | g0067 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01175 | hp2 | a0002 | c0004 | t0002 | g0005 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01192 | hp1 | a0002 | c0004 | t0002 | g0005 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01192 | hp2 | a0003 | c0002 | t0001 | g0247 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01243 | hp1 | a0001 | c0005 | t0001 | g0063 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01243 | hp2 | a0003 | c0002 | t0001 | g0223 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01255 | hp1 | a0001 | c0007 | t0001 | g0264 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01255 | hp2 | a0003 | c0002 | t0001 | g0029 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01257 | hp1 | a0002 | c0004 | t0001 | g0009 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01257 | hp2 | a0003 | c0002 | t0001 | g0010 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01258 | hp2 | a0003 | c0002 | t0001 | g0010 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0190 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0168 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01346 | hp1 | a0003 | c0002 | t0001 | g0180 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01346 | hp2 | a0004 | c0006 | t0001 | g0093 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01358 | hp1 | a0002 | c0003 | t0002 | g0191 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01361 | hp1 | a0004 | c0006 | t0001 | g0109 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01361 | hp2 | a0003 | c0002 | t0001 | g0202 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01433 | hp1 | a0004 | c0006 | t0001 | g0092 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01433 | hp2 | a0001 | c0005 | t0001 | g0061 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01496 | hp2 | a0002 | c0003 | t0001 | g0207 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01516 | hp1 | a0003 | c0002 | t0001 | g0239 | EUR | IBS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01516 | hp2 | a0002 | c0013 | t0001 | g0111 | EUR | IBS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01517 | hp1 | a0002 | c0013 | t0001 | g0112 | EUR | IBS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01517 | hp2 | a0002 | c0004 | t0002 | g0005 | EUR | IBS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01884 | hp1 | a0005 | c0008 | t0001 | g0054 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01884 | hp2 | a0001 | c0005 | t0006 | g0045 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01891 | hp1 | a0007 | c0011 | t0007 | g0271 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01891 | hp2 | a0001 | c0005 | t0005 | g0008 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01934 | hp1 | a0003 | c0002 | t0001 | g0245 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01934 | hp2 | a0001 | c0012 | t0001 | g0153 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01943 | hp1 | a0001 | c0020 | t0001 | g0135 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01943 | hp2 | a0001 | c0001 | t0018 | g0250 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0163 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01952 | hp2 | a0003 | c0002 | t0002 | g0007 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01975 | hp1 | a0001 | c0005 | t0001 | g0100 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01975 | hp2 | a0003 | c0002 | t0001 | g0255 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01981 | hp2 | a0003 | c0002 | t0002 | g0033 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01993 | hp1 | a0003 | c0002 | t0001 | g0248 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01993 | hp2 | a0003 | c0002 | t0001 | g0242 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02004 | hp1 | a0003 | c0002 | t0002 | g0031 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02004 | hp2 | a0001 | c0007 | t0001 | g0266 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02015 | hp2 | a0006 | c0010 | t0002 | g0276 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02040 | hp1 | a0002 | c0003 | t0002 | g0299 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02040 | hp2 | a0003 | c0002 | t0001 | g0234 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02055 | hp2 | a0001 | c0009 | t0007 | g0189 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02071 | hp1 | a0002 | c0004 | t0002 | g0076 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02074 | hp1 | a0002 | c0004 | t0001 | g0052 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02080 | hp1 | a0001 | c0005 | t0001 | g0050 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02129 | hp1 | a0002 | c0004 | t0001 | g0070 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02129 | hp2 | a0002 | c0004 | t0002 | g0084 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02132 | hp2 | a0001 | c0005 | t0002 | g0085 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02145 | hp1 | a0001 | c0005 | t0005 | g0064 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CDX | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02155 | hp2 | a0001 | c0005 | t0001 | g0058 | EAS | CDX | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02257 | hp1 | a0003 | c0002 | t0002 | g0140 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02257 | hp2 | a0001 | c0005 | t0005 | g0003 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02258 | hp1 | a0007 | c0011 | t0007 | g0041 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0331 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02273 | hp1 | a0003 | c0002 | t0001 | g0244 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02273 | hp2 | a0003 | c0002 | t0002 | g0007 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0158 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02280 | hp2 | a0001 | c0001 | t0020 | g0026 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02293 | hp2 | a0001 | c0005 | t0001 | g0062 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02451 | hp1 | a0005 | c0008 | t0001 | g0055 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02451 | hp2 | a0005 | c0008 | t0002 | g0346 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02523 | hp1 | a0002 | c0004 | t0002 | g0075 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02572 | hp1 | a0004 | c0006 | t0001 | g0201 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02572 | hp2 | a0004 | c0006 | t0001 | g0291 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02602 | hp1 | a0002 | c0003 | t0002 | g0309 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02602 | hp2 | a0003 | c0002 | t0001 | g0037 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0325 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02630 | hp2 | a0003 | c0002 | t0001 | g0238 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02647 | hp1 | a0004 | c0006 | t0001 | g0289 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0336 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02683 | hp2 | a0011 | c0026 | t0001 | g0220 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02698 | hp2 | a0002 | c0003 | t0002 | g0173 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02717 | hp2 | a0001 | c0007 | t0001 | g0023 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0337 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02723 | hp2 | a0001 | c0009 | t0008 | g0340 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02738 | hp2 | a0003 | c0002 | t0001 | g0225 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02809 | hp1 | a0001 | c0001 | t0024 | g0356 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02809 | hp2 | a0002 | c0003 | t0002 | g0326 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02818 | hp2 | a0003 | c0002 | t0002 | g0231 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02886 | hp1 | a0001 | c0005 | t0006 | g0073 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02886 | hp2 | a0002 | c0003 | t0002 | g0333 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02895 | hp1 | a0003 | c0002 | t0002 | g0141 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02895 | hp2 | a0005 | c0008 | t0001 | g0022 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02896 | hp1 | a0004 | c0006 | t0001 | g0156 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02896 | hp2 | a0001 | c0009 | t0008 | g0342 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02897 | hp1 | a0005 | c0008 | t0001 | g0021 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02897 | hp2 | a0001 | c0009 | t0008 | g0341 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02922 | hp2 | a0001 | c0001 | t0013 | g0240 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02965 | hp1 | a0009 | c0019 | t0001 | g0096 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02965 | hp2 | a0002 | c0014 | t0002 | g0267 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02970 | hp2 | a0001 | c0005 | t0002 | g0351 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02976 | hp2 | a0005 | c0008 | t0002 | g0347 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03017 | hp2 | a0013 | c0018 | t0001 | g0213 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0316 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03041 | hp2 | a0001 | c0007 | t0006 | g0259 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03098 | hp1 | a0001 | c0005 | t0005 | g0077 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03098 | hp2 | a0001 | c0005 | t0009 | g0025 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0065 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03130 | hp2 | a0001 | c0005 | t0005 | g0003 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03139 | hp1 | a0001 | c0007 | t0001 | g0261 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03139 | hp2 | a0003 | c0002 | t0010 | g0157 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0284 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03195 | hp2 | a0002 | c0003 | t0001 | g0028 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03209 | hp1 | a0001 | c0016 | t0006 | g0150 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03209 | hp2 | a0001 | c0007 | t0021 | g0262 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03225 | hp1 | a0004 | c0006 | t0001 | g0335 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03225 | hp2 | a0001 | c0001 | t0019 | g0305 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03239 | hp1 | a0004 | c0006 | t0002 | g0205 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03239 | hp2 | a0002 | c0013 | t0001 | g0104 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03453 | hp1 | a0003 | c0002 | t0001 | g0290 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03453 | hp2 | a0003 | c0002 | t0006 | g0146 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03486 | hp1 | a0004 | c0006 | t0001 | g0292 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03490 | hp1 | a0002 | c0004 | t0002 | g0047 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03491 | hp1 | a0001 | c0007 | t0002 | g0257 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03492 | hp1 | a0001 | c0007 | t0002 | g0263 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03492 | hp2 | a0002 | c0004 | t0002 | g0046 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03516 | hp1 | a0003 | c0002 | t0002 | g0145 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03516 | hp2 | a0001 | c0009 | t0008 | g0343 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03540 | hp1 | a0003 | c0002 | t0010 | g0155 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03540 | hp2 | a0001 | c0007 | t0002 | g0270 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03579 | hp1 | a0008 | c0021 | t0003 | g0192 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03654 | hp2 | a0004 | c0006 | t0001 | g0237 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03669 | hp1 | a0002 | c0003 | t0001 | g0167 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03704 | hp1 | a0002 | c0004 | t0015 | g0079 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03710 | hp1 | a0003 | c0002 | t0001 | g0188 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03831 | hp1 | a0010 | c0028 | t0002 | g0193 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03831 | hp2 | a0001 | c0012 | t0001 | g0350 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0236 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG04115 | hp2 | a0002 | c0003 | t0002 | g0302 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG04184 | hp1 | a0003 | c0002 | t0002 | g0199 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG04184 | hp2 | a0003 | c0002 | t0001 | g0194 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG04199 | hp1 | a0003 | c0002 | t0002 | g0020 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0348 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG04204 | hp1 | a0004 | c0006 | t0002 | g0204 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG04228 | hp1 | a0002 | c0003 | t0023 | g0030 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18522 | hp1 | a0001 | c0007 | t0001 | g0260 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18747 | hp1 | a0002 | c0004 | t0002 | g0078 | EAS | CHB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18906 | hp1 | a0002 | c0003 | t0001 | g0322 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18906 | hp2 | a0001 | c0009 | t0002 | g0279 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18940 | hp1 | a0003 | c0002 | t0001 | g0209 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18940 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18942 | hp2 | a0003 | c0002 | t0001 | g0228 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18943 | hp1 | a0004 | c0006 | t0002 | g0036 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18944 | hp1 | a0003 | c0002 | t0001 | g0226 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18944 | hp2 | a0002 | c0004 | t0002 | g0049 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18945 | hp1 | a0001 | c0005 | t0002 | g0089 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18945 | hp2 | a0003 | c0002 | t0001 | g0210 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18947 | hp2 | a0002 | c0004 | t0001 | g0090 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18951 | hp1 | a0002 | c0004 | t0002 | g0091 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18954 | hp2 | a0003 | c0002 | t0001 | g0232 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18959 | hp1 | a0001 | c0007 | t0001 | g0268 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18959 | hp2 | a0002 | c0003 | t0001 | g0311 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18960 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18962 | hp1 | a0001 | c0005 | t0001 | g0059 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18962 | hp2 | a0003 | c0002 | t0001 | g0211 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18966 | hp1 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18967 | hp2 | a0003 | c0002 | t0001 | g0224 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18968 | hp1 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18969 | hp1 | a0003 | c0002 | t0001 | g0227 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18969 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18971 | hp2 | a0003 | c0002 | t0002 | g0219 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18975 | hp2 | a0002 | c0004 | t0002 | g0051 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18977 | hp2 | a0002 | c0003 | t0001 | g0138 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18978 | hp1 | a0001 | c0005 | t0002 | g0087 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18979 | hp1 | a0002 | c0003 | t0001 | g0286 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18979 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18983 | hp1 | a0002 | c0003 | t0002 | g0124 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18983 | hp2 | a0003 | c0002 | t0001 | g0230 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18986 | hp2 | a0006 | c0010 | t0002 | g0273 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18991 | hp2 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18993 | hp1 | a0002 | c0003 | t0002 | g0125 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18994 | hp1 | a0002 | c0003 | t0002 | g0329 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18994 | hp2 | a0006 | c0015 | t0001 | g0275 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18995 | hp1 | a0002 | c0003 | t0001 | g0114 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19000 | hp1 | a0002 | c0014 | t0001 | g0258 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19002 | hp1 | a0001 | c0001 | t0014 | g0254 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19004 | hp2 | a0003 | c0002 | t0002 | g0042 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19005 | hp2 | a0001 | c0005 | t0002 | g0081 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19010 | hp2 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19011 | hp2 | a0003 | c0002 | t0001 | g0345 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19012 | hp2 | a0002 | c0003 | t0001 | g0315 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0151 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19030 | hp2 | a0008 | c0022 | t0001 | g0339 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0152 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19043 | hp2 | a0005 | c0008 | t0009 | g0338 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19058 | hp1 | a0002 | c0003 | t0001 | g0113 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19060 | hp1 | a0002 | c0003 | t0001 | g0132 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19060 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19066 | hp2 | a0003 | c0002 | t0001 | g0235 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19068 | hp2 | a0001 | c0005 | t0001 | g0071 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19070 | hp1 | a0003 | c0002 | t0001 | g0344 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19070 | hp2 | a0002 | c0004 | t0001 | g0101 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19072 | hp1 | a0002 | c0003 | t0002 | g0282 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19072 | hp2 | a0002 | c0004 | t0002 | g0082 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19076 | hp2 | a0002 | c0004 | t0002 | g0069 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19077 | hp1 | a0002 | c0014 | t0002 | g0269 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19079 | hp1 | a0006 | c0010 | t0001 | g0277 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19079 | hp2 | a0002 | c0003 | t0001 | g0310 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19080 | hp1 | a0001 | c0023 | t0001 | g0056 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19082 | hp1 | a0002 | c0004 | t0001 | g0043 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19084 | hp1 | a0006 | c0015 | t0002 | g0274 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19084 | hp2 | a0002 | c0003 | t0001 | g0115 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19086 | hp1 | a0002 | c0004 | t0001 | g0102 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19086 | hp2 | a0002 | c0003 | t0001 | g0314 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19088 | hp1 | a0001 | c0007 | t0001 | g0265 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19088 | hp2 | a0002 | c0003 | t0001 | g0313 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19090 | hp1 | a0002 | c0003 | t0001 | g0312 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19090 | hp2 | a0003 | c0002 | t0001 | g0206 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19091 | hp1 | a0002 | c0004 | t0002 | g0088 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0241 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA19240 | hp2 | a0001 | c0005 | t0005 | g0057 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA20129 | hp1 | a0001 | c0016 | t0002 | g0149 | AFR | ASW | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0355 | AFR | ASW | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA20752 | hp1 | a0003 | c0002 | t0001 | g0196 | EUR | TSI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA20752 | hp2 | a0004 | c0006 | t0001 | g0208 | EUR | TSI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01123 | hp1 | a0001 | c0012 | t0001 | g0154 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0161 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02486 | hp1 | a0003 | c0002 | t0006 | g0143 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0354 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02559 | hp1 | a0007 | c0011 | t0007 | g0187 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG02559 | hp2 | a0003 | c0002 | t0010 | g0353 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03471 | hp1 | a0003 | c0002 | t0012 | g0144 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0332 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG06807 | hp1 | a0001 | c0027 | t0001 | g0044 | AFR | USA | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0306 | AFR | USA | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA20300 | hp1 | a0001 | c0005 | t0005 | g0003 | AFR | USA | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | USA | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA21309 | hp1 | a0003 | c0002 | t0008 | g0034 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| NA21309 | hp2 | a0004 | c0006 | t0002 | g0233 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0177 | REF | REF | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| homoSapiens_grch38 | hp1 | a0002 | c0004 | t0001 | g0103 | REF | REF | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:132065886
|
T | A | 2 | a0007a0012 | 4 | HG01167.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1552A>T | p.Thr518Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/17 | 1629/4188 | 1552/1596 | 518/531 | chr8 | 132065886 | ||
| chr8:132077728
|
A | G | 6 | a0001a0003a0006others(3): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
missense_variant&splice_region_variant | MODERATE | c.1169T>C | p.Leu390Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/17 | 1246/4188 | 1169/1596 | 390/531 | chr8 | 132077728 | ||
| chr8:132079844
|
A | G | 1 | a0011 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.799T>C | p.Ser267Pro | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/17 | 876/4188 | 799/1596 | 267/531 | chr8 | 132079844 | ||
| chr8:132079875
|
C | G | 2 | a0005a0008 | 9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.768G>C | p.Gln256His | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/17 | 845/4188 | 768/1596 | 256/531 | chr8 | 132079875 | ||
| chr8:132079891
|
G | A | 5 | a0003a0004a0010others(2): Show | 85 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(82): Show |
missense_variant | MODERATE | c.752C>T | p.Pro251Leu | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/17 | 829/4188 | 752/1596 | 251/531 | chr8 | 132079891 | ||
| chr8:132087856
|
G | A | 1 | a0010 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.578C>T | p.Thr193Ile | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 9/17 | 655/4188 | 578/1596 | 193/531 | chr8 | 132087856 | ||
| chr8:132095718
|
C | T | 1 | a0009 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.349G>A | p.Val117Ile | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 6/17 | 426/4188 | 349/1596 | 117/531 | chr8 | 132095718 | ||
| chr8:132098893
|
C | G | 1 | a0006 | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
missense_variant | MODERATE | c.269G>C | p.Arg90Thr | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/17 | 346/4188 | 269/1596 | 90/531 | chr8 | 132098893 | ||
| chr8:132098954
|
C | T | 1 | a0013 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.208G>A | p.Ala70Thr | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/17 | 285/4188 | 208/1596 | 70/531 | chr8 | 132098954 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:132076512
|
A | G | 1 | a0001c0024 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.1203T>C | p.Ser401Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/17 | 1280/4188 | 1203/1596 | 401/531 | chr8 | 132076512 | ||
| chr8:132077727
|
C | T | 1 | a0001c0023 | 1 | NA19080.hp1 | splice_region_variant&synonymous_variant | LOW | c.1170G>A | p.Leu390Leu | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/17 | 1247/4188 | 1170/1596 | 390/531 | chr8 | 132077727 | ||
| chr8:132077922
|
C | T | 1 | a0008c0021 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.975G>A | p.Thr325Thr | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/17 | 1052/4188 | 975/1596 | 325/531 | chr8 | 132077922 | ||
| chr8:132087672
|
G | A | 1 | a0001c0027 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.657C>T | p.Ser219Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/17 | 734/4188 | 657/1596 | 219/531 | chr8 | 132087672 | ||
| chr8:132089571
|
G | A | 24 | a0001c0001a0001c0007a0001c0009others(21): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
synonymous_variant | LOW | c.477C>T | p.Ile159Ile | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/17 | 554/4188 | 477/1596 | 159/531 | chr8 | 132089571 | ||
| chr8:132095583
|
T | C | 25 | a0001c0001a0001c0007a0001c0009others(22): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
synonymous_variant | LOW | c.384A>G | p.Val128Val | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/17 | 461/4188 | 384/1596 | 128/531 | chr8 | 132095583 | ||
| chr8:132095758
|
A | G | 2 | a0001c0012a0002c0013 | 6 | HG01123.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
synonymous_variant | LOW | c.309T>C | p.Ser103Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 6/17 | 386/4188 | 309/1596 | 103/531 | chr8 | 132095758 | ||
| chr8:132098919
|
T | C | 2 | a0001c0007a0002c0014 | 15 | HG01255.hp1 HG02004.hp2 HG02717.hp2 others(12): Show |
synonymous_variant | LOW | c.243A>G | p.Thr81Thr | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/17 | 320/4188 | 243/1596 | 81/531 | chr8 | 132098919 | ||
| chr8:132098934
|
G | A | 7 | a0001c0007a0001c0009a0001c0012others(4): Show | 30 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(27): Show |
synonymous_variant | LOW | c.228C>T | p.Ser76Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/17 | 305/4188 | 228/1596 | 76/531 | chr8 | 132098934 | ||
| chr8:132100076
|
C | T | 2 | a0001c0009a0002c0017 | 7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.198G>A | p.Thr66Thr | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/17 | 275/4188 | 198/1596 | 66/531 | chr8 | 132100076 | ||
| chr8:132100100
|
C | T | 1 | a0006c0015 | 2 | NA18994.hp2 NA19084.hp1 |
synonymous_variant | LOW | c.174G>A | p.Lys58Lys | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/17 | 251/4188 | 174/1596 | 58/531 | chr8 | 132100100 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:132061707
|
G | A | 1 | a0001c0001t0011 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2288C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2288 | chr8 | 132061707 | |||||
| chr8:132061841
|
G | A | 1 | a0003c0002t0012 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2154C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2154 | chr8 | 132061841 | |||||
| chr8:132061851
|
C | A | 1 | a0004c0006t0016 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2144G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2144 | chr8 | 132061851 | |||||
| chr8:132061852
|
C | T | 1 | a0003c0002t0017 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2143G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2143 | chr8 | 132061852 | |||||
| chr8:132061880
|
T | C | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(6): Show | 20 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2115A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2115 | chr8 | 132061880 | |||||
| chr8:132061898
|
A | C | 1 | a0002c0004t0015 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2097T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2097 | chr8 | 132061898 | |||||
| chr8:132062009
|
G | A | 1 | a0001c0001t0018 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1986C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1986 | chr8 | 132062009 | |||||
| chr8:132062071
|
G | C | 1 | a0004c0006t0016 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1924C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1924 | chr8 | 132062071 | |||||
| chr8:132062230
|
T | C | 15 | a0001c0001t0005a0001c0001t0009a0001c0001t0011others(12): Show | 30 | HG00733.hp1 HG01099.hp2 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1765A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1765 | chr8 | 132062230 | |||||
| chr8:132062304
|
C | A | 5 | a0001c0001t0009a0001c0001t0019a0001c0001t0024others(2): Show | 7 | HG01106.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1691G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1691 | chr8 | 132062304 | |||||
| chr8:132062331
|
T | C | 15 | a0001c0001t0005a0001c0001t0009a0001c0001t0011others(12): Show | 30 | HG00733.hp1 HG01099.hp2 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1664A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1664 | chr8 | 132062331 | |||||
| chr8:132062464
|
A | G | 8 | a0001c0001t0004a0001c0001t0006a0001c0005t0006others(5): Show | 19 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1531T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1531 | chr8 | 132062464 | |||||
| chr8:132062509
|
A | T | 2 | a0001c0001t0003a0008c0021t0003 | 11 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1486T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1486 | chr8 | 132062509 | |||||
| chr8:132062580
|
A | G | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(41): Show | 171 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1415T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1415 | chr8 | 132062580 | |||||
| chr8:132062639
|
G | A | 1 | a0003c0002t0010 | 3 | HG02559.hp2 HG03139.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1356C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1356 | chr8 | 132062639 | |||||
| chr8:132062983
|
G | A | 1 | a0001c0001t0019 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1012C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1012 | chr8 | 132062983 | |||||
| chr8:132063100
|
A | G | 4 | a0001c0001t0011a0001c0009t0007a0007c0011t0007others(1): Show | 6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*895T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 895 | chr8 | 132063100 | |||||
| chr8:132063151
|
G | C | 11 | a0001c0001t0004a0001c0001t0006a0001c0001t0013others(8): Show | 25 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*844C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 844 | chr8 | 132063151 | |||||
| chr8:132063168
|
G | C | 1 | a0001c0001t0020 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*827C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 827 | chr8 | 132063168 | |||||
| chr8:132063415
|
A | G | 2 | a0001c0001t0004a0003c0002t0004 | 10 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*580T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 580 | chr8 | 132063415 | |||||
| chr8:132063490
|
T | C | 1 | a0001c0007t0021 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*505A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 505 | chr8 | 132063490 | |||||
| chr8:132063509
|
T | C | 1 | a0001c0001t0022 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*486A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 486 | chr8 | 132063509 | |||||
| chr8:132063661
|
C | A | 1 | a0002c0003t0023 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*334G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 334 | chr8 | 132063661 | |||||
| chr8:132063755
|
C | T | 1 | a0001c0001t0014 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*240G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 240 | chr8 | 132063755 | |||||
| chr8:132063848
|
A | G | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(14): Show | 41 | HG00609.hp2 HG00733.hp1 HG01099.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*147T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 147 | chr8 | 132063848 | |||||
| chr8:132105277
|
T | C | 1 | a0001c0001t0024 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/17 | 12 | chr8 | 132105277 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:132064133
|
A | G | 1 | a0001c0007t0021g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1553-95T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064133 | ||||||
| chr8:132064249
|
A | C | 1 | a0001c0001t0020g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1553-211T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064249 | ||||||
| chr8:132064501
|
G | A | 6 | a0001c0001t0005g0331a0001c0005t0005g0003a0001c0005t0005g0008others(3): Show | 10 | HG00733.hp1 HG01099.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1553-463C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064501 | ||||||
| chr8:132064508
|
C | A | 4 | a0001c0001t0001g0252a0001c0001t0001g0301a0001c0007t0001g0264others(1): Show | 4 | HG00544.hp2 HG01255.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1553-470G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064508 | ||||||
| chr8:132064508
|
C | G | 14 | a0001c0001t0001g0129a0001c0001t0002g0280a0001c0012t0001g0350others(11): Show | 15 | HG00642.hp1 HG00673.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1553-470G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064508 | ||||||
| chr8:132064624
|
CTG | C | 53 | a0001c0001t0002g0317a0001c0001t0003g0002a0001c0001t0003g0027others(50): Show | 67 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1553-588_1553-587d others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064624 | ||||||
| chr8:132064906
|
A | T | 1 | a0001c0016t0002g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1553-868T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064906 | ||||||
| chr8:132064934
|
A | G | 1 | a0001c0005t0006g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1553-896T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064934 | ||||||
| chr8:132065057
|
G | T | 6 | a0001c0001t0011g0158a0001c0009t0007g0189a0007c0011t0007g0041others(3): Show | 6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1552+829C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065057 | ||||||
| chr8:132065068
|
T | C | 3 | a0001c0001t0001g0252a0001c0001t0001g0301a0003c0002t0001g0235 | 3 | HG00544.hp2 NA18954.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1552+818A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065068 | ||||||
| chr8:132065112
|
A | G | 2 | a0003c0002t0001g0211a0003c0002t0001g0227 | 2 | NA18962.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1552+774T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065112 | ||||||
| chr8:132065124
|
T | G | 95 | a0001c0001t0002g0004a0001c0001t0002g0014a0001c0001t0002g0015others(92): Show | 111 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1552+762A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065124 | ||||||
| chr8:132065153
|
A | G | 6 | a0001c0001t0011g0158a0001c0009t0007g0189a0007c0011t0007g0041others(3): Show | 6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1552+733T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065153 | ||||||
| chr8:132065192
|
G | A | 1 | a0001c0001t0005g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1552+694C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065192 | ||||||
| chr8:132065236
|
T | C | 1 | a0001c0001t0020g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1552+650A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065236 | ||||||
| chr8:132065293
|
G | A | 3 | a0007c0011t0007g0041a0007c0011t0007g0271a0012c0025t0007g0283 | 3 | HG01167.hp1 HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1552+593C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065293 | ||||||
| chr8:132065442
|
T | C | 5 | a0001c0001t0002g0317a0002c0004t0002g0076a0006c0010t0002g0273others(2): Show | 5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1552+444A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065442 | ||||||
| chr8:132065484
|
A | G | 1 | a0003c0002t0001g0010 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1552+402T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065484 | ||||||
| chr8:132065489
|
A | G | 109 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(106): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1552+397T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065489 | ||||||
| chr8:132065555
|
T | C | 1 | a0003c0002t0001g0200 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1552+331A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065555 | ||||||
| chr8:132065564
|
G | A | 2 | a0002c0003t0002g0309a0002c0003t0023g0030 | 2 | HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1552+322C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065564 | ||||||
| chr8:132065574
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1552+312C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065574 | ||||||
| chr8:132065604
|
C | T | 1 | a0001c0005t0006g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1552+282G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065604 | ||||||
| chr8:132065662
|
G | T | 10 | a0001c0001t0002g0148a0001c0001t0002g0169a0001c0001t0002g0170others(7): Show | 10 | HG01070.hp1 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1552+224C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065662 | ||||||
| chr8:132065836
|
G | A | 3 | a0007c0011t0007g0041a0007c0011t0007g0271a0012c0025t0007g0283 | 3 | HG01167.hp1 HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1552+50C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065836 | ||||||
| chr8:132066014
|
G | T | 34 | a0001c0001t0001g0300a0001c0001t0002g0004a0001c0001t0002g0014others(31): Show | 36 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.1470-46C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066014 | ||||||
| chr8:132066127
|
T | C | 1 | a0002c0003t0001g0337 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1470-159A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066127 | ||||||
| chr8:132066146
|
GGAA | G | 4 | a0007c0011t0007g0041a0007c0011t0007g0187a0007c0011t0007g0271others(1): Show | 4 | HG01167.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1470-181_1470-179d others(5): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066146 | ||||||
| chr8:132066178
|
T | C | 1 | a0001c0007t0001g0264 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1470-210A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066178 | ||||||
| chr8:132066202
|
C | T | 2 | a0001c0009t0008g0343a0002c0003t0001g0332 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1470-234G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066202 | ||||||
| chr8:132066245
|
G | A | 6 | a0001c0001t0011g0158a0001c0009t0007g0189a0007c0011t0007g0041others(3): Show | 6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-277C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066245 | ||||||
| chr8:132066291
|
T | A | 1 | a0002c0003t0001g0113 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1470-323A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066291 | ||||||
| chr8:132066362
|
C | T | 5 | a0001c0001t0002g0317a0002c0004t0002g0076a0006c0010t0002g0273others(2): Show | 5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1470-394G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066362 | ||||||
| chr8:132066371
|
T | TG | 6 | a0001c0001t0009g0303a0001c0001t0009g0306a0001c0001t0009g0354others(3): Show | 6 | HG01106.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1470-404dupC | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066371 | ||||||
| chr8:132066384
|
CTGTT | C | 5 | a0001c0001t0002g0317a0002c0004t0002g0076a0006c0010t0002g0273others(2): Show | 5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1470-420_1470-417d others(6): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066384 | ||||||
| chr8:132066440
|
G | C | 1 | a0007c0011t0007g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1470-472C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066440 | ||||||
| chr8:132066463
|
T | G | 6 | a0001c0001t0011g0158a0001c0009t0007g0189a0007c0011t0007g0041others(3): Show | 6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-495A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066463 | ||||||
| chr8:132066568
|
G | A | 5 | a0001c0009t0008g0340a0001c0009t0008g0341a0001c0009t0008g0342others(2): Show | 5 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1470-600C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066568 | ||||||
| chr8:132066831
|
C | T | 6 | a0001c0001t0011g0158a0001c0009t0007g0189a0007c0011t0007g0041others(3): Show | 6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-863G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066831 | ||||||
| chr8:132066907
|
G | A | 6 | a0001c0001t0013g0240a0001c0009t0008g0340a0001c0009t0008g0341others(3): Show | 6 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-939C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066907 | ||||||
| chr8:132067041
|
C | T | 1 | a0001c0005t0002g0085 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1470-1073G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067041 | ||||||
| chr8:132067141
|
C | T | 1 | a0003c0002t0001g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1470-1173G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067141 | ||||||
| chr8:132067218
|
T | A | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1250A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067218 | ||||||
| chr8:132067219
|
G | C | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1251C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067219 | ||||||
| chr8:132067220
|
C | A | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1252G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067220 | ||||||
| chr8:132067222
|
C | T | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1254G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067222 | ||||||
| chr8:132067224
|
A | G | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1256T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067224 | ||||||
| chr8:132067227
|
C | T | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1259G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067227 | ||||||
| chr8:132067228
|
A | T | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1260T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067228 | ||||||
| chr8:132067329
|
G | A | 142 | a0001c0001t0001g0300a0001c0001t0002g0004a0001c0001t0002g0014others(139): Show | 162 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.1470-1361C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067329 | ||||||
| chr8:132067594
|
G | T | 1 | a0003c0002t0002g0231 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1470-1626C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067594 | ||||||
| chr8:132067853
|
G | A | 1 | a0002c0004t0002g0005 | 3 | HG01175.hp2 HG01192.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1470-1885C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067853 | ||||||
| chr8:132068053
|
A | G | 6 | a0001c0001t0011g0158a0001c0009t0007g0189a0007c0011t0007g0041others(3): Show | 6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-2085T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068053 | ||||||
| chr8:132068143
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1470-2175T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068143 | ||||||
| chr8:132068177
|
C | T | 6 | a0001c0001t0013g0240a0001c0009t0008g0340a0001c0009t0008g0341others(3): Show | 6 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-2209G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068177 | ||||||
| chr8:132068213
|
C | A | 1 | a0001c0001t0020g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1470-2245G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068213 | ||||||
| chr8:132068277
|
A | T | 6 | a0001c0009t0002g0279a0001c0016t0002g0149a0001c0027t0001g0044others(3): Show | 6 | HG02257.hp1 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1470-2309T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068277 | ||||||
| chr8:132068291
|
C | T | 1 | a0002c0003t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1470-2323G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068291 | ||||||
| chr8:132068476
|
T | A | 3 | a0003c0002t0010g0155a0003c0002t0010g0157a0003c0002t0010g0353 | 3 | HG02559.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1470-2508A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068476 | ||||||
| chr8:132068486
|
G | T | 5 | a0001c0001t0002g0317a0002c0004t0002g0076a0006c0010t0002g0273others(2): Show | 5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1470-2518C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068486 | ||||||
| chr8:132068583
|
G | T | 17 | a0001c0001t0001g0129a0001c0001t0001g0252a0001c0001t0001g0301others(14): Show | 18 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1470-2615C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068583 | ||||||
| chr8:132068686
|
C | T | 5 | a0001c0001t0002g0317a0002c0004t0002g0076a0006c0010t0002g0273others(2): Show | 5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+2654G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068686 | ||||||
| chr8:132068690
|
C | T | 5 | a0001c0001t0002g0317a0002c0004t0002g0076a0006c0010t0002g0273others(2): Show | 5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+2650G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068690 | ||||||
| chr8:132068710
|
G | A | 4 | a0001c0001t0006g0241a0001c0001t0006g0284a0001c0005t0006g0073others(1): Show | 4 | HG02886.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469+2630C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068710 | ||||||
| chr8:132068755
|
C | G | 45 | a0001c0001t0001g0019a0001c0001t0001g0300a0001c0001t0002g0004others(42): Show | 47 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1469+2585G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068755 | ||||||
| chr8:132068765
|
T | G | 2 | a0002c0003t0002g0173a0004c0006t0002g0205 | 2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1469+2575A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068765 | ||||||
| chr8:132068831
|
A | G | 7 | a0001c0007t0001g0260a0001c0007t0001g0261a0001c0009t0008g0340others(4): Show | 7 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1469+2509T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068831 | ||||||
| chr8:132068996
|
G | GGTAGAAA others(4): Show |
1 | a0002c0003t0001g0113 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1469+2343_1469+234 others(15): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068996 | ||||||
| chr8:132069007
|
C | T | 1 | a0001c0001t0005g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1469+2333G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069007 | ||||||
| chr8:132069013
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1469+2327C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069013 | ||||||
| chr8:132069199
|
C | A | 17 | a0001c0001t0002g0095a0001c0001t0004g0163a0001c0001t0004g0168others(14): Show | 17 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1469+2141G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069199 | ||||||
| chr8:132069245
|
C | A | 5 | a0001c0001t0002g0317a0002c0004t0002g0076a0006c0010t0002g0273others(2): Show | 5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+2095G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069245 | ||||||
| chr8:132069249
|
A | G | 3 | a0003c0002t0010g0155a0003c0002t0010g0157a0003c0002t0010g0353 | 3 | HG02559.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1469+2091T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069249 | ||||||
| chr8:132069355
|
G | GT | 7 | a0001c0001t0009g0303a0001c0001t0009g0306a0001c0001t0009g0354others(4): Show | 7 | HG01106.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469+1984dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069355 | ||||||
| chr8:132069360
|
T | TTTG | 5 | a0001c0001t0002g0317a0002c0004t0002g0076a0006c0010t0002g0273others(2): Show | 5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+1979_1469+198 others(7): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069360 | ||||||
| chr8:132069364
|
G | T | 7 | a0001c0001t0003g0099a0001c0009t0002g0279a0001c0027t0001g0044others(4): Show | 7 | HG02257.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1469+1976C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069364 | ||||||
| chr8:132069400
|
C | T | 1 | a0001c0009t0002g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1469+1940G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069400 | ||||||
| chr8:132069401
|
G | A | 1 | a0003c0002t0001g0255 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1469+1939C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069401 | ||||||
| chr8:132069468
|
G | A | 1 | a0011c0026t0001g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1469+1872C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069468 | ||||||
| chr8:132069594
|
A | G | 1 | a0001c0001t0005g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1469+1746T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069594 | ||||||
| chr8:132069603
|
T | G | 3 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0007t0002g0270 | 3 | HG02922.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1469+1737A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069603 | ||||||
| chr8:132069685
|
G | A | 12 | a0001c0001t0002g0095a0001c0001t0004g0163a0001c0001t0004g0168others(9): Show | 12 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1469+1655C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069685 | ||||||
| chr8:132069736
|
C | T | 1 | a0008c0022t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1469+1604G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069736 | ||||||
| chr8:132069739
|
T | G | 105 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(102): Show | 122 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1469+1601A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069739 | ||||||
| chr8:132069748
|
C | A | 6 | a0001c0001t0009g0303a0001c0001t0009g0306a0001c0001t0009g0354others(3): Show | 6 | HG01106.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469+1592G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069748 | ||||||
| chr8:132069814
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0323 | 2 | NA18966.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1469+1526G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069814 | ||||||
| chr8:132069816
|
G | C | 5 | a0001c0001t0002g0317a0002c0004t0002g0076a0006c0010t0002g0273others(2): Show | 5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+1524C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069816 | ||||||
| chr8:132069898
|
C | T | 1 | a0002c0003t0001g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1469+1442G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069898 | ||||||
| chr8:132069923
|
G | A | 1 | a0007c0011t0007g0041 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1469+1417C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069923 | ||||||
| chr8:132069925
|
A | G | 190 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(187): Show | 213 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.1469+1415T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069925 | ||||||
| chr8:132070010
|
A | C | 3 | a0003c0002t0002g0145a0003c0002t0006g0143a0003c0002t0012g0144 | 3 | HG02486.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1469+1330T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070010 | ||||||
| chr8:132070011
|
C | A | 1 | a0001c0001t0004g0320 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1469+1329G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(3): Show |
14 | a0001c0001t0001g0121a0001c0001t0001g0166a0001c0001t0001g0253others(11): Show | 14 | HG01358.hp2 HG01496.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1469+1319_1469+132 others(14): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(4): Show |
14 | a0001c0001t0001g0178a0001c0001t0004g0334a0001c0005t0001g0059others(11): Show | 15 | HG00609.hp2 HG00735.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1469+1318_1469+132 others(15): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(5): Show |
28 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0107others(25): Show | 28 | HG00280.hp1 HG00544.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1469+1317_1469+132 others(16): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(6): Show |
32 | a0001c0001t0001g0119a0001c0001t0001g0128a0001c0001t0001g0136others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1469+1316_1469+132 others(17): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(7): Show |
30 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0127others(27): Show | 30 | HG00639.hp1 HG01069.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(18): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(8): Show |
22 | a0001c0001t0001g0126a0001c0001t0001g0131a0001c0001t0001g0212others(19): Show | 22 | HG00408.hp2 HG00642.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(19): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(9): Show |
11 | a0001c0001t0001g0139a0001c0001t0004g0168a0001c0007t0001g0268others(8): Show | 11 | HG01070.hp2 HG01261.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(20): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(10): Show |
5 | a0001c0001t0001g0251a0001c0005t0001g0061a0001c0005t0001g0067others(2): Show | 5 | HG01169.hp2 HG01433.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(21): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(11): Show |
6 | a0001c0001t0001g0117a0001c0001t0013g0240a0002c0003t0001g0316others(3): Show | 6 | HG01934.hp1 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(22): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(12): Show |
2 | a0001c0005t0001g0060a0003c0002t0001g0244 | 2 | HG00280.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(23): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(13): Show |
4 | a0001c0001t0003g0098a0003c0002t0001g0242a0004c0006t0001g0094others(1): Show | 4 | HG00733.hp2 HG01993.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(24): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070011
|
C | CGGGGGGG others(14): Show |
1 | a0001c0001t0004g0163 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1469+1328_1469+132 others(25): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | ||||||
| chr8:132070012
|
GGGGGGGG others(6): Show |
G | 65 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 69 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1469+1315_1469+132 others(17): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070012 | ||||||
| chr8:132070015
|
G | GGGGGGGG others(6): Show |
1 | a0001c0009t0008g0343 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1469+1324_1469+132 others(17): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070015 | ||||||
| chr8:132070016
|
G | GGGGGGGG others(3): Show |
1 | a0001c0009t0008g0342 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1469+1323_1469+132 others(14): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070016 | ||||||
| chr8:132070017
|
G | GGGGGGGG others(3): Show |
1 | a0003c0002t0008g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1469+1322_1469+132 others(14): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070017 | ||||||
| chr8:132070019
|
G | T | 61 | a0001c0001t0001g0129a0001c0001t0001g0252a0001c0001t0001g0301others(58): Show | 76 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1469+1321C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070019 | ||||||
| chr8:132070020
|
G | T | 2 | a0002c0004t0002g0069a0004c0006t0002g0036 | 2 | NA18943.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1469+1320C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070020 | ||||||
| chr8:132070020
|
GGGGGA | G | 62 | a0001c0001t0001g0129a0001c0001t0001g0252a0001c0001t0001g0301others(59): Show | 77 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1469+1315_1469+131 others(9): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070020 | ||||||
| chr8:132070021
|
G | GGGGGGGG others(7): Show |
1 | a0003c0002t0001g0225 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1469+1318_1469+131 others(18): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070021 | ||||||
| chr8:132070021
|
G | T | 1 | a0002c0003t0002g0134 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1469+1319C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070021 | ||||||
| chr8:132070024
|
GA | G | 3 | a0001c0001t0002g0172a0001c0001t0002g0278a0001c0001t0004g0321 | 3 | HG03017.hp1 HG03688.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1469+1315delT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070024 | ||||||
| chr8:132070025
|
A | G | 42 | a0001c0001t0002g0095a0001c0001t0002g0148a0001c0001t0002g0169others(39): Show | 46 | HG00609.hp2 HG00733.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1469+1315T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070025 | ||||||
| chr8:132070025
|
A | T | 1 | a0001c0009t0008g0341 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1469+1315T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070025 | ||||||
| chr8:132070028
|
G | GGGGTGGG others(10): Show |
1 | a0001c0007t0001g0261 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1469+1311_1469+131 others(21): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070028 | ||||||
| chr8:132070028
|
G | GGGGTGGG others(8): Show |
1 | a0001c0009t0008g0340 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1469+1311_1469+131 others(19): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070028 | ||||||
| chr8:132070028
|
G | GGGTGGGG others(8): Show |
1 | a0001c0007t0001g0260 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1469+1311_1469+131 others(19): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070028 | ||||||
| chr8:132070028
|
G | T | 3 | a0001c0009t0008g0342a0001c0009t0008g0343a0003c0002t0008g0034 | 3 | HG02896.hp2 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1469+1312C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070028 | ||||||
| chr8:132070247
|
T | G | 157 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(154): Show | 177 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.1469+1093A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070247 | ||||||
| chr8:132070252
|
G | A | 1 | a0001c0001t0002g0324 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1469+1088C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070252 | ||||||
| chr8:132070381
|
C | T | 3 | a0003c0002t0010g0155a0003c0002t0010g0157a0003c0002t0010g0353 | 3 | HG02559.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1469+959G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070381 | ||||||
| chr8:132070408
|
A | T | 1 | a0003c0002t0001g0010 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1469+932T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070408 | ||||||
| chr8:132070568
|
C | T | 1 | a0003c0002t0002g0140 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1469+772G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070568 | ||||||
| chr8:132070587
|
T | C | 2 | a0002c0003t0001g0316a0004c0006t0001g0335 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1469+753A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070587 | ||||||
| chr8:132070669
|
G | A | 1 | a0001c0001t0011g0158 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1469+671C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070669 | ||||||
| chr8:132070676
|
C | T | 1 | a0007c0011t0007g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1469+664G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070676 | ||||||
| chr8:132070722
|
TCATCTCA others(8): Show |
T | 1 | a0001c0001t0002g0106 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1469+603_1469+617d others(17): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070722 | ||||||
| chr8:132071049
|
C | T | 1 | a0002c0003t0002g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1469+291G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132071049 | ||||||
| chr8:132071164
|
C | T | 1 | a0001c0001t0005g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1469+176G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132071164 | ||||||
| chr8:132071284
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0253 | 2 | NA18968.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1469+56G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132071284 | ||||||
| chr8:132071554
|
G | A | 20 | a0001c0001t0003g0002a0001c0001t0003g0027a0001c0001t0003g0098others(17): Show | 25 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1316-61C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071554 | ||||||
| chr8:132071580
|
G | A | 1 | a0001c0001t0013g0240 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1316-87C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071580 | ||||||
| chr8:132071628
|
A | T | 2 | a0004c0006t0001g0291a0004c0006t0001g0292 | 2 | HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1316-135T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071628 | ||||||
| chr8:132071677
|
GT | G | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316-185delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071677 | ||||||
| chr8:132071788
|
G | C | 1 | a0001c0001t0001g0251 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-295C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071788 | ||||||
| chr8:132071789
|
C | A | 1 | a0001c0001t0001g0251 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-296G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071789 | ||||||
| chr8:132071790
|
A | T | 1 | a0001c0001t0001g0251 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-297T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071790 | ||||||
| chr8:132071851
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-358C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071851 | ||||||
| chr8:132071852
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-359T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071852 | ||||||
| chr8:132071921
|
C | T | 1 | a0001c0023t0001g0056 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1316-428G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071921 | ||||||
| chr8:132071940
|
G | A | 5 | a0001c0005t0005g0003a0001c0005t0005g0008a0001c0005t0005g0057others(2): Show | 9 | HG00733.hp1 HG01099.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1316-447C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071940 | ||||||
| chr8:132071951
|
T | C | 3 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0007t0002g0270 | 3 | HG02922.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1316-458A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071951 | ||||||
| chr8:132071960
|
G | A | 1 | a0003c0002t0001g0032 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1316-467C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071960 | ||||||
| chr8:132071967
|
C | A | 1 | a0001c0001t0001g0251 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-474G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071967 | ||||||
| chr8:132071968
|
A | G | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316-475T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071968 | ||||||
| chr8:132072048
|
G | T | 1 | a0001c0001t0001g0251 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-555C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072048 | ||||||
| chr8:132072078
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1316-585T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072078 | ||||||
| chr8:132072097
|
C | T | 1 | a0001c0007t0001g0264 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1316-604G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072097 | ||||||
| chr8:132072249
|
G | A | 48 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(45): Show | 52 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1316-756C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072249 | ||||||
| chr8:132072333
|
T | C | 1 | a0001c0001t0005g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1316-840A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072333 | ||||||
| chr8:132072343
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1316-850C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072343 | ||||||
| chr8:132072416
|
A | C | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316-923T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072416 | ||||||
| chr8:132072427
|
T | A | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1316-934A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072427 | ||||||
| chr8:132072496
|
T | C | 55 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(52): Show | 59 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1316-1003A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072496 | ||||||
| chr8:132072787
|
G | T | 1 | a0001c0001t0001g0251 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-1294C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072787 | ||||||
| chr8:132072905
|
T | TA | 6 | a0001c0001t0009g0303a0001c0001t0009g0306a0001c0001t0009g0354others(3): Show | 6 | HG01106.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316-1413dupT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072905 | ||||||
| chr8:132073064
|
G | T | 1 | a0002c0003t0001g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1316-1571C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073064 | ||||||
| chr8:132073074
|
A | T | 1 | a0002c0003t0001g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1316-1581T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073074 | ||||||
| chr8:132073214
|
T | G | 1 | a0002c0004t0002g0076 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1316-1721A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073214 | ||||||
| chr8:132073416
|
G | T | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316-1923C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073416 | ||||||
| chr8:132073458
|
T | C | 1 | a0002c0003t0001g0190 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1316-1965A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073458 | ||||||
| chr8:132073556
|
G | A | 1 | a0003c0002t0002g0033 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1316-2063C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073556 | ||||||
| chr8:132073619
|
C | G | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316-2126G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073619 | ||||||
| chr8:132073686
|
A | C | 1 | a0008c0021t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1316-2193T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073686 | ||||||
| chr8:132073702
|
C | A | 4 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0005t0001g0100others(1): Show | 4 | HG00639.hp1 HG01496.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1316-2209G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073702 | ||||||
| chr8:132073820
|
G | A | 1 | a0001c0001t0005g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1315+2235C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073820 | ||||||
| chr8:132073836
|
A | G | 2 | a0001c0005t0001g0058a0001c0005t0001g0059 | 2 | HG02155.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1315+2219T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073836 | ||||||
| chr8:132073963
|
CT | C | 5 | a0001c0005t0005g0003a0001c0005t0005g0008a0001c0005t0005g0057others(2): Show | 9 | HG00733.hp1 HG01099.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1315+2091delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073963 | ||||||
| chr8:132073987
|
C | A | 1 | a0002c0003t0001g0316 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1315+2068G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073987 | ||||||
| chr8:132074013
|
A | G | 1 | a0001c0001t0013g0240 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1315+2042T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074013 | ||||||
| chr8:132074042
|
C | T | 1 | a0003c0002t0001g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1315+2013G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074042 | ||||||
| chr8:132074115
|
C | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(60): Show | 67 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1315+1940G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074115 | ||||||
| chr8:132074225
|
T | C | 1 | a0008c0021t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1315+1830A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074225 | ||||||
| chr8:132074233
|
C | T | 4 | a0001c0027t0001g0044a0003c0002t0002g0140a0003c0002t0002g0141others(1): Show | 4 | HG02257.hp1 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315+1822G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074233 | ||||||
| chr8:132074306
|
T | C | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+1749A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074306 | ||||||
| chr8:132074320
|
C | A | 1 | a0002c0003t0001g0113 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1315+1735G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074320 | ||||||
| chr8:132074322
|
A | T | 1 | a0002c0003t0001g0113 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1315+1733T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074322 | ||||||
| chr8:132074329
|
CT | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0184a0001c0001t0001g0287others(3): Show | 8 | HG00423.hp1 HG02074.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315+1725delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074329 | ||||||
| chr8:132074337
|
T | C | 51 | a0001c0001t0001g0129a0001c0001t0001g0252a0001c0001t0001g0301others(48): Show | 57 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1315+1718A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074337 | ||||||
| chr8:132074366
|
G | A | 1 | a0002c0003t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1315+1689C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074366 | ||||||
| chr8:132074407
|
A | T | 6 | a0002c0003t0002g0282a0002c0003t0002g0349a0002c0004t0001g0070others(3): Show | 6 | HG00438.hp1 HG00597.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1315+1648T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074407 | ||||||
| chr8:132074463
|
T | A | 3 | a0001c0001t0002g0214a0001c0001t0002g0216a0001c0001t0002g0218 | 3 | NA18972.hp1 NA19003.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1315+1592A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074463 | ||||||
| chr8:132074533
|
G | A | 4 | a0003c0002t0001g0242a0003c0002t0001g0244a0003c0002t0001g0245others(1): Show | 4 | HG01934.hp1 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+1522C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074533 | ||||||
| chr8:132074561
|
T | G | 3 | a0001c0001t0006g0241a0001c0001t0006g0284a0001c0007t0006g0259 | 3 | HG03041.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1315+1494A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074561 | ||||||
| chr8:132074602
|
A | AT | 22 | a0001c0001t0002g0095a0001c0001t0002g0317a0001c0001t0004g0163others(19): Show | 22 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1315+1452dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074602 | ||||||
| chr8:132074607
|
T | A | 1 | a0002c0003t0002g0349 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1315+1448A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074607 | ||||||
| chr8:132074634
|
G | A | 1 | a0001c0005t0006g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1315+1421C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074634 | ||||||
| chr8:132074814
|
G | A | 1 | a0002c0003t0023g0030 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1315+1241C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074814 | ||||||
| chr8:132074853
|
G | A | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1202C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074853 | ||||||
| chr8:132074854
|
G | C | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1201C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074854 | ||||||
| chr8:132074855
|
G | A | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1200C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074855 | ||||||
| chr8:132074856
|
T | C | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1199A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074856 | ||||||
| chr8:132074857
|
A | T | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1198T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074857 | ||||||
| chr8:132074858
|
G | A | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1197C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074858 | ||||||
| chr8:132074860
|
T | A | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1195A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074860 | ||||||
| chr8:132074862
|
A | C | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1193T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074862 | ||||||
| chr8:132074863
|
A | G | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1192T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074863 | ||||||
| chr8:132074864
|
T | C | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1191A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074864 | ||||||
| chr8:132074865
|
A | G | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1190T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074865 | ||||||
| chr8:132074866
|
A | T | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1189T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074866 | ||||||
| chr8:132074867
|
A | G | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1188T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074867 | ||||||
| chr8:132074869
|
A | T | 1 | a0003c0002t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1186T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074869 | ||||||
| chr8:132075124
|
T | C | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+931A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075124 | ||||||
| chr8:132075241
|
T | A | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+814A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075241 | ||||||
| chr8:132075275
|
C | G | 1 | a0001c0001t0001g0253 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1315+780G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075275 | ||||||
| chr8:132075344
|
C | T | 1 | a0009c0019t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1315+711G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075344 | ||||||
| chr8:132075404
|
G | T | 1 | a0001c0005t0002g0351 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1315+651C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075404 | ||||||
| chr8:132075413
|
C | A | 2 | a0002c0003t0002g0333a0002c0014t0002g0267 | 2 | HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1315+642G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075413 | ||||||
| chr8:132075437
|
C | T | 3 | a0007c0011t0007g0041a0007c0011t0007g0187a0007c0011t0007g0271 | 3 | HG01891.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1315+618G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075437 | ||||||
| chr8:132075510
|
G | T | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+545C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075510 | ||||||
| chr8:132075521
|
T | C | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+534A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075521 | ||||||
| chr8:132075537
|
A | G | 1 | a0003c0002t0001g0234 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1315+518T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075537 | ||||||
| chr8:132075589
|
C | G | 1 | a0002c0004t0002g0005 | 3 | HG01175.hp2 HG01192.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1315+466G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075589 | ||||||
| chr8:132075614
|
T | C | 2 | a0002c0003t0001g0316a0004c0006t0001g0335 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1315+441A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075614 | ||||||
| chr8:132075780
|
A | T | 8 | a0001c0001t0003g0142a0001c0001t0013g0240a0001c0007t0021g0262others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315+275T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075780 | ||||||
| chr8:132076179
|
G | A | 1 | a0001c0016t0006g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1241-50C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076179 | ||||||
| chr8:132076183
|
A | G | 1 | a0003c0002t0001g0010 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1241-54T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076183 | ||||||
| chr8:132076204
|
T | C | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-75A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076204 | ||||||
| chr8:132076246
|
T | C | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-117A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076246 | ||||||
| chr8:132076289
|
A | C | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-160T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076289 | ||||||
| chr8:132076363
|
A | G | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+112T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076363 | ||||||
| chr8:132076388
|
C | T | 1 | a0001c0001t0009g0354 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1240+87G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076388 | ||||||
| chr8:132076398
|
C | A | 1 | a0001c0005t0006g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1240+77G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076398 | ||||||
| chr8:132076429
|
C | T | 1 | a0001c0005t0006g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1240+46G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076429 | ||||||
| chr8:132076603
|
G | A | 1 | a0009c0019t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1172-60C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076603 | ||||||
| chr8:132076713
|
G | A | 1 | a0003c0002t0001g0200 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1172-170C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076713 | ||||||
| chr8:132076729
|
G | A | 1 | a0003c0002t0001g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1172-186C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076729 | ||||||
| chr8:132076757
|
G | A | 1 | a0001c0005t0006g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1172-214C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076757 | ||||||
| chr8:132076907
|
T | C | 1 | a0001c0001t0002g0110 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1172-364A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076907 | ||||||
| chr8:132076941
|
C | T | 6 | a0002c0003t0001g0312a0002c0003t0001g0313a0002c0003t0001g0314others(3): Show | 6 | HG01358.hp1 HG03704.hp1 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.1172-398G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076941 | ||||||
| chr8:132077042
|
G | A | 1 | a0005c0008t0002g0347 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1172-499C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077042 | ||||||
| chr8:132077133
|
G | C | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1172-590C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077133 | ||||||
| chr8:132077243
|
A | C | 1 | a0004c0006t0001g0208 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1171+483T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077243 | ||||||
| chr8:132077468
|
A | C | 1 | a0002c0003t0001g0286 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1171+258T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077468 | ||||||
| chr8:132077511
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1171+215T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077511 | ||||||
| chr8:132077581
|
G | A | 1 | a0001c0009t0007g0189 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1171+145C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077581 | ||||||
| chr8:132077667
|
A | T | 1 | a0002c0004t0001g0052 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1171+59T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077667 | ||||||
| chr8:132077694
|
C | T | 2 | a0001c0001t0002g0080a0001c0001t0002g0097 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1171+32G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077694 | ||||||
| chr8:132078029
|
A | G | 6 | a0001c0005t0005g0003a0001c0005t0005g0008a0001c0005t0005g0057others(3): Show | 10 | HG00733.hp1 HG01099.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-58T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078029 | ||||||
| chr8:132078083
|
G | A | 1 | a0001c0009t0007g0189 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.926-112C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078083 | ||||||
| chr8:132078105
|
G | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(5): Show | 8 | HG01106.hp2 HG02015.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-134C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078105 | ||||||
| chr8:132078171
|
A | AAC | 25 | a0001c0001t0001g0131a0001c0001t0001g0137a0001c0001t0001g0159others(22): Show | 25 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.926-202_926-201dup others(2): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | ||||||
| chr8:132078171
|
A | AACAC | 10 | a0001c0001t0001g0165a0001c0001t0001g0174a0001c0001t0018g0250others(7): Show | 11 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-204_926-201dup others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | ||||||
| chr8:132078171
|
A | C | 1 | a0006c0015t0001g0275 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.926-200T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | ||||||
| chr8:132078171
|
AAC | A | 34 | a0001c0001t0001g0129a0001c0001t0001g0252a0001c0001t0001g0272others(31): Show | 35 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.926-202_926-201del others(2): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | ||||||
| chr8:132078171
|
AACAC | A | 58 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0017others(55): Show | 60 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.926-204_926-201del others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | ||||||
| chr8:132078171
|
AACACAC | A | 80 | a0001c0001t0002g0215a0001c0001t0002g0216a0001c0001t0002g0217others(77): Show | 93 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.926-206_926-201del others(6): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | ||||||
| chr8:132078171
|
AACACACA others(1): Show |
A | 19 | a0001c0001t0002g0169a0001c0001t0006g0241a0001c0001t0013g0240others(16): Show | 19 | HG00438.hp1 HG01175.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.926-208_926-201del others(8): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | ||||||
| chr8:132078171
|
AACACACA others(3): Show |
A | 14 | a0001c0001t0002g0148a0001c0001t0002g0170a0001c0001t0002g0171others(11): Show | 14 | HG01070.hp1 HG02258.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-210_926-201del others(10): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | ||||||
| chr8:132078171
|
AACACACA others(9): Show |
A | 4 | a0001c0001t0002g0317a0006c0010t0002g0273a0006c0010t0002g0276others(1): Show | 4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-216_926-201del others(16): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | ||||||
| chr8:132078238
|
C | T | 2 | a0002c0003t0023g0030a0003c0002t0001g0194 | 2 | HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.926-267G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078238 | ||||||
| chr8:132078249
|
G | C | 3 | a0002c0013t0001g0111a0002c0013t0001g0112a0004c0006t0001g0109 | 3 | HG01361.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.926-278C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078249 | ||||||
| chr8:132078581
|
A | G | 3 | a0001c0001t0006g0241a0001c0001t0006g0284a0001c0001t0013g0240 | 3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.926-610T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078581 | ||||||
| chr8:132078620
|
G | A | 3 | a0004c0006t0001g0289a0004c0006t0001g0291a0004c0006t0001g0292 | 3 | HG02572.hp2 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.926-649C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078620 | ||||||
| chr8:132078665
|
T | C | 3 | a0004c0006t0001g0289a0004c0006t0001g0291a0004c0006t0001g0292 | 3 | HG02572.hp2 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.926-694A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078665 | ||||||
| chr8:132078800
|
A | C | 1 | a0007c0011t0007g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.926-829T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078800 | ||||||
| chr8:132078837
|
G | T | 3 | a0004c0006t0001g0289a0004c0006t0001g0291a0004c0006t0001g0292 | 3 | HG02572.hp2 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.926-866C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078837 | ||||||
| chr8:132078861
|
A | T | 2 | a0005c0008t0001g0054a0005c0008t0001g0055 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.925+857T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078861 | ||||||
| chr8:132078865
|
G | T | 1 | a0001c0005t0006g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.925+853C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078865 | ||||||
| chr8:132078870
|
A | G | 3 | a0001c0007t0001g0260a0001c0007t0001g0261a0001c0007t0021g0262 | 3 | HG03139.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.925+848T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078870 | ||||||
| chr8:132078904
|
T | TTTTG | 7 | a0002c0013t0001g0111a0002c0013t0001g0112a0006c0010t0001g0277others(4): Show | 7 | HG01516.hp2 HG01517.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+810_925+813dup others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078904 | ||||||
| chr8:132078904
|
TTTTG | T | 4 | a0001c0009t0008g0340a0001c0009t0008g0341a0001c0009t0008g0342others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+810_925+813del others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078904 | ||||||
| chr8:132079119
|
C | A | 1 | a0002c0014t0002g0267 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.925+599G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079119 | ||||||
| chr8:132079127
|
G | T | 2 | a0005c0008t0001g0054a0005c0008t0001g0055 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.925+591C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079127 | ||||||
| chr8:132079212
|
A | G | 1 | a0001c0027t0001g0044 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.925+506T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079212 | ||||||
| chr8:132079327
|
C | T | 4 | a0001c0009t0008g0340a0001c0009t0008g0341a0001c0009t0008g0342others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+391G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079327 | ||||||
| chr8:132079342
|
C | T | 2 | a0002c0013t0001g0111a0002c0013t0001g0112 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.925+376G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079342 | ||||||
| chr8:132079423
|
T | C | 6 | a0001c0009t0007g0189a0001c0009t0008g0340a0001c0009t0008g0341others(3): Show | 6 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+295A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079423 | ||||||
| chr8:132079433
|
C | T | 10 | a0001c0001t0002g0040a0001c0007t0001g0023a0001c0007t0001g0264others(7): Show | 10 | HG01255.hp1 HG01891.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+285G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079433 | ||||||
| chr8:132079460
|
G | A | 10 | a0002c0004t0001g0043a0005c0008t0001g0021a0005c0008t0001g0022others(7): Show | 10 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+258C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079460 | ||||||
| chr8:132079514
|
C | A | 2 | a0001c0001t0009g0354a0007c0011t0007g0041 | 2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.925+204G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079514 | ||||||
| chr8:132079565
|
C | T | 1 | a0001c0005t0006g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.925+153G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079565 | ||||||
| chr8:132079615
|
G | C | 1 | a0011c0026t0001g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.925+103C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079615 | ||||||
| chr8:132079658
|
C | T | 85 | a0001c0001t0005g0331a0003c0002t0001g0010a0003c0002t0001g0029others(82): Show | 87 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.925+60G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079658 | ||||||
| chr8:132079700
|
G | T | 6 | a0001c0009t0007g0189a0001c0009t0008g0340a0001c0009t0008g0341others(3): Show | 6 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+18C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079700 | ||||||
| chr8:132079973
|
G | A | 3 | a0001c0001t0011g0158a0002c0003t0001g0151a0002c0003t0001g0152 | 3 | HG02280.hp1 NA19030.hp1 NA19043.hp1 |
splice_region_variant&intron_variant | LOW | c.677-7C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132079973 | ||||||
| chr8:132080080
|
A | G | 1 | a0001c0001t0001g0018 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.677-114T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080080 | ||||||
| chr8:132080084
|
A | T | 1 | a0001c0001t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.677-118T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080084 | ||||||
| chr8:132080310
|
T | G | 3 | a0001c0001t0001g0186a0001c0001t0001g0253a0001c0001t0014g0254 | 3 | NA19002.hp1 NA19012.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.677-344A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080310 | ||||||
| chr8:132080327
|
C | T | 1 | a0001c0009t0007g0189 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.677-361G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080327 | ||||||
| chr8:132080328
|
G | A | 2 | a0001c0005t0009g0025a0002c0003t0002g0333 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.677-362C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080328 | ||||||
| chr8:132080411
|
G | T | 1 | a0010c0028t0002g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.677-445C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080411 | ||||||
| chr8:132080417
|
T | A | 1 | a0001c0005t0002g0351 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.677-451A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080417 | ||||||
| chr8:132080531
|
A | G | 303 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(300): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.677-565T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080531 | ||||||
| chr8:132080581
|
G | A | 27 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.677-615C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080581 | ||||||
| chr8:132080632
|
G | C | 18 | a0001c0001t0002g0040a0001c0001t0002g0080a0001c0001t0002g0097others(15): Show | 23 | HG00741.hp2 HG01255.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.677-666C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080632 | ||||||
| chr8:132080782
|
C | T | 1 | a0002c0003t0001g0286 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.677-816G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080782 | ||||||
| chr8:132080794
|
G | C | 264 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 275 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.677-828C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080794 | ||||||
| chr8:132080808
|
G | A | 1 | a0001c0007t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.677-842C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080808 | ||||||
| chr8:132080823
|
G | A | 3 | a0001c0001t0006g0241a0001c0001t0006g0284a0001c0001t0013g0240 | 3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.677-857C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080823 | ||||||
| chr8:132080876
|
G | A | 261 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(258): Show | 272 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.677-910C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080876 | ||||||
| chr8:132080878
|
G | A | 261 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(258): Show | 272 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.677-912C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080878 | ||||||
| chr8:132080890
|
A | T | 2 | a0005c0008t0001g0054a0005c0008t0001g0055 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.677-924T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080890 | ||||||
| chr8:132080911
|
G | A | 1 | a0002c0003t0001g0138 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.677-945C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080911 | ||||||
| chr8:132080923
|
A | T | 264 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 275 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.677-957T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080923 | ||||||
| chr8:132080930
|
G | A | 6 | a0001c0009t0007g0189a0001c0009t0008g0340a0001c0009t0008g0341others(3): Show | 6 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.677-964C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080930 | ||||||
| chr8:132080935
|
G | A | 2 | a0002c0013t0001g0111a0002c0013t0001g0112 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.677-969C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080935 | ||||||
| chr8:132080940
|
C | T | 6 | a0001c0009t0007g0189a0001c0009t0008g0340a0001c0009t0008g0341others(3): Show | 6 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.677-974G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080940 | ||||||
| chr8:132080941
|
A | G | 2 | a0002c0013t0001g0111a0002c0013t0001g0112 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.677-975T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080941 | ||||||
| chr8:132081115
|
G | A | 2 | a0006c0010t0002g0273a0006c0010t0002g0276 | 2 | HG02015.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.677-1149C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081115 | ||||||
| chr8:132081151
|
CA | C | 303 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(300): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.677-1186delT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081151 | ||||||
| chr8:132081212
|
C | T | 16 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(13): Show | 21 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.677-1246G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081212 | ||||||
| chr8:132081306
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.677-1340A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081306 | ||||||
| chr8:132081309
|
A | G | 2 | a0002c0003t0001g0028a0007c0011t0007g0271 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.677-1343T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081309 | ||||||
| chr8:132081317
|
G | A | 1 | a0001c0005t0006g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.677-1351C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081317 | ||||||
| chr8:132081415
|
C | T | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-1449G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081415 | ||||||
| chr8:132081684
|
G | A | 267 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(264): Show | 278 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.677-1718C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081684 | ||||||
| chr8:132081762
|
C | T | 85 | a0001c0001t0005g0331a0003c0002t0001g0010a0003c0002t0001g0029others(82): Show | 87 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.677-1796G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081762 | ||||||
| chr8:132081763
|
G | A | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-1797C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081763 | ||||||
| chr8:132081780
|
A | G | 1 | a0003c0002t0002g0031 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.677-1814T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081780 | ||||||
| chr8:132081839
|
G | A | 1 | a0001c0001t0001g0300 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.677-1873C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081839 | ||||||
| chr8:132081869
|
A | G | 1 | a0001c0001t0001g0300 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.677-1903T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081869 | ||||||
| chr8:132081917
|
G | A | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-1951C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081917 | ||||||
| chr8:132081930
|
T | C | 9 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0001g0054others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-1964A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081930 | ||||||
| chr8:132081947
|
G | A | 2 | a0001c0005t0006g0045a0001c0005t0009g0025 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.677-1981C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081947 | ||||||
| chr8:132081975
|
T | C | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.677-2009A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081975 | ||||||
| chr8:132081990
|
A | T | 1 | a0001c0027t0001g0044 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.677-2024T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081990 | ||||||
| chr8:132082071
|
A | C | 3 | a0001c0001t0009g0303a0001c0001t0019g0305a0001c0009t0002g0279 | 3 | HG01106.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.677-2105T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082071 | ||||||
| chr8:132082112
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.677-2146C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082112 | ||||||
| chr8:132082166
|
G | A | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-2200C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082166 | ||||||
| chr8:132082171
|
T | C | 9 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0001g0054others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-2205A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082171 | ||||||
| chr8:132082185
|
A | G | 9 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0001g0054others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-2219T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082185 | ||||||
| chr8:132082247
|
C | A | 1 | a0001c0005t0005g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.677-2281G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082247 | ||||||
| chr8:132082253
|
A | G | 1 | a0001c0005t0005g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.677-2287T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082253 | ||||||
| chr8:132082323
|
G | A | 8 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(5): Show | 13 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-2357C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082323 | ||||||
| chr8:132082382
|
G | C | 84 | a0001c0001t0005g0331a0003c0002t0001g0010a0003c0002t0001g0029others(81): Show | 86 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.677-2416C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082382 | ||||||
| chr8:132082438
|
A | G | 73 | a0003c0002t0001g0010a0003c0002t0001g0029a0003c0002t0001g0032others(70): Show | 75 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.677-2472T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082438 | ||||||
| chr8:132082465
|
T | C | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.677-2499A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082465 | ||||||
| chr8:132082493
|
T | C | 287 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(284): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.677-2527A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082493 | ||||||
| chr8:132082536
|
G | A | 1 | a0003c0002t0001g0037 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.677-2570C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082536 | ||||||
| chr8:132082590
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0318 | 2 | NA19005.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.677-2624C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082590 | ||||||
| chr8:132082619
|
T | A | 129 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(126): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.677-2653A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082619 | ||||||
| chr8:132082639
|
T | C | 2 | a0003c0002t0001g0234a0003c0002t0001g0235 | 2 | HG02040.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.677-2673A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082639 | ||||||
| chr8:132082651
|
T | A | 228 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(225): Show | 237 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.677-2685A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082651 | ||||||
| chr8:132082677
|
C | T | 7 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.677-2711G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082677 | ||||||
| chr8:132082683
|
C | A | 67 | a0001c0001t0001g0006a0001c0001t0001g0108a0001c0001t0001g0212others(64): Show | 69 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.677-2717G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082683 | ||||||
| chr8:132082683
|
C | G | 74 | a0003c0002t0001g0010a0003c0002t0001g0029a0003c0002t0001g0032others(71): Show | 76 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.677-2717G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082683 | ||||||
| chr8:132082776
|
C | T | 3 | a0001c0001t0006g0241a0001c0001t0006g0284a0001c0001t0013g0240 | 3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.677-2810G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082776 | ||||||
| chr8:132082879
|
A | G | 303 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(300): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.677-2913T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082879 | ||||||
| chr8:132082886
|
T | G | 9 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0001g0054others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-2920A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082886 | ||||||
| chr8:132082931
|
G | A | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.677-2965C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082931 | ||||||
| chr8:132082968
|
T | C | 286 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(283): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.677-3002A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082968 | ||||||
| chr8:132082969
|
G | A | 278 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(275): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.677-3003C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082969 | ||||||
| chr8:132082985
|
A | G | 10 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(7): Show | 15 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.677-3019T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082985 | ||||||
| chr8:132083018
|
A | G | 1 | a0001c0001t0009g0306 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.677-3052T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083018 | ||||||
| chr8:132083028
|
GGGTGCAT others(4): Show |
G | 8 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(5): Show | 13 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-3073_677-3063d others(13): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083028 | ||||||
| chr8:132083039
|
T | C | 3 | a0001c0007t0001g0268a0006c0015t0001g0275a0006c0015t0002g0274 | 3 | NA18959.hp1 NA18994.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.677-3073A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083039 | ||||||
| chr8:132083044
|
G | A | 8 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(5): Show | 13 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-3078C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083044 | ||||||
| chr8:132083048
|
A | T | 1 | a0001c0012t0001g0350 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.677-3082T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083048 | ||||||
| chr8:132083056
|
G | A | 3 | a0001c0001t0006g0241a0001c0001t0006g0284a0001c0001t0013g0240 | 3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.677-3090C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083056 | ||||||
| chr8:132083142
|
CA | C | 27 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.677-3177delT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083142 | ||||||
| chr8:132083146
|
G | C | 27 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.677-3180C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083146 | ||||||
| chr8:132083200
|
A | G | 259 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(256): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.677-3234T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083200 | ||||||
| chr8:132083315
|
C | A | 2 | a0001c0001t0009g0354a0007c0011t0007g0041 | 2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.677-3349G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083315 | ||||||
| chr8:132083370
|
G | T | 205 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(202): Show | 209 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.677-3404C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083370 | ||||||
| chr8:132083388
|
C | T | 18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 20 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.677-3422G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083388 | ||||||
| chr8:132083393
|
G | A | 102 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(99): Show | 104 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.677-3427C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083393 | ||||||
| chr8:132083452
|
G | A | 27 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.677-3486C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083452 | ||||||
| chr8:132083507
|
G | A | 1 | a0008c0022t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.677-3541C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083507 | ||||||
| chr8:132083525
|
G | A | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.677-3559C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083525 | ||||||
| chr8:132083557
|
C | T | 1 | a0003c0002t0002g0219 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.677-3591G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083557 | ||||||
| chr8:132083570
|
C | G | 1 | a0004c0006t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.677-3604G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083570 | ||||||
| chr8:132083593
|
T | A | 11 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216others(8): Show | 11 | HG00609.hp2 NA18951.hp2 NA18972.hp1 others(8): Show |
intron_variant | MODIFIER | c.677-3627A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083593 | ||||||
| chr8:132083633
|
C | T | 44 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(41): Show | 44 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.677-3667G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083633 | ||||||
| chr8:132083634
|
G | A | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-3668C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083634 | ||||||
| chr8:132083635
|
C | T | 248 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(245): Show | 257 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.677-3669G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083635 | ||||||
| chr8:132083691
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0002g0148 | 2 | HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.677-3725T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083691 | ||||||
| chr8:132083778
|
G | C | 3 | a0001c0007t0001g0260a0001c0007t0001g0261a0001c0007t0021g0262 | 3 | HG03139.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.677-3812C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083778 | ||||||
| chr8:132083931
|
T | C | 7 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185others(4): Show | 7 | HG02280.hp1 HG02683.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+3722A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083931 | ||||||
| chr8:132083942
|
A | T | 243 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(240): Show | 249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.676+3711T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083942 | ||||||
| chr8:132083944
|
T | A | 243 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(240): Show | 249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.676+3709A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083944 | ||||||
| chr8:132083946
|
T | C | 243 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(240): Show | 249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.676+3707A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083946 | ||||||
| chr8:132083948
|
T | A | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+3705A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083948 | ||||||
| chr8:132083948
|
T | G | 243 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(240): Show | 249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.676+3705A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083948 | ||||||
| chr8:132083949
|
T | A | 243 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(240): Show | 249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.676+3704A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083949 | ||||||
| chr8:132083992
|
A | G | 260 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(257): Show | 271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.676+3661T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083992 | ||||||
| chr8:132083998
|
T | C | 287 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(284): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.676+3655A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083998 | ||||||
| chr8:132084019
|
C | G | 4 | a0001c0001t0006g0241a0001c0001t0006g0284a0001c0001t0013g0240others(1): Show | 4 | HG02886.hp2 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+3634G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084019 | ||||||
| chr8:132084058
|
A | G | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185 | 3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.676+3595T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084058 | ||||||
| chr8:132084162
|
G | C | 1 | a0001c0001t0001g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.676+3491C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084162 | ||||||
| chr8:132084196
|
C | T | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+3457G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084196 | ||||||
| chr8:132084197
|
G | A | 15 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0164others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.676+3456C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084197 | ||||||
| chr8:132084248
|
G | A | 270 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(267): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.676+3405C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084248 | ||||||
| chr8:132084259
|
G | A | 1 | a0007c0011t0007g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.676+3394C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084259 | ||||||
| chr8:132084311
|
G | A | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+3342C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084311 | ||||||
| chr8:132084422
|
C | T | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+3231G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084422 | ||||||
| chr8:132084441
|
A | AG | 302 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(299): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.676+3211dupC | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084441 | ||||||
| chr8:132084483
|
A | G | 1 | a0001c0027t0001g0044 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.676+3170T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084483 | ||||||
| chr8:132084508
|
G | A | 2 | a0001c0005t0006g0045a0001c0005t0009g0025 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.676+3145C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084508 | ||||||
| chr8:132084632
|
G | T | 1 | a0002c0003t0001g0337 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.676+3021C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084632 | ||||||
| chr8:132084664
|
T | C | 1 | a0005c0008t0002g0347 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.676+2989A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084664 | ||||||
| chr8:132084748
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.676+2905G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084748 | ||||||
| chr8:132084771
|
G | A | 4 | a0001c0001t0006g0241a0001c0001t0006g0284a0001c0001t0013g0240others(1): Show | 4 | HG02886.hp2 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+2882C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084771 | ||||||
| chr8:132084870
|
C | T | 2 | a0001c0005t0006g0045a0001c0005t0009g0025 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.676+2783G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084870 | ||||||
| chr8:132084888
|
C | T | 94 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(91): Show | 98 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.676+2765G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084888 | ||||||
| chr8:132084930
|
G | A | 1 | a0002c0003t0001g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.676+2723C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084930 | ||||||
| chr8:132084960
|
A | C | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+2693T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084960 | ||||||
| chr8:132084969
|
T | C | 299 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(296): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.676+2684A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084969 | ||||||
| chr8:132085094
|
C | G | 1 | a0001c0005t0009g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.676+2559G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085094 | ||||||
| chr8:132085133
|
C | T | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+2520G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085133 | ||||||
| chr8:132085134
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.676+2519C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085134 | ||||||
| chr8:132085159
|
G | T | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+2494C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085159 | ||||||
| chr8:132085232
|
G | A | 2 | a0001c0016t0006g0150a0004c0006t0001g0335 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.676+2421C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085232 | ||||||
| chr8:132085295
|
T | C | 1 | a0001c0007t0002g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.676+2358A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085295 | ||||||
| chr8:132085313
|
A | G | 297 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(294): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.676+2340T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085313 | ||||||
| chr8:132085461
|
G | A | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+2192C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085461 | ||||||
| chr8:132085534
|
G | A | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+2119C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085534 | ||||||
| chr8:132085560
|
G | A | 9 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0001g0054others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.676+2093C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085560 | ||||||
| chr8:132085601
|
T | C | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+2052A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085601 | ||||||
| chr8:132085603
|
A | T | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+2050T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085603 | ||||||
| chr8:132085604
|
A | G | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+2049T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085604 | ||||||
| chr8:132085630
|
C | T | 12 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(9): Show | 12 | HG01109.hp1 HG02015.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.676+2023G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085630 | ||||||
| chr8:132085642
|
G | A | 2 | a0001c0005t0006g0045a0001c0005t0009g0025 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.676+2011C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085642 | ||||||
| chr8:132085679
|
G | A | 4 | a0003c0002t0010g0155a0003c0002t0010g0157a0003c0002t0010g0353others(1): Show | 4 | HG02559.hp2 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.676+1974C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085679 | ||||||
| chr8:132085756
|
T | A | 296 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0016others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.676+1897A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085756 | ||||||
| chr8:132085790
|
G | C | 2 | a0001c0001t0009g0354a0007c0011t0007g0041 | 2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.676+1863C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085790 | ||||||
| chr8:132085791
|
A | G | 298 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(295): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.676+1862T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085791 | ||||||
| chr8:132085803
|
G | A | 298 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(295): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.676+1850C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085803 | ||||||
| chr8:132085830
|
G | C | 201 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(198): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.676+1823C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085830 | ||||||
| chr8:132085844
|
C | T | 298 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(295): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.676+1809G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085844 | ||||||
| chr8:132085845
|
G | A | 3 | a0001c0005t0001g0050a0001c0005t0001g0071a0002c0004t0002g0005 | 5 | HG01175.hp2 HG01192.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+1808C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085845 | ||||||
| chr8:132085951
|
G | C | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+1702C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085951 | ||||||
| chr8:132085989
|
T | C | 1 | a0001c0005t0002g0085 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.676+1664A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085989 | ||||||
| chr8:132086135
|
T | C | 281 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(278): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.676+1518A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086135 | ||||||
| chr8:132086202
|
A | T | 298 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(295): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.676+1451T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086202 | ||||||
| chr8:132086283
|
T | C | 66 | a0001c0001t0001g0006a0001c0001t0001g0108a0001c0001t0001g0212others(63): Show | 68 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.676+1370A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086283 | ||||||
| chr8:132086421
|
G | A | 1 | a0002c0003t0001g0337 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.676+1232C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086421 | ||||||
| chr8:132086498
|
C | A | 1 | a0003c0002t0002g0024 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.676+1155G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086498 | ||||||
| chr8:132086518
|
A | T | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+1135T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086518 | ||||||
| chr8:132086575
|
G | C | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+1078C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086575 | ||||||
| chr8:132086662
|
C | A | 1 | a0003c0002t0001g0209 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.676+991G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086662 | ||||||
| chr8:132086664
|
C | A | 1 | a0003c0002t0001g0209 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.676+989G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086664 | ||||||
| chr8:132086667
|
A | T | 1 | a0003c0002t0001g0209 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.676+986T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086667 | ||||||
| chr8:132086670
|
A | T | 1 | a0003c0002t0001g0209 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.676+983T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086670 | ||||||
| chr8:132086851
|
G | GT | 29 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0117others(26): Show | 29 | HG00323.hp1 HG00544.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.676+801dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086851 | ||||||
| chr8:132086918
|
G | C | 1 | a0003c0002t0001g0238 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.676+735C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086918 | ||||||
| chr8:132086942
|
A | G | 4 | a0001c0001t0011g0158a0001c0027t0001g0044a0002c0003t0001g0151others(1): Show | 4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+711T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086942 | ||||||
| chr8:132087032
|
C | T | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+621G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087032 | ||||||
| chr8:132087052
|
C | A | 1 | a0001c0001t0002g0181 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.676+601G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087052 | ||||||
| chr8:132087072
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.676+581G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087072 | ||||||
| chr8:132087073
|
G | A | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+580C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087073 | ||||||
| chr8:132087229
|
G | A | 4 | a0001c0001t0011g0158a0001c0027t0001g0044a0002c0003t0001g0151others(1): Show | 4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+424C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087229 | ||||||
| chr8:132087240
|
G | T | 11 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(8): Show | 16 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.676+413C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087240 | ||||||
| chr8:132087274
|
T | C | 4 | a0001c0001t0011g0158a0001c0027t0001g0044a0002c0003t0001g0151others(1): Show | 4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+379A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087274 | ||||||
| chr8:132087395
|
C | G | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185 | 3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.676+258G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087395 | ||||||
| chr8:132087427
|
A | C | 288 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(285): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.676+226T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087427 | ||||||
| chr8:132087607
|
C | T | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+46G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087607 | ||||||
| chr8:132087816
|
A | T | 7 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.589+29T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 9/16 | chr8 | 132087816 | ||||||
| chr8:132088135
|
C | T | 7 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(4): Show | 12 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.533-234G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088135 | ||||||
| chr8:132088176
|
T | C | 298 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(295): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.533-275A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088176 | ||||||
| chr8:132088203
|
G | T | 6 | a0001c0012t0001g0153a0001c0012t0001g0154a0001c0012t0001g0350others(3): Show | 6 | HG01123.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.533-302C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088203 | ||||||
| chr8:132088287
|
G | A | 3 | a0001c0007t0001g0260a0001c0007t0001g0261a0001c0007t0021g0262 | 3 | HG03139.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.533-386C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088287 | ||||||
| chr8:132088296
|
G | A | 4 | a0001c0001t0011g0158a0001c0027t0001g0044a0002c0003t0001g0151others(1): Show | 4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.533-395C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088296 | ||||||
| chr8:132088377
|
A | G | 302 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(299): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.533-476T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088377 | ||||||
| chr8:132088457
|
C | T | 6 | a0001c0012t0001g0153a0001c0012t0001g0154a0001c0012t0001g0350others(3): Show | 6 | HG01123.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.533-556G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088457 | ||||||
| chr8:132088539
|
G | A | 241 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(238): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.533-638C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088539 | ||||||
| chr8:132088581
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.533-680T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088581 | ||||||
| chr8:132088679
|
T | A | 3 | a0001c0001t0006g0241a0001c0001t0006g0284a0001c0001t0013g0240 | 3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.533-778A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088679 | ||||||
| chr8:132088744
|
T | C | 1 | a0003c0002t0001g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.532+772A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088744 | ||||||
| chr8:132088917
|
A | G | 1 | a0002c0004t0001g0101 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.532+599T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088917 | ||||||
| chr8:132088981
|
G | T | 4 | a0001c0001t0011g0158a0001c0027t0001g0044a0002c0003t0001g0151others(1): Show | 4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+535C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088981 | ||||||
| chr8:132089067
|
G | A | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.532+449C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089067 | ||||||
| chr8:132089097
|
G | C | 1 | a0001c0005t0002g0351 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.532+419C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089097 | ||||||
| chr8:132089187
|
A | G | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.532+329T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089187 | ||||||
| chr8:132089253
|
G | C | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+263C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089253 | ||||||
| chr8:132089329
|
T | G | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185 | 3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.532+187A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089329 | ||||||
| chr8:132089359
|
A | G | 7 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(4): Show | 12 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.532+157T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089359 | ||||||
| chr8:132089389
|
T | C | 4 | a0001c0001t0011g0158a0001c0027t0001g0044a0002c0003t0001g0151others(1): Show | 4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+127A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089389 | ||||||
| chr8:132089486
|
G | A | 1 | a0003c0002t0001g0188 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.532+30C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089486 | ||||||
| chr8:132089515
|
C | A | 1 | a0001c0001t0002g0014 | 1 | NA18960.hp1 | splice_donor_variant&intron_variant | HIGH | c.532+1G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089515 | ||||||
| chr8:132089741
|
A | T | 3 | a0001c0001t0006g0241a0001c0001t0006g0284a0001c0001t0013g0240 | 3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.449-142T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132089741 | ||||||
| chr8:132089762
|
T | C | 301 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(298): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.449-163A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132089762 | ||||||
| chr8:132089929
|
G | A | 1 | a0002c0003t0023g0030 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.449-330C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132089929 | ||||||
| chr8:132089929
|
G | C | 5 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0002g0346others(2): Show | 5 | HG02451.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.449-330C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132089929 | ||||||
| chr8:132089931
|
C | A | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.449-332G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132089931 | ||||||
| chr8:132090059
|
T | G | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.449-460A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090059 | ||||||
| chr8:132090107
|
C | G | 5 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(2): Show | 5 | HG01074.hp1 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-508G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090107 | ||||||
| chr8:132090122
|
C | T | 1 | a0001c0005t0002g0351 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.449-523G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090122 | ||||||
| chr8:132090328
|
A | G | 4 | a0001c0012t0001g0153a0001c0012t0001g0154a0001c0012t0001g0350others(1): Show | 4 | HG01123.hp1 HG01934.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-729T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090328 | ||||||
| chr8:132090389
|
C | T | 1 | a0001c0005t0006g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449-790G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090389 | ||||||
| chr8:132090404
|
A | G | 298 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(295): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.449-805T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090404 | ||||||
| chr8:132090527
|
G | A | 1 | a0003c0002t0002g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.449-928C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090527 | ||||||
| chr8:132090684
|
A | G | 1 | a0002c0003t0002g0333 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.449-1085T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090684 | ||||||
| chr8:132090755
|
CT | C | 256 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(253): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.449-1157delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090755 | ||||||
| chr8:132090755
|
CTT | C | 15 | a0001c0001t0001g0131a0001c0001t0002g0014a0001c0001t0002g0218others(12): Show | 15 | HG01069.hp2 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.449-1158_449-1157d others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090755 | ||||||
| chr8:132090755
|
CTTTT | C | 11 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(8): Show | 16 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.449-1160_449-1157d others(6): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090755 | ||||||
| chr8:132090756
|
T | TC | 5 | a0001c0007t0001g0260a0001c0007t0001g0261a0001c0007t0021g0262others(2): Show | 5 | HG02257.hp1 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.449-1158_449-1157i others(3): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090756 | ||||||
| chr8:132090757
|
T | C | 14 | a0001c0001t0001g0133a0001c0001t0001g0304a0001c0001t0002g0040others(11): Show | 14 | HG01255.hp1 HG01891.hp1 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.449-1158A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090757 | ||||||
| chr8:132090758
|
T | C | 254 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.449-1159A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090758 | ||||||
| chr8:132090759
|
T | C | 9 | a0001c0001t0001g0131a0001c0001t0002g0014a0001c0001t0002g0218others(6): Show | 9 | HG01069.hp2 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.449-1160A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090759 | ||||||
| chr8:132090760
|
T | C | 1 | a0005c0008t0001g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-1161A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090760 | ||||||
| chr8:132090776
|
T | G | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1177A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090776 | ||||||
| chr8:132090820
|
G | A | 7 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-1221C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090820 | ||||||
| chr8:132090907
|
C | T | 1 | a0001c0001t0011g0158 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.449-1308G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090907 | ||||||
| chr8:132090917
|
C | T | 1 | a0001c0005t0005g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.449-1318G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090917 | ||||||
| chr8:132090952
|
G | A | 2 | a0001c0005t0006g0045a0001c0005t0009g0025 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.449-1353C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090952 | ||||||
| chr8:132090980
|
C | G | 2 | a0001c0001t0009g0354a0007c0011t0007g0041 | 2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.449-1381G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090980 | ||||||
| chr8:132091011
|
G | A | 2 | a0002c0003t0001g0322a0012c0025t0007g0283 | 2 | HG01167.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.449-1412C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091011 | ||||||
| chr8:132091020
|
C | A | 2 | a0002c0003t0001g0151a0002c0003t0001g0152 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.449-1421G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091020 | ||||||
| chr8:132091043
|
T | C | 68 | a0001c0001t0001g0006a0001c0001t0001g0108a0001c0001t0001g0212others(65): Show | 70 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.449-1444A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091043 | ||||||
| chr8:132091082
|
CTTAG | C | 7 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(4): Show | 12 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.449-1487_449-1484d others(6): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091082 | ||||||
| chr8:132091534
|
C | T | 2 | a0001c0016t0002g0149a0001c0016t0006g0150 | 2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.449-1935G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091534 | ||||||
| chr8:132091574
|
T | C | 1 | a0002c0003t0001g0132 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.449-1975A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091574 | ||||||
| chr8:132091651
|
A | G | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185 | 3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.449-2052T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091651 | ||||||
| chr8:132092051
|
G | T | 4 | a0001c0009t0008g0340a0001c0009t0008g0341a0001c0009t0008g0342others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-2452C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092051 | ||||||
| chr8:132092068
|
G | A | 297 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(294): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.449-2469C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092068 | ||||||
| chr8:132092186
|
G | A | 86 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(83): Show | 90 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.449-2587C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092186 | ||||||
| chr8:132092359
|
T | A | 1 | a0001c0001t0002g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.449-2760A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092359 | ||||||
| chr8:132092360
|
C | A | 6 | a0001c0012t0001g0153a0001c0012t0001g0154a0001c0012t0001g0350others(3): Show | 6 | HG01123.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-2761G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092360 | ||||||
| chr8:132092361
|
A | G | 7 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-2762T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092361 | ||||||
| chr8:132092447
|
G | T | 286 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(283): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.449-2848C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092447 | ||||||
| chr8:132092539
|
G | A | 1 | a0002c0004t0001g0090 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.449-2940C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092539 | ||||||
| chr8:132092811
|
C | T | 2 | a0001c0001t0003g0027a0001c0001t0020g0026 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.448+2708G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092811 | ||||||
| chr8:132092830
|
G | A | 4 | a0001c0001t0006g0241a0001c0001t0006g0284a0001c0001t0013g0240others(1): Show | 4 | HG02886.hp2 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+2689C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092830 | ||||||
| chr8:132092851
|
C | T | 7 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.448+2668G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092851 | ||||||
| chr8:132092872
|
A | G | 281 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(278): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.448+2647T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092872 | ||||||
| chr8:132092900
|
A | G | 1 | a0001c0001t0009g0303 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.448+2619T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092900 | ||||||
| chr8:132092922
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.448+2597G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092922 | ||||||
| chr8:132093000
|
T | C | 10 | a0001c0001t0002g0040a0001c0007t0001g0023a0001c0007t0001g0264others(7): Show | 10 | HG01255.hp1 HG01891.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.448+2519A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093000 | ||||||
| chr8:132093137
|
G | C | 2 | a0001c0005t0006g0045a0001c0005t0009g0025 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448+2382C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093137 | ||||||
| chr8:132093145
|
G | A | 11 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(8): Show | 16 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.448+2374C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093145 | ||||||
| chr8:132093207
|
T | C | 1 | a0001c0001t0011g0158 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.448+2312A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093207 | ||||||
| chr8:132093256
|
G | A | 1 | a0001c0001t0011g0158 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.448+2263C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093256 | ||||||
| chr8:132093386
|
G | A | 287 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(284): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.448+2133C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093386 | ||||||
| chr8:132093493
|
G | A | 1 | a0001c0007t0021g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.448+2026C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093493 | ||||||
| chr8:132093527
|
G | A | 9 | a0003c0002t0001g0290a0003c0002t0010g0155a0003c0002t0010g0157others(6): Show | 9 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.448+1992C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093527 | ||||||
| chr8:132093543
|
G | T | 2 | a0001c0005t0006g0045a0001c0005t0009g0025 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448+1976C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093543 | ||||||
| chr8:132093551
|
T | A | 2 | a0001c0005t0006g0045a0001c0005t0009g0025 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448+1968A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093551 | ||||||
| chr8:132093586
|
G | T | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.448+1933C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093586 | ||||||
| chr8:132093688
|
A | C | 96 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(93): Show | 100 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.448+1831T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093688 | ||||||
| chr8:132093713
|
C | T | 1 | a0001c0005t0002g0351 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.448+1806G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093713 | ||||||
| chr8:132093720
|
A | G | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185 | 3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.448+1799T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093720 | ||||||
| chr8:132093818
|
A | T | 68 | a0001c0001t0001g0006a0001c0001t0001g0108a0001c0001t0001g0212others(65): Show | 70 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.448+1701T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093818 | ||||||
| chr8:132093868
|
A | T | 287 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(284): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.448+1651T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093868 | ||||||
| chr8:132094034
|
T | A | 2 | a0001c0001t0001g0133a0002c0003t0002g0134 | 2 | HG00673.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.448+1485A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094034 | ||||||
| chr8:132094039
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.448+1480C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094039 | ||||||
| chr8:132094093
|
C | G | 9 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0001g0054others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.448+1426G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094093 | ||||||
| chr8:132094151
|
T | C | 287 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(284): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.448+1368A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094151 | ||||||
| chr8:132094153
|
A | G | 1 | a0001c0005t0002g0085 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.448+1366T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094153 | ||||||
| chr8:132094192
|
G | GT | 287 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(284): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.448+1326_448+1327i others(3): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094192 | ||||||
| chr8:132094236
|
T | C | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.448+1283A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094236 | ||||||
| chr8:132094292
|
T | C | 302 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(299): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.448+1227A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094292 | ||||||
| chr8:132094320
|
C | T | 2 | a0001c0005t0006g0045a0001c0005t0009g0025 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448+1199G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094320 | ||||||
| chr8:132094357
|
C | T | 1 | a0003c0002t0002g0020 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.448+1162G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094357 | ||||||
| chr8:132094377
|
C | A | 1 | a0001c0007t0002g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.448+1142G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094377 | ||||||
| chr8:132094378
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.448+1141C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094378 | ||||||
| chr8:132094490
|
G | A | 68 | a0001c0001t0001g0006a0001c0001t0001g0108a0001c0001t0001g0212others(65): Show | 70 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.448+1029C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094490 | ||||||
| chr8:132094520
|
C | A | 1 | a0001c0009t0008g0343 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.448+999G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094520 | ||||||
| chr8:132094545
|
G | A | 2 | a0001c0001t0001g0323a0001c0001t0002g0324 | 2 | NA18966.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.448+974C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094545 | ||||||
| chr8:132094569
|
A | G | 5 | a0001c0001t0020g0026a0002c0003t0001g0113a0002c0003t0001g0114others(2): Show | 5 | HG02280.hp2 NA18968.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.448+950T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094569 | ||||||
| chr8:132094651
|
T | C | 302 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(299): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.448+868A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094651 | ||||||
| chr8:132094665
|
C | T | 281 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(278): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.448+854G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094665 | ||||||
| chr8:132094732
|
C | T | 1 | a0002c0003t0002g0333 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.448+787G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094732 | ||||||
| chr8:132094745
|
C | T | 287 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(284): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.448+774G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094745 | ||||||
| chr8:132094758
|
A | G | 104 | a0001c0001t0001g0006a0001c0001t0001g0108a0001c0001t0001g0147others(101): Show | 106 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.448+761T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094758 | ||||||
| chr8:132094777
|
G | T | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.448+742C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094777 | ||||||
| chr8:132094799
|
G | T | 3 | a0002c0003t0001g0325a0002c0003t0001g0336a0002c0003t0001g0337 | 3 | HG02622.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.448+720C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094799 | ||||||
| chr8:132094881
|
C | T | 2 | a0001c0001t0024g0356a0001c0005t0001g0100 | 2 | HG01975.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.448+638G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094881 | ||||||
| chr8:132094898
|
C | T | 1 | a0003c0002t0001g0188 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.448+621G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094898 | ||||||
| chr8:132095122
|
T | C | 2 | a0001c0005t0006g0045a0001c0005t0009g0025 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448+397A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132095122 | ||||||
| chr8:132095265
|
T | C | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.448+254A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132095265 | ||||||
| chr8:132095277
|
C | T | 1 | a0002c0004t0002g0084 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.448+242G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132095277 | ||||||
| chr8:132095410
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.448+109A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132095410 | ||||||
| chr8:132095421
|
A | C | 2 | a0002c0014t0001g0258a0002c0014t0002g0269 | 2 | NA19000.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.448+98T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132095421 | ||||||
| chr8:132095610
|
G | A | 11 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(8): Show | 16 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.365-8C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 6/16 | chr8 | 132095610 | ||||||
| chr8:132095646
|
A | G | 299 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(296): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.365-44T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 6/16 | chr8 | 132095646 | ||||||
| chr8:132095660
|
T | A | 7 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.364+43A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 6/16 | chr8 | 132095660 | ||||||
| chr8:132095860
|
C | T | 9 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0001g0054others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-74G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132095860 | ||||||
| chr8:132095863
|
T | C | 37 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.281-77A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132095863 | ||||||
| chr8:132095982
|
A | G | 2 | a0001c0005t0006g0045a0001c0005t0009g0025 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.281-196T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132095982 | ||||||
| chr8:132096021
|
G | A | 9 | a0003c0002t0001g0290a0003c0002t0010g0155a0003c0002t0010g0157others(6): Show | 9 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-235C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096021 | ||||||
| chr8:132096212
|
T | G | 166 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(163): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.281-426A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096212 | ||||||
| chr8:132096217
|
C | T | 1 | a0001c0001t0003g0142 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.281-431G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096217 | ||||||
| chr8:132096304
|
T | C | 7 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(4): Show | 12 | HG00741.hp2 HG02145.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.281-518A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096304 | ||||||
| chr8:132096335
|
C | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185 | 3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.281-549G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096335 | ||||||
| chr8:132096404
|
C | T | 124 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(121): Show | 131 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.281-618G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096404 | ||||||
| chr8:132096512
|
A | AT | 9 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(6): Show | 14 | HG00741.hp2 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.281-727dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096512 | ||||||
| chr8:132096696
|
G | T | 1 | a0001c0001t0004g0163 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.281-910C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096696 | ||||||
| chr8:132096700
|
C | A | 7 | a0003c0002t0001g0290a0003c0002t0010g0155a0003c0002t0010g0157others(4): Show | 7 | HG02572.hp2 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-914G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096700 | ||||||
| chr8:132096835
|
G | C | 7 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.281-1049C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096835 | ||||||
| chr8:132096842
|
C | T | 1 | a0001c0001t0009g0303 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.281-1056G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096842 | ||||||
| chr8:132096868
|
C | T | 37 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.281-1082G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096868 | ||||||
| chr8:132096881
|
C | G | 1 | a0001c0001t0001g0256 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.281-1095G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096881 | ||||||
| chr8:132096895
|
C | A | 5 | a0006c0010t0001g0277a0006c0010t0002g0273a0006c0010t0002g0276others(2): Show | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-1109G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096895 | ||||||
| chr8:132096895
|
C | G | 294 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(291): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.281-1109G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096895 | ||||||
| chr8:132096939
|
C | T | 264 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.281-1153G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096939 | ||||||
| chr8:132096960
|
C | G | 1 | a0001c0001t0001g0011 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.281-1174G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096960 | ||||||
| chr8:132096965
|
G | A | 2 | a0001c0001t0009g0354a0007c0011t0007g0041 | 2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.281-1179C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096965 | ||||||
| chr8:132097000
|
T | G | 3 | a0003c0002t0010g0155a0003c0002t0010g0157a0004c0006t0001g0156 | 3 | HG02896.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.281-1214A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097000 | ||||||
| chr8:132097029
|
G | A | 2 | a0001c0016t0002g0149a0001c0016t0006g0150 | 2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.281-1243C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097029 | ||||||
| chr8:132097123
|
T | C | 294 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(291): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.281-1337A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097123 | ||||||
| chr8:132097132
|
C | T | 10 | a0001c0001t0001g0281a0001c0001t0001g0295a0001c0001t0001g0296others(7): Show | 10 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-1346G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097132 | ||||||
| chr8:132097133
|
G | A | 1 | a0001c0001t0009g0354 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.281-1347C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097133 | ||||||
| chr8:132097234
|
A | G | 1 | a0002c0003t0002g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.281-1448T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097234 | ||||||
| chr8:132097394
|
T | C | 2 | a0001c0001t0024g0356a0001c0005t0001g0355 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.280+1488A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097394 | ||||||
| chr8:132097400
|
A | T | 7 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0002g0346others(4): Show | 7 | HG02451.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+1482T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097400 | ||||||
| chr8:132097554
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.280+1328A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097554 | ||||||
| chr8:132097682
|
C | T | 3 | a0001c0005t0006g0045a0001c0005t0009g0025a0003c0002t0010g0353 | 3 | HG01884.hp2 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.280+1200G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097682 | ||||||
| chr8:132097943
|
A | T | 27 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.280+939T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097943 | ||||||
| chr8:132098042
|
C | A | 2 | a0002c0003t0001g0325a0002c0003t0002g0326 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.280+840G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098042 | ||||||
| chr8:132098173
|
G | A | 1 | a0001c0020t0001g0135 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.280+709C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098173 | ||||||
| chr8:132098244
|
T | C | 1 | a0002c0004t0002g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.280+638A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098244 | ||||||
| chr8:132098327
|
A | G | 5 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0003g0002others(2): Show | 10 | HG00741.hp2 HG02145.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.280+555T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098327 | ||||||
| chr8:132098394
|
G | A | 1 | a0002c0004t0002g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.280+488C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098394 | ||||||
| chr8:132098425
|
A | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0002c0003t0001g0161others(1): Show | 4 | HG00280.hp1 HG01081.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+457T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098425 | ||||||
| chr8:132098623
|
A | C | 5 | a0001c0005t0001g0100a0002c0004t0001g0009a0002c0004t0001g0053others(2): Show | 6 | HG01099.hp1 HG01257.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+259T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098623 | ||||||
| chr8:132098813
|
A | G | 1 | a0001c0001t0002g0095 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.280+69T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098813 | ||||||
| chr8:132098816
|
G | T | 1 | a0003c0002t0001g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.280+66C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098816 | ||||||
| chr8:132098839
|
GA | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0281a0001c0001t0001g0287others(10): Show | 15 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.280+42delT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098839 | ||||||
| chr8:132098990
|
T | C | 1 | a0001c0005t0002g0351 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.200-28A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132098990 | ||||||
| chr8:132099005
|
G | A | 5 | a0001c0005t0006g0073a0003c0002t0001g0242a0003c0002t0001g0243others(2): Show | 5 | HG00639.hp1 HG01934.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.200-43C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099005 | ||||||
| chr8:132099060
|
C | G | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(194): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.200-98G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099060 | ||||||
| chr8:132099093
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.200-131G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099093 | ||||||
| chr8:132099116
|
G | A | 3 | a0003c0002t0010g0155a0003c0002t0010g0157a0004c0006t0001g0156 | 3 | HG02896.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.200-154C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099116 | ||||||
| chr8:132099122
|
G | A | 3 | a0001c0005t0006g0045a0001c0005t0009g0025a0003c0002t0010g0353 | 3 | HG01884.hp2 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.200-160C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099122 | ||||||
| chr8:132099167
|
A | T | 1 | a0001c0001t0001g0293 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.200-205T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099167 | ||||||
| chr8:132099182
|
A | G | 2 | a0005c0008t0001g0021a0005c0008t0001g0022 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.200-220T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099182 | ||||||
| chr8:132099273
|
T | C | 1 | a0001c0001t0003g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.200-311A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099273 | ||||||
| chr8:132099391
|
A | C | 7 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-429T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099391 | ||||||
| chr8:132099422
|
C | T | 15 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(12): Show | 15 | HG01109.hp1 HG01123.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.200-460G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099422 | ||||||
| chr8:132099459
|
A | G | 2 | a0001c0001t0024g0356a0001c0005t0001g0355 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.200-497T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099459 | ||||||
| chr8:132099470
|
A | C | 7 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-508T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099470 | ||||||
| chr8:132099472
|
TGGAG | T | 7 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0002g0346others(4): Show | 7 | HG02451.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.200-514_200-511del others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099472 | ||||||
| chr8:132099480
|
G | T | 4 | a0001c0001t0003g0027a0001c0001t0020g0026a0002c0003t0001g0028others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-518C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099480 | ||||||
| chr8:132099600
|
T | A | 7 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0002g0346others(4): Show | 7 | HG02451.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+475A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099600 | ||||||
| chr8:132099656
|
C | G | 1 | a0002c0017t0002g0352 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.199+419G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099656 | ||||||
| chr8:132099683
|
A | G | 180 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(177): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.199+392T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099683 | ||||||
| chr8:132099686
|
G | T | 180 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(177): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.199+389C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099686 | ||||||
| chr8:132099760
|
A | G | 3 | a0001c0001t0005g0331a0004c0006t0001g0335a0007c0011t0007g0187 | 3 | HG02258.hp2 HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.199+315T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099760 | ||||||
| chr8:132099768
|
C | T | 2 | a0003c0002t0002g0140a0003c0002t0002g0141 | 2 | HG02257.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.199+307G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099768 | ||||||
| chr8:132099846
|
C | T | 1 | a0003c0002t0002g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.199+229G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099846 | ||||||
| chr8:132100145
|
G | A | 225 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(222): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.140-11C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100145 | ||||||
| chr8:132100234
|
G | A | 15 | a0001c0007t0001g0023a0001c0007t0001g0260a0001c0007t0001g0261others(12): Show | 15 | HG01255.hp1 HG02004.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.140-100C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100234 | ||||||
| chr8:132100362
|
C | T | 3 | a0003c0002t0001g0209a0003c0002t0001g0210a0003c0002t0001g0211 | 3 | NA18940.hp1 NA18945.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.140-228G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100362 | ||||||
| chr8:132100376
|
G | A | 2 | a0001c0001t0001g0327a0001c0001t0022g0328 | 2 | HG00323.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.140-242C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100376 | ||||||
| chr8:132100416
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.140-282A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100416 | ||||||
| chr8:132100513
|
C | G | 120 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(117): Show | 133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.140-379G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100513 | ||||||
| chr8:132100553
|
G | A | 1 | a0003c0002t0010g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.140-419C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100553 | ||||||
| chr8:132100555
|
G | T | 1 | a0001c0001t0002g0280 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.140-421C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100555 | ||||||
| chr8:132100621
|
TCATTCAA others(25): Show |
T | 1 | a0001c0001t0001g0182 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.140-519_140-488del others(32): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100621 | ||||||
| chr8:132100667
|
G | A | 72 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0080others(69): Show | 85 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.140-533C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100667 | ||||||
| chr8:132100670
|
A | G | 15 | a0002c0003t0001g0207a0003c0002t0001g0194a0003c0002t0001g0196others(12): Show | 15 | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.140-536T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100670 | ||||||
| chr8:132100713
|
C | T | 103 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(100): Show | 116 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.140-579G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100713 | ||||||
| chr8:132100738
|
G | A | 1 | a0001c0027t0001g0044 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.140-604C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100738 | ||||||
| chr8:132100756
|
G | A | 4 | a0001c0001t0002g0097a0001c0001t0003g0002a0001c0001t0003g0098others(1): Show | 9 | HG00741.hp2 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.140-622C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100756 | ||||||
| chr8:132100779
|
C | T | 2 | a0001c0001t0024g0356a0001c0005t0001g0355 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.140-645G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100779 | ||||||
| chr8:132100845
|
A | G | 7 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0002g0346others(4): Show | 7 | HG02451.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.140-711T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100845 | ||||||
| chr8:132100991
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.140-857A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100991 | ||||||
| chr8:132101000
|
A | T | 3 | a0003c0002t0001g0196a0004c0006t0001g0197a0004c0006t0001g0198 | 3 | HG01069.hp2 HG01071.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.140-866T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101000 | ||||||
| chr8:132101228
|
G | A | 1 | a0002c0003t0002g0329 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.140-1094C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101228 | ||||||
| chr8:132101235
|
T | A | 1 | a0002c0003t0001g0138 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.140-1101A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101235 | ||||||
| chr8:132101284
|
A | T | 182 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(179): Show | 191 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(188): Show |
intron_variant | MODIFIER | c.140-1150T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101284 | ||||||
| chr8:132101433
|
G | C | 220 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(217): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.140-1299C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101433 | ||||||
| chr8:132101434
|
G | A | 1 | a0007c0011t0007g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.140-1300C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101434 | ||||||
| chr8:132101464
|
C | T | 1 | a0002c0004t0002g0083 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.140-1330G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101464 | ||||||
| chr8:132101528
|
A | T | 182 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(179): Show | 191 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(188): Show |
intron_variant | MODIFIER | c.140-1394T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101528 | ||||||
| chr8:132101582
|
A | AT | 97 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(94): Show | 106 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.140-1449dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101582 | ||||||
| chr8:132101582
|
AT | A | 101 | a0001c0001t0001g0139a0001c0001t0001g0147a0001c0001t0001g0159others(98): Show | 114 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.140-1449delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101582 | ||||||
| chr8:132101621
|
C | T | 2 | a0001c0001t0024g0356a0001c0005t0001g0355 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.140-1487G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101621 | ||||||
| chr8:132101640
|
G | A | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 94 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.140-1506C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101640 | ||||||
| chr8:132101654
|
A | G | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185others(2): Show | 5 | HG02486.hp2 HG02683.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-1520T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101654 | ||||||
| chr8:132101663
|
T | C | 2 | a0001c0001t0024g0356a0001c0005t0001g0355 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.140-1529A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101663 | ||||||
| chr8:132101670
|
G | A | 1 | a0003c0002t0004g0246 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.140-1536C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101670 | ||||||
| chr8:132101704
|
G | A | 183 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(180): Show | 192 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.140-1570C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101704 | ||||||
| chr8:132101749
|
T | A | 183 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(180): Show | 192 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.140-1615A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101749 | ||||||
| chr8:132101797
|
C | G | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185others(2): Show | 5 | HG02486.hp2 HG02683.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-1663G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101797 | ||||||
| chr8:132101827
|
T | C | 222 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(219): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.140-1693A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101827 | ||||||
| chr8:132101896
|
A | G | 37 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.140-1762T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101896 | ||||||
| chr8:132101977
|
A | G | 4 | a0003c0002t0010g0155a0003c0002t0010g0157a0004c0006t0001g0156others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-1843T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101977 | ||||||
| chr8:132102065
|
T | C | 1 | a0001c0001t0005g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.140-1931A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102065 | ||||||
| chr8:132102246
|
A | G | 1 | a0006c0010t0002g0273 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.139+1862T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102246 | ||||||
| chr8:132102394
|
G | A | 3 | a0002c0003t0001g0151a0002c0003t0001g0152a0003c0002t0002g0042 | 3 | NA19004.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.139+1714C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102394 | ||||||
| chr8:132102439
|
C | T | 14 | a0001c0007t0001g0260a0001c0007t0001g0261a0001c0007t0001g0264others(11): Show | 14 | HG01255.hp1 HG02004.hp2 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.139+1669G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102439 | ||||||
| chr8:132102545
|
G | A | 1 | a0002c0003t0001g0332 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.139+1563C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102545 | ||||||
| chr8:132102568
|
C | T | 4 | a0001c0001t0002g0097a0001c0001t0003g0002a0001c0001t0003g0098others(1): Show | 9 | HG00741.hp2 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.139+1540G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102568 | ||||||
| chr8:132102593
|
A | G | 37 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.139+1515T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102593 | ||||||
| chr8:132102602
|
G | T | 2 | a0001c0001t0001g0285a0002c0003t0001g0286 | 2 | NA18979.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.139+1506C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102602 | ||||||
| chr8:132102603
|
C | T | 9 | a0003c0002t0010g0155a0003c0002t0010g0157a0004c0006t0001g0156others(6): Show | 9 | HG02451.hp2 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.139+1505G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102603 | ||||||
| chr8:132102604
|
A | G | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(220): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.139+1504T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102604 | ||||||
| chr8:132102640
|
G | A | 37 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.139+1468C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102640 | ||||||
| chr8:132102686
|
C | T | 7 | a0001c0009t0002g0279a0001c0009t0007g0189a0001c0009t0008g0340others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.139+1422G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102686 | ||||||
| chr8:132102687
|
G | A | 2 | a0001c0001t0009g0354a0001c0027t0001g0044 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.139+1421C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102687 | ||||||
| chr8:132102706
|
G | GATGCCCC others(12): Show |
2 | a0001c0001t0024g0356a0001c0005t0001g0355 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.139+1401_139+1402i others(21): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102706 | ||||||
| chr8:132102710
|
A | C | 352 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(349): Show | 376 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.139+1398T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102710 | ||||||
| chr8:132102752
|
C | T | 186 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(183): Show | 195 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(192): Show |
intron_variant | MODIFIER | c.139+1356G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102752 | ||||||
| chr8:132102792
|
A | AT | 5 | a0001c0005t0001g0050a0002c0004t0001g0052a0002c0004t0002g0005others(2): Show | 7 | HG01175.hp2 HG01192.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.139+1315dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | ||||||
| chr8:132102792
|
AT | A | 10 | a0001c0001t0002g0080a0001c0005t0002g0351a0001c0005t0005g0008others(7): Show | 11 | HG01099.hp2 HG01891.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.139+1315delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | ||||||
| chr8:132102792
|
ATTTTTTT | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0108a0001c0001t0001g0272others(60): Show | 65 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.139+1309_139+1315d others(9): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | ||||||
| chr8:132102792
|
ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0009g0354a0001c0016t0002g0149a0001c0016t0006g0150others(4): Show | 7 | HG02015.hp2 HG02486.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.139+1306_139+1315d others(12): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | ||||||
| chr8:132102792
|
ATTTTTTT others(4): Show |
A | 44 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.139+1305_139+1315d others(13): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | ||||||
| chr8:132102792
|
ATTTTTTT others(5): Show |
A | 177 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(174): Show | 186 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.139+1304_139+1315d others(14): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | ||||||
| chr8:132102826
|
T | C | 2 | a0001c0001t0024g0356a0001c0005t0001g0355 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.139+1282A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102826 | ||||||
| chr8:132102844
|
G | A | 4 | a0001c0001t0002g0097a0001c0001t0003g0002a0001c0001t0003g0098others(1): Show | 9 | HG00741.hp2 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.139+1264C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102844 | ||||||
| chr8:132103042
|
C | T | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185others(2): Show | 5 | HG02486.hp2 HG02683.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+1066G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103042 | ||||||
| chr8:132103056
|
A | G | 2 | a0001c0001t0024g0356a0001c0005t0001g0355 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.139+1052T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103056 | ||||||
| chr8:132103110
|
G | A | 1 | a0002c0014t0002g0269 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.139+998C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103110 | ||||||
| chr8:132103232
|
A | C | 4 | a0001c0012t0001g0153a0001c0012t0001g0154a0001c0012t0001g0350others(1): Show | 4 | HG01123.hp1 HG01934.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+876T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103232 | ||||||
| chr8:132103247
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.139+861C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103247 | ||||||
| chr8:132103400
|
C | T | 184 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(181): Show | 193 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.139+708G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103400 | ||||||
| chr8:132103412
|
G | T | 184 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(181): Show | 193 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.139+696C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103412 | ||||||
| chr8:132103417
|
T | A | 184 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(181): Show | 193 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.139+691A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103417 | ||||||
| chr8:132103543
|
T | G | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(220): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.139+565A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103543 | ||||||
| chr8:132103618
|
A | AAAAT | 6 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185others(3): Show | 6 | HG00735.hp1 HG02647.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.139+486_139+489dup others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103618 | ||||||
| chr8:132103618
|
AAAATAAA others(1): Show |
A | 58 | a0001c0001t0002g0080a0001c0005t0001g0050a0001c0005t0001g0058others(55): Show | 71 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.139+482_139+489del others(8): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103618 | ||||||
| chr8:132103704
|
A | C | 184 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(181): Show | 193 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.139+404T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103704 | ||||||
| chr8:132103739
|
A | T | 286 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(283): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.139+369T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103739 | ||||||
| chr8:132103807
|
A | G | 184 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(181): Show | 193 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.139+301T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103807 | ||||||
| chr8:132103862
|
G | A | 286 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(283): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.139+246C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103862 | ||||||
| chr8:132104004
|
C | T | 186 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(183): Show | 195 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(192): Show |
intron_variant | MODIFIER | c.139+104G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132104004 | ||||||
| chr8:132104005
|
G | A | 2 | a0001c0016t0002g0149a0001c0016t0006g0150 | 2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.139+103C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132104005 | ||||||
| chr8:132104055
|
A | G | 1 | a0003c0002t0001g0194 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.139+53T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132104055 | ||||||
| chr8:132104063
|
G | T | 32 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(29): Show | 32 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.139+45C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132104063 | ||||||
| chr8:132104085
|
A | G | 1 | a0001c0001t0002g0015 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.139+23T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132104085 | ||||||
| chr8:132104328
|
G | A | 34 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(31): Show | 34 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.80-161C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104328 | ||||||
| chr8:132104353
|
A | G | 187 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(184): Show | 196 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(193): Show |
intron_variant | MODIFIER | c.80-186T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104353 | ||||||
| chr8:132104370
|
C | A | 1 | a0003c0002t0001g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.80-203G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104370 | ||||||
| chr8:132104487
|
G | A | 14 | a0001c0007t0001g0260a0001c0007t0001g0261a0001c0007t0001g0264others(11): Show | 14 | HG01255.hp1 HG02004.hp2 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-320C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104487 | ||||||
| chr8:132104523
|
G | GTGAGTCT others(29): Show |
1 | a0001c0001t0001g0182 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.80-357_80-356insGC others(34): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104523 | ||||||
| chr8:132104661
|
A | T | 67 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(64): Show | 67 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.80-494T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104661 | ||||||
| chr8:132104676
|
A | G | 1 | a0010c0028t0002g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.80-509T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104676 | ||||||
| chr8:132104782
|
A | G | 4 | a0005c0008t0002g0346a0005c0008t0002g0347a0005c0008t0009g0338others(1): Show | 4 | HG02451.hp2 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+405T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104782 | ||||||
| chr8:132104786
|
C | T | 2 | a0001c0005t0002g0081a0002c0004t0002g0048 | 2 | HG00738.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.79+401G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104786 | ||||||
| chr8:132104956
|
G | A | 1 | a0002c0003t0002g0333 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.79+231C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104956 | ||||||
| chr8:132104969
|
G | A | 1 | a0001c0007t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79+218C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104969 | ||||||
| chr8:132104991
|
G | T | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 94 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.79+196C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104991 | ||||||
| chr8:132105115
|
T | A | 120 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(117): Show | 129 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.79+72A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132105115 | ||||||
| chr8:132105356
|
G | A | 74 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(71): Show | 74 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.-21-70C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132105356 | ||||||
| chr8:132105623
|
G | C | 96 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(93): Show | 109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.-21-337C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132105623 | ||||||
| chr8:132105716
|
C | T | 2 | a0001c0016t0002g0149a0001c0016t0006g0150 | 2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-21-430G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132105716 | ||||||
| chr8:132105818
|
G | A | 69 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(66): Show | 69 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.-21-532C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132105818 | ||||||
| chr8:132105909
|
TCCTTCTC others(18): Show |
T | 1 | a0001c0001t0001g0108 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21-648_-21-624del others(25): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132105909 | ||||||
| chr8:132106054
|
T | A | 163 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(160): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-21-768A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106054 | ||||||
| chr8:132106106
|
T | C | 1 | a0001c0001t0004g0334 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-21-820A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106106 | ||||||
| chr8:132106142
|
T | G | 2 | a0001c0001t0024g0356a0001c0005t0001g0355 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-21-856A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106142 | ||||||
| chr8:132106169
|
C | T | 67 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(64): Show | 67 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.-21-883G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106169 | ||||||
| chr8:132106179
|
G | T | 4 | a0001c0001t0002g0097a0001c0001t0003g0002a0001c0001t0003g0098others(1): Show | 9 | HG00741.hp2 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21-893C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106179 | ||||||
| chr8:132106235
|
G | A | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 94 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.-21-949C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106235 | ||||||
| chr8:132106325
|
G | C | 163 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(160): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-21-1039C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106325 | ||||||
| chr8:132106387
|
C | A | 297 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(294): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-21-1101G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106387 | ||||||
| chr8:132106394
|
A | T | 1 | a0003c0002t0002g0024 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-21-1108T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106394 | ||||||
| chr8:132106494
|
A | G | 2 | a0001c0001t0009g0354a0001c0027t0001g0044 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-21-1208T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106494 | ||||||
| chr8:132106506
|
C | T | 163 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(160): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-21-1220G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106506 | ||||||
| chr8:132106752
|
C | T | 1 | a0001c0007t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-21-1466G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106752 | ||||||
| chr8:132106838
|
G | C | 11 | a0001c0005t0001g0086a0001c0005t0002g0081a0001c0005t0002g0085others(8): Show | 11 | HG00408.hp1 HG00438.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21-1552C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106838 | ||||||
| chr8:132106859
|
G | A | 36 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-21-1573C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106859 | ||||||
| chr8:132106867
|
A | G | 1 | a0001c0027t0001g0044 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-21-1581T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106867 | ||||||
| chr8:132106913
|
G | A | 1 | a0001c0007t0002g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-21-1627C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106913 | ||||||
| chr8:132106944
|
G | A | 36 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-21-1658C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106944 | ||||||
| chr8:132107074
|
C | G | 2 | a0001c0001t0024g0356a0001c0005t0001g0355 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-21-1788G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107074 | ||||||
| chr8:132107356
|
AGTGGTAC others(32): Show |
A | 1 | a0001c0001t0003g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-21-2109_-21-2071d others(41): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107356 | ||||||
| chr8:132107404
|
G | T | 67 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(64): Show | 67 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.-21-2118C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107404 | ||||||
| chr8:132107420
|
A | C | 94 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(91): Show | 107 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-21-2134T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107420 | ||||||
| chr8:132107528
|
G | A | 94 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(91): Show | 107 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-21-2242C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107528 | ||||||
| chr8:132107552
|
A | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185 | 3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-21-2266T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107552 | ||||||
| chr8:132107568
|
G | A | 94 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(91): Show | 107 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-21-2282C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107568 | ||||||
| chr8:132107591
|
C | T | 94 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(91): Show | 107 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-21-2305G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107591 | ||||||
| chr8:132107592
|
G | A | 67 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(64): Show | 67 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.-21-2306C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107592 | ||||||
| chr8:132107714
|
C | A | 55 | a0001c0001t0002g0080a0001c0005t0001g0050a0001c0005t0001g0058others(52): Show | 68 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-21-2428G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107714 | ||||||
| chr8:132107835
|
T | TTTGGAGA others(1): Show |
187 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(184): Show | 196 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(193): Show |
intron_variant | MODIFIER | c.-21-2557_-21-2550d others(10): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107835 | ||||||
| chr8:132107839
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21-2553C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107839 | ||||||
| chr8:132107840
|
A | AGAGTTG | 96 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(93): Show | 109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.-21-2555_-21-2554i others(8): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107840 | ||||||
| chr8:132108188
|
G | T | 2 | a0003c0002t0001g0010a0003c0002t0001g0188 | 3 | HG01257.hp2 HG01258.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-21-2902C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108188 | ||||||
| chr8:132108220
|
C | T | 58 | a0001c0001t0002g0080a0001c0001t0002g0095a0001c0005t0001g0050others(55): Show | 71 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.-22+2882G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108220 | ||||||
| chr8:132108442
|
T | G | 1 | a0001c0001t0011g0158 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-22+2660A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108442 | ||||||
| chr8:132108457
|
C | T | 6 | a0001c0001t0001g0272a0006c0010t0001g0277a0006c0010t0002g0273others(3): Show | 6 | HG02015.hp2 NA18977.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+2645G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108457 | ||||||
| chr8:132108492
|
T | C | 2 | a0005c0008t0002g0346a0005c0008t0002g0347 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-22+2610A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108492 | ||||||
| chr8:132108536
|
C | A | 28 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(25): Show | 29 | HG00408.hp2 HG00597.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-22+2566G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108536 | ||||||
| chr8:132108537
|
G | A | 44 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(41): Show | 44 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.-22+2565C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108537 | ||||||
| chr8:132108630
|
C | T | 2 | a0002c0004t0002g0046a0002c0004t0002g0047 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-22+2472G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108630 | ||||||
| chr8:132108641
|
G | A | 2 | a0003c0002t0002g0140a0003c0002t0002g0141 | 2 | HG02257.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-22+2461C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108641 | ||||||
| chr8:132108764
|
CT | C | 4 | a0001c0005t0001g0100a0002c0004t0001g0009a0002c0004t0001g0101others(1): Show | 5 | HG01257.hp1 HG01975.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+2337delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108764 | ||||||
| chr8:132108791
|
G | A | 134 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(131): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-22+2311C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108791 | ||||||
| chr8:132108845
|
A | C | 25 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(22): Show | 26 | HG00408.hp2 HG00597.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-22+2257T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108845 | ||||||
| chr8:132108886
|
G | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0002g0106 | 3 | HG00609.hp1 NA18968.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-22+2216C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108886 | ||||||
| chr8:132108887
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0002g0106 | 3 | HG00609.hp1 NA18968.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-22+2215G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108887 | ||||||
| chr8:132108911
|
C | T | 1 | a0001c0001t0002g0014 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-22+2191G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108911 | ||||||
| chr8:132108948
|
A | T | 221 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(218): Show | 226 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.-22+2154T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108948 | ||||||
| chr8:132109045
|
T | C | 1 | a0001c0001t0001g0348 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-22+2057A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109045 | ||||||
| chr8:132109047
|
G | T | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(42): Show | 45 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.-22+2055C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109047 | ||||||
| chr8:132109063
|
A | G | 1 | a0001c0001t0009g0354 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-22+2039T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109063 | ||||||
| chr8:132109095
|
C | A | 1 | a0002c0003t0002g0349 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-22+2007G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109095 | ||||||
| chr8:132109163
|
T | G | 136 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(133): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-22+1939A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109163 | ||||||
| chr8:132109330
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0002g0106 | 3 | HG00609.hp1 NA18968.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-22+1772G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109330 | ||||||
| chr8:132109331
|
G | A | 26 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(23): Show | 26 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-22+1771C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109331 | ||||||
| chr8:132109345
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0002g0148 | 2 | HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-22+1757T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109345 | ||||||
| chr8:132109433
|
GA | G | 227 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(224): Show | 249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.-22+1668delT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109433 | ||||||
| chr8:132109449
|
C | A | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0185 | 3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-22+1653G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109449 | ||||||
| chr8:132109638
|
A | T | 134 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0160others(131): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-22+1464T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109638 | ||||||
| chr8:132109717
|
G | T | 63 | a0001c0001t0002g0080a0001c0001t0002g0095a0001c0001t0002g0097others(60): Show | 81 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-22+1385C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109717 | ||||||
| chr8:132109774
|
A | C | 1 | a0007c0011t0007g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-22+1328T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109774 | ||||||
| chr8:132109937
|
A | T | 27 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(24): Show | 28 | HG00408.hp2 HG00597.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-22+1165T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109937 | ||||||
| chr8:132110007
|
C | T | 221 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(218): Show | 226 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.-22+1095G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110007 | ||||||
| chr8:132110047
|
G | A | 221 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(218): Show | 226 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.-22+1055C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110047 | ||||||
| chr8:132110147
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-22+955T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110147 | ||||||
| chr8:132110155
|
T | C | 5 | a0001c0001t0003g0142a0003c0002t0002g0145a0003c0002t0006g0143others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+947A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110155 | ||||||
| chr8:132110219
|
T | C | 221 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(218): Show | 226 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.-22+883A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110219 | ||||||
| chr8:132110254
|
C | T | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(42): Show | 45 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.-22+848G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110254 | ||||||
| chr8:132110280
|
C | T | 1 | a0002c0013t0001g0104 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-22+822G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110280 | ||||||
| chr8:132110304
|
C | G | 2 | a0001c0001t0024g0356a0001c0005t0001g0355 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-22+798G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110304 | ||||||
| chr8:132110326
|
G | C | 1 | a0001c0012t0001g0350 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-22+776C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110326 | ||||||
| chr8:132110537
|
G | A | 3 | a0001c0005t0002g0351a0002c0017t0002g0352a0003c0002t0010g0353 | 3 | HG01109.hp1 HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-22+565C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110537 | ||||||
| chr8:132110540
|
C | T | 265 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(262): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-22+562G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110540 | ||||||
| chr8:132110591
|
G | C | 1 | a0001c0001t0009g0354 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-22+511C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110591 | ||||||
| chr8:132110651
|
G | T | 263 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-22+451C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110651 | ||||||
| chr8:132110713
|
A | G | 27 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(24): Show | 28 | HG00408.hp2 HG00597.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-22+389T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110713 | ||||||
| chr8:132110752
|
G | T | 266 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.-22+350C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110752 | ||||||
| chr8:132110794
|
T | G | 265 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(262): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-22+308A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110794 | ||||||
| chr8:132110915
|
C | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 9 | HG00558.hp2 HG02080.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22+187G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110915 | ||||||
| chr8:132111038
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0002c0003t0001g0013 | 3 | HG02071.hp2 NA18971.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-22+64G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132111038 |