Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79618 |
|---|---|
| ensemblid | ENSG00000147421.18 |
| hgncid | 26137 |
| symbol | HMBOX1 |
| name | homeobox containing 1 |
| refseq_nuc | NM_001135726.3 |
| refseq_prot | NP_001129198.1 |
| ensembl_nuc | ENST00000287701.15 |
| ensembl_prot | ENSP00000287701.10 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 28890395 |
| end | 29053262 |
| strand | + |
| ver | v1.2 |
| region | chr8:28890395-29053262 |
| region5000 | chr8:28885395-29058262 |
| regionname0 | HMBOX1_chr8_28890395_29053262 |
| regionname5000 | HMBOX1_chr8_28885395_29058262 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 420 | 344 | 90 | 50 | 158 | 12 | 32 | 122 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1263 | 343 | 90 | 49 | 158 | 12 | 32 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| c0002 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2448 | 77 | 18 | 14 | 32 | 5 | 7 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0002 | 1/0 | 2449 | 76 | 2 | 9 | 55 | 0 | 9 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0003 | 0/0 | 2454 | 60 | 17 | 4 | 32 | 0 | 7 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0004 | 0/0 | 2445 | 50 | 16 | 16 | 7 | 4 | 7 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0005 | 0/0 | 2449 | 16 | 11 | 1 | 0 | 3 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0006 | 0/0 | 2455 | 14 | 2 | 0 | 12 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0007 | 0/0 | 2445 | 12 | 11 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0008 | 0/0 | 2453 | 10 | 5 | 1 | 3 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0009 | 0/0 | 2454 | 5 | 0 | 0 | 5 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0010 | 0/0 | 2449 | 4 | 2 | 2 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0011 | 0/0 | 2450 | 3 | 0 | 0 | 3 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0012 | 0/0 | 2449 | 2 | 2 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0013 | 0/0 | 2445 | 2 | 0 | 0 | 2 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0014 | 0/0 | 2454 | 2 | 2 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0015 | 0/0 | 2452 | 2 | 0 | 2 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0016 | 0/0 | 2455 | 2 | 0 | 0 | 2 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0017 | 0/0 | 2449 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0018 | 0/0 | 2450 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0019 | 0/0 | 2448 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0020 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0021 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0022 | 0/0 | 2477 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| t0023 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0293 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1263 | 343 | 90 | 49 | 158 | 12 | 32 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0002 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3710 | 77 | 18 | 14 | 32 | 5 | 7 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0002 | 1/0 | 3711 | 75 | 2 | 8 | 55 | 0 | 9 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0003 | 0/0 | 3716 | 60 | 17 | 4 | 32 | 0 | 7 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0004 | 0/0 | 3707 | 50 | 16 | 16 | 7 | 4 | 7 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0005 | 0/0 | 3711 | 16 | 11 | 1 | 0 | 3 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0006 | 0/0 | 3717 | 14 | 2 | 0 | 12 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0007 | 0/0 | 3707 | 12 | 11 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0008 | 0/0 | 3715 | 10 | 5 | 1 | 3 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0009 | 0/0 | 3716 | 5 | 0 | 0 | 5 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0010 | 0/0 | 3711 | 4 | 2 | 2 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0011 | 0/0 | 3712 | 3 | 0 | 0 | 3 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0012 | 0/0 | 3711 | 2 | 2 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0013 | 0/0 | 3707 | 2 | 0 | 0 | 2 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0014 | 0/0 | 3716 | 2 | 2 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0015 | 0/0 | 3714 | 2 | 0 | 2 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0016 | 0/0 | 3717 | 2 | 0 | 0 | 2 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0017 | 0/0 | 3711 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0018 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0019 | 0/0 | 3710 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0020 | 0/0 | 3680 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0021 | 0/0 | 3716 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0022 | 0/0 | 3739 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0001t0023 | 0/0 | 3716 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| a0001c0002t0002 | 0/0 | 3711 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | copy fasta | chr8 | 28885395 | 29058262 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0293 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0006g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0007g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0009g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0009g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0009g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0010g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0010g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0010g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0010g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0011g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0011g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0011g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0012g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0012g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0013g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0013g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0014g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0014g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0015g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0015g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0016g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0016g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0017g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0018g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0019g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0020g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0021g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0022g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0001t0023g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | GBR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0021 | EUR | GBR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0034 | EUR | FIN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0177 | EUR | FIN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0268 | EUR | FIN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0028 | EUR | FIN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00408 | hp1 | a0001 | c0001 | t0017 | g0195 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0330 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00621 | hp2 | a0001 | c0001 | t0008 | g0097 | EAS | CHS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0343 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0076 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00735 | hp2 | a0001 | c0001 | t0015 | g0260 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0038 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0062 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01069 | hp1 | a0001 | c0001 | t0015 | g0274 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01167 | hp2 | a0001 | c0001 | t0010 | g0311 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0063 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0011 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0211 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0292 | EUR | IBS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01928 | hp1 | a0001 | c0001 | t0010 | g0216 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02027 | hp1 | a0001 | c0001 | t0013 | g0050 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02055 | hp1 | a0001 | c0001 | t0018 | g0304 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0302 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0331 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02080 | hp2 | a0001 | c0001 | t0009 | g0080 | EAS | KHV | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0301 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02155 | hp1 | a0001 | c0001 | t0008 | g0098 | EAS | CDX | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CDX | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | CDX | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | CDX | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0262 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0106 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02572 | hp1 | a0001 | c0001 | t0014 | g0117 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0313 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02717 | hp1 | a0001 | c0001 | t0021 | g0344 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0162 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0230 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0327 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0297 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02886 | hp2 | a0001 | c0001 | t0014 | g0116 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0064 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0122 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0166 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0326 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0325 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0180 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0120 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0340 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0342 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0065 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0030 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0061 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0043 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0023 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0088 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0042 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0075 | SAS | PJL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0040 | SAS | BEB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0103 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0039 | SAS | STU | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0121 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0215 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | CHB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | CHB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | CHB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0338 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18947 | hp1 | a0001 | c0001 | t0016 | g0332 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0107 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18953 | hp1 | a0001 | c0001 | t0011 | g0210 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18956 | hp1 | a0001 | c0001 | t0006 | g0336 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18956 | hp2 | a0001 | c0001 | t0011 | g0224 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0341 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18959 | hp2 | a0001 | c0001 | t0008 | g0102 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18965 | hp2 | a0001 | c0001 | t0011 | g0314 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18972 | hp2 | a0001 | c0001 | t0022 | g0334 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18974 | hp2 | a0001 | c0001 | t0009 | g0131 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18981 | hp2 | a0001 | c0001 | t0006 | g0337 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18982 | hp2 | a0001 | c0001 | t0023 | g0333 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18988 | hp1 | a0001 | c0001 | t0009 | g0128 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA18999 | hp2 | a0001 | c0001 | t0013 | g0037 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0074 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19002 | hp1 | a0001 | c0001 | t0009 | g0129 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19010 | hp2 | a0001 | c0001 | t0020 | g0052 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19011 | hp2 | a0001 | c0001 | t0019 | g0173 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19012 | hp2 | a0001 | c0001 | t0016 | g0329 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | LWK | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | LWK | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | LWK | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | LWK | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19057 | hp1 | a0001 | c0001 | t0006 | g0339 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19062 | hp1 | a0001 | c0001 | t0006 | g0328 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19062 | hp2 | a0001 | c0001 | t0009 | g0130 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19079 | hp1 | a0001 | c0001 | t0006 | g0335 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19083 | hp1 | a0001 | c0001 | t0006 | g0112 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0156 | AFR | YRI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | ASW | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ASW | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | TSI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0025 | EUR | TSI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | TSI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0155 | EUR | TSI | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0213 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0199 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | MSL | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | USA | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | USA | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0293 | REF | REF | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0036 | REF | REF | HMBOX1_chr8_28885395_29058262 | HMBOX1 | chr8 | 28885395 | 29058262 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28970316
|
G | A | 1 | a0001c0002 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.297G>A | p.Pro99Pro | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/10 | 638/3711 | 297/1263 | 99/420 | chr8 | 28970316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28890402
|
T | C | 1 | a0001c0001t0012 | 2 | HG02886.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-334T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/10 | 73466 | chr8 | 28890402 | |||||
| chr8:28963863
|
A | G | 2 | a0001c0001t0016a0001c0001t0023 | 3 | NA18947.hp1 NA18982.hp2 NA19012.hp2 |
5_prime_UTR_variant | MODIFIER | c.-5A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/10 | 5 | chr8 | 28963863 | |||||
| chr8:29051357
|
T | TAACC | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(11): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*217_*220dupCCAA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 221 | INFO_REALIGN_3_PRIME | chr8 | 29051357 | ||||
| chr8:29051484
|
T | C | 2 | a0001c0001t0013a0001c0001t0020 | 3 | HG02027.hp1 NA18999.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*329T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 329 | chr8 | 29051484 | |||||
| chr8:29051898
|
T | TA | 7 | a0001c0001t0003a0001c0001t0009a0001c0001t0011others(4): Show | 73 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*763dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 764 | INFO_REALIGN_3_PRIME | chr8 | 29051898 | ||||
| chr8:29051898
|
T | TAA | 2 | a0001c0001t0006a0001c0001t0016 | 16 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*762_*763dupAA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 764 | INFO_REALIGN_3_PRIME | chr8 | 29051898 | ||||
| chr8:29051898
|
TA | T | 3 | a0001c0001t0001a0001c0001t0015a0001c0001t0019 | 80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*763delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 763 | INFO_REALIGN_3_PRIME | chr8 | 29051898 | ||||
| chr8:29051898
|
TAAAAAAA others(1): Show |
T | 4 | a0001c0001t0004a0001c0001t0007a0001c0001t0013others(1): Show | 65 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*756_*763delAAAAAA others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 756 | INFO_REALIGN_3_PRIME | chr8 | 29051898 | ||||
| chr8:29051919
|
C | A | 1 | a0001c0001t0017 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 764 | chr8 | 29051919 | |||||
| chr8:29052006
|
C | T | 4 | a0001c0001t0004a0001c0001t0007a0001c0001t0013others(1): Show | 65 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*851C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 851 | chr8 | 29052006 | |||||
| chr8:29052200
|
A | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1045A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1045 | chr8 | 29052200 | |||||
| chr8:29052210
|
A | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1055A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1055 | chr8 | 29052210 | |||||
| chr8:29052212
|
T | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1057T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1057 | chr8 | 29052212 | |||||
| chr8:29052217
|
T | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1062T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1062 | chr8 | 29052217 | |||||
| chr8:29052224
|
GCTTATCA others(20): Show |
G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1070_*1096delCTTA others(23): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1070 | chr8 | 29052224 | |||||
| chr8:29052254
|
T | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1099T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1099 | chr8 | 29052254 | |||||
| chr8:29052442
|
T | A | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1287T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1287 | chr8 | 29052442 | |||||
| chr8:29052526
|
T | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1371T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1371 | chr8 | 29052526 | |||||
| chr8:29052560
|
A | ATCTATTT others(17): Show |
1 | a0001c0001t0022 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1405_*1406insTCTA others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1406 | chr8 | 29052560 | |||||
| chr8:29052561
|
A | G | 1 | a0001c0001t0022 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1406A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1406 | chr8 | 29052561 | |||||
| chr8:29052569
|
C | T | 1 | a0001c0001t0022 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1414C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1414 | chr8 | 29052569 | |||||
| chr8:29052571
|
G | C | 1 | a0001c0001t0022 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1416G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1416 | chr8 | 29052571 | |||||
| chr8:29052798
|
C | T | 2 | a0001c0001t0005a0001c0001t0012 | 18 | HG00280.hp2 HG01123.hp1 HG01516.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1643C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1643 | chr8 | 29052798 | |||||
| chr8:29052799
|
G | A | 1 | a0001c0001t0014 | 2 | HG02572.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1644G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1644 | chr8 | 29052799 | |||||
| chr8:29052863
|
A | T | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1708A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1708 | chr8 | 29052863 | |||||
| chr8:29052880
|
G | A | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(13): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*1725G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1725 | chr8 | 29052880 | |||||
| chr8:29052976
|
A | T | 1 | a0001c0001t0021 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1821A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1821 | chr8 | 29052976 | |||||
| chr8:29053055
|
G | T | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1900G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1900 | chr8 | 29053055 | |||||
| chr8:29053056
|
T | G | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1901T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 1901 | chr8 | 29053056 | |||||
| chr8:29053184
|
A | T | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2029A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 2029 | chr8 | 29053184 | |||||
| chr8:29053230
|
G | T | 1 | a0001c0001t0007 | 12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2075G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 10/10 | 2075 | chr8 | 29053230 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28891597
|
A | G | 1 | a0001c0001t0021g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-58+919A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28891597 | ||||||
| chr8:28891687
|
G | C | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+1009G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28891687 | ||||||
| chr8:28891978
|
C | G | 1 | a0001c0001t0004g0343 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-58+1300C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28891978 | ||||||
| chr8:28892419
|
C | T | 1 | a0001c0001t0002g0342 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-58+1741C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892419 | ||||||
| chr8:28892436
|
A | G | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+1758A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892436 | ||||||
| chr8:28892468
|
C | T | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-58+1790C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892468 | ||||||
| chr8:28892564
|
A | G | 5 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 5 | HG02165.hp1 NA18954.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+1886A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892564 | ||||||
| chr8:28892901
|
G | A | 1 | a0001c0001t0004g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-58+2223G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892901 | ||||||
| chr8:28892912
|
A | C | 198 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(195): Show | 198 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-58+2234A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892912 | ||||||
| chr8:28892967
|
T | A | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-58+2289T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28892967 | ||||||
| chr8:28893347
|
C | G | 1 | a0001c0001t0002g0342 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-58+2669C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893347 | ||||||
| chr8:28893609
|
T | G | 1 | a0001c0001t0006g0327 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-58+2931T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893609 | ||||||
| chr8:28893747
|
A | T | 1 | a0001c0001t0002g0319 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-58+3069A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893747 | ||||||
| chr8:28893789
|
G | A | 1 | a0001c0001t0007g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-58+3111G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893789 | ||||||
| chr8:28893864
|
C | T | 201 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(198): Show | 201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-58+3186C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893864 | ||||||
| chr8:28893905
|
C | T | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+3227C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28893905 | ||||||
| chr8:28894031
|
A | G | 1 | a0001c0001t0002g0318 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-58+3353A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894031 | ||||||
| chr8:28894040
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-58+3362G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894040 | ||||||
| chr8:28894045
|
G | A | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | NA18968.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-58+3367G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894045 | ||||||
| chr8:28894268
|
A | G | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+3590A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894268 | ||||||
| chr8:28894428
|
T | G | 2 | a0001c0001t0003g0007a0001c0001t0003g0008 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-58+3750T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894428 | ||||||
| chr8:28894476
|
T | C | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-58+3798T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894476 | ||||||
| chr8:28894522
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-58+3844C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894522 | ||||||
| chr8:28894588
|
C | T | 58 | a0001c0001t0001g0084a0001c0001t0002g0083a0001c0001t0003g0005others(55): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-58+3910C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894588 | ||||||
| chr8:28894717
|
A | T | 1 | a0001c0001t0007g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-58+4039A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894717 | ||||||
| chr8:28894897
|
C | A | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+4219C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894897 | ||||||
| chr8:28894942
|
C | CA | 9 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0002g0134others(6): Show | 9 | HG00423.hp2 HG00558.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58+4276dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28894942 | |||||
| chr8:28894942
|
CA | C | 20 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(17): Show | 20 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-58+4276delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28894942 | |||||
| chr8:28894954
|
A | C | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+4276A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894954 | ||||||
| chr8:28894959
|
A | G | 2 | a0001c0001t0003g0121a0001c0001t0008g0120 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+4281A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894959 | ||||||
| chr8:28894990
|
C | G | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+4312C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28894990 | ||||||
| chr8:28895445
|
T | C | 231 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(228): Show | 231 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-58+4767T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895445 | ||||||
| chr8:28895495
|
C | T | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+4817C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895495 | ||||||
| chr8:28895631
|
C | T | 1 | a0001c0001t0003g0114 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-58+4953C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895631 | ||||||
| chr8:28895635
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG03834.hp2 NA18975.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+4957G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895635 | ||||||
| chr8:28895669
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-58+4991A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895669 | ||||||
| chr8:28895674
|
C | CAAAAAAA others(4): Show |
5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+4999_-58+5009d others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28895674 | |||||
| chr8:28895674
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-58+4998_-58+5009d others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28895674 | |||||
| chr8:28895674
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+4997_-58+5009d others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28895674 | |||||
| chr8:28895674
|
CA | C | 6 | a0001c0001t0001g0140a0001c0001t0002g0138a0001c0001t0002g0139others(3): Show | 6 | HG01975.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+5009delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28895674 | |||||
| chr8:28895687
|
A | T | 1 | a0001c0001t0003g0113 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-58+5009A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895687 | ||||||
| chr8:28895688
|
T | A | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+5010T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895688 | ||||||
| chr8:28895714
|
A | C | 1 | a0001c0001t0001g0315 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-58+5036A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895714 | ||||||
| chr8:28895765
|
A | G | 1 | a0001c0001t0011g0314 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-58+5087A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895765 | ||||||
| chr8:28895808
|
A | G | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-58+5130A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895808 | ||||||
| chr8:28895851
|
T | C | 312 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(309): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.-58+5173T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895851 | ||||||
| chr8:28895891
|
A | G | 1 | a0001c0001t0004g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-58+5213A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895891 | ||||||
| chr8:28895988
|
T | C | 2 | a0001c0001t0004g0029a0001c0001t0004g0030 | 2 | HG01975.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-58+5310T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28895988 | ||||||
| chr8:28896004
|
CTCCTCAG others(18): Show |
C | 1 | a0001c0001t0003g0113 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-58+5327_-58+5351d others(27): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896004 | ||||||
| chr8:28896107
|
A | G | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-58+5429A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896107 | ||||||
| chr8:28896165
|
T | C | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-58+5487T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896165 | ||||||
| chr8:28896176
|
T | C | 1 | a0001c0001t0002g0319 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-58+5498T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896176 | ||||||
| chr8:28896216
|
T | C | 11 | a0001c0001t0007g0004a0001c0001t0007g0009a0001c0001t0007g0010others(8): Show | 11 | HG01261.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-58+5538T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896216 | ||||||
| chr8:28896343
|
T | G | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+5665T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896343 | ||||||
| chr8:28896382
|
GTGTGTAG others(231): Show |
G | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+5705_-58+5942d others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896382 | ||||||
| chr8:28896546
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-58+5868A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896546 | ||||||
| chr8:28896630
|
A | T | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+5952A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896630 | ||||||
| chr8:28896631
|
CTGTACTT others(76): Show |
C | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+5954_-58+6036d others(85): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896631 | ||||||
| chr8:28896674
|
C | T | 1 | a0001c0001t0002g0312 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-58+5996C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896674 | ||||||
| chr8:28896810
|
C | T | 4 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0310others(1): Show | 4 | HG01167.hp2 HG01358.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+6132C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896810 | ||||||
| chr8:28896817
|
C | T | 5 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+6139C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896817 | ||||||
| chr8:28896915
|
T | C | 1 | a0001c0001t0001g0315 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-58+6237T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28896915 | ||||||
| chr8:28896978
|
G | GT | 19 | a0001c0001t0003g0105a0001c0001t0003g0106a0001c0001t0003g0118others(16): Show | 19 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-58+6314dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28896978 | |||||
| chr8:28897078
|
A | T | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-58+6400A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28897078 | ||||||
| chr8:28897080
|
G | T | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-58+6402G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28897080 | ||||||
| chr8:28897388
|
T | TAAATGAG others(14): Show |
1 | a0001c0001t0003g0113 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-58+6711_-58+6731d others(23): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28897388 | |||||
| chr8:28897536
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-58+6858C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28897536 | ||||||
| chr8:28897628
|
G | A | 312 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(309): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.-58+6950G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28897628 | ||||||
| chr8:28898158
|
C | CA | 16 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.-58+7483dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28898158 | |||||
| chr8:28898237
|
T | C | 320 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(317): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.-58+7559T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898237 | ||||||
| chr8:28898238
|
A | AC | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+7560_-58+7561i others(3): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898238 | ||||||
| chr8:28898240
|
T | G | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+7562T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898240 | ||||||
| chr8:28898240
|
T | TG | 297 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(294): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.-58+7562_-58+7563i others(3): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898240 | ||||||
| chr8:28898248
|
G | A | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+7570G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898248 | ||||||
| chr8:28898375
|
T | G | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+7697T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898375 | ||||||
| chr8:28898471
|
C | T | 202 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(199): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.-58+7793C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898471 | ||||||
| chr8:28898498
|
G | C | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+7820G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898498 | ||||||
| chr8:28898591
|
G | T | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-58+7913G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898591 | ||||||
| chr8:28898671
|
C | T | 1 | a0001c0001t0012g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-58+7993C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898671 | ||||||
| chr8:28898769
|
A | G | 312 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(309): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.-58+8091A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898769 | ||||||
| chr8:28898874
|
G | T | 2 | a0001c0001t0002g0295a0001c0001t0002g0296 | 2 | NA18968.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-58+8196G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898874 | ||||||
| chr8:28898948
|
T | A | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+8270T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898948 | ||||||
| chr8:28898950
|
G | A | 2 | a0001c0001t0007g0010a0001c0001t0007g0017 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-58+8272G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28898950 | ||||||
| chr8:28899221
|
G | A | 227 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(224): Show | 227 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-58+8543G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28899221 | ||||||
| chr8:28899261
|
G | C | 1 | a0001c0001t0008g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-58+8583G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28899261 | ||||||
| chr8:28899730
|
T | A | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-58+9052T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28899730 | ||||||
| chr8:28900115
|
A | G | 227 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(224): Show | 227 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-58+9437A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900115 | ||||||
| chr8:28900152
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-58+9474G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900152 | ||||||
| chr8:28900254
|
C | CAAA | 6 | a0001c0001t0006g0330a0001c0001t0006g0331a0001c0001t0006g0341others(3): Show | 6 | HG00544.hp1 HG02056.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+9592_-58+9594d others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900254 | |||||
| chr8:28900265
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0294 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-58+9588_-58+9589i others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900265 | |||||
| chr8:28900267
|
A | AATATATA others(3): Show |
6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG00423.hp1 HG01123.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+9590_-58+9591i others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900267 | |||||
| chr8:28900267
|
A | ATAT | 8 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(5): Show | 8 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+9589_-58+9590i others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900267 | ||||||
| chr8:28900267
|
A | ATATATAT others(4): Show |
5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG01070.hp2 HG01516.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+9589_-58+9590i others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900267 | ||||||
| chr8:28900267
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0289 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-58+9589_-58+9590i others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900267 | ||||||
| chr8:28900267
|
A | T | 2 | a0001c0001t0001g0294a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-58+9589A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900267 | ||||||
| chr8:28900269
|
A | AATAT | 27 | a0001c0001t0001g0243a0001c0001t0002g0132a0001c0001t0002g0137others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.-58+9592_-58+9593i others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900269 | |||||
| chr8:28900269
|
A | AATATATA others(3): Show |
3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0307 | 3 | HG02071.hp1 HG02559.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-58+9592_-58+9593i others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900269 | |||||
| chr8:28900269
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0229 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+9592_-58+9593i others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900269 | |||||
| chr8:28900269
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+9592_-58+9593i others(24): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900269 | |||||
| chr8:28900269
|
A | AT | 3 | a0001c0001t0001g0287a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG01243.hp1 HG02004.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(3): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | ||||||
| chr8:28900269
|
A | ATATAT | 4 | a0001c0001t0001g0285a0001c0001t0002g0286a0001c0001t0002g0342others(1): Show | 4 | HG03239.hp1 NA19062.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | ||||||
| chr8:28900269
|
A | ATATATAT others(2): Show |
22 | a0001c0001t0001g0140a0001c0001t0001g0144a0001c0001t0001g0148others(19): Show | 22 | HG00140.hp1 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(11): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | ||||||
| chr8:28900269
|
A | ATATATAT others(4): Show |
9 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0263others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | ||||||
| chr8:28900269
|
A | ATATATAT others(6): Show |
5 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(2): Show | 5 | HG00735.hp2 HG01109.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | ||||||
| chr8:28900269
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0317 | 3 | HG02040.hp2 HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(17): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | ||||||
| chr8:28900269
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG01175.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-58+9591_-58+9592i others(23): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | ||||||
| chr8:28900269
|
A | T | 28 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(25): Show | 28 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.-58+9591A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900269 | ||||||
| chr8:28900271
|
A | AAAAAT | 8 | a0001c0001t0002g0138a0001c0001t0003g0007a0001c0001t0003g0066others(5): Show | 8 | HG01109.hp2 HG03490.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+9594_-58+9595i others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | |||||
| chr8:28900271
|
A | AAAAT | 14 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(11): Show | 14 | HG02258.hp1 HG02647.hp1 HG03017.hp2 others(11): Show |
intron_variant | MODIFIER | c.-58+9594_-58+9595i others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | |||||
| chr8:28900271
|
A | AAAT | 6 | a0001c0001t0003g0096a0001c0001t0003g0133a0001c0001t0004g0127others(3): Show | 6 | HG01928.hp2 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+9594_-58+9595i others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | |||||
| chr8:28900271
|
A | AAATAT | 34 | a0001c0001t0001g0084a0001c0001t0002g0083a0001c0001t0002g0139others(31): Show | 34 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-58+9594_-58+9595i others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | |||||
| chr8:28900271
|
A | AAATATAT | 6 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0071others(3): Show | 6 | NA18961.hp2 NA18986.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+9594_-58+9595i others(9): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | |||||
| chr8:28900271
|
A | AATAT | 52 | a0001c0001t0001g0176a0001c0001t0002g0134a0001c0001t0002g0135others(49): Show | 52 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-58+9610_-58+9613d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | |||||
| chr8:28900271
|
A | AATATAT | 6 | a0001c0001t0002g0295a0001c0001t0003g0104a0001c0001t0005g0166others(3): Show | 6 | HG00621.hp2 HG02145.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+9608_-58+9613d others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | |||||
| chr8:28900271
|
A | AATATATA others(3): Show |
2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18966.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-58+9604_-58+9613d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28900271 | |||||
| chr8:28900271
|
A | ATAT | 4 | a0001c0001t0002g0227a0001c0001t0002g0228a0001c0001t0004g0003others(1): Show | 4 | HG00741.hp2 HG02074.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+9593_-58+9594i others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | ||||||
| chr8:28900271
|
A | ATATAT | 7 | a0001c0001t0002g0223a0001c0001t0002g0225a0001c0001t0003g0101others(4): Show | 7 | HG04115.hp1 NA18956.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+9593_-58+9594i others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | ||||||
| chr8:28900271
|
A | ATATATAT | 4 | a0001c0001t0001g0136a0001c0001t0001g0221a0001c0001t0002g0222others(1): Show | 4 | HG01168.hp2 HG02109.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+9593_-58+9594i others(9): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | ||||||
| chr8:28900271
|
A | ATATATAT others(2): Show |
9 | a0001c0001t0001g0220a0001c0001t0001g0299a0001c0001t0001g0305others(6): Show | 9 | HG01167.hp2 HG01358.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-58+9593_-58+9594i others(11): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | ||||||
| chr8:28900271
|
A | ATATATAT others(4): Show |
6 | a0001c0001t0001g0141a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02055.hp1 HG02155.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+9593_-58+9594i others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | ||||||
| chr8:28900271
|
A | T | 122 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0143others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.-58+9593A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900271 | ||||||
| chr8:28900273
|
T | A | 1 | a0001c0001t0007g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-58+9595T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900273 | ||||||
| chr8:28900310
|
C | A | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-58+9632C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900310 | ||||||
| chr8:28900405
|
G | C | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+9727G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900405 | ||||||
| chr8:28900507
|
T | C | 1 | a0001c0001t0005g0162 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-58+9829T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900507 | ||||||
| chr8:28900529
|
C | G | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-58+9851C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900529 | ||||||
| chr8:28900750
|
G | A | 1 | a0001c0001t0004g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-58+10072G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900750 | ||||||
| chr8:28900780
|
G | T | 5 | a0001c0001t0003g0070a0001c0001t0003g0071a0001c0001t0003g0072others(2): Show | 5 | NA18986.hp1 NA18998.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+10102G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900780 | ||||||
| chr8:28900851
|
C | T | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+10173C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28900851 | ||||||
| chr8:28901169
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-58+10491A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901169 | ||||||
| chr8:28901175
|
T | C | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+10497T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901175 | ||||||
| chr8:28901543
|
T | A | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-58+10865T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901543 | ||||||
| chr8:28901779
|
C | T | 1 | a0001c0001t0005g0213 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-58+11101C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901779 | ||||||
| chr8:28901936
|
G | T | 4 | a0001c0001t0009g0128a0001c0001t0009g0129a0001c0001t0009g0130others(1): Show | 4 | NA18974.hp2 NA18988.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+11258G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901936 | ||||||
| chr8:28901937
|
T | C | 4 | a0001c0001t0009g0128a0001c0001t0009g0129a0001c0001t0009g0130others(1): Show | 4 | NA18974.hp2 NA18988.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+11259T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901937 | ||||||
| chr8:28901950
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-58+11272T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901950 | ||||||
| chr8:28901961
|
A | G | 320 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(317): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.-58+11283A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28901961 | ||||||
| chr8:28902537
|
C | T | 1 | a0001c0001t0004g0051 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-58+11859C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28902537 | ||||||
| chr8:28902578
|
A | G | 1 | a0001c0001t0004g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-58+11900A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28902578 | ||||||
| chr8:28902608
|
A | T | 1 | a0001c0001t0003g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-58+11930A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28902608 | ||||||
| chr8:28902678
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-58+12000G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28902678 | ||||||
| chr8:28902773
|
C | CT | 222 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(219): Show | 222 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.-58+12096dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28902773 | |||||
| chr8:28902902
|
C | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-58+12224C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28902902 | ||||||
| chr8:28903106
|
T | TAC | 15 | a0001c0001t0003g0168a0001c0001t0006g0327a0001c0001t0006g0328others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+12444_-58+1244 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28903106 | |||||
| chr8:28903124
|
T | C | 16 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(13): Show | 16 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.-58+12446T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28903124 | ||||||
| chr8:28903220
|
C | T | 202 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(199): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.-58+12542C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28903220 | ||||||
| chr8:28903447
|
G | A | 2 | a0001c0001t0002g0295a0001c0001t0002g0296 | 2 | NA18968.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-58+12769G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28903447 | ||||||
| chr8:28903458
|
C | T | 3 | a0001c0001t0002g0212a0001c0001t0002g0248a0001c0002t0002g0211 | 3 | HG01358.hp2 HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-58+12780C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28903458 | ||||||
| chr8:28903556
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-58+12878G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28903556 | ||||||
| chr8:28903857
|
AT | A | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+13183delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28903857 | |||||
| chr8:28904002
|
G | C | 312 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(309): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.-58+13324G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904002 | ||||||
| chr8:28904090
|
G | A | 1 | a0001c0001t0006g0074 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-58+13412G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904090 | ||||||
| chr8:28904098
|
A | G | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+13420A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904098 | ||||||
| chr8:28904113
|
A | G | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+13435A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904113 | ||||||
| chr8:28904162
|
T | C | 1 | a0001c0001t0002g0169 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-58+13484T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904162 | ||||||
| chr8:28904212
|
A | G | 1 | a0001c0001t0005g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-58+13534A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904212 | ||||||
| chr8:28904286
|
T | C | 1 | a0001c0001t0009g0131 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-58+13608T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904286 | ||||||
| chr8:28904338
|
C | T | 1 | a0001c0001t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+13660C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904338 | ||||||
| chr8:28904357
|
C | T | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+13679C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904357 | ||||||
| chr8:28904378
|
G | A | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+13700G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904378 | ||||||
| chr8:28904380
|
G | A | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+13702G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904380 | ||||||
| chr8:28904526
|
C | G | 1 | a0001c0001t0003g0226 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-58+13848C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904526 | ||||||
| chr8:28904676
|
C | A | 1 | a0001c0001t0003g0113 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-58+13998C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904676 | ||||||
| chr8:28904679
|
A | G | 2 | a0001c0001t0003g0007a0001c0001t0003g0008 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-58+14001A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28904679 | ||||||
| chr8:28905209
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-58+14531G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905209 | ||||||
| chr8:28905210
|
C | G | 1 | a0001c0001t0002g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-58+14532C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905210 | ||||||
| chr8:28905211
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-58+14533A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905211 | ||||||
| chr8:28905212
|
G | A | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+14534G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905212 | ||||||
| chr8:28905233
|
G | T | 4 | a0001c0001t0001g0268a0001c0001t0001g0283a0001c0001t0001g0288others(1): Show | 4 | HG00323.hp1 HG01123.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+14555G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905233 | ||||||
| chr8:28905281
|
A | G | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+14603A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905281 | ||||||
| chr8:28905340
|
C | T | 4 | a0001c0001t0004g0123a0001c0001t0004g0124a0001c0001t0004g0125others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+14662C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905340 | ||||||
| chr8:28905355
|
G | GCGCACAC others(7): Show |
5 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0247others(2): Show | 5 | NA18612.hp1 NA18953.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+14678_-58+1467 others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28905355 | |||||
| chr8:28905355
|
GCA | G | 17 | a0001c0001t0001g0285a0001c0001t0002g0201a0001c0001t0002g0202others(14): Show | 17 | HG00609.hp2 HG02074.hp2 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+14693_-58+1469 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28905355 | |||||
| chr8:28905357
|
A | G | 5 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0247others(2): Show | 5 | NA18612.hp1 NA18953.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+14679A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905357 | ||||||
| chr8:28905367
|
A | C | 1 | a0001c0001t0004g0027 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-58+14689A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905367 | ||||||
| chr8:28905856
|
C | A | 1 | a0001c0001t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+15178C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905856 | ||||||
| chr8:28905969
|
A | G | 5 | a0001c0001t0003g0091a0001c0001t0003g0092a0001c0001t0003g0093others(2): Show | 5 | NA18960.hp2 NA18980.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+15291A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905969 | ||||||
| chr8:28905974
|
A | G | 1 | a0001c0001t0002g0244 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-58+15296A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28905974 | ||||||
| chr8:28906050
|
A | G | 1 | a0001c0001t0021g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-58+15372A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906050 | ||||||
| chr8:28906108
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-58+15430C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906108 | ||||||
| chr8:28906317
|
G | T | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+15639G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906317 | ||||||
| chr8:28906355
|
CTTAG | C | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+15681_-58+1568 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28906355 | |||||
| chr8:28906374
|
A | G | 4 | a0001c0001t0009g0128a0001c0001t0009g0129a0001c0001t0009g0130others(1): Show | 4 | NA18974.hp2 NA18988.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+15696A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906374 | ||||||
| chr8:28906506
|
T | C | 1 | a0001c0001t0006g0328 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-58+15828T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906506 | ||||||
| chr8:28906525
|
C | A | 115 | a0001c0001t0001g0176a0001c0001t0001g0285a0001c0001t0001g0290others(112): Show | 115 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-58+15847C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906525 | ||||||
| chr8:28906531
|
A | T | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+15853A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906531 | ||||||
| chr8:28906629
|
CCTCAGGC others(24): Show |
C | 1 | a0001c0001t0008g0097 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-58+15956_-58+1598 others(35): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28906629 | |||||
| chr8:28906643
|
A | ATGTCCCT others(4): Show |
1 | a0001c0001t0010g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-58+15965_-58+1596 others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906643 | ||||||
| chr8:28906664
|
A | G | 79 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-58+15986A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906664 | ||||||
| chr8:28906839
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-58+16161G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906839 | ||||||
| chr8:28906920
|
C | G | 1 | a0001c0001t0003g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-58+16242C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28906920 | ||||||
| chr8:28907030
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-58+16352A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907030 | ||||||
| chr8:28907044
|
ATAAT | A | 54 | a0001c0001t0001g0084a0001c0001t0002g0083a0001c0001t0003g0005others(51): Show | 54 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-58+16370_-58+1637 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28907044 | |||||
| chr8:28907438
|
T | G | 1 | a0001c0001t0002g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-58+16760T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907438 | ||||||
| chr8:28907575
|
A | C | 2 | a0001c0001t0003g0121a0001c0001t0008g0120 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+16897A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907575 | ||||||
| chr8:28907718
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-58+17040G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907718 | ||||||
| chr8:28907805
|
C | T | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-58+17127C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907805 | ||||||
| chr8:28907852
|
T | TC | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+17174_-58+1717 others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907852 | ||||||
| chr8:28907853
|
T | C | 8 | a0001c0001t0001g0268a0001c0001t0001g0283a0001c0001t0001g0288others(5): Show | 8 | HG00323.hp1 HG01123.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+17175T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907853 | ||||||
| chr8:28907877
|
G | T | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+17199G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907877 | ||||||
| chr8:28907917
|
T | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0250 | 2 | NA18978.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-58+17239T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907917 | ||||||
| chr8:28907976
|
T | G | 230 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(227): Show | 230 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.-58+17298T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28907976 | ||||||
| chr8:28908128
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-58+17450C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908128 | ||||||
| chr8:28908157
|
A | G | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+17479A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908157 | ||||||
| chr8:28908566
|
C | G | 3 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120 | 3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+17888C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908566 | ||||||
| chr8:28908616
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-58+17938A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908616 | ||||||
| chr8:28908718
|
A | T | 1 | a0001c0001t0009g0130 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-58+18040A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908718 | ||||||
| chr8:28908720
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-58+18042T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908720 | ||||||
| chr8:28908726
|
A | C | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+18048A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908726 | ||||||
| chr8:28908816
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-58+18138G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908816 | ||||||
| chr8:28908921
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-58+18243G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908921 | ||||||
| chr8:28908925
|
C | T | 1 | a0001c0001t0003g0090 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-58+18247C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908925 | ||||||
| chr8:28908958
|
C | T | 3 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120 | 3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+18280C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28908958 | ||||||
| chr8:28909064
|
C | T | 9 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0003g0325others(6): Show | 9 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-58+18386C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909064 | ||||||
| chr8:28909076
|
C | T | 1 | a0001c0001t0003g0073 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-58+18398C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909076 | ||||||
| chr8:28909086
|
C | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-58+18408C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909086 | ||||||
| chr8:28909095
|
T | TA | 6 | a0001c0001t0001g0229a0001c0001t0001g0282a0001c0001t0001g0321others(3): Show | 6 | HG02738.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+18435dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28909095 | |||||
| chr8:28909212
|
A | G | 1 | a0001c0001t0008g0098 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-58+18534A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909212 | ||||||
| chr8:28909256
|
A | G | 1 | a0001c0001t0003g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-58+18578A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909256 | ||||||
| chr8:28909316
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-58+18638C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909316 | ||||||
| chr8:28909329
|
C | A | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+18651C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909329 | ||||||
| chr8:28909510
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-58+18832G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909510 | ||||||
| chr8:28909773
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+19095C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28909773 | ||||||
| chr8:28910020
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-58+19342C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910020 | ||||||
| chr8:28910026
|
T | C | 1 | a0001c0001t0006g0330 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-58+19348T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910026 | ||||||
| chr8:28910152
|
T | C | 2 | a0001c0001t0001g0272a0001c0001t0001g0287 | 2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-58+19474T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910152 | ||||||
| chr8:28910193
|
C | G | 1 | a0001c0001t0007g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-58+19515C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910193 | ||||||
| chr8:28910347
|
G | A | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+19669G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910347 | ||||||
| chr8:28910456
|
C | G | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-58+19778C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910456 | ||||||
| chr8:28910560
|
A | G | 8 | a0001c0001t0007g0010a0001c0001t0007g0012a0001c0001t0007g0013others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+19882A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910560 | ||||||
| chr8:28910576
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-58+19898G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910576 | ||||||
| chr8:28910808
|
A | G | 2 | a0001c0001t0001g0320a0001c0001t0001g0323 | 2 | NA18954.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-58+20130A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910808 | ||||||
| chr8:28910876
|
C | T | 4 | a0001c0001t0005g0161a0001c0001t0005g0199a0001c0001t0005g0200others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+20198C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910876 | ||||||
| chr8:28910882
|
C | T | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-58+20204C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28910882 | ||||||
| chr8:28911017
|
GTGTTTCA others(7): Show |
G | 1 | a0001c0001t0007g0009 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-58+20341_-58+2035 others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28911017 | |||||
| chr8:28911164
|
C | G | 2 | a0001c0001t0003g0121a0001c0001t0008g0120 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+20486C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911164 | ||||||
| chr8:28911238
|
A | G | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-58+20560A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911238 | ||||||
| chr8:28911253
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-58+20575G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911253 | ||||||
| chr8:28911259
|
G | T | 1 | a0001c0001t0005g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-58+20581G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911259 | ||||||
| chr8:28911365
|
G | C | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-58+20687G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911365 | ||||||
| chr8:28911403
|
T | G | 2 | a0001c0001t0003g0119a0001c0001t0010g0302 | 2 | HG02055.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-58+20725T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911403 | ||||||
| chr8:28911484
|
TAGCTAGG others(2636): Show |
T | 1 | a0001c0001t0006g0331 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-58+20808_-58+2345 others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28911484 | |||||
| chr8:28911535
|
T | A | 3 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120 | 3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+20857T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911535 | ||||||
| chr8:28911589
|
C | G | 2 | a0001c0001t0001g0272a0001c0001t0001g0287 | 2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-58+20911C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911589 | ||||||
| chr8:28911596
|
T | G | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+20918T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911596 | ||||||
| chr8:28911617
|
A | G | 1 | a0001c0001t0002g0198 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-58+20939A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911617 | ||||||
| chr8:28911645
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-58+20967C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911645 | ||||||
| chr8:28911679
|
G | T | 1 | a0001c0001t0001g0293 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-58+21001G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911679 | ||||||
| chr8:28911730
|
G | T | 335 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(332): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.-58+21052G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911730 | ||||||
| chr8:28911731
|
T | C | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+21053T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28911731 | ||||||
| chr8:28912164
|
T | G | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+21486T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912164 | ||||||
| chr8:28912368
|
A | C | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-58+21690A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912368 | ||||||
| chr8:28912404
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-58+21726A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912404 | ||||||
| chr8:28912438
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-58+21760A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912438 | ||||||
| chr8:28912448
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-58+21770T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912448 | ||||||
| chr8:28912615
|
C | T | 54 | a0001c0001t0001g0084a0001c0001t0002g0083a0001c0001t0003g0005others(51): Show | 54 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-58+21937C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912615 | ||||||
| chr8:28912631
|
C | G | 1 | a0001c0001t0003g0088 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-58+21953C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912631 | ||||||
| chr8:28912697
|
T | A | 1 | a0001c0001t0005g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-58+22019T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912697 | ||||||
| chr8:28912808
|
C | T | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-58+22130C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912808 | ||||||
| chr8:28912901
|
A | G | 1 | a0001c0001t0002g0241 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-58+22223A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912901 | ||||||
| chr8:28912955
|
G | T | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+22277G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28912955 | ||||||
| chr8:28913342
|
A | T | 1 | a0001c0001t0001g0280 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-58+22664A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28913342 | ||||||
| chr8:28913840
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-58+23162T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28913840 | ||||||
| chr8:28913855
|
C | CT | 16 | a0001c0001t0001g0140a0001c0001t0001g0282a0001c0001t0002g0138others(13): Show | 16 | HG02027.hp1 HG02056.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+23198dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28913855 | |||||
| chr8:28913855
|
CT | C | 13 | a0001c0001t0001g0084a0001c0001t0001g0303a0001c0001t0001g0307others(10): Show | 13 | HG02027.hp2 HG02559.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-58+23198delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28913855 | |||||
| chr8:28913855
|
CTT | C | 44 | a0001c0001t0002g0083a0001c0001t0002g0171a0001c0001t0003g0005others(41): Show | 44 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.-58+23197_-58+2319 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28913855 | |||||
| chr8:28913884
|
C | CGG | 5 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0090others(2): Show | 5 | NA18968.hp2 NA18982.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+23207_-58+2320 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28913884 | |||||
| chr8:28914129
|
A | C | 1 | a0001c0001t0006g0331 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-58+23451A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914129 | ||||||
| chr8:28914321
|
C | T | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+23643C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914321 | ||||||
| chr8:28914413
|
T | C | 1 | a0001c0001t0004g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-58+23735T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914413 | ||||||
| chr8:28914450
|
A | T | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+23772A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914450 | ||||||
| chr8:28914619
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-58+23941A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914619 | ||||||
| chr8:28914626
|
C | T | 312 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(309): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.-58+23948C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914626 | ||||||
| chr8:28914721
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-58+24043G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28914721 | ||||||
| chr8:28915056
|
C | A | 1 | a0001c0001t0018g0304 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-58+24378C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915056 | ||||||
| chr8:28915140
|
C | A | 1 | a0001c0001t0004g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-58+24462C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915140 | ||||||
| chr8:28915160
|
C | G | 1 | a0001c0001t0003g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-58+24482C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915160 | ||||||
| chr8:28915279
|
T | C | 15 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(12): Show | 15 | HG00741.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-58+24601T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915279 | ||||||
| chr8:28915327
|
G | A | 1 | a0001c0001t0008g0065 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-58+24649G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915327 | ||||||
| chr8:28915332
|
C | T | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-58+24654C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915332 | ||||||
| chr8:28915384
|
C | G | 1 | a0001c0001t0002g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-58+24706C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915384 | ||||||
| chr8:28915430
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-58+24752G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915430 | ||||||
| chr8:28915556
|
C | CA | 24 | a0001c0001t0003g0007a0001c0001t0003g0099a0001c0001t0003g0113others(21): Show | 24 | HG00738.hp1 HG00741.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-58+24901dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28915556 | |||||
| chr8:28915556
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0009g0131 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-58+24892_-58+2490 others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28915556 | |||||
| chr8:28915556
|
CAAAAAAA others(4): Show |
C | 195 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(192): Show | 195 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-58+24891_-58+2490 others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28915556 | |||||
| chr8:28915578
|
A | G | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+24900A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28915578 | ||||||
| chr8:28916459
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(1): Show | 4 | NA18947.hp2 NA18990.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+25781G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28916459 | ||||||
| chr8:28916523
|
A | C | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+25845A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28916523 | ||||||
| chr8:28916615
|
A | G | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+25937A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28916615 | ||||||
| chr8:28916789
|
A | C | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-58+26111A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28916789 | ||||||
| chr8:28916912
|
TA | T | 3 | a0001c0001t0002g0244a0001c0001t0003g0086a0001c0001t0006g0107 | 3 | NA18949.hp1 NA18949.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-58+26239delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28916912 | |||||
| chr8:28917066
|
C | CA | 67 | a0001c0001t0001g0084a0001c0001t0001g0221a0001c0001t0001g0257others(64): Show | 67 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.-58+26407dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28917066 | |||||
| chr8:28917103
|
T | C | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+26425T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28917103 | ||||||
| chr8:28917477
|
A | G | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-58+26799A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28917477 | ||||||
| chr8:28917623
|
T | G | 2 | a0001c0001t0003g0232a0001c0001t0003g0269 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-58+26945T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28917623 | ||||||
| chr8:28918022
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-58+27344A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918022 | ||||||
| chr8:28918105
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+27427C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918105 | ||||||
| chr8:28918595
|
A | T | 3 | a0001c0001t0005g0199a0001c0001t0005g0200a0001c0001t0005g0215 | 3 | HG02559.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-58+27917A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918595 | ||||||
| chr8:28918596
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-58+27918C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918596 | ||||||
| chr8:28918611
|
C | G | 2 | a0001c0001t0003g0121a0001c0001t0008g0120 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+27933C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918611 | ||||||
| chr8:28918717
|
C | T | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-58+28039C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918717 | ||||||
| chr8:28918721
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-58+28043G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918721 | ||||||
| chr8:28918767
|
TAGTA | T | 52 | a0001c0001t0001g0084a0001c0001t0002g0171a0001c0001t0002g0244others(49): Show | 52 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.-58+28094_-58+2809 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28918767 | |||||
| chr8:28918966
|
T | C | 3 | a0001c0001t0013g0037a0001c0001t0013g0050a0001c0001t0020g0052 | 3 | HG02027.hp1 NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-58+28288T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28918966 | ||||||
| chr8:28919364
|
C | G | 2 | a0001c0001t0004g0025a0001c0001t0004g0028 | 2 | HG00323.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-58+28686C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28919364 | ||||||
| chr8:28919392
|
T | C | 312 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(309): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.-58+28714T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28919392 | ||||||
| chr8:28919510
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-58+28832G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28919510 | ||||||
| chr8:28919817
|
C | G | 1 | a0001c0001t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+29139C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28919817 | ||||||
| chr8:28919971
|
T | TTG | 4 | a0001c0001t0003g0091a0001c0001t0003g0099a0001c0001t0004g0059others(1): Show | 4 | HG02145.hp1 HG03540.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+29323_-58+2932 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28919971 | |||||
| chr8:28919971
|
TTG | T | 33 | a0001c0001t0001g0243a0001c0001t0001g0257a0001c0001t0001g0308others(30): Show | 33 | HG00544.hp1 HG00609.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.-58+29323_-58+2932 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28919971 | |||||
| chr8:28919971
|
TTGTG | T | 176 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(173): Show | 176 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-58+29321_-58+2932 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28919971 | |||||
| chr8:28919971
|
TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+29317_-58+2932 others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28919971 | |||||
| chr8:28919971
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-58+29315_-58+2932 others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28919971 | |||||
| chr8:28920022
|
G | C | 2 | a0001c0001t0003g0121a0001c0001t0008g0120 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+29344G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920022 | ||||||
| chr8:28920084
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-58+29406G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920084 | ||||||
| chr8:28920160
|
T | G | 1 | a0001c0001t0002g0242 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-58+29482T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920160 | ||||||
| chr8:28920235
|
G | A | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+29557G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920235 | ||||||
| chr8:28920333
|
A | T | 1 | a0001c0001t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+29655A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920333 | ||||||
| chr8:28920525
|
C | T | 11 | a0001c0001t0002g0202a0001c0001t0002g0208a0001c0001t0002g0209others(8): Show | 11 | NA18612.hp1 NA18941.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+29847C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920525 | ||||||
| chr8:28920579
|
C | G | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+29901C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920579 | ||||||
| chr8:28920715
|
G | A | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+30037G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28920715 | ||||||
| chr8:28921246
|
G | T | 1 | a0001c0001t0014g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-58+30568G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921246 | ||||||
| chr8:28921312
|
G | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0279 | 2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-58+30634G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921312 | ||||||
| chr8:28921344
|
C | T | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+30666C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921344 | ||||||
| chr8:28921347
|
A | T | 4 | a0001c0001t0004g0123a0001c0001t0004g0124a0001c0001t0004g0125others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+30669A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921347 | ||||||
| chr8:28921367
|
A | C | 1 | a0001c0001t0001g0289 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-58+30689A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921367 | ||||||
| chr8:28921553
|
A | G | 3 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0028 | 3 | HG00323.hp2 HG02004.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-58+30875A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921553 | ||||||
| chr8:28921686
|
A | C | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+31008A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921686 | ||||||
| chr8:28921695
|
A | G | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+31017A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921695 | ||||||
| chr8:28921707
|
A | T | 1 | a0001c0001t0002g0240 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-58+31029A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921707 | ||||||
| chr8:28921720
|
A | C | 1 | a0001c0001t0017g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-58+31042A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921720 | ||||||
| chr8:28921805
|
A | G | 1 | a0001c0001t0002g0198 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-58+31127A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921805 | ||||||
| chr8:28921929
|
A | G | 1 | a0001c0001t0006g0328 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-58+31251A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28921929 | ||||||
| chr8:28922215
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-58+31537G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922215 | ||||||
| chr8:28922283
|
C | T | 1 | a0001c0001t0003g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-58+31605C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922283 | ||||||
| chr8:28922305
|
C | T | 1 | a0001c0001t0021g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-58+31627C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922305 | ||||||
| chr8:28922366
|
G | A | 1 | a0001c0001t0004g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-58+31688G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922366 | ||||||
| chr8:28922562
|
C | G | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+31884C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922562 | ||||||
| chr8:28922613
|
A | G | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+31935A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922613 | ||||||
| chr8:28922841
|
G | A | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+32163G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922841 | ||||||
| chr8:28922896
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-58+32218A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922896 | ||||||
| chr8:28922943
|
T | C | 79 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-58+32265T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922943 | ||||||
| chr8:28922986
|
G | A | 1 | a0001c0001t0005g0300 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-58+32308G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28922986 | ||||||
| chr8:28923216
|
T | C | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-58+32538T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923216 | ||||||
| chr8:28923226
|
T | A | 1 | a0001c0001t0004g0039 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-58+32548T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923226 | ||||||
| chr8:28923272
|
G | A | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-58+32594G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923272 | ||||||
| chr8:28923347
|
C | G | 1 | a0001c0001t0002g0241 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-58+32669C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923347 | ||||||
| chr8:28923443
|
A | C | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+32765A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923443 | ||||||
| chr8:28923753
|
G | A | 1 | a0001c0001t0002g0172 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-58+33075G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923753 | ||||||
| chr8:28923831
|
T | G | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58+33153T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923831 | ||||||
| chr8:28923861
|
T | C | 1 | a0001c0001t0010g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-58+33183T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28923861 | ||||||
| chr8:28924016
|
G | T | 1 | a0001c0001t0004g0023 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-58+33338G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924016 | ||||||
| chr8:28924044
|
A | G | 1 | a0001c0001t0004g0049 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-58+33366A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924044 | ||||||
| chr8:28924050
|
C | T | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+33372C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924050 | ||||||
| chr8:28924101
|
G | GT | 84 | a0001c0001t0001g0283a0001c0001t0002g0083a0001c0001t0002g0132others(81): Show | 84 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-58+33432dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28924101 | |||||
| chr8:28924112
|
G | T | 3 | a0001c0001t0001g0316a0001c0001t0002g0184a0001c0001t0002g0240 | 3 | HG00642.hp1 NA19043.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-58+33434G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924112 | ||||||
| chr8:28924112
|
GTT | G | 8 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(5): Show | 8 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+33445_-58+3344 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28924112 | |||||
| chr8:28924175
|
T | C | 1 | a0001c0001t0003g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-58+33497T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924175 | ||||||
| chr8:28924194
|
C | T | 2 | a0001c0001t0003g0087a0001c0001t0003g0103 | 2 | HG02040.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-58+33516C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924194 | ||||||
| chr8:28924208
|
G | A | 1 | a0001c0001t0004g0040 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-58+33530G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924208 | ||||||
| chr8:28924359
|
C | T | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-58+33681C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924359 | ||||||
| chr8:28924450
|
A | AT | 7 | a0001c0001t0002g0193a0001c0001t0002g0212a0001c0001t0003g0325others(4): Show | 7 | HG00741.hp2 HG01358.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+33791dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28924450 | |||||
| chr8:28924450
|
AT | A | 118 | a0001c0001t0001g0084a0001c0001t0001g0148a0001c0001t0001g0317others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-58+33791delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28924450 | |||||
| chr8:28924451
|
T | A | 2 | a0001c0001t0002g0223a0001c0001t0011g0224 | 2 | NA18956.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-58+33773T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924451 | ||||||
| chr8:28924471
|
G | A | 2 | a0001c0001t0003g0075a0001c0001t0003g0088 | 2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-58+33793G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924471 | ||||||
| chr8:28924471
|
G | T | 1 | a0001c0001t0004g0022 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-58+33793G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924471 | ||||||
| chr8:28924526
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-58+33848A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924526 | ||||||
| chr8:28924619
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-58+33941A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924619 | ||||||
| chr8:28924698
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-58+34020C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924698 | ||||||
| chr8:28924703
|
C | T | 8 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(5): Show | 8 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+34025C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924703 | ||||||
| chr8:28924768
|
G | A | 2 | a0001c0001t0007g0061a0001c0001t0010g0313 | 2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-58+34090G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924768 | ||||||
| chr8:28924800
|
C | A | 1 | a0001c0001t0001g0250 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-58+34122C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924800 | ||||||
| chr8:28924901
|
C | T | 11 | a0001c0001t0003g0133a0001c0001t0003g0168a0001c0001t0003g0170others(8): Show | 11 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+34223C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924901 | ||||||
| chr8:28924903
|
C | T | 1 | a0001c0001t0003g0066 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-58+34225C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28924903 | ||||||
| chr8:28924913
|
CT | C | 8 | a0001c0001t0001g0273a0001c0001t0002g0186a0001c0001t0004g0031others(5): Show | 8 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+34253delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28924913 | |||||
| chr8:28925002
|
C | T | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+34324C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925002 | ||||||
| chr8:28925011
|
AT | A | 8 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0004g0003others(5): Show | 8 | HG00741.hp2 HG01069.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+34346delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28925011 | |||||
| chr8:28925160
|
T | C | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-58+34482T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925160 | ||||||
| chr8:28925336
|
C | G | 1 | a0001c0001t0002g0153 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-58+34658C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925336 | ||||||
| chr8:28925515
|
T | G | 2 | a0001c0001t0004g0025a0001c0001t0004g0028 | 2 | HG00323.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-58+34837T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925515 | ||||||
| chr8:28925640
|
GA | G | 231 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(228): Show | 231 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-58+34972delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28925640 | |||||
| chr8:28925761
|
A | G | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+35083A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925761 | ||||||
| chr8:28925986
|
T | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-58+35308T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28925986 | ||||||
| chr8:28926178
|
T | C | 1 | a0001c0001t0003g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-58+35500T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926178 | ||||||
| chr8:28926210
|
A | G | 6 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+35532A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926210 | ||||||
| chr8:28926219
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(1): Show | 4 | NA18947.hp2 NA18990.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+35541C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926219 | ||||||
| chr8:28926282
|
GAT | G | 22 | a0001c0001t0002g0241a0001c0001t0003g0113a0001c0001t0004g0031others(19): Show | 22 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.-58+35626_-58+3562 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926282 | |||||
| chr8:28926300
|
T | C | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+35622T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926300 | ||||||
| chr8:28926302
|
T | C | 12 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+35624T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926302 | ||||||
| chr8:28926302
|
T | TAC | 7 | a0001c0001t0001g0136a0001c0001t0001g0263a0001c0001t0001g0272others(4): Show | 7 | HG00140.hp1 HG00741.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+35625_-58+3562 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926302 | |||||
| chr8:28926302
|
T | TACAC | 8 | a0001c0001t0001g0084a0001c0001t0003g0082a0001c0001t0003g0086others(5): Show | 8 | HG02027.hp2 HG03195.hp2 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+35625_-58+3562 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926302 | |||||
| chr8:28926304
|
T | C | 176 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-58+35626T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926304 | ||||||
| chr8:28926304
|
T | TAC | 127 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0148others(124): Show | 127 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-58+35644_-58+3564 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | |||||
| chr8:28926304
|
T | TACAC | 4 | a0001c0001t0002g0193a0001c0001t0003g0067a0001c0001t0005g0177others(1): Show | 4 | HG00280.hp2 HG01123.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+35642_-58+3564 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | |||||
| chr8:28926304
|
T | TACACAC | 3 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0010g0302 | 3 | HG02055.hp2 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-58+35640_-58+3564 others(10): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | |||||
| chr8:28926304
|
T | TATACACA others(7): Show |
1 | a0001c0001t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+35627_-58+3562 others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | |||||
| chr8:28926304
|
T | TATACACA others(9): Show |
2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-58+35627_-58+3562 others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | |||||
| chr8:28926304
|
T | TATATACA others(9): Show |
1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-58+35627_-58+3562 others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | |||||
| chr8:28926304
|
T | TATATATA others(23): Show |
1 | a0001c0001t0003g0326 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-58+35627_-58+3562 others(34): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | |||||
| chr8:28926304
|
T | TATATATA others(25): Show |
1 | a0001c0001t0003g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-58+35627_-58+3562 others(36): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28926304 | |||||
| chr8:28926306
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-58+35628C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926306 | ||||||
| chr8:28926324
|
T | C | 1 | a0001c0001t0002g0233 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-58+35646T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926324 | ||||||
| chr8:28926416
|
A | C | 2 | a0001c0001t0003g0121a0001c0001t0008g0120 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-58+35738A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926416 | ||||||
| chr8:28926498
|
T | C | 200 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(197): Show | 200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.-58+35820T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926498 | ||||||
| chr8:28926591
|
C | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | NA18975.hp2 NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-58+35913C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926591 | ||||||
| chr8:28926635
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-58+35957G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926635 | ||||||
| chr8:28926705
|
C | A | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+36027C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926705 | ||||||
| chr8:28926825
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-58+36147G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926825 | ||||||
| chr8:28926867
|
A | G | 2 | a0001c0001t0003g0066a0001c0001t0003g0068 | 2 | NA18962.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-58+36189A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28926867 | ||||||
| chr8:28927047
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-58+36369A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927047 | ||||||
| chr8:28927159
|
ATAAAATG others(1): Show |
A | 4 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+36483_-58+3649 others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927159 | |||||
| chr8:28927169
|
T | G | 4 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+36491T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927169 | ||||||
| chr8:28927369
|
A | G | 1 | a0001c0001t0010g0216 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-57-36442A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927369 | ||||||
| chr8:28927389
|
T | C | 113 | a0001c0001t0001g0290a0001c0001t0002g0083a0001c0001t0002g0132others(110): Show | 113 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-57-36422T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927389 | ||||||
| chr8:28927424
|
C | T | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-36387C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927424 | ||||||
| chr8:28927524
|
TAGG | T | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-36276_-57-3627 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927524 | |||||
| chr8:28927696
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57-36115A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927696 | ||||||
| chr8:28927718
|
C | A | 343 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(340): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.-57-36093C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927718 | ||||||
| chr8:28927734
|
T | C | 343 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(340): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.-57-36077T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927734 | ||||||
| chr8:28927736
|
A | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-57-36075A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927736 | ||||||
| chr8:28927741
|
A | G | 343 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(340): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.-57-36070A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927741 | ||||||
| chr8:28927809
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-57-36002C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927809 | ||||||
| chr8:28927831
|
C | CA | 99 | a0001c0001t0001g0084a0001c0001t0001g0140a0001c0001t0001g0141others(96): Show | 99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-57-35956dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927831 | |||||
| chr8:28927831
|
C | CAA | 21 | a0001c0001t0001g0136a0001c0001t0001g0148a0001c0001t0001g0149others(18): Show | 21 | HG00423.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-57-35957_-57-3595 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927831 | |||||
| chr8:28927831
|
CA | C | 107 | a0001c0001t0001g0290a0001c0001t0002g0083a0001c0001t0002g0132others(104): Show | 107 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-57-35956delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927831 | |||||
| chr8:28927831
|
CAA | C | 9 | a0001c0001t0002g0201a0001c0001t0002g0225a0001c0001t0002g0228others(6): Show | 9 | HG02572.hp1 HG02897.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-35957_-57-3595 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28927831 | |||||
| chr8:28927856
|
G | A | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG00423.hp1 HG02071.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-35955G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927856 | ||||||
| chr8:28927872
|
C | G | 111 | a0001c0001t0001g0290a0001c0001t0002g0083a0001c0001t0002g0132others(108): Show | 111 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-57-35939C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927872 | ||||||
| chr8:28927874
|
C | T | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-35937C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927874 | ||||||
| chr8:28927893
|
T | A | 4 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-35918T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28927893 | ||||||
| chr8:28928010
|
C | G | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57-35801C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28928010 | ||||||
| chr8:28928093
|
C | G | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57-35718C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28928093 | ||||||
| chr8:28928133
|
CA | C | 9 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0003g0325others(6): Show | 9 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-35666delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28928133 | |||||
| chr8:28928468
|
A | T | 70 | a0001c0001t0001g0084a0001c0001t0003g0005a0001c0001t0003g0006others(67): Show | 70 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.-57-35343A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28928468 | ||||||
| chr8:28928708
|
C | T | 2 | a0001c0001t0008g0097a0001c0001t0008g0098 | 2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-57-35103C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28928708 | ||||||
| chr8:28929150
|
G | T | 7 | a0001c0001t0004g0044a0001c0001t0004g0045a0001c0001t0004g0046others(4): Show | 7 | HG00544.hp2 HG00597.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57-34661G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929150 | ||||||
| chr8:28929160
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-57-34651A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929160 | ||||||
| chr8:28929203
|
G | A | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-34608G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929203 | ||||||
| chr8:28929256
|
C | G | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-34555C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929256 | ||||||
| chr8:28929262
|
C | T | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-34549C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929262 | ||||||
| chr8:28929348
|
A | T | 1 | a0001c0001t0002g0238 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-57-34463A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929348 | ||||||
| chr8:28929498
|
A | G | 2 | a0001c0001t0002g0157a0001c0001t0002g0158 | 2 | NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-57-34313A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929498 | ||||||
| chr8:28929585
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57-34226T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929585 | ||||||
| chr8:28929624
|
A | C | 1 | a0001c0001t0007g0009 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-57-34187A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929624 | ||||||
| chr8:28929731
|
A | C | 1 | a0001c0001t0004g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-57-34080A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929731 | ||||||
| chr8:28929846
|
G | A | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-33965G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929846 | ||||||
| chr8:28929926
|
G | GC | 7 | a0001c0001t0001g0084a0001c0001t0001g0142a0001c0001t0001g0306others(4): Show | 7 | HG02027.hp2 HG02615.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-33879dupC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28929926 | |||||
| chr8:28929933
|
G | GC | 24 | a0001c0001t0001g0147a0001c0001t0001g0276a0001c0001t0001g0284others(21): Show | 24 | HG01167.hp1 HG01261.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.-57-33875dupC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28929933 | |||||
| chr8:28929937
|
G | A | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-33874G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929937 | ||||||
| chr8:28929937
|
G | C | 2 | a0001c0001t0008g0102a0001c0002t0002g0211 | 2 | HG01496.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-57-33874G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929937 | ||||||
| chr8:28929937
|
G | GC | 8 | a0001c0001t0001g0220a0001c0001t0001g0254a0001c0001t0001g0279others(5): Show | 8 | HG00741.hp2 HG01175.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57-33868dupC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28929937 | |||||
| chr8:28929938
|
C | G | 1 | a0001c0001t0008g0102 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-57-33873C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929938 | ||||||
| chr8:28929942
|
C | T | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-33869C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28929942 | ||||||
| chr8:28930008
|
C | G | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-33803C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930008 | ||||||
| chr8:28930272
|
T | C | 1 | a0001c0001t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-57-33539T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930272 | ||||||
| chr8:28930296
|
G | T | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-33515G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930296 | ||||||
| chr8:28930325
|
A | G | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-33486A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930325 | ||||||
| chr8:28930442
|
A | T | 2 | a0001c0001t0004g0124a0001c0001t0004g0126 | 2 | HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-57-33369A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930442 | ||||||
| chr8:28930516
|
G | A | 194 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(191): Show | 194 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-57-33295G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930516 | ||||||
| chr8:28930575
|
C | G | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57-33236C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930575 | ||||||
| chr8:28930815
|
A | G | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-57-32996A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930815 | ||||||
| chr8:28930840
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-57-32971C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930840 | ||||||
| chr8:28930846
|
A | G | 6 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-32965A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28930846 | ||||||
| chr8:28931124
|
T | C | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-32687T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931124 | ||||||
| chr8:28931549
|
T | G | 1 | a0001c0001t0012g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-57-32262T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931549 | ||||||
| chr8:28931581
|
A | G | 1 | a0001c0001t0004g0051 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-57-32230A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931581 | ||||||
| chr8:28931623
|
C | T | 2 | a0001c0001t0003g0232a0001c0001t0003g0269 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57-32188C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931623 | ||||||
| chr8:28931734
|
C | T | 11 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57-32077C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931734 | ||||||
| chr8:28931758
|
C | G | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-32053C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931758 | ||||||
| chr8:28931816
|
C | T | 110 | a0001c0001t0001g0290a0001c0001t0002g0083a0001c0001t0002g0132others(107): Show | 110 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-57-31995C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931816 | ||||||
| chr8:28931833
|
A | T | 1 | a0001c0001t0005g0162 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-57-31978A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28931833 | ||||||
| chr8:28932193
|
C | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31618C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932193 | ||||||
| chr8:28932195
|
G | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31616G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932195 | ||||||
| chr8:28932200
|
A | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31611A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932200 | ||||||
| chr8:28932201
|
C | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31610C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932201 | ||||||
| chr8:28932202
|
G | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31609G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932202 | ||||||
| chr8:28932209
|
G | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31602G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932209 | ||||||
| chr8:28932211
|
G | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31600G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932211 | ||||||
| chr8:28932213
|
C | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31598C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932213 | ||||||
| chr8:28932214
|
T | C | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31597T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932214 | ||||||
| chr8:28932215
|
A | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31596A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932215 | ||||||
| chr8:28932216
|
G | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31595G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932216 | ||||||
| chr8:28932217
|
G | A | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31594G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932217 | ||||||
| chr8:28932218
|
G | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31593G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932218 | ||||||
| chr8:28932220
|
A | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31591A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932220 | ||||||
| chr8:28932221
|
T | C | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31590T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932221 | ||||||
| chr8:28932222
|
G | C | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31589G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932222 | ||||||
| chr8:28932223
|
G | A | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31588G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932223 | ||||||
| chr8:28932230
|
A | C | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31581A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932230 | ||||||
| chr8:28932232
|
G | A | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31579G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932232 | ||||||
| chr8:28932233
|
G | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31578G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932233 | ||||||
| chr8:28932234
|
G | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31577G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932234 | ||||||
| chr8:28932237
|
G | C | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31574G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932237 | ||||||
| chr8:28932238
|
A | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31573A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932238 | ||||||
| chr8:28932240
|
G | C | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31571G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932240 | ||||||
| chr8:28932241
|
C | A | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31570C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932241 | ||||||
| chr8:28932243
|
A | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31568A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932243 | ||||||
| chr8:28932247
|
C | G | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31564C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932247 | ||||||
| chr8:28932249
|
T | G | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31562T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932249 | ||||||
| chr8:28932252
|
A | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31559A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932252 | ||||||
| chr8:28932253
|
A | G | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31558A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932253 | ||||||
| chr8:28932254
|
G | T | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31557G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932254 | ||||||
| chr8:28932255
|
G | C | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-57-31556G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932255 | ||||||
| chr8:28932274
|
G | A | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-57-31537G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932274 | ||||||
| chr8:28932414
|
G | A | 2 | a0001c0001t0012g0156a0001c0001t0012g0297 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-57-31397G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932414 | ||||||
| chr8:28932683
|
A | G | 1 | a0001c0001t0007g0011 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-57-31128A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932683 | ||||||
| chr8:28932725
|
T | G | 11 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57-31086T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932725 | ||||||
| chr8:28932794
|
G | T | 1 | a0001c0001t0007g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57-31017G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932794 | ||||||
| chr8:28932795
|
C | T | 1 | a0001c0001t0007g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57-31016C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932795 | ||||||
| chr8:28932810
|
C | G | 1 | a0001c0001t0003g0108 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-57-31001C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28932810 | ||||||
| chr8:28933069
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-57-30742C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933069 | ||||||
| chr8:28933101
|
G | C | 336 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(333): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(333): Show |
intron_variant | MODIFIER | c.-57-30710G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933101 | ||||||
| chr8:28933121
|
G | A | 3 | a0001c0001t0001g0291a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG01070.hp2 HG03704.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-57-30690G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933121 | ||||||
| chr8:28933378
|
C | T | 3 | a0001c0001t0001g0291a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG01070.hp2 HG03704.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-57-30433C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933378 | ||||||
| chr8:28933571
|
A | G | 2 | a0001c0001t0002g0152a0001c0001t0002g0154 | 2 | HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-57-30240A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933571 | ||||||
| chr8:28933598
|
C | A | 1 | a0001c0001t0005g0162 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-57-30213C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933598 | ||||||
| chr8:28933598
|
C | G | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-57-30213C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933598 | ||||||
| chr8:28933642
|
G | A | 219 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(216): Show | 219 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-57-30169G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933642 | ||||||
| chr8:28933949
|
A | G | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-29862A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933949 | ||||||
| chr8:28933990
|
A | C | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-29821A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28933990 | ||||||
| chr8:28934281
|
T | G | 1 | a0001c0001t0003g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-57-29530T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934281 | ||||||
| chr8:28934445
|
A | G | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-29366A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934445 | ||||||
| chr8:28934582
|
T | G | 1 | a0001c0001t0007g0015 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57-29229T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934582 | ||||||
| chr8:28934647
|
C | T | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-29164C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934647 | ||||||
| chr8:28934705
|
C | T | 1 | a0001c0001t0004g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-57-29106C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934705 | ||||||
| chr8:28934926
|
C | CA | 83 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(80): Show | 83 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-57-28868dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28934926 | |||||
| chr8:28934968
|
C | T | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-28843C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28934968 | ||||||
| chr8:28935264
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-57-28547G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935264 | ||||||
| chr8:28935385
|
A | T | 1 | a0001c0001t0003g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-57-28426A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935385 | ||||||
| chr8:28935475
|
C | T | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-28336C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935475 | ||||||
| chr8:28935505
|
T | A | 1 | a0001c0001t0021g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57-28306T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935505 | ||||||
| chr8:28935506
|
T | A | 3 | a0001c0001t0001g0268a0001c0001t0001g0283a0001c0001t0001g0288 | 3 | HG00323.hp1 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-57-28305T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935506 | ||||||
| chr8:28935780
|
C | T | 1 | a0001c0001t0021g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57-28031C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28935780 | ||||||
| chr8:28936390
|
G | A | 1 | a0001c0001t0004g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-57-27421G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936390 | ||||||
| chr8:28936410
|
T | C | 206 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(203): Show | 206 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.-57-27401T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936410 | ||||||
| chr8:28936488
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0003g0118 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-57-27323C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936488 | ||||||
| chr8:28936513
|
A | T | 1 | a0001c0001t0004g0039 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-57-27298A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936513 | ||||||
| chr8:28936544
|
C | T | 1 | a0001c0001t0007g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-57-27267C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936544 | ||||||
| chr8:28936799
|
T | TA | 123 | a0001c0001t0001g0290a0001c0001t0002g0083a0001c0001t0002g0132others(120): Show | 123 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-57-26996dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28936799 | |||||
| chr8:28936799
|
TA | T | 6 | a0001c0001t0001g0316a0001c0001t0003g0325a0001c0001t0003g0326others(3): Show | 6 | HG00738.hp2 HG01243.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-26996delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28936799 | |||||
| chr8:28936849
|
G | C | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-26962G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936849 | ||||||
| chr8:28936874
|
A | T | 3 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120 | 3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57-26937A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28936874 | ||||||
| chr8:28937161
|
C | T | 214 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(211): Show | 214 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-57-26650C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937161 | ||||||
| chr8:28937339
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0256 | 2 | HG02040.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-57-26472G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937339 | ||||||
| chr8:28937505
|
A | G | 2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-57-26306A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937505 | ||||||
| chr8:28937617
|
C | T | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-26194C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937617 | ||||||
| chr8:28937630
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-57-26181A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937630 | ||||||
| chr8:28937829
|
G | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0090others(2): Show | 5 | NA18968.hp2 NA18982.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-25982G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937829 | ||||||
| chr8:28937879
|
ATACT | A | 54 | a0001c0001t0001g0084a0001c0001t0003g0005a0001c0001t0003g0006others(51): Show | 54 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-57-25929_-57-2592 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28937879 | |||||
| chr8:28937890
|
T | A | 2 | a0001c0001t0012g0156a0001c0001t0012g0297 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-57-25921T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28937890 | ||||||
| chr8:28938058
|
A | C | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-25753A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938058 | ||||||
| chr8:28938320
|
T | G | 1 | a0001c0001t0003g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-57-25491T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938320 | ||||||
| chr8:28938487
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57-25324G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938487 | ||||||
| chr8:28938675
|
T | A | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57-25136T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938675 | ||||||
| chr8:28938690
|
CTTT | C | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-25120_-57-2511 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938690 | ||||||
| chr8:28938714
|
G | A | 3 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120 | 3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57-25097G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938714 | ||||||
| chr8:28938791
|
T | TAGC | 230 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(227): Show | 230 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.-57-25020_-57-2501 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938791 | ||||||
| chr8:28938807
|
G | A | 54 | a0001c0001t0001g0084a0001c0001t0003g0005a0001c0001t0003g0006others(51): Show | 54 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-57-25004G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938807 | ||||||
| chr8:28938869
|
C | T | 1 | a0001c0001t0007g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57-24942C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28938869 | ||||||
| chr8:28939211
|
C | T | 81 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(78): Show | 81 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.-57-24600C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939211 | ||||||
| chr8:28939294
|
A | G | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-57-24517A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939294 | ||||||
| chr8:28939304
|
A | G | 1 | a0001c0001t0009g0131 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-57-24507A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939304 | ||||||
| chr8:28939496
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57-24315G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939496 | ||||||
| chr8:28939511
|
T | A | 4 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-24300T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939511 | ||||||
| chr8:28939570
|
C | T | 1 | a0001c0001t0004g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57-24241C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939570 | ||||||
| chr8:28939576
|
C | T | 9 | a0001c0001t0007g0010a0001c0001t0007g0011a0001c0001t0007g0012others(6): Show | 9 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-24235C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939576 | ||||||
| chr8:28939600
|
C | G | 1 | a0001c0001t0002g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-57-24211C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939600 | ||||||
| chr8:28939674
|
T | G | 1 | a0001c0001t0002g0318 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-57-24137T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939674 | ||||||
| chr8:28939730
|
G | A | 3 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120 | 3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57-24081G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939730 | ||||||
| chr8:28939735
|
C | T | 2 | a0001c0001t0001g0272a0001c0001t0001g0287 | 2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-57-24076C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939735 | ||||||
| chr8:28939927
|
A | C | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-23884A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939927 | ||||||
| chr8:28939971
|
A | G | 1 | a0001c0001t0004g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-57-23840A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939971 | ||||||
| chr8:28939973
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-23838A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28939973 | ||||||
| chr8:28940021
|
T | C | 2 | a0001c0001t0003g0121a0001c0001t0008g0120 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57-23790T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940021 | ||||||
| chr8:28940036
|
G | A | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-23775G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940036 | ||||||
| chr8:28940402
|
C | T | 1 | a0001c0001t0004g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-57-23409C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940402 | ||||||
| chr8:28940429
|
A | G | 8 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-23382A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940429 | ||||||
| chr8:28940859
|
C | T | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-22952C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940859 | ||||||
| chr8:28940923
|
T | A | 1 | a0001c0001t0003g0079 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-57-22888T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940923 | ||||||
| chr8:28940975
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0219 | 2 | NA18961.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-57-22836A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28940975 | ||||||
| chr8:28941111
|
C | T | 54 | a0001c0001t0001g0084a0001c0001t0003g0005a0001c0001t0003g0006others(51): Show | 54 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-57-22700C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941111 | ||||||
| chr8:28941117
|
A | T | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-57-22694A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941117 | ||||||
| chr8:28941267
|
C | T | 2 | a0001c0001t0001g0272a0001c0001t0001g0287 | 2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-57-22544C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941267 | ||||||
| chr8:28941276
|
G | T | 1 | a0001c0001t0004g0022 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-57-22535G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941276 | ||||||
| chr8:28941287
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-57-22524T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941287 | ||||||
| chr8:28941350
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-57-22461A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941350 | ||||||
| chr8:28941388
|
T | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0250a0001c0001t0001g0285 | 3 | NA18978.hp1 NA19065.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.-57-22423T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941388 | ||||||
| chr8:28941718
|
T | TA | 9 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0070others(6): Show | 9 | NA18968.hp2 NA18982.hp1 NA18985.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57-22084dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28941718 | |||||
| chr8:28941749
|
C | T | 21 | a0001c0001t0001g0140a0001c0001t0001g0229a0001c0001t0001g0243others(18): Show | 21 | HG00544.hp1 HG02056.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.-57-22062C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941749 | ||||||
| chr8:28941790
|
A | G | 3 | a0001c0001t0013g0037a0001c0001t0013g0050a0001c0001t0020g0052 | 3 | HG02027.hp1 NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-57-22021A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941790 | ||||||
| chr8:28941940
|
G | A | 1 | a0001c0001t0004g0045 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-57-21871G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941940 | ||||||
| chr8:28941982
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-57-21829C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28941982 | ||||||
| chr8:28942208
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-57-21603C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942208 | ||||||
| chr8:28942219
|
G | A | 1 | a0001c0001t0004g0043 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-57-21592G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942219 | ||||||
| chr8:28942248
|
G | C | 9 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0003g0325others(6): Show | 9 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-21563G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942248 | ||||||
| chr8:28942252
|
T | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0266 | 2 | HG01109.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-57-21559T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942252 | ||||||
| chr8:28942435
|
A | C | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-21376A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942435 | ||||||
| chr8:28942443
|
G | C | 1 | a0001c0001t0007g0012 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57-21368G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942443 | ||||||
| chr8:28942841
|
G | A | 1 | a0001c0001t0004g0035 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-57-20970G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942841 | ||||||
| chr8:28942868
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-57-20943C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28942868 | ||||||
| chr8:28943092
|
A | G | 11 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57-20719A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943092 | ||||||
| chr8:28943273
|
C | T | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-20538C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943273 | ||||||
| chr8:28943305
|
G | A | 5 | a0001c0001t0003g0070a0001c0001t0003g0071a0001c0001t0003g0072others(2): Show | 5 | NA18986.hp1 NA18998.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-20506G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943305 | ||||||
| chr8:28943528
|
G | T | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-20283G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943528 | ||||||
| chr8:28943683
|
G | C | 1 | a0001c0001t0004g0027 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-57-20128G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943683 | ||||||
| chr8:28943898
|
A | C | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-57-19913A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943898 | ||||||
| chr8:28943906
|
G | T | 1 | a0001c0001t0003g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-57-19905G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28943906 | ||||||
| chr8:28944000
|
T | C | 6 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-19811T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28944000 | ||||||
| chr8:28944380
|
T | C | 1 | a0001c0001t0004g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-57-19431T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28944380 | ||||||
| chr8:28944665
|
A | G | 1 | a0001c0001t0002g0186 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-57-19146A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28944665 | ||||||
| chr8:28944974
|
G | A | 2 | a0001c0001t0003g0239a0001c0001t0007g0061 | 2 | HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-57-18837G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28944974 | ||||||
| chr8:28945018
|
T | G | 1 | a0001c0001t0005g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-57-18793T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945018 | ||||||
| chr8:28945191
|
G | A | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-18620G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945191 | ||||||
| chr8:28945235
|
T | C | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-18576T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945235 | ||||||
| chr8:28945415
|
A | G | 238 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(235): Show | 238 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-57-18396A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945415 | ||||||
| chr8:28945558
|
G | C | 194 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(191): Show | 194 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-57-18253G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945558 | ||||||
| chr8:28945559
|
G | A | 1 | a0001c0001t0002g0206 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-57-18252G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945559 | ||||||
| chr8:28945698
|
T | G | 1 | a0001c0001t0002g0187 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-57-18113T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945698 | ||||||
| chr8:28945775
|
T | A | 2 | a0001c0001t0003g0093a0001c0001t0003g0095 | 2 | NA18980.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-57-18036T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945775 | ||||||
| chr8:28945799
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-57-18012A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945799 | ||||||
| chr8:28945823
|
G | A | 2 | a0001c0001t0002g0152a0001c0001t0002g0154 | 2 | HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-57-17988G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945823 | ||||||
| chr8:28945856
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-57-17955G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945856 | ||||||
| chr8:28945881
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-57-17930T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945881 | ||||||
| chr8:28945900
|
A | G | 1 | a0001c0001t0004g0048 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-57-17911A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945900 | ||||||
| chr8:28945937
|
G | C | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57-17874G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28945937 | ||||||
| chr8:28945944
|
C | CT | 30 | a0001c0001t0001g0143a0001c0001t0001g0250a0001c0001t0001g0254others(27): Show | 30 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57-17849dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28945944 | |||||
| chr8:28946102
|
A | G | 8 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-17709A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946102 | ||||||
| chr8:28946214
|
A | G | 12 | a0001c0001t0007g0004a0001c0001t0007g0009a0001c0001t0007g0010others(9): Show | 12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-17597A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946214 | ||||||
| chr8:28946227
|
A | C | 1 | a0001c0001t0005g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-57-17584A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946227 | ||||||
| chr8:28946296
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-57-17515G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946296 | ||||||
| chr8:28946579
|
A | AT | 7 | a0001c0001t0002g0295a0001c0001t0002g0296a0001c0001t0003g0121others(4): Show | 7 | HG02572.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-17232_-57-1723 others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946579 | ||||||
| chr8:28946579
|
A | T | 89 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(86): Show | 89 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-57-17232A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946579 | ||||||
| chr8:28946581
|
A | AT | 3 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0010g0302 | 3 | HG02055.hp2 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-57-17230_-57-1722 others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946581 | ||||||
| chr8:28946581
|
A | T | 202 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(199): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.-57-17230A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946581 | ||||||
| chr8:28946582
|
AT | A | 14 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-17228delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946582 | ||||||
| chr8:28946805
|
G | A | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-17006G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28946805 | ||||||
| chr8:28947089
|
C | T | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-16722C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28947089 | ||||||
| chr8:28947221
|
C | T | 1 | a0001c0001t0006g0328 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-57-16590C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28947221 | ||||||
| chr8:28947400
|
G | A | 1 | a0001c0001t0017g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-57-16411G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28947400 | ||||||
| chr8:28947636
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-16175A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28947636 | ||||||
| chr8:28947797
|
C | T | 77 | a0001c0001t0002g0083a0001c0001t0002g0132a0001c0001t0002g0134others(74): Show | 77 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-57-16014C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28947797 | ||||||
| chr8:28948132
|
G | A | 219 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(216): Show | 219 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-57-15679G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948132 | ||||||
| chr8:28948326
|
A | G | 2 | a0001c0001t0003g0101a0001c0001t0008g0102 | 2 | NA18959.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-57-15485A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948326 | ||||||
| chr8:28948340
|
A | T | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57-15471A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948340 | ||||||
| chr8:28948391
|
G | A | 16 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57-15420G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948391 | ||||||
| chr8:28948609
|
C | G | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-15202C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948609 | ||||||
| chr8:28948972
|
A | G | 1 | a0001c0001t0003g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-57-14839A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28948972 | ||||||
| chr8:28949284
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57-14527G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949284 | ||||||
| chr8:28949341
|
G | T | 1 | a0001c0001t0006g0327 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-57-14470G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949341 | ||||||
| chr8:28949504
|
T | C | 10 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(7): Show | 10 | HG00423.hp1 HG02071.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-14307T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949504 | ||||||
| chr8:28949797
|
A | C | 1 | a0001c0001t0007g0011 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-57-14014A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949797 | ||||||
| chr8:28949839
|
T | G | 223 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(220): Show | 223 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-57-13972T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949839 | ||||||
| chr8:28949870
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-57-13941A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28949870 | ||||||
| chr8:28950105
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-57-13706G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28950105 | ||||||
| chr8:28950383
|
A | G | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-13428A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28950383 | ||||||
| chr8:28950881
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-57-12930A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28950881 | ||||||
| chr8:28950885
|
G | A | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-12926G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28950885 | ||||||
| chr8:28950925
|
G | C | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-12886G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28950925 | ||||||
| chr8:28951136
|
T | C | 6 | a0001c0001t0006g0336a0001c0001t0006g0337a0001c0001t0006g0338others(3): Show | 6 | NA18943.hp2 NA18956.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-12675T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951136 | ||||||
| chr8:28951196
|
G | A | 1 | a0001c0001t0008g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57-12615G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951196 | ||||||
| chr8:28951219
|
A | C | 1 | a0001c0001t0002g0192 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-57-12592A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951219 | ||||||
| chr8:28951236
|
G | A | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57-12575G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951236 | ||||||
| chr8:28951240
|
C | G | 3 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120 | 3 | HG02280.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57-12571C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951240 | ||||||
| chr8:28951277
|
C | T | 5 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(2): Show | 5 | HG00140.hp2 HG00323.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-12534C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951277 | ||||||
| chr8:28951289
|
C | T | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-12522C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951289 | ||||||
| chr8:28951386
|
C | T | 9 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0003g0325others(6): Show | 9 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-12425C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951386 | ||||||
| chr8:28951806
|
G | A | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-12005G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951806 | ||||||
| chr8:28951821
|
C | G | 4 | a0001c0001t0009g0128a0001c0001t0009g0129a0001c0001t0009g0130others(1): Show | 4 | NA18974.hp2 NA18988.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11990C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28951821 | ||||||
| chr8:28952158
|
T | TA | 71 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0142others(68): Show | 71 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-57-11636dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28952158 | |||||
| chr8:28952158
|
TA | T | 15 | a0001c0001t0002g0171a0001c0001t0002g0319a0001c0001t0003g0072others(12): Show | 15 | HG00558.hp2 HG01167.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-11636delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28952158 | |||||
| chr8:28952279
|
G | A | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-11532G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952279 | ||||||
| chr8:28952346
|
G | C | 1 | a0001c0001t0003g0078 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-57-11465G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952346 | ||||||
| chr8:28952394
|
C | T | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-57-11417C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952394 | ||||||
| chr8:28952400
|
A | C | 1 | a0001c0001t0001g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-57-11411A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952400 | ||||||
| chr8:28952409
|
T | A | 3 | a0001c0001t0001g0289a0001c0001t0008g0001a0001c0001t0008g0002 | 3 | HG03225.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-57-11402T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952409 | ||||||
| chr8:28952434
|
A | G | 199 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(196): Show | 199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-57-11377A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28952434 | ||||||
| chr8:28953003
|
C | A | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-10808C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28953003 | ||||||
| chr8:28953917
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-57-9894C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28953917 | ||||||
| chr8:28954172
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-57-9639A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954172 | ||||||
| chr8:28954494
|
C | G | 1 | a0001c0001t0002g0191 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-57-9317C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954494 | ||||||
| chr8:28954573
|
C | G | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-9238C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954573 | ||||||
| chr8:28954691
|
A | T | 1 | a0001c0001t0002g0227 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-57-9120A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954691 | ||||||
| chr8:28954956
|
A | T | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-8855A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954956 | ||||||
| chr8:28954983
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-57-8828A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28954983 | ||||||
| chr8:28955327
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-57-8484C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955327 | ||||||
| chr8:28955366
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-57-8445A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955366 | ||||||
| chr8:28955631
|
T | A | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-57-8180T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955631 | ||||||
| chr8:28955638
|
C | T | 220 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(217): Show | 220 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-57-8173C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955638 | ||||||
| chr8:28955733
|
C | T | 1 | a0001c0001t0004g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-57-8078C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955733 | ||||||
| chr8:28955865
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-57-7946A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955865 | ||||||
| chr8:28955924
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-7887A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955924 | ||||||
| chr8:28955926
|
T | G | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-57-7885T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955926 | ||||||
| chr8:28955970
|
A | AAAAG | 117 | a0001c0001t0001g0084a0001c0001t0001g0220a0001c0001t0001g0289others(114): Show | 117 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-57-7838_-57-7837i others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28955970 | |||||
| chr8:28955970
|
A | AAAG | 188 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(185): Show | 188 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-57-7839_-57-7838i others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28955970 | |||||
| chr8:28955970
|
A | G | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57-7841A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28955970 | ||||||
| chr8:28956155
|
G | A | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-7656G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956155 | ||||||
| chr8:28956242
|
G | A | 1 | a0001c0001t0002g0241 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-57-7569G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956242 | ||||||
| chr8:28956261
|
G | C | 22 | a0001c0001t0001g0084a0001c0001t0003g0007a0001c0001t0003g0008others(19): Show | 22 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.-57-7550G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956261 | ||||||
| chr8:28956262
|
A | G | 2 | a0001c0001t0002g0192a0001c0001t0002g0242 | 2 | HG02071.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-57-7549A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956262 | ||||||
| chr8:28956317
|
A | C | 1 | a0001c0001t0004g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-57-7494A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956317 | ||||||
| chr8:28956492
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0279 | 2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-57-7319A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956492 | ||||||
| chr8:28956504
|
A | AT | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-7306dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28956504 | |||||
| chr8:28956517
|
TG | T | 3 | a0001c0001t0001g0289a0001c0001t0008g0001a0001c0001t0008g0002 | 3 | HG03225.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-57-7293delG | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956517 | ||||||
| chr8:28956636
|
A | G | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-7175A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956636 | ||||||
| chr8:28956675
|
G | C | 340 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(337): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.-57-7136G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956675 | ||||||
| chr8:28956809
|
C | G | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-7002C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28956809 | ||||||
| chr8:28957046
|
A | G | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-6765A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957046 | ||||||
| chr8:28957346
|
T | A | 340 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(337): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.-57-6465T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957346 | ||||||
| chr8:28957378
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-57-6433T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957378 | ||||||
| chr8:28957393
|
C | T | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-6418C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957393 | ||||||
| chr8:28957425
|
C | T | 1 | a0001c0001t0005g0300 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-57-6386C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957425 | ||||||
| chr8:28957470
|
C | A | 1 | a0001c0001t0001g0320 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-57-6341C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957470 | ||||||
| chr8:28957537
|
C | A | 4 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0008g0120others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-6274C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957537 | ||||||
| chr8:28957571
|
A | AAAAC | 312 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(309): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.-57-6236_-57-6233d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28957571 | |||||
| chr8:28957583
|
T | C | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-6228T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957583 | ||||||
| chr8:28957657
|
C | G | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-6154C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957657 | ||||||
| chr8:28957717
|
G | T | 8 | a0001c0001t0003g0121a0001c0001t0003g0325a0001c0001t0003g0326others(5): Show | 8 | HG02572.hp1 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-6094G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957717 | ||||||
| chr8:28957973
|
C | T | 1 | a0001c0001t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-57-5838C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28957973 | ||||||
| chr8:28958033
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57-5778A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958033 | ||||||
| chr8:28958375
|
A | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-57-5436A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958375 | ||||||
| chr8:28958601
|
A | C | 1 | a0001c0001t0003g0066 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-57-5210A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958601 | ||||||
| chr8:28958670
|
T | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-57-5141T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958670 | ||||||
| chr8:28958675
|
C | A | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-5136C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958675 | ||||||
| chr8:28958677
|
A | C | 84 | a0001c0001t0001g0316a0001c0001t0002g0083a0001c0001t0002g0132others(81): Show | 84 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-57-5134A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958677 | ||||||
| chr8:28958858
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-4953A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28958858 | ||||||
| chr8:28959255
|
C | G | 12 | a0001c0001t0007g0004a0001c0001t0007g0009a0001c0001t0007g0010others(9): Show | 12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-4556C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959255 | ||||||
| chr8:28959295
|
A | G | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-4516A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959295 | ||||||
| chr8:28959335
|
G | A | 220 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(217): Show | 220 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-57-4476G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959335 | ||||||
| chr8:28959362
|
C | G | 2 | a0001c0001t0008g0097a0001c0001t0008g0098 | 2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-57-4449C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959362 | ||||||
| chr8:28959460
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0243 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-57-4351C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959460 | ||||||
| chr8:28959472
|
G | A | 1 | a0001c0001t0010g0216 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-57-4339G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959472 | ||||||
| chr8:28959520
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-57-4291A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959520 | ||||||
| chr8:28959796
|
A | G | 2 | a0001c0001t0012g0156a0001c0001t0012g0297 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-57-4015A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28959796 | ||||||
| chr8:28959875
|
G | GT | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-3932dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28959875 | |||||
| chr8:28960165
|
A | G | 3 | a0001c0001t0005g0199a0001c0001t0005g0200a0001c0001t0005g0215 | 3 | HG02559.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-57-3646A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960165 | ||||||
| chr8:28960219
|
A | AATATTTA others(372): Show |
8 | a0001c0001t0003g0118a0001c0001t0003g0121a0001c0001t0003g0325others(5): Show | 8 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-3590_-57-3589i others(381): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960219 | |||||
| chr8:28960219
|
A | AATATTTA others(373): Show |
1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-3590_-57-3589i others(382): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960219 | |||||
| chr8:28960219
|
A | AATATTTA others(372): Show |
1 | a0001c0001t0003g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-57-3590_-57-3589i others(381): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960219 | |||||
| chr8:28960427
|
T | C | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57-3384T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960427 | ||||||
| chr8:28960737
|
A | T | 343 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(340): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.-57-3074A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960737 | ||||||
| chr8:28960745
|
CTCTTTTT others(5): Show |
C | 51 | a0001c0001t0001g0145a0001c0001t0001g0151a0001c0001t0001g0219others(48): Show | 51 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3041d others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960745 | |||||
| chr8:28960753
|
CTTTTTCT others(6): Show |
C | 139 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(136): Show | 139 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3040d others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | |||||
| chr8:28960753
|
CTTTTTCT others(7): Show |
C | 4 | a0001c0001t0007g0061a0001c0001t0008g0002a0001c0001t0008g0122others(1): Show | 4 | HG02630.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3039d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | |||||
| chr8:28960753
|
CTTTTTCT others(8): Show |
C | 3 | a0001c0001t0001g0316a0001c0001t0006g0331a0001c0001t0008g0001 | 3 | HG02056.hp1 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57-3052_-57-3038d others(17): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | |||||
| chr8:28960753
|
CTTTTTCT others(9): Show |
C | 24 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(21): Show | 24 | HG00544.hp1 HG01261.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3037d others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | |||||
| chr8:28960753
|
CTTTTTCT others(11): Show |
C | 1 | a0001c0001t0003g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-57-3052_-57-3035d others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | |||||
| chr8:28960753
|
CTTTTTCT others(17): Show |
C | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3029d others(26): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | |||||
| chr8:28960753
|
CTTTTTCT others(27): Show |
C | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3019d others(36): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | |||||
| chr8:28960753
|
CTTTTTCT others(28): Show |
C | 56 | a0001c0001t0001g0084a0001c0001t0003g0007a0001c0001t0003g0008others(53): Show | 56 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3018d others(37): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | |||||
| chr8:28960753
|
CTTTTTCT others(29): Show |
C | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | NA18968.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-57-3052_-57-3017d others(38): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960753 | |||||
| chr8:28960754
|
TTTTTCTT others(4): Show |
T | 11 | a0001c0001t0001g0257a0001c0001t0003g0298a0001c0001t0004g0063others(8): Show | 11 | HG01123.hp1 HG01243.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57-3052_-57-3042d others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960754 | |||||
| chr8:28960765
|
C | T | 3 | a0001c0001t0003g0119a0001c0001t0004g0003a0001c0001t0004g0125 | 3 | HG00741.hp2 HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-57-3046C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960765 | ||||||
| chr8:28960765
|
CT | C | 6 | a0001c0001t0004g0029a0001c0001t0004g0032a0001c0001t0004g0039others(3): Show | 6 | HG00639.hp1 HG00738.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-3007delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960765 | |||||
| chr8:28960765
|
CTTTTTTT others(11): Show |
C | 8 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-3024_-57-3007d others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28960765 | |||||
| chr8:28960779
|
T | G | 6 | a0001c0001t0001g0257a0001c0001t0003g0298a0001c0001t0005g0200others(3): Show | 6 | HG01123.hp1 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-3032T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960779 | ||||||
| chr8:28960780
|
T | G | 48 | a0001c0001t0001g0145a0001c0001t0001g0151a0001c0001t0001g0219others(45): Show | 48 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-57-3031T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960780 | ||||||
| chr8:28960781
|
T | G | 137 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(134): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-57-3030T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960781 | ||||||
| chr8:28960782
|
T | G | 5 | a0001c0001t0001g0316a0001c0001t0007g0004a0001c0001t0008g0002others(2): Show | 5 | HG02630.hp2 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-3029T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960782 | ||||||
| chr8:28960783
|
T | G | 3 | a0001c0001t0006g0331a0001c0001t0007g0061a0001c0001t0008g0001 | 3 | HG02056.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-57-3028T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960783 | ||||||
| chr8:28960784
|
T | C | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-3027T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960784 | ||||||
| chr8:28960784
|
T | G | 24 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(21): Show | 24 | HG00544.hp1 HG01261.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-57-3027T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960784 | ||||||
| chr8:28960789
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-57-3022T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960789 | ||||||
| chr8:28960792
|
T | G | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-3019T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960792 | ||||||
| chr8:28960794
|
T | G | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-3017T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960794 | ||||||
| chr8:28960816
|
C | T | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-2995C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960816 | ||||||
| chr8:28960943
|
T | C | 225 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(222): Show | 225 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-57-2868T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960943 | ||||||
| chr8:28960944
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-57-2867G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28960944 | ||||||
| chr8:28961312
|
A | G | 2 | a0001c0001t0003g0114a0001c0001t0006g0112 | 2 | NA18945.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-57-2499A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961312 | ||||||
| chr8:28961314
|
A | G | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-57-2497A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961314 | ||||||
| chr8:28961894
|
AT | A | 10 | a0001c0001t0001g0281a0001c0001t0003g0121a0001c0001t0003g0298others(7): Show | 10 | HG02451.hp2 HG03041.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-1899delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28961894 | |||||
| chr8:28961898
|
T | TG | 5 | a0001c0001t0002g0184a0001c0001t0004g0057a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-1913_-57-1912i others(3): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961898 | ||||||
| chr8:28961899
|
T | G | 328 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(325): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-57-1912T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961899 | ||||||
| chr8:28961900
|
T | G | 10 | a0001c0001t0001g0281a0001c0001t0003g0121a0001c0001t0003g0298others(7): Show | 10 | HG02451.hp2 HG03041.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-1911T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961900 | ||||||
| chr8:28961920
|
C | CT | 199 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(196): Show | 199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-57-1878dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 28961920 | |||||
| chr8:28961943
|
A | G | 1 | a0001c0001t0015g0274 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-57-1868A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28961943 | ||||||
| chr8:28962448
|
A | G | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-57-1363A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962448 | ||||||
| chr8:28962485
|
C | T | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57-1326C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962485 | ||||||
| chr8:28962496
|
G | T | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-1315G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962496 | ||||||
| chr8:28962522
|
A | G | 4 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0003g0079others(1): Show | 4 | NA18612.hp2 NA18952.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-1289A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962522 | ||||||
| chr8:28962580
|
A | G | 1 | a0001c0001t0005g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-57-1231A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962580 | ||||||
| chr8:28962723
|
T | G | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | NA18968.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-57-1088T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962723 | ||||||
| chr8:28962897
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57-914A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28962897 | ||||||
| chr8:28963047
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-57-764C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963047 | ||||||
| chr8:28963289
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-57-522T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963289 | ||||||
| chr8:28963393
|
T | C | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-57-418T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963393 | ||||||
| chr8:28963459
|
A | G | 1 | a0001c0001t0004g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-57-352A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963459 | ||||||
| chr8:28963467
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-57-344G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963467 | ||||||
| chr8:28963509
|
C | T | 2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-57-302C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963509 | ||||||
| chr8:28963511
|
T | A | 2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-57-300T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963511 | ||||||
| chr8:28963620
|
A | C | 1 | a0001c0001t0001g0279 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-57-191A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 1/9 | chr8 | 28963620 | ||||||
| chr8:28964020
|
C | A | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.23+130C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964020 | ||||||
| chr8:28964505
|
C | T | 5 | a0001c0001t0004g0123a0001c0001t0004g0124a0001c0001t0004g0125others(2): Show | 5 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.23+615C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964505 | ||||||
| chr8:28964514
|
C | G | 1 | a0001c0001t0007g0009 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.23+624C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964514 | ||||||
| chr8:28964561
|
T | G | 2 | a0001c0001t0002g0214a0001c0001t0002g0270 | 2 | NA18973.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.23+671T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964561 | ||||||
| chr8:28964613
|
G | C | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.23+723G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964613 | ||||||
| chr8:28964687
|
A | G | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.23+797A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964687 | ||||||
| chr8:28964710
|
T | C | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.23+820T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964710 | ||||||
| chr8:28964935
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.23+1045A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28964935 | ||||||
| chr8:28965036
|
G | A | 1 | a0001c0001t0008g0076 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.23+1146G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965036 | ||||||
| chr8:28965157
|
C | A | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.23+1267C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965157 | ||||||
| chr8:28965317
|
T | C | 1 | a0001c0001t0003g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.23+1427T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965317 | ||||||
| chr8:28965534
|
C | T | 193 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(190): Show | 193 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.23+1644C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965534 | ||||||
| chr8:28965578
|
A | G | 86 | a0001c0001t0001g0084a0001c0001t0003g0005a0001c0001t0003g0006others(83): Show | 86 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.23+1688A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965578 | ||||||
| chr8:28965592
|
G | T | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.23+1702G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965592 | ||||||
| chr8:28965636
|
G | A | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.23+1746G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965636 | ||||||
| chr8:28965643
|
C | T | 4 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0206others(1): Show | 4 | HG00609.hp2 HG02074.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.23+1753C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965643 | ||||||
| chr8:28965983
|
A | G | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.23+2093A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28965983 | ||||||
| chr8:28966052
|
G | C | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.23+2162G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966052 | ||||||
| chr8:28966166
|
A | G | 1 | a0001c0001t0011g0314 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.23+2276A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966166 | ||||||
| chr8:28966238
|
G | T | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+2348G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966238 | ||||||
| chr8:28966306
|
T | C | 1 | a0001c0001t0023g0333 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.23+2416T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966306 | ||||||
| chr8:28966648
|
T | C | 1 | a0001c0001t0002g0242 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.23+2758T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966648 | ||||||
| chr8:28966705
|
T | C | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.23+2815T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966705 | ||||||
| chr8:28966754
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0283a0001c0001t0001g0288 | 3 | HG00323.hp1 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.23+2864C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966754 | ||||||
| chr8:28966764
|
T | C | 4 | a0001c0001t0002g0083a0001c0001t0002g0187a0001c0001t0002g0249others(1): Show | 4 | NA18946.hp1 NA18990.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+2874T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28966764 | ||||||
| chr8:28967193
|
G | A | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.24-2850G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967193 | ||||||
| chr8:28967337
|
T | A | 2 | a0001c0001t0012g0156a0001c0001t0012g0297 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.24-2706T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967337 | ||||||
| chr8:28967812
|
A | C | 1 | a0001c0001t0008g0065 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.24-2231A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967812 | ||||||
| chr8:28967905
|
C | G | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.24-2138C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967905 | ||||||
| chr8:28967935
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.24-2108G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967935 | ||||||
| chr8:28967957
|
T | A | 221 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(218): Show | 221 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.24-2086T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28967957 | ||||||
| chr8:28968098
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.24-1945T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968098 | ||||||
| chr8:28968161
|
C | T | 111 | a0001c0001t0001g0267a0001c0001t0002g0083a0001c0001t0002g0132others(108): Show | 111 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.24-1882C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968161 | ||||||
| chr8:28968271
|
A | G | 3 | a0001c0001t0001g0289a0001c0001t0008g0001a0001c0001t0008g0002 | 3 | HG03225.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.24-1772A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968271 | ||||||
| chr8:28968351
|
T | C | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.24-1692T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968351 | ||||||
| chr8:28968561
|
G | A | 4 | a0001c0001t0001g0263a0001c0001t0001g0272a0001c0001t0001g0275others(1): Show | 4 | HG00140.hp1 HG01884.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-1482G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968561 | ||||||
| chr8:28968615
|
C | T | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.24-1428C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968615 | ||||||
| chr8:28968686
|
A | G | 1 | a0001c0001t0004g0343 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.24-1357A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968686 | ||||||
| chr8:28968752
|
C | T | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-1291C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28968752 | ||||||
| chr8:28969225
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0289 | 2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.24-818A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28969225 | ||||||
| chr8:28969306
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.24-737A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28969306 | ||||||
| chr8:28969541
|
CAAA | C | 69 | a0001c0001t0001g0136a0001c0001t0001g0141a0001c0001t0001g0142others(66): Show | 69 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.24-501_24-499delAA others(1): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 2/9 | chr8 | 28969541 | ||||||
| chr8:28970751
|
C | G | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.500+232C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28970751 | ||||||
| chr8:28970874
|
T | G | 197 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(194): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.500+355T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28970874 | ||||||
| chr8:28970894
|
G | A | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.500+375G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28970894 | ||||||
| chr8:28970941
|
T | TG | 7 | a0001c0001t0002g0083a0001c0001t0002g0169a0001c0001t0003g0092others(4): Show | 7 | HG01175.hp2 HG01928.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.500+426dupG | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970941 | |||||
| chr8:28970981
|
G | GAC | 27 | a0001c0001t0001g0219a0001c0001t0001g0255a0001c0001t0002g0137others(24): Show | 27 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.500+510_500+511dup others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28970981
|
G | GACAC | 16 | a0001c0001t0002g0152a0001c0001t0002g0174a0001c0001t0002g0198others(13): Show | 16 | HG01261.hp1 HG01884.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.500+508_500+511dup others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28970981
|
GAC | G | 54 | a0001c0001t0001g0084a0001c0001t0001g0145a0001c0001t0001g0147others(51): Show | 54 | HG00280.hp1 HG01081.hp1 HG01123.hp1 others(51): Show |
intron_variant | MODIFIER | c.500+510_500+511del others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28970981
|
GACAC | G | 88 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0148others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.500+508_500+511del others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28970981
|
GACACAC | G | 44 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0143others(41): Show | 44 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.500+506_500+511del others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28970981
|
GACACACA others(1): Show |
G | 15 | a0001c0001t0001g0142a0001c0001t0001g0266a0001c0001t0001g0317others(12): Show | 15 | HG00558.hp2 HG01256.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.500+504_500+511del others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28970981
|
GACACACA others(3): Show |
G | 6 | a0001c0001t0001g0258a0001c0001t0001g0283a0001c0001t0003g0170others(3): Show | 6 | HG01109.hp1 HG01255.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.500+502_500+511del others(10): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28970981
|
GACACACA others(5): Show |
G | 5 | a0001c0001t0001g0254a0001c0001t0005g0199a0001c0001t0005g0200others(2): Show | 5 | HG01175.hp1 HG02559.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.500+500_500+511del others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28970981
|
GACACACA others(7): Show |
G | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.500+498_500+511del others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28970981
|
GACACACA others(9): Show |
G | 6 | a0001c0001t0002g0132a0001c0001t0002g0190a0001c0001t0002g0214others(3): Show | 6 | HG00438.hp2 HG01943.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.500+496_500+511del others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28970981
|
GACACACA others(11): Show |
G | 1 | a0001c0001t0004g0023 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.500+494_500+511del others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28970981
|
GACACACA others(13): Show |
G | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.500+492_500+511del others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28970981 | |||||
| chr8:28971083
|
C | G | 2 | a0001c0001t0012g0156a0001c0001t0012g0297 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.500+564C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971083 | ||||||
| chr8:28971086
|
CT | C | 43 | a0001c0001t0001g0316a0001c0001t0002g0152a0001c0001t0002g0175others(40): Show | 43 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.500+589delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28971086 | |||||
| chr8:28971086
|
CTT | C | 255 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(252): Show | 255 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.500+588_500+589del others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28971086 | |||||
| chr8:28971086
|
CTTT | C | 14 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0285others(11): Show | 14 | HG01496.hp2 HG02647.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.500+587_500+589del others(3): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28971086 | |||||
| chr8:28971148
|
A | G | 1 | a0001c0001t0004g0051 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.500+629A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971148 | ||||||
| chr8:28971255
|
G | A | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.500+736G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971255 | ||||||
| chr8:28971337
|
C | T | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.500+818C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971337 | ||||||
| chr8:28971338
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.500+819G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971338 | ||||||
| chr8:28971642
|
G | A | 7 | a0001c0001t0004g0044a0001c0001t0004g0045a0001c0001t0004g0046others(4): Show | 7 | HG00544.hp2 HG00597.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.500+1123G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971642 | ||||||
| chr8:28971799
|
T | G | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.500+1280T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971799 | ||||||
| chr8:28971900
|
C | A | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.500+1381C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28971900 | ||||||
| chr8:28972213
|
T | A | 3 | a0001c0001t0002g0193a0001c0001t0002g0222a0001c0001t0017g0195 | 3 | HG00408.hp1 HG01168.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.500+1694T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972213 | ||||||
| chr8:28972276
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0279 | 3 | HG02486.hp2 HG02897.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.500+1757G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972276 | ||||||
| chr8:28972287
|
A | T | 1 | a0001c0001t0001g0257 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.500+1768A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972287 | ||||||
| chr8:28972358
|
G | C | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.500+1839G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972358 | ||||||
| chr8:28972592
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.500+2073A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972592 | ||||||
| chr8:28972622
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.500+2103G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972622 | ||||||
| chr8:28972783
|
C | G | 209 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(206): Show | 209 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.500+2264C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972783 | ||||||
| chr8:28972948
|
C | T | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.500+2429C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972948 | ||||||
| chr8:28972958
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.500+2439G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28972958 | ||||||
| chr8:28973192
|
A | G | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.500+2673A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973192 | ||||||
| chr8:28973568
|
A | G | 2 | a0001c0001t0004g0038a0001c0001t0004g0041 | 2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.500+3049A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973568 | ||||||
| chr8:28973636
|
G | T | 2 | a0001c0001t0003g0087a0001c0001t0003g0103 | 2 | HG02040.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.500+3117G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973636 | ||||||
| chr8:28973754
|
C | T | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.500+3235C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973754 | ||||||
| chr8:28973765
|
C | T | 100 | a0001c0001t0001g0316a0001c0001t0002g0083a0001c0001t0002g0132others(97): Show | 100 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.500+3246C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973765 | ||||||
| chr8:28973787
|
C | T | 4 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(1): Show | 4 | HG00140.hp2 HG00323.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.500+3268C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973787 | ||||||
| chr8:28973803
|
G | GTTTTTTT others(4): Show |
3 | a0001c0001t0003g0077a0001c0001t0004g0041a0001c0001t0004g0048 | 3 | HG01070.hp1 HG02074.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.500+3305_500+3315d others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
G | GTTTTTTT others(5): Show |
8 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0008others(5): Show | 8 | HG00738.hp1 HG01928.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.500+3304_500+3315d others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
G | GTTTTTTT others(6): Show |
3 | a0001c0001t0003g0089a0001c0001t0004g0043a0001c0001t0004g0046 | 3 | HG00558.hp2 HG03654.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.500+3303_500+3315d others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
G | GTTTTTTT others(7): Show |
3 | a0001c0001t0003g0114a0001c0001t0004g0029a0001c0001t0004g0042 | 3 | HG01975.hp1 HG03710.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.500+3302_500+3315d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
G | GTTTTTTT others(8): Show |
4 | a0001c0001t0004g0034a0001c0001t0004g0035a0001c0001t0004g0039others(1): Show | 4 | HG00280.hp1 HG01081.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.500+3301_500+3315d others(17): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
G | GTTTTTTT others(9): Show |
3 | a0001c0001t0004g0031a0001c0001t0004g0047a0001c0001t0020g0052 | 3 | HG00544.hp2 HG00741.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.500+3300_500+3315d others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
G | GTTTTTTT others(10): Show |
2 | a0001c0001t0008g0076a0001c0001t0013g0050 | 2 | HG00735.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.500+3299_500+3315d others(19): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
G | GTTTTTTT others(13): Show |
2 | a0001c0001t0004g0032a0001c0001t0004g0033 | 2 | HG00639.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.500+3296_500+3315d others(22): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
G | GTTTTTTT others(14): Show |
1 | a0001c0001t0004g0030 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.500+3295_500+3315d others(23): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
G | GTTTTTTT others(17): Show |
1 | a0001c0001t0004g0051 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.500+3292_500+3315d others(26): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
G | GTTTTTTT others(30): Show |
1 | a0001c0001t0004g0040 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.500+3315_500+3316i others(39): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
GTTTT | G | 16 | a0001c0001t0002g0083a0001c0001t0002g0157a0001c0001t0002g0175others(13): Show | 16 | HG00621.hp1 HG01168.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.500+3312_500+3315d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
GTTTTT | G | 83 | a0001c0001t0001g0316a0001c0001t0002g0132a0001c0001t0002g0134others(80): Show | 83 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.500+3311_500+3315d others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
GTTTTTTT | G | 7 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0012others(4): Show | 7 | HG02257.hp2 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.500+3309_500+3315d others(9): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
GTTTTTTT others(3): Show |
G | 27 | a0001c0001t0001g0084a0001c0001t0001g0145a0001c0001t0001g0147others(24): Show | 27 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.500+3306_500+3315d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
GTTTTTTT others(4): Show |
G | 82 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(79): Show | 82 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.500+3305_500+3315d others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0003g0106 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.500+3302_500+3315d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973803
|
GTTTTTTT others(8): Show |
G | 8 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.500+3301_500+3315d others(17): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973803 | |||||
| chr8:28973811
|
T | TTTTTTTT others(7): Show |
2 | a0001c0001t0003g0082a0001c0001t0003g0226 | 2 | NA18941.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.500+3305_500+3306i others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973811 | |||||
| chr8:28973812
|
T | TTTTTTTT others(5): Show |
1 | a0001c0001t0003g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.500+3304_500+3305i others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973812 | |||||
| chr8:28973812
|
T | TTTTTTTT others(6): Show |
13 | a0001c0001t0003g0086a0001c0001t0003g0099a0001c0001t0003g0101others(10): Show | 13 | HG01109.hp2 HG02257.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.500+3305_500+3306i others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973812 | |||||
| chr8:28973812
|
T | TTTTTTTT others(7): Show |
2 | a0001c0001t0003g0073a0001c0001t0006g0074 | 2 | NA18998.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.500+3306_500+3307i others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973812 | |||||
| chr8:28973813
|
T | TGTTTTTT others(5): Show |
1 | a0001c0001t0003g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.500+3294_500+3295i others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973813 | ||||||
| chr8:28973813
|
T | TTTG | 15 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(12): Show | 15 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.500+3296_500+3297i others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | |||||
| chr8:28973813
|
T | TTTTTGTT others(5): Show |
2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.500+3298_500+3299i others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | |||||
| chr8:28973813
|
T | TTTTTTGT others(5): Show |
1 | a0001c0001t0003g0092 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.500+3299_500+3300i others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | |||||
| chr8:28973813
|
T | TTTTTTTT others(5): Show |
37 | a0001c0001t0003g0006a0001c0001t0003g0066a0001c0001t0003g0067others(34): Show | 37 | HG00609.hp1 HG00621.hp2 HG01975.hp2 others(34): Show |
intron_variant | MODIFIER | c.500+3305_500+3306i others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | |||||
| chr8:28973813
|
T | TTTTTTTT others(23): Show |
1 | a0001c0001t0003g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.500+3305_500+3306i others(32): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | |||||
| chr8:28973813
|
T | TTTTTTTT others(6): Show |
1 | a0001c0001t0003g0108 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.500+3306_500+3307i others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28973813 | |||||
| chr8:28973814
|
T | G | 1 | a0001c0001t0002g0191 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.500+3295T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973814 | ||||||
| chr8:28973820
|
T | G | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.500+3301T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973820 | ||||||
| chr8:28973822
|
T | G | 1 | a0001c0001t0004g0062 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.500+3303T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973822 | ||||||
| chr8:28973900
|
C | T | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.500+3381C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973900 | ||||||
| chr8:28973917
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.500+3398C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973917 | ||||||
| chr8:28973918
|
G | A | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.500+3399G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973918 | ||||||
| chr8:28973920
|
T | A | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.500+3401T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973920 | ||||||
| chr8:28973942
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.500+3423G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28973942 | ||||||
| chr8:28974034
|
A | G | 209 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(206): Show | 209 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.500+3515A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974034 | ||||||
| chr8:28974105
|
T | C | 312 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(309): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.500+3586T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974105 | ||||||
| chr8:28974106
|
G | A | 1 | a0001c0001t0004g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.500+3587G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974106 | ||||||
| chr8:28974248
|
A | G | 1 | a0001c0001t0006g0331 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.500+3729A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974248 | ||||||
| chr8:28974360
|
A | C | 8 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.500+3841A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974360 | ||||||
| chr8:28974578
|
C | T | 83 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(80): Show | 83 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.500+4059C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974578 | ||||||
| chr8:28974726
|
T | C | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.500+4207T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974726 | ||||||
| chr8:28974750
|
G | A | 1 | a0001c0001t0004g0060 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.500+4231G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974750 | ||||||
| chr8:28974771
|
T | C | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.500+4252T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974771 | ||||||
| chr8:28974778
|
A | T | 1 | a0001c0001t0007g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.500+4259A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974778 | ||||||
| chr8:28974875
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.500+4356A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974875 | ||||||
| chr8:28974987
|
C | A | 11 | a0001c0001t0003g0133a0001c0001t0003g0168a0001c0001t0003g0170others(8): Show | 11 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.500+4468C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28974987 | ||||||
| chr8:28975091
|
A | G | 4 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(1): Show | 4 | NA18947.hp2 NA18990.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.500+4572A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28975091 | ||||||
| chr8:28975314
|
A | C | 1 | a0001c0001t0002g0193 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.501-4757A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28975314 | ||||||
| chr8:28976059
|
G | T | 3 | a0001c0001t0002g0286a0001c0001t0005g0292a0001c0001t0005g0301 | 3 | HG01516.hp1 HG02145.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.501-4012G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976059 | ||||||
| chr8:28976264
|
T | G | 1 | a0001c0001t0003g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.501-3807T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976264 | ||||||
| chr8:28976273
|
T | A | 1 | a0001c0001t0006g0336 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.501-3798T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976273 | ||||||
| chr8:28976283
|
T | A | 1 | a0001c0001t0002g0083 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.501-3788T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976283 | ||||||
| chr8:28976393
|
C | A | 80 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(77): Show | 80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.501-3678C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976393 | ||||||
| chr8:28976687
|
T | C | 69 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(66): Show | 69 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.501-3384T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976687 | ||||||
| chr8:28976690
|
CTTTTCTT others(7): Show |
C | 1 | a0001c0001t0001g0277 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.501-3371_501-3358d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28976690 | |||||
| chr8:28976709
|
C | CT | 7 | a0001c0001t0003g0073a0001c0001t0006g0115a0001c0001t0008g0001others(4): Show | 7 | HG02572.hp1 HG02886.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.501-3347dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28976709 | |||||
| chr8:28976731
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.501-3340G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976731 | ||||||
| chr8:28976738
|
A | G | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.501-3333A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28976738 | ||||||
| chr8:28977264
|
G | A | 3 | a0001c0001t0016g0329a0001c0001t0016g0332a0001c0001t0023g0333 | 3 | NA18947.hp1 NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.501-2807G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977264 | ||||||
| chr8:28977531
|
C | T | 1 | a0001c0001t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.501-2540C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977531 | ||||||
| chr8:28977681
|
C | G | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-2390C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977681 | ||||||
| chr8:28977737
|
A | G | 312 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(309): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.501-2334A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977737 | ||||||
| chr8:28977743
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.501-2328A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977743 | ||||||
| chr8:28977875
|
C | T | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501-2196C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977875 | ||||||
| chr8:28977959
|
GA | G | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.501-2109delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28977959 | |||||
| chr8:28977972
|
A | T | 3 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0002g0312 | 3 | NA18952.hp2 NA18974.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.501-2099A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28977972 | ||||||
| chr8:28978026
|
C | A | 1 | a0001c0001t0001g0282 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.501-2045C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978026 | ||||||
| chr8:28978052
|
G | T | 1 | a0001c0001t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.501-2019G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978052 | ||||||
| chr8:28978212
|
T | G | 6 | a0001c0001t0006g0336a0001c0001t0006g0337a0001c0001t0006g0338others(3): Show | 6 | NA18943.hp2 NA18956.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-1859T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978212 | ||||||
| chr8:28978286
|
T | C | 1 | a0001c0001t0004g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.501-1785T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978286 | ||||||
| chr8:28978326
|
A | T | 1 | a0001c0001t0001g0271 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.501-1745A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978326 | ||||||
| chr8:28978346
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.501-1725A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978346 | ||||||
| chr8:28978564
|
C | T | 1 | a0001c0001t0002g0319 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.501-1507C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978564 | ||||||
| chr8:28978591
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.501-1480C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978591 | ||||||
| chr8:28978595
|
C | T | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.501-1476C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978595 | ||||||
| chr8:28978645
|
G | C | 1 | a0001c0001t0002g0227 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.501-1426G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978645 | ||||||
| chr8:28978713
|
G | T | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-1358G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978713 | ||||||
| chr8:28978786
|
C | CA | 277 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(274): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.501-1265dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28978786 | |||||
| chr8:28978786
|
C | CAA | 29 | a0001c0001t0001g0148a0001c0001t0001g0258a0001c0001t0001g0310others(26): Show | 29 | HG01081.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.501-1266_501-1265d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 28978786 | |||||
| chr8:28978875
|
A | C | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-1196A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978875 | ||||||
| chr8:28978900
|
C | T | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.501-1171C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28978900 | ||||||
| chr8:28979104
|
C | T | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501-967C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979104 | ||||||
| chr8:28979429
|
C | T | 1 | a0001c0001t0004g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.501-642C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979429 | ||||||
| chr8:28979463
|
T | C | 5 | a0001c0001t0001g0254a0001c0001t0001g0264a0001c0001t0001g0265others(2): Show | 5 | HG00735.hp2 HG01175.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-608T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979463 | ||||||
| chr8:28979465
|
G | A | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.501-606G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979465 | ||||||
| chr8:28979487
|
G | C | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.501-584G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979487 | ||||||
| chr8:28979567
|
G | A | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501-504G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979567 | ||||||
| chr8:28979591
|
T | C | 3 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0005g0162 | 3 | HG02735.hp2 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.501-480T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979591 | ||||||
| chr8:28979718
|
C | T | 1 | a0001c0001t0004g0039 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.501-353C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979718 | ||||||
| chr8:28979757
|
T | C | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.501-314T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979757 | ||||||
| chr8:28979765
|
A | G | 1 | a0001c0001t0006g0330 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.501-306A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979765 | ||||||
| chr8:28979955
|
T | G | 1 | a0001c0001t0001g0281 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.501-116T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979955 | ||||||
| chr8:28979992
|
T | C | 1 | a0001c0001t0017g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.501-79T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 3/9 | chr8 | 28979992 | ||||||
| chr8:28980193
|
G | A | 1 | a0001c0001t0003g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.586+37G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980193 | ||||||
| chr8:28980268
|
G | C | 1 | a0001c0001t0003g0197 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.586+112G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980268 | ||||||
| chr8:28980318
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.586+162C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980318 | ||||||
| chr8:28980322
|
C | T | 11 | a0001c0001t0003g0133a0001c0001t0003g0168a0001c0001t0003g0170others(8): Show | 11 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+166C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980322 | ||||||
| chr8:28980545
|
T | A | 1 | a0001c0001t0021g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.586+389T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980545 | ||||||
| chr8:28980820
|
C | T | 6 | a0001c0001t0005g0155a0001c0001t0005g0162a0001c0001t0005g0177others(3): Show | 6 | HG00280.hp2 HG01123.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+664C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980820 | ||||||
| chr8:28980846
|
C | T | 6 | a0001c0001t0006g0336a0001c0001t0006g0337a0001c0001t0006g0338others(3): Show | 6 | NA18943.hp2 NA18956.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+690C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980846 | ||||||
| chr8:28980908
|
C | T | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+752C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28980908 | ||||||
| chr8:28981056
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.586+900T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981056 | ||||||
| chr8:28981084
|
A | C | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586+928A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981084 | ||||||
| chr8:28981085
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586+929G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981085 | ||||||
| chr8:28981289
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.586+1133T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981289 | ||||||
| chr8:28981382
|
T | C | 1 | a0001c0001t0004g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.586+1226T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981382 | ||||||
| chr8:28981414
|
G | T | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.586+1258G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981414 | ||||||
| chr8:28981590
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.586+1434T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981590 | ||||||
| chr8:28981618
|
C | T | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+1462C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981618 | ||||||
| chr8:28981621
|
AT | A | 7 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(4): Show | 7 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+1476delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28981621 | |||||
| chr8:28981685
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.586+1529G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981685 | ||||||
| chr8:28981963
|
C | T | 3 | a0001c0001t0002g0212a0001c0001t0002g0248a0001c0002t0002g0211 | 3 | HG01358.hp2 HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.586+1807C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981963 | ||||||
| chr8:28981972
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.586+1816T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28981972 | ||||||
| chr8:28982054
|
G | A | 1 | a0001c0001t0003g0085 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.586+1898G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982054 | ||||||
| chr8:28982093
|
C | T | 2 | a0001c0001t0004g0040a0001c0001t0004g0042 | 2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.586+1937C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982093 | ||||||
| chr8:28982168
|
G | A | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+2012G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982168 | ||||||
| chr8:28982398
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.586+2242T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982398 | ||||||
| chr8:28982405
|
G | C | 227 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(224): Show | 227 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.586+2249G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982405 | ||||||
| chr8:28982498
|
A | G | 1 | a0001c0001t0003g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.586+2342A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982498 | ||||||
| chr8:28982712
|
G | A | 79 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.586+2556G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982712 | ||||||
| chr8:28982753
|
G | A | 1 | a0001c0001t0004g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+2597G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982753 | ||||||
| chr8:28982812
|
C | T | 1 | a0001c0001t0004g0038 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.586+2656C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982812 | ||||||
| chr8:28982815
|
G | A | 5 | a0001c0001t0002g0132a0001c0001t0002g0190a0001c0001t0002g0214others(2): Show | 5 | HG00438.hp2 NA18949.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+2659G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982815 | ||||||
| chr8:28982828
|
C | T | 1 | a0001c0001t0004g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.586+2672C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28982828 | ||||||
| chr8:28983129
|
A | G | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.586+2973A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28983129 | ||||||
| chr8:28983151
|
A | G | 1 | a0001c0001t0002g0319 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.586+2995A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28983151 | ||||||
| chr8:28983581
|
A | G | 1 | a0001c0001t0004g0048 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.586+3425A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28983581 | ||||||
| chr8:28983879
|
C | T | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+3723C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28983879 | ||||||
| chr8:28984040
|
G | A | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.586+3884G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28984040 | ||||||
| chr8:28984065
|
C | T | 2 | a0001c0001t0002g0207a0001c0001t0002g0286 | 2 | NA19072.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.586+3909C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28984065 | ||||||
| chr8:28984161
|
G | A | 1 | a0001c0001t0005g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.586+4005G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28984161 | ||||||
| chr8:28984304
|
G | A | 184 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(181): Show | 184 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.586+4148G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28984304 | ||||||
| chr8:28984789
|
T | A | 1 | a0001c0001t0021g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.586+4633T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28984789 | ||||||
| chr8:28985034
|
A | G | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+4878A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985034 | ||||||
| chr8:28985307
|
T | C | 1 | a0001c0001t0003g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.586+5151T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985307 | ||||||
| chr8:28985359
|
T | C | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+5203T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985359 | ||||||
| chr8:28985468
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.586+5312G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985468 | ||||||
| chr8:28985540
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.586+5384C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985540 | ||||||
| chr8:28985585
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.586+5429T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985585 | ||||||
| chr8:28985849
|
A | G | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+5693A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985849 | ||||||
| chr8:28985919
|
A | G | 1 | a0001c0001t0004g0043 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.586+5763A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28985919 | ||||||
| chr8:28986113
|
T | C | 2 | a0001c0001t0005g0292a0001c0001t0005g0301 | 2 | HG01516.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.586+5957T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986113 | ||||||
| chr8:28986204
|
G | A | 209 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(206): Show | 209 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.586+6048G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986204 | ||||||
| chr8:28986271
|
ATAT | A | 181 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(178): Show | 181 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.586+6117_586+6119d others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28986271 | |||||
| chr8:28986305
|
A | G | 1 | a0001c0001t0003g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.586+6149A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986305 | ||||||
| chr8:28986316
|
G | A | 2 | a0001c0001t0005g0292a0001c0001t0005g0301 | 2 | HG01516.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.586+6160G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986316 | ||||||
| chr8:28986367
|
A | G | 1 | a0001c0001t0003g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.586+6211A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986367 | ||||||
| chr8:28986666
|
A | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0283a0001c0001t0001g0288 | 3 | HG00323.hp1 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.586+6510A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986666 | ||||||
| chr8:28986877
|
A | G | 1 | a0001c0001t0003g0106 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.586+6721A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28986877 | ||||||
| chr8:28987082
|
A | G | 1 | a0001c0001t0003g0092 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.586+6926A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987082 | ||||||
| chr8:28987214
|
T | A | 2 | a0001c0001t0002g0223a0001c0001t0011g0224 | 2 | NA18956.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.586+7058T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987214 | ||||||
| chr8:28987227
|
A | G | 2 | a0001c0001t0002g0157a0001c0001t0002g0158 | 2 | NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.586+7071A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987227 | ||||||
| chr8:28987319
|
G | A | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.586+7163G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987319 | ||||||
| chr8:28987417
|
C | T | 13 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.586+7261C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987417 | ||||||
| chr8:28987525
|
C | T | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.586+7369C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987525 | ||||||
| chr8:28987878
|
G | C | 1 | a0001c0001t0003g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.586+7722G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28987878 | ||||||
| chr8:28988031
|
T | C | 16 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.586+7875T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988031 | ||||||
| chr8:28988134
|
A | G | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+7978A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988134 | ||||||
| chr8:28988157
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.586+8001T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988157 | ||||||
| chr8:28988291
|
A | G | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+8135A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988291 | ||||||
| chr8:28988463
|
G | C | 1 | a0001c0001t0006g0335 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.586+8307G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988463 | ||||||
| chr8:28988482
|
G | A | 73 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.586+8326G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988482 | ||||||
| chr8:28988531
|
A | G | 10 | a0001c0001t0002g0202a0001c0001t0002g0209a0001c0001t0002g0228others(7): Show | 10 | NA18612.hp1 NA18941.hp1 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+8375A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988531 | ||||||
| chr8:28988886
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.586+8730A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988886 | ||||||
| chr8:28988911
|
A | T | 1 | a0001c0001t0003g0110 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.586+8755A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28988911 | ||||||
| chr8:28989044
|
G | A | 184 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(181): Show | 184 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.586+8888G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28989044 | ||||||
| chr8:28989133
|
A | G | 184 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(181): Show | 184 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.586+8977A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28989133 | ||||||
| chr8:28989362
|
C | A | 6 | a0001c0001t0001g0140a0001c0001t0001g0229a0001c0001t0001g0243others(3): Show | 6 | HG02486.hp2 HG02723.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+9206C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28989362 | ||||||
| chr8:28989953
|
A | G | 336 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(333): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(333): Show |
intron_variant | MODIFIER | c.586+9797A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28989953 | ||||||
| chr8:28990161
|
G | A | 99 | a0001c0001t0002g0083a0001c0001t0002g0132a0001c0001t0002g0134others(96): Show | 99 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.586+10005G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990161 | ||||||
| chr8:28990166
|
T | C | 13 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.586+10010T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990166 | ||||||
| chr8:28990252
|
T | C | 1 | a0001c0001t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.586+10096T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990252 | ||||||
| chr8:28990256
|
C | T | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.586+10100C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990256 | ||||||
| chr8:28990341
|
T | C | 1 | a0001c0001t0002g0242 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.586+10185T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990341 | ||||||
| chr8:28990628
|
TTTTTTTG others(5): Show |
T | 1 | a0001c0001t0001g0282 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.586+10483_586+1049 others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28990628 | |||||
| chr8:28990686
|
T | A | 1 | a0001c0001t0010g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.586+10530T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990686 | ||||||
| chr8:28990883
|
A | G | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+10727A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28990883 | ||||||
| chr8:28991022
|
G | T | 16 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.586+10866G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991022 | ||||||
| chr8:28991027
|
G | A | 1 | a0001c0001t0002g0342 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.586+10871G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991027 | ||||||
| chr8:28991055
|
G | A | 2 | a0001c0001t0005g0179a0001c0001t0005g0180 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.586+10899G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991055 | ||||||
| chr8:28991293
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586+11137T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991293 | ||||||
| chr8:28991509
|
C | T | 1 | a0001c0001t0008g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.586+11353C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991509 | ||||||
| chr8:28991535
|
C | T | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.586+11379C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991535 | ||||||
| chr8:28991698
|
T | G | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+11542T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991698 | ||||||
| chr8:28991727
|
C | T | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586+11571C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991727 | ||||||
| chr8:28991754
|
G | T | 1 | a0001c0001t0007g0012 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.586+11598G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28991754 | ||||||
| chr8:28992125
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.586+11969G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992125 | ||||||
| chr8:28992200
|
A | G | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586+12044A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992200 | ||||||
| chr8:28992203
|
G | C | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586+12047G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992203 | ||||||
| chr8:28992372
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.586+12216T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992372 | ||||||
| chr8:28992391
|
C | G | 4 | a0001c0001t0005g0166a0001c0001t0005g0178a0001c0001t0005g0179others(1): Show | 4 | HG02922.hp2 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+12235C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992391 | ||||||
| chr8:28992413
|
C | G | 1 | a0001c0001t0003g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.586+12257C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992413 | ||||||
| chr8:28992528
|
T | A | 2 | a0001c0001t0005g0166a0001c0001t0005g0178 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.586+12372T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992528 | ||||||
| chr8:28992597
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.586+12441G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992597 | ||||||
| chr8:28992602
|
G | T | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.586+12446G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992602 | ||||||
| chr8:28992635
|
C | G | 1 | a0001c0001t0004g0044 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.586+12479C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28992635 | ||||||
| chr8:28992869
|
C | CA | 167 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(164): Show | 167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.586+12738dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | |||||
| chr8:28992869
|
C | CAA | 122 | a0001c0001t0001g0084a0001c0001t0001g0146a0001c0001t0001g0149others(119): Show | 122 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.586+12737_586+1273 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | |||||
| chr8:28992869
|
C | CAAA | 21 | a0001c0001t0002g0132a0001c0001t0002g0163a0001c0001t0002g0169others(18): Show | 21 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.586+12736_586+1273 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | |||||
| chr8:28992869
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0002g0172a0001c0001t0002g0225 | 2 | NA18950.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.586+12729_586+1273 others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | |||||
| chr8:28992869
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0228 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.586+12728_586+1273 others(15): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | |||||
| chr8:28992869
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.586+12727_586+1273 others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28992869 | |||||
| chr8:28993049
|
GT | G | 310 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.586+12904delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28993049 | |||||
| chr8:28993099
|
A | G | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+12943A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28993099 | ||||||
| chr8:28993660
|
A | C | 115 | a0001c0001t0002g0083a0001c0001t0002g0132a0001c0001t0002g0134others(112): Show | 115 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.586+13504A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28993660 | ||||||
| chr8:28993706
|
C | T | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.586+13550C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28993706 | ||||||
| chr8:28994014
|
G | A | 8 | a0001c0001t0007g0010a0001c0001t0007g0012a0001c0001t0007g0013others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+13858G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994014 | ||||||
| chr8:28994023
|
C | T | 2 | a0001c0001t0002g0152a0001c0001t0002g0154 | 2 | HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.586+13867C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994023 | ||||||
| chr8:28994111
|
G | A | 2 | a0001c0001t0012g0156a0001c0001t0012g0297 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.586+13955G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994111 | ||||||
| chr8:28994167
|
C | CA | 98 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.586+14024dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 28994167 | |||||
| chr8:28994221
|
C | T | 4 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0001g0307others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+14065C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994221 | ||||||
| chr8:28994701
|
A | G | 1 | a0001c0001t0004g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.587-14371A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994701 | ||||||
| chr8:28994817
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587-14255G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994817 | ||||||
| chr8:28994837
|
C | A | 98 | a0001c0001t0002g0083a0001c0001t0002g0132a0001c0001t0002g0134others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.587-14235C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994837 | ||||||
| chr8:28994911
|
G | A | 1 | a0001c0001t0009g0131 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.587-14161G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994911 | ||||||
| chr8:28994934
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0279 | 2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.587-14138A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28994934 | ||||||
| chr8:28995168
|
C | T | 1 | a0001c0001t0001g0293 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.587-13904C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995168 | ||||||
| chr8:28995238
|
C | T | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.587-13834C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995238 | ||||||
| chr8:28995440
|
A | G | 2 | a0001c0001t0008g0097a0001c0001t0008g0098 | 2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.587-13632A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995440 | ||||||
| chr8:28995545
|
T | G | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.587-13527T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995545 | ||||||
| chr8:28995575
|
A | C | 1 | a0001c0001t0002g0196 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.587-13497A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995575 | ||||||
| chr8:28995703
|
T | C | 1 | a0001c0001t0007g0009 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.587-13369T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995703 | ||||||
| chr8:28995868
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.587-13204C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995868 | ||||||
| chr8:28995869
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.587-13203G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995869 | ||||||
| chr8:28995874
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.587-13198G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28995874 | ||||||
| chr8:28996031
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.587-13041G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996031 | ||||||
| chr8:28996070
|
C | T | 1 | a0001c0001t0004g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.587-13002C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996070 | ||||||
| chr8:28996269
|
CAAG | C | 69 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12802_587-1280 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996269 | ||||||
| chr8:28996275
|
G | A | 69 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12797G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996275 | ||||||
| chr8:28996276
|
A | C | 69 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12796A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996276 | ||||||
| chr8:28996278
|
T | TA | 69 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12794_587-1279 others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996278 | ||||||
| chr8:28996279
|
T | A | 69 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12793T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996279 | ||||||
| chr8:28996280
|
C | A | 69 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12792C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996280 | ||||||
| chr8:28996281
|
T | C | 69 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.587-12791T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996281 | ||||||
| chr8:28996434
|
T | C | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-12638T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996434 | ||||||
| chr8:28996509
|
T | C | 1 | a0001c0001t0004g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.587-12563T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996509 | ||||||
| chr8:28996722
|
G | C | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-12350G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996722 | ||||||
| chr8:28996736
|
G | A | 12 | a0001c0001t0007g0004a0001c0001t0007g0009a0001c0001t0007g0010others(9): Show | 12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-12336G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996736 | ||||||
| chr8:28996901
|
T | C | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.587-12171T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28996901 | ||||||
| chr8:28997359
|
T | A | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.587-11713T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997359 | ||||||
| chr8:28997482
|
T | A | 1 | a0001c0001t0004g0027 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.587-11590T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997482 | ||||||
| chr8:28997545
|
G | A | 1 | a0001c0001t0010g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.587-11527G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997545 | ||||||
| chr8:28997585
|
C | T | 200 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(197): Show | 200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.587-11487C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997585 | ||||||
| chr8:28997702
|
C | T | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-11370C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997702 | ||||||
| chr8:28997792
|
C | G | 1 | a0001c0001t0002g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.587-11280C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28997792 | ||||||
| chr8:28998009
|
C | T | 184 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(181): Show | 184 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.587-11063C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998009 | ||||||
| chr8:28998265
|
A | G | 1 | a0001c0001t0002g0174 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.587-10807A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998265 | ||||||
| chr8:28998368
|
C | G | 1 | a0001c0001t0003g0090 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.587-10704C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998368 | ||||||
| chr8:28998374
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.587-10698C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998374 | ||||||
| chr8:28998689
|
A | C | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.587-10383A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998689 | ||||||
| chr8:28998776
|
C | T | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587-10296C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28998776 | ||||||
| chr8:28999341
|
C | T | 3 | a0001c0001t0007g0010a0001c0001t0007g0017a0001c0001t0007g0262 | 3 | HG02257.hp2 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.587-9731C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28999341 | ||||||
| chr8:28999393
|
A | G | 3 | a0001c0001t0007g0010a0001c0001t0007g0017a0001c0001t0007g0262 | 3 | HG02257.hp2 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.587-9679A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 28999393 | ||||||
| chr8:29000064
|
A | G | 1 | a0001c0001t0003g0073 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.587-9008A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000064 | ||||||
| chr8:29000076
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.587-8996G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000076 | ||||||
| chr8:29000212
|
C | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.587-8860C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000212 | ||||||
| chr8:29000276
|
G | A | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-8796G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000276 | ||||||
| chr8:29000290
|
T | C | 2 | a0001c0001t0003g0075a0001c0001t0003g0088 | 2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.587-8782T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000290 | ||||||
| chr8:29000333
|
C | T | 12 | a0001c0001t0007g0004a0001c0001t0007g0009a0001c0001t0007g0010others(9): Show | 12 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-8739C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000333 | ||||||
| chr8:29000943
|
T | G | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587-8129T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29000943 | ||||||
| chr8:29001057
|
A | C | 2 | a0001c0001t0002g0214a0001c0001t0002g0270 | 2 | NA18973.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.587-8015A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001057 | ||||||
| chr8:29001060
|
C | A | 98 | a0001c0001t0002g0083a0001c0001t0002g0132a0001c0001t0002g0134others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.587-8012C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001060 | ||||||
| chr8:29001376
|
C | T | 1 | a0001c0001t0003g0094 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.587-7696C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001376 | ||||||
| chr8:29001476
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.587-7596G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001476 | ||||||
| chr8:29001510
|
G | A | 4 | a0001c0001t0001g0291a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG01070.hp2 HG01261.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-7562G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001510 | ||||||
| chr8:29001512
|
G | T | 2 | a0001c0001t0006g0337a0001c0001t0006g0338 | 2 | NA18943.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.587-7560G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001512 | ||||||
| chr8:29001536
|
C | T | 11 | a0001c0001t0003g0133a0001c0001t0003g0168a0001c0001t0003g0170others(8): Show | 11 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-7536C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001536 | ||||||
| chr8:29001537
|
G | A | 1 | a0001c0001t0003g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.587-7535G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001537 | ||||||
| chr8:29001547
|
C | G | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.587-7525C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001547 | ||||||
| chr8:29001549
|
C | CAAACAAA others(3): Show |
1 | a0001c0001t0004g0060 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.587-7486_587-7477d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29001549 | |||||
| chr8:29001549
|
CAAACA | C | 113 | a0001c0001t0001g0142a0001c0001t0001g0243a0001c0001t0001g0261others(110): Show | 113 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.587-7481_587-7477d others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29001549 | |||||
| chr8:29001549
|
CAAACAAA others(3): Show |
C | 186 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(183): Show | 186 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.587-7486_587-7477d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29001549 | |||||
| chr8:29001549
|
CAAACAAA others(8): Show |
C | 4 | a0001c0001t0001g0303a0001c0001t0001g0307a0001c0001t0014g0116others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-7491_587-7477d others(17): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29001549 | |||||
| chr8:29001718
|
A | C | 1 | a0001c0001t0010g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.587-7354A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29001718 | ||||||
| chr8:29002114
|
G | T | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.587-6958G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29002114 | ||||||
| chr8:29002294
|
G | A | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-6778G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29002294 | ||||||
| chr8:29002863
|
A | G | 2 | a0001c0001t0004g0040a0001c0001t0004g0042 | 2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.587-6209A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29002863 | ||||||
| chr8:29002901
|
C | A | 1 | a0001c0001t0006g0330 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.587-6171C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29002901 | ||||||
| chr8:29003084
|
C | CT | 67 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(64): Show | 67 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.587-5977dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003084 | |||||
| chr8:29003084
|
CT | C | 14 | a0001c0001t0001g0218a0001c0001t0002g0184a0001c0001t0004g0018others(11): Show | 14 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.587-5977delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003084 | |||||
| chr8:29003140
|
T | C | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-5932T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003140 | ||||||
| chr8:29003342
|
T | C | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.587-5730T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003342 | ||||||
| chr8:29003496
|
GTA | G | 101 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.587-5556_587-5555d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003496 | |||||
| chr8:29003496
|
GTATA | G | 210 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(207): Show | 210 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.587-5558_587-5555d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003496 | |||||
| chr8:29003500
|
A | G | 17 | a0001c0001t0003g0108a0001c0001t0004g0018a0001c0001t0004g0019others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(14): Show |
intron_variant | MODIFIER | c.587-5572A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003500 | ||||||
| chr8:29003543
|
T | A | 1 | a0001c0001t0002g0248 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5529T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003543 | ||||||
| chr8:29003545
|
T | A | 1 | a0001c0001t0002g0248 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5527T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003545 | ||||||
| chr8:29003547
|
C | A | 1 | a0001c0001t0002g0248 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5525C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003547 | ||||||
| chr8:29003549
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5523G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003549 | ||||||
| chr8:29003552
|
T | TATATATA others(4): Show |
1 | a0001c0001t0002g0248 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5520_587-5519i others(13): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003552 | ||||||
| chr8:29003555
|
A | AAT | 10 | a0001c0001t0004g0040a0001c0001t0004g0042a0001c0001t0004g0048others(7): Show | 10 | HG02074.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-5496_587-5495d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATAAATA others(9): Show |
1 | a0001c0001t0003g0066 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.587-5514_587-5513i others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATAT | 7 | a0001c0001t0001g0220a0001c0001t0001g0256a0001c0001t0001g0276others(4): Show | 7 | HG02040.hp2 HG02738.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.587-5498_587-5495d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATAT | 8 | a0001c0001t0001g0257a0001c0001t0004g0019a0001c0001t0004g0020others(5): Show | 8 | HG00140.hp2 HG00642.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-5500_587-5495d others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(1): Show |
8 | a0001c0001t0001g0316a0001c0001t0003g0070a0001c0001t0003g0071others(5): Show | 8 | HG01069.hp2 HG02717.hp1 NA18986.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-5502_587-5495d others(10): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(3): Show |
8 | a0001c0001t0002g0175a0001c0001t0002g0185a0001c0001t0003g0007others(5): Show | 8 | HG00735.hp1 HG02896.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-5504_587-5495d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(5): Show |
28 | a0001c0001t0002g0152a0001c0001t0003g0008a0001c0001t0003g0068others(25): Show | 28 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.587-5506_587-5495d others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(7): Show |
16 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0001g0287others(13): Show | 16 | HG01167.hp2 HG01884.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.587-5508_587-5495d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(9): Show |
25 | a0001c0001t0001g0084a0001c0001t0001g0141a0001c0001t0001g0142others(22): Show | 25 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.587-5510_587-5495d others(18): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(11): Show |
16 | a0001c0001t0001g0136a0001c0001t0001g0146a0001c0001t0001g0147others(13): Show | 16 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.587-5512_587-5495d others(20): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(13): Show |
17 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0219others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.587-5514_587-5495d others(22): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(15): Show |
12 | a0001c0001t0001g0140a0001c0001t0001g0164a0001c0001t0001g0221others(9): Show | 12 | HG01123.hp2 HG01496.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.587-5516_587-5495d others(24): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(17): Show |
12 | a0001c0001t0001g0148a0001c0001t0001g0253a0001c0001t0001g0261others(9): Show | 12 | HG00408.hp1 HG01243.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(26): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(19): Show |
17 | a0001c0001t0001g0165a0001c0001t0001g0229a0001c0001t0001g0281others(14): Show | 17 | HG00438.hp2 HG01070.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(28): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(21): Show |
22 | a0001c0001t0001g0282a0001c0001t0001g0289a0001c0001t0001g0303others(19): Show | 22 | HG00621.hp2 HG02055.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(30): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(23): Show |
18 | a0001c0001t0001g0217a0001c0001t0001g0277a0001c0001t0001g0323others(15): Show | 18 | HG00280.hp2 HG00558.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(32): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(25): Show |
32 | a0001c0001t0001g0271a0001c0001t0001g0299a0001c0001t0001g0322others(29): Show | 32 | HG00597.hp2 HG00642.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(34): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(27): Show |
15 | a0001c0001t0001g0321a0001c0001t0002g0135a0001c0001t0002g0137others(12): Show | 15 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(36): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(29): Show |
9 | a0001c0001t0001g0176a0001c0001t0001g0305a0001c0001t0002g0138others(6): Show | 9 | HG01168.hp1 HG01175.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(38): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(31): Show |
11 | a0001c0001t0001g0218a0001c0001t0002g0196a0001c0001t0002g0214others(8): Show | 11 | HG00544.hp1 HG00621.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-5495_587-5494i others(40): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(33): Show |
1 | a0001c0001t0002g0235 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.587-5495_587-5494i others(42): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | AATATATA others(35): Show |
1 | a0001c0001t0002g0236 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.587-5495_587-5494i others(44): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
A | ATATATAT others(22): Show |
3 | a0001c0001t0005g0199a0001c0001t0006g0328a0001c0001t0009g0130 | 3 | HG02559.hp1 NA19062.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.587-5517_587-5516i others(31): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003555 | ||||||
| chr8:29003555
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0002g0252 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.587-5517_587-5516i others(37): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003555 | ||||||
| chr8:29003555
|
A | T | 1 | a0001c0001t0002g0248 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587-5517A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003555 | ||||||
| chr8:29003555
|
AATAT | A | 11 | a0001c0001t0003g0133a0001c0001t0003g0168a0001c0001t0003g0170others(8): Show | 11 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-5498_587-5495d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003555
|
AATATATA others(3): Show |
A | 3 | a0001c0001t0002g0153a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | NA18943.hp1 NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.587-5504_587-5495d others(12): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003555 | |||||
| chr8:29003565
|
T | TATATATA others(13): Show |
1 | a0001c0001t0001g0250 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.587-5495_587-5494i others(22): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29003565 | |||||
| chr8:29003700
|
G | A | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-5372G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003700 | ||||||
| chr8:29003774
|
G | T | 2 | a0001c0001t0003g0121a0001c0001t0008g0120 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.587-5298G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003774 | ||||||
| chr8:29003799
|
A | G | 1 | a0001c0001t0006g0331 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.587-5273A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003799 | ||||||
| chr8:29003866
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.587-5206A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003866 | ||||||
| chr8:29003884
|
A | G | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-5188A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003884 | ||||||
| chr8:29003943
|
G | A | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.587-5129G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29003943 | ||||||
| chr8:29004292
|
T | C | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-4780T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004292 | ||||||
| chr8:29004433
|
G | C | 1 | a0001c0001t0001g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.587-4639G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004433 | ||||||
| chr8:29004670
|
A | T | 3 | a0001c0001t0002g0153a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | NA18943.hp1 NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.587-4402A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004670 | ||||||
| chr8:29004776
|
G | T | 3 | a0001c0001t0016g0329a0001c0001t0016g0332a0001c0001t0023g0333 | 3 | NA18947.hp1 NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.587-4296G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004776 | ||||||
| chr8:29004809
|
A | C | 1 | a0001c0001t0003g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.587-4263A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004809 | ||||||
| chr8:29004855
|
C | T | 2 | a0001c0001t0002g0157a0001c0001t0002g0158 | 2 | NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.587-4217C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004855 | ||||||
| chr8:29004856
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.587-4216G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004856 | ||||||
| chr8:29004886
|
A | G | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.587-4186A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29004886 | ||||||
| chr8:29005213
|
T | G | 2 | a0001c0001t0003g0121a0001c0001t0008g0120 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.587-3859T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29005213 | ||||||
| chr8:29005420
|
G | T | 209 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(206): Show | 209 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.587-3652G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29005420 | ||||||
| chr8:29005786
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.587-3286G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29005786 | ||||||
| chr8:29005911
|
A | G | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.587-3161A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29005911 | ||||||
| chr8:29005990
|
A | AT | 93 | a0001c0001t0001g0142a0001c0001t0001g0149a0001c0001t0001g0250others(90): Show | 93 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.587-3062dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 29005990 | |||||
| chr8:29006021
|
G | A | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.587-3051G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006021 | ||||||
| chr8:29006210
|
G | C | 336 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(333): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(333): Show |
intron_variant | MODIFIER | c.587-2862G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006210 | ||||||
| chr8:29006241
|
C | A | 1 | a0001c0001t0003g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.587-2831C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006241 | ||||||
| chr8:29006266
|
T | A | 1 | a0001c0001t0004g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-2806T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006266 | ||||||
| chr8:29006285
|
G | T | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.587-2787G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006285 | ||||||
| chr8:29006292
|
C | T | 1 | a0001c0001t0008g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.587-2780C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006292 | ||||||
| chr8:29006558
|
C | T | 181 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(178): Show | 181 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.587-2514C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006558 | ||||||
| chr8:29006681
|
T | G | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.587-2391T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006681 | ||||||
| chr8:29006708
|
C | T | 1 | a0001c0001t0007g0015 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.587-2364C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006708 | ||||||
| chr8:29006756
|
G | C | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-2316G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006756 | ||||||
| chr8:29006795
|
A | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0188 | 2 | NA19004.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.587-2277A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29006795 | ||||||
| chr8:29007016
|
C | T | 1 | a0001c0001t0008g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.587-2056C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007016 | ||||||
| chr8:29007158
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.587-1914G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007158 | ||||||
| chr8:29007421
|
A | G | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.587-1651A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007421 | ||||||
| chr8:29007640
|
G | A | 1 | a0001c0001t0008g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.587-1432G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007640 | ||||||
| chr8:29007749
|
G | A | 2 | a0001c0001t0004g0020a0001c0001t0004g0343 | 2 | HG00642.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.587-1323G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007749 | ||||||
| chr8:29007831
|
T | C | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.587-1241T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007831 | ||||||
| chr8:29007930
|
C | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.587-1142C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007930 | ||||||
| chr8:29007984
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.587-1088T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29007984 | ||||||
| chr8:29008087
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.587-985G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29008087 | ||||||
| chr8:29008468
|
T | C | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG00738.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.587-604T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29008468 | ||||||
| chr8:29008740
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.587-332G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 4/9 | chr8 | 29008740 | ||||||
| chr8:29009267
|
T | G | 1 | a0001c0001t0012g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.697+85T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009267 | ||||||
| chr8:29009343
|
A | T | 3 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0343 | 3 | HG00642.hp2 HG01081.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.697+161A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009343 | ||||||
| chr8:29009380
|
AG | A | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.697+199delG | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009380 | ||||||
| chr8:29009457
|
C | T | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+275C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009457 | ||||||
| chr8:29009465
|
ATGTT | A | 53 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(50): Show | 53 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.697+284_697+287del others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009465 | ||||||
| chr8:29009506
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.697+324C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009506 | ||||||
| chr8:29009516
|
C | T | 1 | a0001c0001t0003g0100 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.697+334C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009516 | ||||||
| chr8:29009523
|
CT | C | 241 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(238): Show | 241 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.697+362delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 29009523 | |||||
| chr8:29009523
|
CTT | C | 37 | a0001c0001t0001g0164a0001c0001t0001g0303a0001c0001t0002g0208others(34): Show | 37 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.697+361_697+362del others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 29009523 | |||||
| chr8:29009523
|
CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(4): Show | 7 | HG02055.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.697+355_697+362del others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 29009523 | |||||
| chr8:29009619
|
C | G | 1 | a0001c0001t0008g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.697+437C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009619 | ||||||
| chr8:29009929
|
C | T | 82 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(79): Show | 82 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.697+747C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29009929 | ||||||
| chr8:29010285
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0279 | 2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.697+1103C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29010285 | ||||||
| chr8:29010563
|
A | T | 26 | a0001c0001t0001g0150a0001c0001t0001g0271a0001c0001t0003g0006others(23): Show | 26 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.697+1381A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29010563 | ||||||
| chr8:29010915
|
T | G | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.697+1733T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29010915 | ||||||
| chr8:29010918
|
A | G | 1 | a0001c0001t0010g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.697+1736A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29010918 | ||||||
| chr8:29011000
|
T | G | 1 | a0001c0001t0003g0096 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.697+1818T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29011000 | ||||||
| chr8:29011188
|
T | C | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.697+2006T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29011188 | ||||||
| chr8:29011711
|
C | T | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.697+2529C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29011711 | ||||||
| chr8:29011714
|
G | T | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.697+2532G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29011714 | ||||||
| chr8:29011724
|
T | A | 1 | a0001c0001t0001g0288 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.697+2542T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29011724 | ||||||
| chr8:29012014
|
A | G | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.697+2832A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012014 | ||||||
| chr8:29012109
|
G | A | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.697+2927G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012109 | ||||||
| chr8:29012120
|
C | T | 224 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(221): Show | 224 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.697+2938C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012120 | ||||||
| chr8:29012418
|
T | C | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.697+3236T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012418 | ||||||
| chr8:29012427
|
A | G | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.697+3245A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012427 | ||||||
| chr8:29012454
|
A | G | 2 | a0001c0001t0004g0040a0001c0001t0004g0042 | 2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.697+3272A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012454 | ||||||
| chr8:29012570
|
A | C | 1 | a0001c0001t0009g0131 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.697+3388A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012570 | ||||||
| chr8:29012596
|
G | A | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.697+3414G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012596 | ||||||
| chr8:29012611
|
G | A | 50 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(47): Show | 50 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.697+3429G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29012611 | ||||||
| chr8:29013053
|
A | C | 1 | a0001c0001t0007g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.697+3871A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013053 | ||||||
| chr8:29013245
|
C | T | 1 | a0001c0001t0002g0249 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.697+4063C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013245 | ||||||
| chr8:29013267
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.697+4085C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013267 | ||||||
| chr8:29013282
|
C | T | 1 | a0001c0001t0003g0101 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.697+4100C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013282 | ||||||
| chr8:29013335
|
C | G | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.697+4153C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013335 | ||||||
| chr8:29013362
|
C | T | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.697+4180C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013362 | ||||||
| chr8:29013386
|
G | A | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.697+4204G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013386 | ||||||
| chr8:29013474
|
T | G | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.697+4292T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013474 | ||||||
| chr8:29013640
|
G | A | 1 | a0001c0001t0004g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.697+4458G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013640 | ||||||
| chr8:29013730
|
T | A | 1 | a0001c0001t0001g0294 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.697+4548T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29013730 | ||||||
| chr8:29014086
|
TC | T | 336 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(333): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.698-4670delC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 29014086 | |||||
| chr8:29014126
|
T | C | 1 | a0001c0001t0004g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.698-4634T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014126 | ||||||
| chr8:29014208
|
A | G | 1 | a0001c0001t0007g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.698-4552A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014208 | ||||||
| chr8:29014212
|
G | T | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.698-4548G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014212 | ||||||
| chr8:29014270
|
GA | G | 119 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(116): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.698-4484delA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 29014270 | |||||
| chr8:29014286
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.698-4474A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014286 | ||||||
| chr8:29014336
|
T | A | 3 | a0001c0001t0005g0199a0001c0001t0005g0200a0001c0001t0005g0215 | 3 | HG02559.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.698-4424T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014336 | ||||||
| chr8:29014573
|
C | T | 2 | a0001c0001t0003g0121a0001c0001t0008g0120 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.698-4187C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014573 | ||||||
| chr8:29014719
|
G | A | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-4041G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014719 | ||||||
| chr8:29014780
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0244 | 2 | HG00438.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.698-3980A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014780 | ||||||
| chr8:29014943
|
G | A | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.698-3817G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014943 | ||||||
| chr8:29014975
|
C | T | 1 | a0001c0001t0003g0092 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.698-3785C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29014975 | ||||||
| chr8:29015058
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.698-3702T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015058 | ||||||
| chr8:29015305
|
T | C | 1 | a0001c0001t0003g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.698-3455T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015305 | ||||||
| chr8:29015365
|
A | G | 1 | a0001c0001t0004g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.698-3395A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015365 | ||||||
| chr8:29015395
|
C | G | 1 | a0001c0001t0003g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.698-3365C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015395 | ||||||
| chr8:29015438
|
A | G | 1 | a0001c0001t0003g0269 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.698-3322A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015438 | ||||||
| chr8:29015466
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.698-3294T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015466 | ||||||
| chr8:29015472
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.698-3288C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015472 | ||||||
| chr8:29015527
|
C | T | 6 | a0001c0001t0006g0336a0001c0001t0006g0337a0001c0001t0006g0338others(3): Show | 6 | NA18943.hp2 NA18956.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.698-3233C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015527 | ||||||
| chr8:29015701
|
G | A | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.698-3059G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015701 | ||||||
| chr8:29015774
|
G | C | 1 | a0001c0001t0007g0009 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.698-2986G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29015774 | ||||||
| chr8:29016113
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.698-2647T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29016113 | ||||||
| chr8:29016114
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.698-2646T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29016114 | ||||||
| chr8:29016232
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.698-2528T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29016232 | ||||||
| chr8:29016995
|
A | C | 15 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.698-1765A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29016995 | ||||||
| chr8:29017001
|
A | G | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-1759A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29017001 | ||||||
| chr8:29017309
|
A | G | 1 | a0001c0001t0007g0011 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.698-1451A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29017309 | ||||||
| chr8:29017581
|
A | T | 1 | a0001c0001t0003g0108 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.698-1179A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29017581 | ||||||
| chr8:29017914
|
C | T | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-846C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29017914 | ||||||
| chr8:29017991
|
G | C | 2 | a0001c0001t0002g0163a0001c0001t0002g0234 | 2 | HG00438.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.698-769G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29017991 | ||||||
| chr8:29018399
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.698-361A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29018399 | ||||||
| chr8:29018704
|
T | C | 163 | a0001c0001t0001g0149a0001c0001t0003g0005a0001c0001t0003g0006others(160): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.698-56T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 5/9 | chr8 | 29018704 | ||||||
| chr8:29018935
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.851+22G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29018935 | ||||||
| chr8:29019049
|
A | G | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851+136A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019049 | ||||||
| chr8:29019076
|
C | G | 245 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.851+163C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019076 | ||||||
| chr8:29019119
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.851+206C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019119 | ||||||
| chr8:29019345
|
A | T | 12 | a0001c0001t0003g0133a0001c0001t0003g0168a0001c0001t0003g0170others(9): Show | 12 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+432A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019345 | ||||||
| chr8:29019436
|
C | T | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851+523C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019436 | ||||||
| chr8:29019671
|
C | T | 1 | a0001c0001t0007g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.851+758C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019671 | ||||||
| chr8:29019773
|
T | C | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.851+860T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019773 | ||||||
| chr8:29019788
|
T | C | 5 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0247others(2): Show | 5 | NA18612.hp1 NA18953.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.851+875T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019788 | ||||||
| chr8:29019872
|
G | A | 2 | a0001c0001t0005g0292a0001c0001t0005g0301 | 2 | HG01516.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.851+959G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29019872 | ||||||
| chr8:29020109
|
A | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0187a0001c0001t0019g0173 | 3 | NA18990.hp1 NA18992.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.851+1196A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020109 | ||||||
| chr8:29020188
|
A | G | 1 | a0001c0001t0008g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.851+1275A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020188 | ||||||
| chr8:29020243
|
G | A | 4 | a0001c0001t0004g0123a0001c0001t0004g0124a0001c0001t0004g0125others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+1330G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020243 | ||||||
| chr8:29020480
|
C | T | 1 | a0001c0001t0005g0300 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.851+1567C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020480 | ||||||
| chr8:29020562
|
A | G | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+1649A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020562 | ||||||
| chr8:29020753
|
A | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG02027.hp2 NA18975.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+1840A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29020753 | ||||||
| chr8:29021574
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.851+2661G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021574 | ||||||
| chr8:29021621
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.851+2708C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021621 | ||||||
| chr8:29021622
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.851+2709G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021622 | ||||||
| chr8:29021631
|
G | A | 2 | a0001c0001t0002g0295a0001c0001t0002g0296 | 2 | NA18968.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.851+2718G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021631 | ||||||
| chr8:29021638
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.851+2725G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021638 | ||||||
| chr8:29021717
|
G | T | 3 | a0001c0001t0003g0119a0001c0001t0003g0121a0001c0001t0008g0120 | 3 | HG03195.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.851+2804G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021717 | ||||||
| chr8:29021728
|
C | T | 1 | a0001c0001t0010g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.851+2815C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021728 | ||||||
| chr8:29021801
|
G | A | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+2888G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29021801 | ||||||
| chr8:29021859
|
C | CA | 123 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0316others(120): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.851+2963dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29021859 | |||||
| chr8:29021859
|
C | CAA | 16 | a0001c0001t0003g0092a0001c0001t0003g0133a0001c0001t0003g0168others(13): Show | 16 | HG01069.hp2 HG01167.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.851+2962_851+2963d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29021859 | |||||
| chr8:29021989
|
T | TGGGC | 81 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(78): Show | 81 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.851+3077_851+3080d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29021989 | |||||
| chr8:29022182
|
T | A | 2 | a0001c0001t0003g0121a0001c0001t0008g0120 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.851+3269T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022182 | ||||||
| chr8:29022234
|
T | C | 1 | a0001c0001t0007g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.851+3321T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022234 | ||||||
| chr8:29022494
|
A | G | 31 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0031others(28): Show | 31 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.851+3581A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022494 | ||||||
| chr8:29022524
|
G | A | 1 | a0001c0001t0004g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.851+3611G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022524 | ||||||
| chr8:29022643
|
C | T | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+3730C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022643 | ||||||
| chr8:29022882
|
A | G | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.851+3969A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29022882 | ||||||
| chr8:29023060
|
T | TAA | 6 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0077others(3): Show | 6 | HG00735.hp1 HG01928.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.851+4149_851+4150d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29023060 | |||||
| chr8:29023235
|
T | C | 245 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.851+4322T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023235 | ||||||
| chr8:29023514
|
C | T | 14 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0068others(11): Show | 14 | HG00609.hp1 HG02080.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.851+4601C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023514 | ||||||
| chr8:29023543
|
C | CA | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.851+4631dupA | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29023543 | |||||
| chr8:29023646
|
C | T | 6 | a0001c0001t0004g0003a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.851+4733C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023646 | ||||||
| chr8:29023662
|
A | G | 2 | a0001c0001t0007g0004a0001c0001t0007g0061 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.851+4749A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023662 | ||||||
| chr8:29023744
|
C | A | 2 | a0001c0001t0002g0202a0001c0001t0002g0252 | 2 | NA18941.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.851+4831C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023744 | ||||||
| chr8:29023763
|
A | T | 3 | a0001c0001t0016g0329a0001c0001t0016g0332a0001c0001t0023g0333 | 3 | NA18947.hp1 NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.851+4850A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023763 | ||||||
| chr8:29023811
|
A | C | 261 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(258): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.851+4898A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29023811 | ||||||
| chr8:29024393
|
G | A | 80 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(77): Show | 80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.851+5480G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29024393 | ||||||
| chr8:29024412
|
G | C | 1 | a0001c0001t0004g0062 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.851+5499G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29024412 | ||||||
| chr8:29024612
|
T | C | 12 | a0001c0001t0003g0133a0001c0001t0003g0168a0001c0001t0003g0170others(9): Show | 12 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+5699T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29024612 | ||||||
| chr8:29024920
|
C | T | 12 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+6007C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29024920 | ||||||
| chr8:29024984
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+6071G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29024984 | ||||||
| chr8:29025093
|
A | G | 2 | a0001c0001t0001g0229a0001c0001t0001g0243 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.851+6180A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29025093 | ||||||
| chr8:29025398
|
A | G | 1 | a0001c0001t0009g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.851+6485A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29025398 | ||||||
| chr8:29025473
|
GTTA | G | 10 | a0001c0001t0007g0009a0001c0001t0007g0010a0001c0001t0007g0011others(7): Show | 10 | HG01261.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+6565_851+6567d others(5): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29025473 | |||||
| chr8:29025871
|
C | A | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.851+6958C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29025871 | ||||||
| chr8:29025897
|
T | C | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.851+6984T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29025897 | ||||||
| chr8:29026043
|
T | TAC | 12 | a0001c0001t0001g0268a0001c0001t0001g0283a0001c0001t0001g0288others(9): Show | 12 | HG00323.hp1 HG01123.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+7168_851+7169d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | |||||
| chr8:29026043
|
T | TACAC | 7 | a0001c0001t0001g0316a0001c0001t0002g0137a0001c0001t0002g0196others(4): Show | 7 | HG00423.hp2 HG01943.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.851+7166_851+7169d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | |||||
| chr8:29026043
|
T | TACACACA others(5): Show |
1 | a0001c0001t0003g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.851+7158_851+7169d others(14): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | |||||
| chr8:29026043
|
TAC | T | 151 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(148): Show | 151 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.851+7168_851+7169d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | |||||
| chr8:29026043
|
TACAC | T | 48 | a0001c0001t0002g0167a0001c0001t0002g0233a0001c0001t0002g0295others(45): Show | 48 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.851+7166_851+7169d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | |||||
| chr8:29026043
|
TACACAC | T | 43 | a0001c0001t0004g0003a0001c0001t0004g0018a0001c0001t0004g0019others(40): Show | 43 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.851+7164_851+7169d others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | |||||
| chr8:29026043
|
TACACACA others(7): Show |
T | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851+7156_851+7169d others(16): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29026043 | |||||
| chr8:29026179
|
C | G | 1 | a0001c0001t0002g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.851+7266C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29026179 | ||||||
| chr8:29026235
|
A | G | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.851+7322A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29026235 | ||||||
| chr8:29026398
|
T | C | 1 | a0001c0001t0008g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.851+7485T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29026398 | ||||||
| chr8:29026445
|
G | T | 1 | a0001c0001t0002g0198 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.851+7532G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29026445 | ||||||
| chr8:29026517
|
T | C | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.851+7604T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29026517 | ||||||
| chr8:29027037
|
G | T | 1 | a0001c0001t0002g0172 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.851+8124G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027037 | ||||||
| chr8:29027131
|
C | T | 1 | a0001c0001t0003g0326 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.851+8218C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027131 | ||||||
| chr8:29027178
|
G | C | 1 | a0001c0001t0004g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.851+8265G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027178 | ||||||
| chr8:29027236
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.851+8323G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027236 | ||||||
| chr8:29027289
|
C | G | 2 | a0001c0001t0006g0337a0001c0001t0006g0338 | 2 | NA18943.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.851+8376C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027289 | ||||||
| chr8:29027374
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.851+8461G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027374 | ||||||
| chr8:29027396
|
G | T | 2 | a0001c0001t0002g0318a0001c0001t0003g0089 | 2 | HG00558.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.851+8483G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027396 | ||||||
| chr8:29027953
|
T | C | 81 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(78): Show | 81 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.851+9040T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29027953 | ||||||
| chr8:29028087
|
A | T | 7 | a0001c0001t0001g0220a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02040.hp2 NA18964.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+9174A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028087 | ||||||
| chr8:29028112
|
C | T | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851+9199C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028112 | ||||||
| chr8:29028144
|
T | C | 118 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.851+9231T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028144 | ||||||
| chr8:29028387
|
A | G | 1 | a0001c0001t0002g0193 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.851+9474A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028387 | ||||||
| chr8:29028462
|
T | C | 11 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(8): Show | 11 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.851+9549T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028462 | ||||||
| chr8:29028559
|
A | G | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851+9646A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028559 | ||||||
| chr8:29028573
|
CT | C | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+9661delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028573 | ||||||
| chr8:29028577
|
C | G | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.851+9664C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028577 | ||||||
| chr8:29028766
|
G | A | 2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.851+9853G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028766 | ||||||
| chr8:29028774
|
T | A | 11 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(8): Show | 11 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.851+9861T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028774 | ||||||
| chr8:29028832
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+9919G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29028832 | ||||||
| chr8:29029106
|
C | T | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.851+10193C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029106 | ||||||
| chr8:29029486
|
C | G | 2 | a0001c0001t0002g0202a0001c0001t0002g0252 | 2 | NA18941.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.851+10573C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029486 | ||||||
| chr8:29029578
|
G | A | 1 | a0001c0001t0007g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.851+10665G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029578 | ||||||
| chr8:29029611
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.851+10698G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029611 | ||||||
| chr8:29029666
|
A | G | 1 | a0001c0001t0004g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.851+10753A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029666 | ||||||
| chr8:29029706
|
C | T | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+10793C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029706 | ||||||
| chr8:29029713
|
G | C | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.851+10800G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029713 | ||||||
| chr8:29029743
|
T | G | 1 | a0001c0001t0006g0327 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.851+10830T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029743 | ||||||
| chr8:29029903
|
T | C | 1 | a0001c0001t0006g0328 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.851+10990T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29029903 | ||||||
| chr8:29029943
|
CT | C | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.851+11039delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29029943 | |||||
| chr8:29030008
|
T | C | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.851+11095T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030008 | ||||||
| chr8:29030169
|
T | A | 12 | a0001c0001t0006g0330a0001c0001t0006g0331a0001c0001t0006g0335others(9): Show | 12 | HG00544.hp1 HG02056.hp1 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+11256T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030169 | ||||||
| chr8:29030179
|
G | GT | 122 | a0001c0001t0001g0149a0001c0001t0002g0244a0001c0001t0003g0005others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.851+11282dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29030179 | |||||
| chr8:29030179
|
G | GTT | 11 | a0001c0001t0003g0085a0001c0001t0003g0103a0001c0001t0003g0181others(8): Show | 11 | HG00642.hp2 HG01261.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.851+11281_851+1128 others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29030179 | |||||
| chr8:29030179
|
GT | G | 9 | a0001c0001t0001g0148a0001c0001t0001g0299a0001c0001t0003g0118others(6): Show | 9 | HG01167.hp2 HG02280.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.851+11282delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29030179 | |||||
| chr8:29030185
|
T | G | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.851+11272T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030185 | ||||||
| chr8:29030239
|
C | T | 1 | a0001c0001t0003g0093 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.851+11326C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030239 | ||||||
| chr8:29030299
|
C | T | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.851+11386C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030299 | ||||||
| chr8:29030428
|
A | G | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.851+11515A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030428 | ||||||
| chr8:29030518
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+11605C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030518 | ||||||
| chr8:29030531
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.851+11618A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030531 | ||||||
| chr8:29030572
|
A | G | 1 | a0001c0001t0004g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.851+11659A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030572 | ||||||
| chr8:29030940
|
A | G | 10 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(7): Show | 10 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+12027A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29030940 | ||||||
| chr8:29031192
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.851+12279A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29031192 | ||||||
| chr8:29031372
|
T | C | 69 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(66): Show | 69 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.851+12459T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29031372 | ||||||
| chr8:29031513
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.851+12600T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29031513 | ||||||
| chr8:29031532
|
A | AT | 70 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(67): Show | 70 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.851+12631dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29031532 | |||||
| chr8:29031643
|
T | C | 1 | a0001c0001t0005g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.851+12730T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29031643 | ||||||
| chr8:29031649
|
A | G | 146 | a0001c0001t0001g0149a0001c0001t0003g0005a0001c0001t0003g0006others(143): Show | 146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.851+12736A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29031649 | ||||||
| chr8:29032224
|
T | C | 1 | a0001c0001t0003g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.852-13137T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032224 | ||||||
| chr8:29032280
|
A | C | 1 | a0001c0001t0001g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.852-13081A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032280 | ||||||
| chr8:29032352
|
A | C | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0027 | 3 | HG01069.hp2 HG01167.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.852-13009A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032352 | ||||||
| chr8:29032418
|
C | T | 2 | a0001c0001t0001g0320a0001c0001t0001g0323 | 2 | NA18954.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.852-12943C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032418 | ||||||
| chr8:29032442
|
A | C | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-12919A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032442 | ||||||
| chr8:29032697
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.852-12664G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032697 | ||||||
| chr8:29032802
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.852-12559T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032802 | ||||||
| chr8:29032862
|
G | A | 1 | a0001c0001t0004g0051 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.852-12499G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29032862 | ||||||
| chr8:29032923
|
GATA | G | 8 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(5): Show | 8 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-12429_852-1242 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29032923 | |||||
| chr8:29033023
|
A | G | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-12338A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033023 | ||||||
| chr8:29033099
|
C | CTAT | 7 | a0001c0001t0001g0220a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02040.hp2 NA18964.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.852-12261_852-1225 others(7): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29033099 | |||||
| chr8:29033200
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0243 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.852-12161G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033200 | ||||||
| chr8:29033267
|
G | A | 2 | a0001c0001t0002g0228a0001c0001t0005g0161 | 2 | HG02258.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.852-12094G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033267 | ||||||
| chr8:29033270
|
A | C | 123 | a0001c0001t0001g0149a0001c0001t0003g0005a0001c0001t0003g0006others(120): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.852-12091A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033270 | ||||||
| chr8:29033425
|
A | G | 4 | a0001c0001t0002g0167a0001c0001t0002g0184a0001c0001t0002g0233others(1): Show | 4 | HG02165.hp2 NA18965.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-11936A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033425 | ||||||
| chr8:29033646
|
C | T | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.852-11715C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033646 | ||||||
| chr8:29033769
|
G | A | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.852-11592G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29033769 | ||||||
| chr8:29034092
|
C | A | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.852-11269C>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034092 | ||||||
| chr8:29034260
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.852-11101C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034260 | ||||||
| chr8:29034521
|
T | C | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-10840T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034521 | ||||||
| chr8:29034573
|
G | A | 53 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(50): Show | 53 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.852-10788G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034573 | ||||||
| chr8:29034586
|
G | A | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.852-10775G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034586 | ||||||
| chr8:29034837
|
G | A | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-10524G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034837 | ||||||
| chr8:29034862
|
A | AAAAT | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-10483_852-1048 others(8): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29034862 | |||||
| chr8:29034885
|
A | G | 6 | a0001c0001t0005g0155a0001c0001t0005g0162a0001c0001t0005g0177others(3): Show | 6 | HG00280.hp2 HG01123.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.852-10476A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034885 | ||||||
| chr8:29034906
|
T | A | 2 | a0001c0001t0003g0075a0001c0001t0003g0088 | 2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.852-10455T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034906 | ||||||
| chr8:29034991
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.852-10370A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29034991 | ||||||
| chr8:29035030
|
C | T | 2 | a0001c0001t0008g0001a0001c0001t0008g0002 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.852-10331C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035030 | ||||||
| chr8:29035140
|
G | T | 1 | a0001c0001t0002g0206 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.852-10221G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035140 | ||||||
| chr8:29035194
|
G | C | 1 | a0001c0001t0002g0184 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.852-10167G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035194 | ||||||
| chr8:29035362
|
A | T | 2 | a0001c0001t0004g0043a0001c0001t0008g0340 | 2 | HG03209.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.852-9999A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035362 | ||||||
| chr8:29035376
|
T | G | 160 | a0001c0001t0001g0149a0001c0001t0003g0005a0001c0001t0003g0006others(157): Show | 160 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.852-9985T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035376 | ||||||
| chr8:29035629
|
G | A | 1 | a0001c0001t0003g0079 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.852-9732G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035629 | ||||||
| chr8:29035890
|
A | G | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-9471A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29035890 | ||||||
| chr8:29036023
|
C | T | 1 | a0001c0001t0008g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.852-9338C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036023 | ||||||
| chr8:29036156
|
G | T | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.852-9205G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036156 | ||||||
| chr8:29036256
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.852-9105A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036256 | ||||||
| chr8:29036619
|
C | T | 2 | a0001c0001t0002g0202a0001c0001t0002g0252 | 2 | NA18941.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.852-8742C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036619 | ||||||
| chr8:29036720
|
C | T | 118 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.852-8641C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036720 | ||||||
| chr8:29036774
|
A | G | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-8587A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036774 | ||||||
| chr8:29036869
|
A | C | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-8492A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036869 | ||||||
| chr8:29036878
|
C | T | 81 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(78): Show | 81 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.852-8483C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29036878 | ||||||
| chr8:29037062
|
C | T | 13 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.852-8299C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037062 | ||||||
| chr8:29037161
|
G | T | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.852-8200G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037161 | ||||||
| chr8:29037317
|
G | T | 1 | a0001c0001t0001g0276 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.852-8044G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037317 | ||||||
| chr8:29037472
|
C | T | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.852-7889C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037472 | ||||||
| chr8:29037474
|
G | A | 146 | a0001c0001t0001g0316a0001c0001t0003g0005a0001c0001t0003g0006others(143): Show | 146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.852-7887G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037474 | ||||||
| chr8:29037612
|
T | C | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-7749T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037612 | ||||||
| chr8:29037651
|
G | A | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-7710G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037651 | ||||||
| chr8:29037741
|
TTGTTTTG others(992): Show |
T | 1 | a0001c0001t0002g0137 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.852-7617_852-6619d others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29037741 | |||||
| chr8:29037904
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.852-7457T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29037904 | ||||||
| chr8:29038048
|
C | T | 1 | a0001c0001t0010g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.852-7313C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038048 | ||||||
| chr8:29038184
|
AC | A | 6 | a0001c0001t0005g0166a0001c0001t0005g0178a0001c0001t0005g0179others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.852-7176delC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038184 | ||||||
| chr8:29038258
|
T | C | 4 | a0001c0001t0004g0123a0001c0001t0004g0124a0001c0001t0004g0125others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-7103T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038258 | ||||||
| chr8:29038299
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.852-7062T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038299 | ||||||
| chr8:29038464
|
A | G | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.852-6897A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038464 | ||||||
| chr8:29038985
|
G | A | 2 | a0001c0001t0003g0114a0001c0001t0006g0112 | 2 | NA18945.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.852-6376G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038985 | ||||||
| chr8:29038997
|
T | C | 81 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(78): Show | 81 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.852-6364T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29038997 | ||||||
| chr8:29039203
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.852-6158T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29039203 | ||||||
| chr8:29039345
|
T | G | 5 | a0001c0001t0003g0325a0001c0001t0003g0326a0001c0001t0006g0115others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-6016T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29039345 | ||||||
| chr8:29039491
|
T | A | 1 | a0001c0001t0003g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.852-5870T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29039491 | ||||||
| chr8:29039654
|
T | C | 2 | a0001c0001t0005g0292a0001c0001t0005g0301 | 2 | HG01516.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.852-5707T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29039654 | ||||||
| chr8:29039912
|
G | T | 1 | a0001c0001t0003g0096 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.852-5449G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29039912 | ||||||
| chr8:29040310
|
A | T | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-5051A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29040310 | ||||||
| chr8:29040347
|
T | C | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.852-5014T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29040347 | ||||||
| chr8:29040729
|
T | A | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.852-4632T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29040729 | ||||||
| chr8:29040916
|
C | T | 261 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(258): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.852-4445C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29040916 | ||||||
| chr8:29041006
|
C | G | 8 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(5): Show | 8 | HG02280.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-4355C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041006 | ||||||
| chr8:29041012
|
A | G | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.852-4349A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041012 | ||||||
| chr8:29041126
|
GTGTT | G | 53 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(50): Show | 53 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.852-4233_852-4230d others(6): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29041126 | |||||
| chr8:29041181
|
T | A | 1 | a0001c0001t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.852-4180T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041181 | ||||||
| chr8:29041182
|
A | T | 58 | a0001c0001t0001g0149a0001c0001t0003g0005a0001c0001t0003g0006others(55): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.852-4179A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041182 | ||||||
| chr8:29041310
|
G | A | 1 | a0001c0001t0004g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.852-4051G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041310 | ||||||
| chr8:29041340
|
C | G | 2 | a0001c0001t0002g0157a0001c0001t0002g0158 | 2 | NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.852-4021C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041340 | ||||||
| chr8:29041818
|
T | G | 3 | a0001c0001t0005g0199a0001c0001t0005g0200a0001c0001t0005g0215 | 3 | HG02559.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.852-3543T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041818 | ||||||
| chr8:29041820
|
C | G | 244 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.852-3541C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29041820 | ||||||
| chr8:29042083
|
C | T | 2 | a0001c0001t0003g0075a0001c0001t0003g0088 | 2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.852-3278C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042083 | ||||||
| chr8:29042106
|
A | G | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.852-3255A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042106 | ||||||
| chr8:29042146
|
A | G | 1 | a0001c0001t0004g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.852-3215A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042146 | ||||||
| chr8:29042180
|
C | G | 159 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(156): Show | 159 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.852-3181C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042180 | ||||||
| chr8:29042257
|
G | A | 8 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-3104G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042257 | ||||||
| chr8:29042277
|
A | G | 1 | a0001c0001t0003g0326 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.852-3084A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042277 | ||||||
| chr8:29042455
|
G | C | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852-2906G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042455 | ||||||
| chr8:29042480
|
G | A | 122 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.852-2881G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042480 | ||||||
| chr8:29042514
|
A | C | 14 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0330others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.852-2847A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042514 | ||||||
| chr8:29042570
|
T | C | 149 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(146): Show | 149 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.852-2791T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29042570 | ||||||
| chr8:29043049
|
A | G | 1 | a0001c0001t0002g0244 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.852-2312A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043049 | ||||||
| chr8:29043150
|
A | C | 1 | a0001c0001t0004g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.852-2211A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043150 | ||||||
| chr8:29043295
|
C | T | 1 | a0001c0001t0003g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.852-2066C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043295 | ||||||
| chr8:29043297
|
TC | T | 16 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0020others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.852-2062delC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29043297 | |||||
| chr8:29043790
|
A | T | 1 | a0001c0001t0003g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.852-1571A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043790 | ||||||
| chr8:29043826
|
A | C | 82 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0140others(79): Show | 82 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.852-1535A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043826 | ||||||
| chr8:29043869
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.852-1492G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043869 | ||||||
| chr8:29043985
|
C | G | 1 | a0001c0001t0001g0288 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.852-1376C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29043985 | ||||||
| chr8:29044175
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0273a0001c0001t0015g0274 | 3 | HG00639.hp2 HG01069.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.852-1186G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29044175 | ||||||
| chr8:29044260
|
G | C | 70 | a0001c0001t0001g0084a0001c0001t0001g0136a0001c0001t0001g0141others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.852-1101G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29044260 | ||||||
| chr8:29044310
|
C | G | 2 | a0001c0001t0002g0184a0001c0001t0011g0314 | 2 | NA18965.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.852-1051C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29044310 | ||||||
| chr8:29044352
|
T | C | 1 | a0001c0001t0004g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.852-1009T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29044352 | ||||||
| chr8:29044453
|
G | C | 1 | a0001c0001t0001g0280 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.852-908G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29044453 | ||||||
| chr8:29044793
|
ACT | A | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.852-565_852-564del others(2): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29044793 | |||||
| chr8:29045005
|
TC | T | 3 | a0001c0001t0001g0176a0001c0001t0001g0273a0001c0001t0015g0274 | 3 | HG00639.hp2 HG01069.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.852-354delC | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 29045005 | |||||
| chr8:29045242
|
C | T | 31 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0031others(28): Show | 31 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.852-119C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29045242 | ||||||
| chr8:29045298
|
G | T | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.852-63G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 6/9 | chr8 | 29045298 | ||||||
| chr8:29046496
|
A | T | 1 | a0001c0001t0004g0026 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.935-862A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29046496 | ||||||
| chr8:29046569
|
G | T | 117 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.935-789G>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29046569 | ||||||
| chr8:29046706
|
T | G | 2 | a0001c0001t0001g0272a0001c0001t0001g0287 | 2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.935-652T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29046706 | ||||||
| chr8:29046785
|
A | C | 1 | a0001c0001t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.935-573A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29046785 | ||||||
| chr8:29047018
|
T | A | 1 | a0001c0001t0002g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.935-340T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29047018 | ||||||
| chr8:29047258
|
C | T | 1 | a0001c0001t0002g0234 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.935-100C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 7/9 | chr8 | 29047258 | ||||||
| chr8:29047501
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1030+48G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29047501 | ||||||
| chr8:29047527
|
A | G | 4 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0121others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1030+74A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29047527 | ||||||
| chr8:29047539
|
G | A | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1030+86G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29047539 | ||||||
| chr8:29047564
|
C | CT | 30 | a0001c0001t0001g0149a0001c0001t0001g0258a0001c0001t0002g0241others(27): Show | 30 | HG00544.hp1 HG01109.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.1030+131dupT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 29047564 | |||||
| chr8:29047564
|
CT | C | 70 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0001t0001g0277others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1030+131delT | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 29047564 | |||||
| chr8:29047602
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1030+149T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29047602 | ||||||
| chr8:29047830
|
A | G | 161 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(158): Show | 161 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1030+377A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29047830 | ||||||
| chr8:29048029
|
C | G | 1 | a0001c0001t0001g0267 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1030+576C>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048029 | ||||||
| chr8:29048113
|
C | T | 1 | a0001c0001t0008g0065 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1030+660C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048113 | ||||||
| chr8:29048228
|
AAT | A | 3 | a0001c0001t0006g0115a0001c0001t0014g0116a0001c0001t0014g0117 | 3 | HG02572.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1031-723_1031-722d others(4): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 29048228 | |||||
| chr8:29048234
|
G | A | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1031-720G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048234 | ||||||
| chr8:29048440
|
T | C | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1031-514T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048440 | ||||||
| chr8:29048440
|
T | G | 2 | a0001c0001t0012g0156a0001c0001t0012g0297 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1031-514T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048440 | ||||||
| chr8:29048735
|
C | T | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1031-219C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 8/9 | chr8 | 29048735 | ||||||
| chr8:29049300
|
A | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | NA18975.hp2 NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1125+252A>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29049300 | ||||||
| chr8:29049718
|
C | T | 7 | a0001c0001t0004g0040a0001c0001t0004g0042a0001c0001t0007g0010others(4): Show | 7 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1125+670C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29049718 | ||||||
| chr8:29049894
|
T | C | 1 | a0001c0001t0008g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1125+846T>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29049894 | ||||||
| chr8:29049910
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1125+862C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29049910 | ||||||
| chr8:29049916
|
T | A | 68 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(65): Show | 68 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1125+868T>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29049916 | ||||||
| chr8:29050224
|
T | G | 1 | a0001c0001t0003g0008 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1126-794T>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050224 | ||||||
| chr8:29050245
|
A | T | 1 | a0001c0001t0001g0164 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1126-773A>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050245 | ||||||
| chr8:29050404
|
C | T | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1126-614C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050404 | ||||||
| chr8:29050459
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1126-559C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050459 | ||||||
| chr8:29050460
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1126-558G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050460 | ||||||
| chr8:29050466
|
G | A | 2 | a0001c0001t0012g0156a0001c0001t0012g0297 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1126-552G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050466 | ||||||
| chr8:29050503
|
ATTCTTTT others(1): Show |
A | 8 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126-504_1126-497d others(10): Show |
HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 29050503 | |||||
| chr8:29050550
|
G | A | 11 | a0001c0001t0002g0202a0001c0001t0002g0208a0001c0001t0002g0209others(8): Show | 11 | NA18612.hp1 NA18941.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1126-468G>A | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050550 | ||||||
| chr8:29050704
|
G | C | 1 | a0001c0001t0010g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1126-314G>C | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050704 | ||||||
| chr8:29050879
|
A | G | 1 | a0001c0001t0008g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1126-139A>G | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050879 | ||||||
| chr8:29050904
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1126-114C>T | HMBOX1 | ENSG00000147421.18 | transcript | ENST00000287701.15 | protein_coding | 9/9 | chr8 | 29050904 |