Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23199 |
|---|---|
| ensemblid | ENSG00000131149.19 |
| hgncid | 28979 |
| symbol | GSE1 |
| name | Gse1 coiled-coil protein |
| refseq_nuc | NM_014615.5 |
| refseq_prot | NP_055430.1 |
| ensembl_nuc | ENST00000253458.12 |
| ensembl_prot | ENSP00000253458.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 85613322 |
| end | 85676200 |
| strand | + |
| ver | v1.2 |
| region | chr16:85613322-85676200 |
| region5000 | chr16:85608322-85681200 |
| regionname0 | GSE1_chr16_85613322_85676200 |
| regionname5000 | GSE1_chr16_85608322_85681200 |
| 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 | 1217 | 202 | 47 | 48 | 61 | 9 | 35 | 36 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002 | 0/0 | 1215 | 40 | 18 | 9 | 3 | 2 | 8 | 2 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0003 | 0/0 | 349 | 6 | 1 | 2 | 1 | 0 | 2 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0004 | 0/0 | 1217 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0005 | 0/0 | 1213 | 3 | 1 | 0 | 2 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0006 | 0/0 | 1217 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0007 | 0/0 | 1215 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0008 | 0/0 | 1217 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0009 | 0/0 | 1217 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0010 | 0/0 | 1217 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0011 | 0/0 | 1217 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0012 | 0/0 | 351 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0013 | 0/0 | 355 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0014 | 0/0 | 1217 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0015 | 0/0 | 1217 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0016 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0017 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0018 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0019 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0020 | 0/0 | 1215 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0021 | 0/0 | 1217 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0022 | 0/0 | 1217 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0023 | 0/0 | 1217 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0024 | 0/0 | 1217 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0025 | 0/0 | 1217 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0026 | 0/0 | 1217 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0027 | 0/0 | 1221 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0028 | 0/0 | 1225 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0029 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0030 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0031 | 0/0 | 1217 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0032 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3654 | 124 | 15 | 29 | 54 | 4 | 22 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0002 | 1/1 | 3654 | 56 | 26 | 8 | 4 | 5 | 11 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0003 | 0/0 | 3654 | 12 | 1 | 9 | 2 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0004 | 0/0 | 3648 | 11 | 2 | 1 | 1 | 0 | 7 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0005 | 0/0 | 3648 | 8 | 2 | 5 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0006 | 0/0 | 3648 | 7 | 6 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0007 | 0/0 | 3654 | 6 | 6 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0008 | 0/0 | 3648 | 4 | 3 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0009 | 0/0 | 3655 | 3 | 1 | 1 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0010 | 0/0 | 3655 | 3 | 0 | 1 | 0 | 0 | 2 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0011 | 0/0 | 3654 | 3 | 2 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0012 | 0/0 | 3648 | 2 | 1 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0013 | 0/0 | 3654 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0014 | 0/0 | 3654 | 2 | 0 | 2 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0015 | 0/0 | 3654 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0016 | 0/0 | 3648 | 2 | 0 | 0 | 1 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0017 | 0/0 | 3648 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0018 | 0/0 | 3648 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0019 | 0/0 | 3654 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0020 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0021 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0022 | 0/0 | 3673 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0023 | 0/0 | 3655 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0024 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0025 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0026 | 0/0 | 3678 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0027 | 0/0 | 3666 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0028 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0029 | 0/0 | 3659 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0030 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0031 | 0/0 | 3654 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0032 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0033 | 0/0 | 3654 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0034 | 0/0 | 3654 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0035 | 0/0 | 3654 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0036 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0037 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0038 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0039 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0040 | 0/0 | 3648 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0041 | 0/0 | 3654 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0042 | 0/0 | 3648 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0043 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0044 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0045 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0046 | 0/0 | 3642 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0047 | 0/0 | 3642 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0048 | 0/0 | 3642 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0049 | 0/0 | 3654 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0050 | 0/0 | 3654 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0051 | 0/0 | 3654 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0052 | 0/0 | 3654 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0053 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0054 | 0/0 | 3648 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0055 | 0/0 | 3654 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0056 | 0/0 | 3654 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| c0057 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3732 | 65 | 31 | 14 | 8 | 4 | 7 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0002 | 0/0 | 3732 | 56 | 0 | 15 | 27 | 1 | 13 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0003 | 0/0 | 3728 | 26 | 3 | 7 | 11 | 1 | 4 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0004 | 0/0 | 3736 | 19 | 4 | 1 | 9 | 0 | 5 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0005 | 0/1 | 3732 | 12 | 1 | 5 | 0 | 2 | 3 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0006 | 0/0 | 3732 | 9 | 9 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0007 | 0/0 | 3736 | 8 | 2 | 5 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0008 | 0/0 | 3734 | 7 | 0 | 3 | 0 | 0 | 4 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0009 | 0/0 | 3733 | 7 | 0 | 1 | 1 | 1 | 4 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0010 | 0/0 | 3735 | 5 | 5 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0011 | 0/0 | 3728 | 3 | 0 | 2 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0012 | 0/0 | 3736 | 3 | 3 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0013 | 0/0 | 3718 | 3 | 2 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0014 | 0/0 | 3733 | 3 | 0 | 2 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0015 | 0/0 | 3728 | 2 | 0 | 0 | 0 | 0 | 2 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0016 | 0/0 | 3728 | 2 | 0 | 2 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0017 | 0/0 | 3737 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0018 | 0/0 | 3729 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0019 | 0/0 | 3716 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0020 | 0/0 | 3719 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0021 | 0/0 | 3733 | 2 | 1 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0022 | 0/0 | 3732 | 2 | 0 | 0 | 2 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0023 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0024 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0025 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0026 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0027 | 0/0 | 3728 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0028 | 0/0 | 3729 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0029 | 0/0 | 3729 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0030 | 0/0 | 3728 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0031 | 0/0 | 3732 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0032 | 0/0 | 3734 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0033 | 0/0 | 3737 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0034 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0035 | 0/0 | 3737 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0036 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0037 | 0/0 | 3736 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0038 | 0/0 | 3736 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0039 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0040 | 0/0 | 3736 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0041 | 0/0 | 3736 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0042 | 0/0 | 3736 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0043 | 0/0 | 3710 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0044 | 0/0 | 3734 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0045 | 0/0 | 3734 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0046 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0047 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0048 | 0/0 | 3727 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0049 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0050 | 0/0 | 3718 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0051 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0052 | 0/0 | 3726 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0053 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0054 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0055 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0056 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0057 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0058 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0059 | 0/0 | 3732 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0060 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0061 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0062 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0063 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0064 | 0/0 | 3736 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0065 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0066 | 0/0 | 3731 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0067 | 0/0 | 3735 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0068 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0069 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| t0070 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| 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 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3654 | 124 | 15 | 29 | 54 | 4 | 22 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002 | 1/1 | 3654 | 56 | 26 | 8 | 4 | 5 | 11 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0003 | 0/0 | 3654 | 12 | 1 | 9 | 2 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0020 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0021 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0028 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0035 | 0/0 | 3654 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0036 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0037 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0050 | 0/0 | 3654 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0051 | 0/0 | 3654 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0055 | 0/0 | 3654 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0056 | 0/0 | 3654 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0004 | 0/0 | 3648 | 11 | 2 | 1 | 1 | 0 | 7 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0005 | 0/0 | 3648 | 8 | 2 | 5 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0006 | 0/0 | 3648 | 7 | 6 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0008 | 0/0 | 3648 | 4 | 3 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0016 | 0/0 | 3648 | 2 | 0 | 0 | 1 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0017 | 0/0 | 3648 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0018 | 0/0 | 3648 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0030 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0040 | 0/0 | 3648 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0045 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0054 | 0/0 | 3648 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0003c0009 | 0/0 | 3655 | 3 | 1 | 1 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0003c0010 | 0/0 | 3655 | 3 | 0 | 1 | 0 | 0 | 2 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0004c0007 | 0/0 | 3654 | 6 | 6 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0005c0046 | 0/0 | 3642 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0005c0047 | 0/0 | 3642 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0005c0048 | 0/0 | 3642 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0006c0011 | 0/0 | 3654 | 3 | 2 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0007c0012 | 0/0 | 3648 | 2 | 1 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0008c0013 | 0/0 | 3654 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0009c0014 | 0/0 | 3654 | 2 | 0 | 2 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0010c0015 | 0/0 | 3654 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0011c0052 | 0/0 | 3654 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0012c0023 | 0/0 | 3655 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0013c0022 | 0/0 | 3673 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0014c0049 | 0/0 | 3654 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0015c0041 | 0/0 | 3654 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0016c0029 | 0/0 | 3659 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0017c0044 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0018c0043 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0019c0025 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0020c0042 | 0/0 | 3648 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0021c0039 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0022c0038 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0023c0031 | 0/0 | 3654 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0024c0034 | 0/0 | 3654 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0025c0033 | 0/0 | 3654 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0026c0032 | 0/0 | 3654 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0027c0027 | 0/0 | 3666 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0028c0026 | 0/0 | 3678 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0029c0024 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0030c0053 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0031c0019 | 0/0 | 3654 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0032c0057 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7385 | 8 | 1 | 1 | 4 | 1 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0002 | 0/0 | 7385 | 42 | 0 | 11 | 25 | 0 | 6 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0003 | 0/0 | 7381 | 13 | 1 | 4 | 5 | 0 | 3 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0004 | 0/0 | 7389 | 14 | 1 | 1 | 9 | 0 | 3 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0005 | 0/0 | 7385 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0007 | 0/0 | 7389 | 4 | 1 | 3 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0009 | 0/0 | 7386 | 7 | 0 | 1 | 1 | 1 | 4 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0011 | 0/0 | 7381 | 3 | 0 | 2 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0012 | 0/0 | 7389 | 3 | 3 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0015 | 0/0 | 7381 | 2 | 0 | 0 | 0 | 0 | 2 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0016 | 0/0 | 7381 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0017 | 0/0 | 7390 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0020 | 0/0 | 7372 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0022 | 0/0 | 7385 | 2 | 0 | 0 | 2 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0027 | 0/0 | 7381 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0028 | 0/0 | 7382 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0029 | 0/0 | 7382 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0035 | 0/0 | 7390 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0039 | 0/0 | 7385 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0040 | 0/0 | 7389 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0041 | 0/0 | 7389 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0042 | 0/0 | 7389 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0043 | 0/0 | 7363 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0046 | 0/0 | 7387 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0051 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0056 | 0/0 | 7385 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0057 | 0/0 | 7385 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0058 | 0/0 | 7385 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0059 | 0/0 | 7385 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0061 | 0/0 | 7385 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0066 | 0/0 | 7384 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0067 | 0/0 | 7388 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0068 | 0/0 | 7385 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0001t0069 | 0/0 | 7388 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0001 | 1/0 | 7385 | 25 | 14 | 2 | 1 | 2 | 5 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0002 | 0/0 | 7385 | 4 | 0 | 2 | 0 | 0 | 2 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0005 | 0/1 | 7385 | 9 | 0 | 3 | 0 | 2 | 3 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0006 | 0/0 | 7385 | 8 | 8 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0007 | 0/0 | 7389 | 2 | 0 | 1 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0014 | 0/0 | 7386 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0018 | 0/0 | 7382 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0019 | 0/0 | 7369 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0026 | 0/0 | 7385 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0031 | 0/0 | 7385 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0049 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0002t0062 | 0/0 | 7385 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0003t0001 | 0/0 | 7385 | 11 | 1 | 8 | 2 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0003t0014 | 0/0 | 7386 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0020t0001 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0021t0033 | 0/0 | 7390 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0028t0053 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0035t0004 | 0/0 | 7389 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0036t0006 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0037t0060 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0050t0002 | 0/0 | 7385 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0051t0002 | 0/0 | 7385 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0055t0048 | 0/0 | 7380 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0001c0056t0014 | 0/0 | 7386 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0004t0002 | 0/0 | 7379 | 2 | 0 | 0 | 0 | 0 | 2 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0004t0003 | 0/0 | 7375 | 3 | 1 | 1 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0004t0004 | 0/0 | 7383 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0004t0008 | 0/0 | 7381 | 3 | 0 | 0 | 0 | 0 | 3 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0004t0025 | 0/0 | 7381 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0004t0045 | 0/0 | 7381 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0005t0001 | 0/0 | 7379 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0005t0007 | 0/0 | 7383 | 2 | 1 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0005t0008 | 0/0 | 7381 | 3 | 0 | 3 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0005t0044 | 0/0 | 7381 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0005t0063 | 0/0 | 7379 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0006t0001 | 0/0 | 7379 | 7 | 6 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0008t0001 | 0/0 | 7379 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0008t0036 | 0/0 | 7379 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0008t0070 | 0/0 | 7379 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0016t0003 | 0/0 | 7375 | 2 | 0 | 0 | 1 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0017t0001 | 0/0 | 7379 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0018t0004 | 0/0 | 7383 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0030t0003 | 0/0 | 7375 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0040t0001 | 0/0 | 7379 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0045t0047 | 0/0 | 7381 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0002c0054t0032 | 0/0 | 7381 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0003c0009t0002 | 0/0 | 7386 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0003c0009t0005 | 0/0 | 7386 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0003c0009t0050 | 0/0 | 7372 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0003c0010t0002 | 0/0 | 7386 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0003c0010t0004 | 0/0 | 7390 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0003c0010t0016 | 0/0 | 7382 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0004c0007t0010 | 0/0 | 7388 | 4 | 4 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0004c0007t0052 | 0/0 | 7379 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0004c0007t0064 | 0/0 | 7389 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0005c0046t0003 | 0/0 | 7369 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0005c0047t0065 | 0/0 | 7373 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0005c0048t0003 | 0/0 | 7369 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0006c0011t0013 | 0/0 | 7371 | 2 | 1 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0006c0011t0019 | 0/0 | 7369 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0007c0012t0021 | 0/0 | 7380 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0007c0012t0034 | 0/0 | 7380 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0008c0013t0021 | 0/0 | 7386 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0008c0013t0055 | 0/0 | 7386 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0009c0014t0005 | 0/0 | 7385 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0009c0014t0054 | 0/0 | 7386 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0010c0015t0001 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0011c0052t0002 | 0/0 | 7385 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0012c0023t0001 | 0/0 | 7386 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0013c0022t0030 | 0/0 | 7400 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0014c0049t0037 | 0/0 | 7389 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0015c0041t0001 | 0/0 | 7385 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0016c0029t0003 | 0/0 | 7386 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0017c0044t0002 | 0/0 | 7379 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0018c0043t0003 | 0/0 | 7375 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0019c0025t0024 | 0/0 | 7379 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0020c0042t0008 | 0/0 | 7381 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0021c0039t0001 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0022c0038t0013 | 0/0 | 7371 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0023c0031t0002 | 0/0 | 7385 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0024c0034t0001 | 0/0 | 7385 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0025c0033t0038 | 0/0 | 7389 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0026c0032t0010 | 0/0 | 7388 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0027c0027t0003 | 0/0 | 7393 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0028c0026t0003 | 0/0 | 7405 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0029c0024t0023 | 0/0 | 7381 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0030c0053t0001 | 0/0 | 7379 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0031c0019t0002 | 0/0 | 7385 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| a0032c0057t0003 | 0/0 | 7375 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | copy fasta | chr16 | 85608322 | 85681200 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0009g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0009g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0009g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0009g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0011g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0011g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0015g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0015g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0016g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0017g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0017g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0020g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0020g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0022g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0022g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0027g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0028g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0029g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0035g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0039g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0040g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0041g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0042g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0043g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0046g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0051g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0056g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0057g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0058g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0059g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0061g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0066g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0067g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0068g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0001t0069g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0005g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0007g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0007g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0014g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0018g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0018g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0019g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0026g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0031g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0049g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0002t0062g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0003t0014g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0020t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0021t0033g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0028t0053g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0035t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0036t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0037t0060g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0050t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0051t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0055t0048g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0001c0056t0014g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0004t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0004t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0004t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0004t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0004t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0004t0008g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0004t0008g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0004t0008g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0004t0025g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0004t0045g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0005t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0005t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0005t0007g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0005t0008g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0005t0008g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0005t0008g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0005t0044g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0005t0063g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0006t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0006t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0006t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0006t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0006t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0006t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0006t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0008t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0008t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0008t0036g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0008t0070g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0016t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0016t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0017t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0017t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0018t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0018t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0030t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0040t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0045t0047g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0002c0054t0032g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0003c0009t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0003c0009t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0003c0009t0050g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0003c0010t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0003c0010t0004g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0003c0010t0016g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0004c0007t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0004c0007t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0004c0007t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0004c0007t0010g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0004c0007t0052g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0004c0007t0064g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0005c0046t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0005c0047t0065g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0005c0048t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0006c0011t0013g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0006c0011t0013g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0006c0011t0019g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0007c0012t0021g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0007c0012t0034g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0008c0013t0021g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0008c0013t0055g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0009c0014t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0009c0014t0054g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0010c0015t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0010c0015t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0011c0052t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0012c0023t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0013c0022t0030g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0014c0049t0037g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0015c0041t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0016c0029t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0017c0044t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0018c0043t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0019c0025t0024g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0020c0042t0008g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0021c0039t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0022c0038t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0023c0031t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0024c0034t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0025c0033t0038g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0026c0032t0010g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0027c0027t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0028c0026t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0029c0024t0023g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0030c0053t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0031c0019t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| a0032c0057t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0016 | t0003 | g0104 | EUR | GBR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0198 | EUR | GBR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00140 | hp1 | a0001 | c0002 | t0005 | g0079 | EUR | GBR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0269 | EUR | GBR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0157 | EUR | FIN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00323 | hp2 | a0023 | c0031 | t0002 | g0280 | EUR | FIN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00423 | hp2 | a0001 | c0002 | t0026 | g0203 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00438 | hp1 | a0001 | c0002 | t0062 | g0167 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00597 | hp1 | a0001 | c0001 | t0041 | g0035 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00639 | hp1 | a0007 | c0012 | t0021 | g0239 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00639 | hp2 | a0003 | c0010 | t0016 | g0067 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00735 | hp2 | a0001 | c0003 | t0014 | g0022 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00738 | hp1 | a0031 | c0019 | t0002 | g0249 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00738 | hp2 | a0002 | c0008 | t0070 | g0060 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG00741 | hp2 | a0001 | c0002 | t0007 | g0267 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0165 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0135 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01070 | hp1 | a0001 | c0001 | t0028 | g0129 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01070 | hp2 | a0001 | c0002 | t0005 | g0143 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0038 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01071 | hp2 | a0001 | c0002 | t0005 | g0043 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0186 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01081 | hp2 | a0001 | c0001 | t0035 | g0286 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01099 | hp1 | a0015 | c0041 | t0001 | g0095 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01106 | hp1 | a0001 | c0001 | t0057 | g0185 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0108 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01109 | hp2 | a0002 | c0006 | t0001 | g0216 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01167 | hp1 | a0001 | c0055 | t0048 | g0241 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01167 | hp2 | a0025 | c0033 | t0038 | g0209 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01175 | hp1 | a0009 | c0014 | t0054 | g0257 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01175 | hp2 | a0001 | c0001 | t0011 | g0002 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0137 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01243 | hp2 | a0001 | c0001 | t0067 | g0111 | AMR | PUR | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01255 | hp1 | a0006 | c0011 | t0013 | g0270 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01255 | hp2 | a0001 | c0001 | t0011 | g0136 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01257 | hp1 | a0002 | c0005 | t0008 | g0159 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0174 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01258 | hp1 | a0002 | c0005 | t0008 | g0160 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0205 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01261 | hp1 | a0009 | c0014 | t0005 | g0176 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0086 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01358 | hp1 | a0001 | c0001 | t0016 | g0162 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01358 | hp2 | a0001 | c0002 | t0005 | g0197 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0263 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01433 | hp1 | a0001 | c0056 | t0014 | g0189 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01496 | hp2 | a0002 | c0040 | t0001 | g0064 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01515 | hp1 | a0001 | c0002 | t0031 | g0256 | EUR | IBS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01884 | hp2 | a0004 | c0007 | t0010 | g0045 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01891 | hp1 | a0008 | c0013 | t0055 | g0119 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01891 | hp2 | a0002 | c0008 | t0001 | g0168 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0206 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01934 | hp2 | a0002 | c0004 | t0003 | g0065 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01943 | hp1 | a0002 | c0005 | t0044 | g0169 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0163 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01978 | hp1 | a0003 | c0009 | t0002 | g0109 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01978 | hp2 | a0028 | c0026 | t0003 | g0183 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0075 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0188 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02027 | hp1 | a0003 | c0009 | t0050 | g0134 | EAS | KHV | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02027 | hp2 | a0002 | c0016 | t0003 | g0046 | EAS | KHV | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02055 | hp1 | a0004 | c0007 | t0052 | g0076 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0210 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02056 | hp1 | a0001 | c0001 | t0058 | g0051 | EAS | KHV | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02056 | hp2 | a0030 | c0053 | t0001 | g0047 | EAS | KHV | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02129 | hp1 | a0001 | c0001 | t0061 | g0158 | EAS | KHV | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02145 | hp1 | a0001 | c0028 | t0053 | g0287 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02145 | hp2 | a0002 | c0018 | t0004 | g0266 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02155 | hp1 | a0001 | c0001 | t0068 | g0054 | EAS | CDX | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CDX | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02165 | hp2 | a0014 | c0049 | t0037 | g0125 | EAS | CDX | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02258 | hp1 | a0002 | c0005 | t0007 | g0080 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02258 | hp2 | a0021 | c0039 | t0001 | g0271 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0032 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02293 | hp2 | a0002 | c0005 | t0008 | g0085 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02300 | hp1 | a0027 | c0027 | t0003 | g0181 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02451 | hp2 | a0002 | c0008 | t0036 | g0277 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0290 | EAS | KHV | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02572 | hp1 | a0008 | c0013 | t0021 | g0284 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02572 | hp2 | a0002 | c0017 | t0001 | g0237 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02602 | hp2 | a0002 | c0004 | t0008 | g0093 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02615 | hp1 | a0001 | c0002 | t0019 | g0145 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02615 | hp2 | a0007 | c0012 | t0034 | g0214 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0092 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02630 | hp1 | a0001 | c0001 | t0020 | g0156 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02630 | hp2 | a0019 | c0025 | t0024 | g0275 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02647 | hp1 | a0001 | c0002 | t0006 | g0285 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02683 | hp1 | a0001 | c0001 | t0009 | g0262 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02683 | hp2 | a0002 | c0004 | t0045 | g0252 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02698 | hp1 | a0002 | c0004 | t0002 | g0019 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02698 | hp2 | a0001 | c0002 | t0007 | g0264 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02717 | hp1 | a0002 | c0004 | t0003 | g0276 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02723 | hp1 | a0001 | c0002 | t0006 | g0215 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0178 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02735 | hp2 | a0024 | c0034 | t0001 | g0117 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02738 | hp1 | a0001 | c0001 | t0029 | g0044 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0288 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02809 | hp2 | a0002 | c0045 | t0047 | g0056 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02818 | hp1 | a0001 | c0002 | t0006 | g0213 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02818 | hp2 | a0001 | c0002 | t0018 | g0283 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02886 | hp1 | a0001 | c0002 | t0006 | g0281 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02886 | hp2 | a0001 | c0001 | t0020 | g0217 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02895 | hp1 | a0001 | c0001 | t0051 | g0140 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02895 | hp2 | a0001 | c0002 | t0018 | g0194 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02896 | hp1 | a0004 | c0007 | t0064 | g0258 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02896 | hp2 | a0001 | c0002 | t0006 | g0211 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02922 | hp1 | a0001 | c0037 | t0060 | g0114 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02965 | hp1 | a0002 | c0005 | t0063 | g0208 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02965 | hp2 | a0001 | c0036 | t0006 | g0112 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02970 | hp1 | a0002 | c0017 | t0001 | g0219 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02970 | hp2 | a0002 | c0006 | t0001 | g0222 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0261 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03041 | hp1 | a0001 | c0002 | t0049 | g0233 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03098 | hp1 | a0018 | c0043 | t0003 | g0098 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03098 | hp2 | a0026 | c0032 | t0010 | g0061 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03130 | hp1 | a0004 | c0007 | t0010 | g0091 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03130 | hp2 | a0002 | c0006 | t0001 | g0113 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03139 | hp1 | a0002 | c0006 | t0001 | g0242 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03139 | hp2 | a0002 | c0008 | t0001 | g0218 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03225 | hp1 | a0006 | c0011 | t0019 | g0282 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03225 | hp2 | a0002 | c0006 | t0001 | g0253 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03239 | hp1 | a0002 | c0004 | t0002 | g0124 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03239 | hp2 | a0002 | c0054 | t0032 | g0084 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03453 | hp2 | a0001 | c0001 | t0017 | g0243 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03486 | hp1 | a0001 | c0001 | t0012 | g0010 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03486 | hp2 | a0005 | c0047 | t0065 | g0088 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03490 | hp1 | a0001 | c0001 | t0015 | g0127 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0274 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03492 | hp1 | a0001 | c0001 | t0015 | g0128 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03492 | hp2 | a0011 | c0052 | t0002 | g0122 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03516 | hp1 | a0001 | c0001 | t0017 | g0090 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03516 | hp2 | a0004 | c0007 | t0010 | g0265 | AFR | ESN | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03540 | hp2 | a0001 | c0020 | t0001 | g0028 | AFR | GWD | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0155 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03579 | hp2 | a0010 | c0015 | t0001 | g0154 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03654 | hp2 | a0001 | c0001 | t0009 | g0171 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03669 | hp1 | a0001 | c0001 | t0009 | g0152 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03688 | hp1 | a0001 | c0001 | t0042 | g0103 | SAS | STU | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | STU | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03704 | hp2 | a0001 | c0001 | t0059 | g0273 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03710 | hp2 | a0001 | c0035 | t0004 | g0070 | SAS | PJL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0052 | SAS | BEB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03831 | hp2 | a0001 | c0002 | t0005 | g0118 | SAS | BEB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03834 | hp1 | a0002 | c0004 | t0003 | g0226 | SAS | BEB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03927 | hp2 | a0001 | c0051 | t0002 | g0106 | SAS | BEB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0053 | SAS | BEB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03942 | hp2 | a0020 | c0042 | t0008 | g0042 | SAS | BEB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG04115 | hp1 | a0001 | c0002 | t0005 | g0078 | SAS | STU | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | STU | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | BEB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG04184 | hp2 | a0003 | c0010 | t0002 | g0110 | SAS | BEB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG04199 | hp1 | a0003 | c0010 | t0004 | g0008 | SAS | STU | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG04199 | hp2 | a0002 | c0004 | t0008 | g0015 | SAS | STU | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG04204 | hp1 | a0001 | c0001 | t0009 | g0196 | SAS | STU | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0195 | SAS | STU | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | STU | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0248 | SAS | STU | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18522 | hp1 | a0004 | c0007 | t0010 | g0116 | AFR | YRI | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18522 | hp2 | a0002 | c0006 | t0001 | g0221 | AFR | YRI | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | CHB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18612 | hp2 | a0005 | c0046 | t0003 | g0034 | EAS | CHB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18906 | hp1 | a0002 | c0018 | t0004 | g0006 | AFR | YRI | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18906 | hp2 | a0001 | c0001 | t0043 | g0014 | AFR | YRI | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18947 | hp2 | a0017 | c0044 | t0002 | g0024 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18950 | hp1 | a0013 | c0022 | t0030 | g0072 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18952 | hp1 | a0005 | c0048 | t0003 | g0050 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18962 | hp1 | a0001 | c0001 | t0066 | g0192 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18966 | hp1 | a0001 | c0001 | t0056 | g0179 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18981 | hp1 | a0001 | c0001 | t0040 | g0033 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18981 | hp2 | a0001 | c0050 | t0002 | g0180 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19004 | hp2 | a0001 | c0001 | t0009 | g0029 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19011 | hp1 | a0032 | c0057 | t0003 | g0058 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19011 | hp2 | a0001 | c0001 | t0022 | g0031 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19043 | hp1 | a0003 | c0009 | t0005 | g0244 | AFR | LWK | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19043 | hp2 | a0022 | c0038 | t0013 | g0089 | AFR | LWK | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19056 | hp1 | a0001 | c0002 | t0014 | g0204 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19065 | hp2 | a0001 | c0001 | t0022 | g0021 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19066 | hp1 | a0002 | c0004 | t0025 | g0048 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19066 | hp2 | a0002 | c0030 | t0003 | g0023 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0259 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19079 | hp2 | a0029 | c0024 | t0023 | g0055 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19087 | hp1 | a0001 | c0001 | t0039 | g0147 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19090 | hp2 | a0016 | c0029 | t0003 | g0100 | EAS | JPT | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0212 | AFR | YRI | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA19240 | hp2 | a0002 | c0006 | t0001 | g0255 | AFR | YRI | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | ASW | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA20129 | hp2 | a0001 | c0021 | t0033 | g0225 | AFR | ASW | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA20752 | hp1 | a0001 | c0002 | t0005 | g0081 | EUR | TSI | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0057 | EUR | TSI | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA20805 | hp1 | a0001 | c0001 | t0027 | g0063 | EUR | TSI | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA20805 | hp2 | a0002 | c0005 | t0001 | g0077 | EUR | TSI | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA20905 | hp1 | a0002 | c0004 | t0008 | g0068 | SAS | GIH | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | GIH | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01123 | hp1 | a0002 | c0005 | t0007 | g0191 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0250 | AMR | CLM | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02109 | hp1 | a0006 | c0011 | t0013 | g0230 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02559 | hp1 | a0002 | c0004 | t0004 | g0001 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0272 | AFR | ACB | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03471 | hp1 | a0010 | c0015 | t0001 | g0246 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG03471 | hp2 | a0001 | c0001 | t0046 | g0105 | AFR | MSL | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0049 | AFR | USA | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0245 | AFR | USA | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA20300 | hp1 | a0012 | c0023 | t0001 | g0175 | AFR | USA | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0138 | AFR | USA | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA21309 | hp1 | a0001 | c0002 | t0006 | g0184 | AFR | LWK | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| NA21309 | hp2 | a0001 | c0001 | t0069 | g0121 | AFR | LWK | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0005 | g0126 | REF | REF | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0132 | REF | REF | GSE1_chr16_85608322_85681200 | GSE1 | chr16 | 85608322 | 85681200 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:85634051
|
G | A | 1 | a0031 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.145G>A | p.Ala49Thr | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/16 | 215/7385 | 145/3654 | 49/1217 | chr16 | 85634051 | ||
| chr16:85634052
|
C | T | 1 | a0032 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.146C>T | p.Ala49Val | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/16 | 216/7385 | 146/3654 | 49/1217 | chr16 | 85634052 | ||
| chr16:85648615
|
C | T | 1 | a0030 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.290C>T | p.Ala97Val | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/16 | 360/7385 | 290/3654 | 97/1217 | chr16 | 85648615 | ||
| chr16:85654299
|
A | C | 1 | a0011 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.448A>C | p.Ser150Arg | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 4/16 | 518/7385 | 448/3654 | 150/1217 | chr16 | 85654299 | ||
| chr16:85654328
|
G | GC | 3 | a0003a0012a0013 | 8 | HG00639.hp2 HG01978.hp1 HG02027.hp1 others(5): Show |
frameshift_variant | HIGH | c.482dupC | p.Leu162fs | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 4/16 | 553/7385 | 483/3654 | 161/1217 | INFO_REALIGN_3_PRIME | chr16 | 85654328 | |
| chr16:85654822
|
C | A | 1 | a0029 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.628C>A | p.Pro210Thr | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 5/16 | 698/7385 | 628/3654 | 210/1217 | chr16 | 85654822 | ||
| chr16:85655727
|
A | T | 1 | a0014 | 1 | HG02165.hp2 | missense_variant&splice_region_variant | MODERATE | c.799A>T | p.Met267Leu | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 6/16 | 869/7385 | 799/3654 | 267/1217 | chr16 | 85655727 | ||
| chr16:85656376
|
G | GGAGCGCG others(5): Show |
1 | a0027 | 1 | HG02300.hp1 | disruptive_inframe_insertion | MODERATE | c.1035_1046dupCGAGCG others(6): Show |
p.Arg349_Glu350insGl others(10): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1117/7385 | 1047/3654 | 349/1217 | INFO_REALIGN_3_PRIME | chr16 | 85656376 | |
| chr16:85656376
|
G | GGAGCGCG others(11): Show |
1 | a0013 | 1 | NA18950.hp1 | disruptive_inframe_insertion | MODERATE | c.1029_1046dupCGAGCG others(12): Show |
p.Arg349_Glu350insGl others(16): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1117/7385 | 1047/3654 | 349/1217 | INFO_REALIGN_3_PRIME | chr16 | 85656376 | |
| chr16:85656376
|
G | GGAGCGCG others(17): Show |
1 | a0028 | 1 | HG01978.hp2 | disruptive_inframe_insertion | MODERATE | c.1046_1047insCGAGCG others(18): Show |
p.Arg349_Glu350insGl others(22): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1117/7385 | 1047/3654 | 349/1217 | INFO_REALIGN_3_PRIME | chr16 | 85656376 | |
| chr16:85656376
|
GGAGCGC | G | 7 | a0002a0007a0017others(4): Show | 32 | HG00639.hp1 HG01123.hp1 HG01257.hp1 others(29): Show |
disruptive_inframe_deletion | MODERATE | c.1041_1046delCGAGCG | p.Glu348_Arg349del | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1111/7385 | 1041/3654 | 347/1217 | INFO_REALIGN_3_PRIME | chr16 | 85656376 | |
| chr16:85656376
|
GGAGCGCG others(5): Show |
G | 1 | a0005 | 2 | HG03486.hp2 NA18952.hp1 |
disruptive_inframe_deletion | MODERATE | c.1035_1046delCGAGCG others(6): Show |
p.Glu346_Arg349del | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1105/7385 | 1035/3654 | 345/1217 | INFO_REALIGN_3_PRIME | chr16 | 85656376 | |
| chr16:85656388
|
CGAGCGCG others(5): Show |
C | 1 | a0005 | 1 | NA18612.hp2 | disruptive_inframe_deletion | MODERATE | c.1041_1052delCGAGCG others(6): Show |
p.Glu348_Arg351del | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1111/7385 | 1041/3654 | 347/1217 | INFO_REALIGN_3_PRIME | chr16 | 85656388 | |
| chr16:85656394
|
CGAGCGT | C | 4 | a0002a0016a0019others(1): Show | 18 | HG00099.hp1 HG00738.hp2 HG01109.hp2 others(15): Show |
conservative_inframe_deletion | MODERATE | c.1051_1056delCGTGAG | p.Arg351_Glu352del | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1121/7385 | 1051/3654 | 351/1217 | INFO_REALIGN_3_PRIME | chr16 | 85656394 | |
| chr16:85656398
|
C | T | 1 | a0015 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1045C>T | p.Arg349Cys | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1115/7385 | 1045/3654 | 349/1217 | chr16 | 85656398 | ||
| chr16:85656519
|
G | T | 1 | a0021 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1166G>T | p.Arg389Leu | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1236/7385 | 1166/3654 | 389/1217 | chr16 | 85656519 | ||
| chr16:85656563
|
C | G | 1 | a0010 | 2 | HG03471.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.1210C>G | p.Leu404Val | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1280/7385 | 1210/3654 | 404/1217 | chr16 | 85656563 | ||
| chr16:85657287
|
G | GGATGCCG others(4): Show |
1 | a0016 | 1 | NA19090.hp2 | frameshift_variant | HIGH | c.1325_1335dupATGCCG others(5): Show |
p.Gln446fs | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/16 | 1406/7385 | 1336/3654 | 446/1217 | INFO_REALIGN_3_PRIME | chr16 | 85657287 | |
| chr16:85657294
|
G | A | 1 | a0004 | 6 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.1330G>A | p.Gly444Ser | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/16 | 1400/7385 | 1330/3654 | 444/1217 | chr16 | 85657294 | ||
| chr16:85657436
|
C | G | 1 | a0022 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1472C>G | p.Thr491Ser | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/16 | 1542/7385 | 1472/3654 | 491/1217 | chr16 | 85657436 | ||
| chr16:85657571
|
C | A | 1 | a0020 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1607C>A | p.Ala536Glu | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/16 | 1677/7385 | 1607/3654 | 536/1217 | chr16 | 85657571 | ||
| chr16:85661449
|
G | C | 1 | a0019 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1944G>C | p.Lys648Asn | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/16 | 2014/7385 | 1944/3654 | 648/1217 | chr16 | 85661449 | ||
| chr16:85661556
|
C | A | 1 | a0023 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.2051C>A | p.Thr684Asn | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/16 | 2121/7385 | 2051/3654 | 684/1217 | chr16 | 85661556 | ||
| chr16:85663029
|
A | T | 1 | a0009 | 2 | HG01175.hp1 HG01261.hp1 |
missense_variant | MODERATE | c.2309A>T | p.Glu770Val | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 10/16 | 2379/7385 | 2309/3654 | 770/1217 | chr16 | 85663029 | ||
| chr16:85666056
|
G | A | 1 | a0026 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.2839G>A | p.Ala947Thr | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/16 | 2909/7385 | 2839/3654 | 947/1217 | chr16 | 85666056 | ||
| chr16:85666074
|
G | A | 1 | a0018 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.2857G>A | p.Glu953Lys | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/16 | 2927/7385 | 2857/3654 | 953/1217 | chr16 | 85666074 | ||
| chr16:85666149
|
G | A | 1 | a0006 | 3 | HG01255.hp1 HG02109.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.2932G>A | p.Glu978Lys | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/16 | 3002/7385 | 2932/3654 | 978/1217 | chr16 | 85666149 | ||
| chr16:85668311
|
C | T | 1 | a0024 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.3302C>T | p.Ser1101Leu | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/16 | 3372/7385 | 3302/3654 | 1101/1217 | chr16 | 85668311 | ||
| chr16:85668333
|
T | G | 1 | a0025 | 1 | HG01167.hp2 | missense_variant | MODERATE | c.3324T>G | p.Asp1108Glu | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/16 | 3394/7385 | 3324/3654 | 1108/1217 | chr16 | 85668333 | ||
| chr16:85668423
|
A | C | 2 | a0007a0008 | 4 | HG00639.hp1 HG01891.hp1 HG02572.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.3414A>C | p.Glu1138Asp | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/16 | 3484/7385 | 3414/3654 | 1138/1217 | chr16 | 85668423 | ||
| chr16:85671037
|
G | A | 1 | a0017 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.3458G>A | p.Arg1153Gln | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/16 | 3528/7385 | 3458/3654 | 1153/1217 | chr16 | 85671037 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:85634077
|
C | T | 1 | a0001c0056 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.171C>T | p.Ser57Ser | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/16 | 241/7385 | 171/3654 | 57/1217 | chr16 | 85634077 | ||
| chr16:85634089
|
C | T | 1 | a0001c0055 | 1 | HG01167.hp1 | synonymous_variant | LOW | c.183C>T | p.Ala61Ala | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/16 | 253/7385 | 183/3654 | 61/1217 | chr16 | 85634089 | ||
| chr16:85634119
|
G | A | 2 | a0001c0020a0001c0021 | 2 | HG03540.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.213G>A | p.Ala71Ala | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/16 | 283/7385 | 213/3654 | 71/1217 | chr16 | 85634119 | ||
| chr16:85648580
|
C | T | 1 | a0002c0054 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.255C>T | p.Pro85Pro | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/16 | 325/7385 | 255/3654 | 85/1217 | chr16 | 85648580 | ||
| chr16:85648592
|
G | A | 1 | a0007c0012 | 2 | HG00639.hp1 HG02615.hp2 |
synonymous_variant | LOW | c.267G>A | p.Pro89Pro | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/16 | 337/7385 | 267/3654 | 89/1217 | chr16 | 85648592 | ||
| chr16:85654878
|
C | T | 1 | a0001c0051 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.684C>T | p.Thr228Thr | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 5/16 | 754/7385 | 684/3654 | 228/1217 | chr16 | 85654878 | ||
| chr16:85654974
|
C | T | 1 | a0001c0050 | 1 | NA18981.hp2 | synonymous_variant | LOW | c.780C>T | p.Phe260Phe | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 5/16 | 850/7385 | 780/3654 | 260/1217 | chr16 | 85654974 | ||
| chr16:85655888
|
G | A | 2 | a0002c0006a0019c0025 | 8 | HG01109.hp2 HG02630.hp2 HG02970.hp2 others(5): Show |
synonymous_variant | LOW | c.960G>A | p.Ser320Ser | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 6/16 | 1030/7385 | 960/3654 | 320/1217 | chr16 | 85655888 | ||
| chr16:85656400
|
T | C | 2 | a0001c0028a0012c0023 | 2 | HG02145.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.1047T>C | p.Arg349Arg | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1117/7385 | 1047/3654 | 349/1217 | chr16 | 85656400 | ||
| chr16:85656406
|
T | C | 3 | a0002c0030a0016c0029a0032c0057 | 3 | NA19011.hp1 NA19066.hp2 NA19090.hp2 |
synonymous_variant | LOW | c.1053T>C | p.Arg351Arg | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1123/7385 | 1053/3654 | 351/1217 | chr16 | 85656406 | ||
| chr16:85656583
|
C | T | 1 | a0002c0018 | 2 | HG02145.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.1230C>T | p.Pro410Pro | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/16 | 1300/7385 | 1230/3654 | 410/1217 | chr16 | 85656583 | ||
| chr16:85657512
|
C | T | 2 | a0001c0037a0002c0017 | 3 | HG02572.hp2 HG02922.hp1 HG02970.hp1 |
synonymous_variant | LOW | c.1548C>T | p.Ser516Ser | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/16 | 1618/7385 | 1548/3654 | 516/1217 | chr16 | 85657512 | ||
| chr16:85661149
|
A | G | 1 | a0001c0036 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.1644A>G | p.Pro548Pro | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/16 | 1714/7385 | 1644/3654 | 548/1217 | chr16 | 85661149 | ||
| chr16:85661362
|
C | T | 1 | a0001c0003 | 12 | HG00735.hp2 HG01106.hp2 HG01243.hp1 others(9): Show |
synonymous_variant | LOW | c.1857C>T | p.Ala619Ala | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/16 | 1927/7385 | 1857/3654 | 619/1217 | chr16 | 85661362 | ||
| chr16:85661692
|
C | T | 1 | a0004c0007 | 6 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
synonymous_variant | LOW | c.2187C>T | p.Phe729Phe | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/16 | 2257/7385 | 2187/3654 | 729/1217 | chr16 | 85661692 | ||
| chr16:85663012
|
C | T | 5 | a0001c0037a0002c0006a0002c0008others(2): Show | 14 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(11): Show |
synonymous_variant | LOW | c.2292C>T | p.Asp764Asp | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 10/16 | 2362/7385 | 2292/3654 | 764/1217 | chr16 | 85663012 | ||
| chr16:85663514
|
C | T | 1 | a0001c0035 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.2544C>T | p.Arg848Arg | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/16 | 2614/7385 | 2544/3654 | 848/1217 | chr16 | 85663514 | ||
| chr16:85672441
|
A | C | 37 | a0001c0001a0001c0021a0001c0035others(34): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
synonymous_variant | LOW | c.3556A>C | p.Arg1186Arg | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 3626/7385 | 3556/3654 | 1186/1217 | chr16 | 85672441 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:85672541
|
G | A | 2 | a0019c0025t0024a0029c0024t0023 | 2 | HG02630.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2 | chr16 | 85672541 | |||||
| chr16:85672542
|
G | A | 1 | a0002c0004t0025 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 3 | chr16 | 85672542 | |||||
| chr16:85672617
|
C | T | 1 | a0002c0008t0070 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 78 | chr16 | 85672617 | |||||
| chr16:85672644
|
G | A | 2 | a0001c0002t0006a0001c0036t0006 | 9 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*105G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 105 | chr16 | 85672644 | |||||
| chr16:85672743
|
G | A | 1 | a0001c0002t0026 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*204G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 204 | chr16 | 85672743 | |||||
| chr16:85672744
|
A | C | 1 | a0001c0001t0069 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 205 | chr16 | 85672744 | |||||
| chr16:85672810
|
ATTATTTC | A | 19 | a0001c0001t0003a0001c0001t0011a0001c0001t0015others(16): Show | 37 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*275_*281delTTTCTT others(1): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 275 | INFO_REALIGN_3_PRIME | chr16 | 85672810 | ||||
| chr16:85672890
|
G | C | 1 | a0001c0001t0027 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*351G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 351 | chr16 | 85672890 | |||||
| chr16:85672958
|
G | A | 19 | a0001c0001t0003a0001c0001t0011a0001c0001t0015others(16): Show | 37 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*419G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 419 | chr16 | 85672958 | |||||
| chr16:85672963
|
G | A | 1 | a0001c0002t0031 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*424G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 424 | chr16 | 85672963 | |||||
| chr16:85673027
|
T | C | 47 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(44): Show | 86 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*488T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 488 | chr16 | 85673027 | |||||
| chr16:85673077
|
CTTCAAAG others(7): Show |
C | 8 | a0001c0002t0018a0001c0002t0019a0001c0002t0049others(5): Show | 10 | HG01167.hp1 HG01255.hp1 HG02027.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*540_*553delTCAAAG others(8): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 540 | INFO_REALIGN_3_PRIME | chr16 | 85673077 | ||||
| chr16:85673178
|
G | A | 1 | a0001c0055t0048 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*639G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 639 | chr16 | 85673178 | |||||
| chr16:85673195
|
C | A | 1 | a0001c0001t0015 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*656C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 656 | chr16 | 85673195 | |||||
| chr16:85673254
|
T | G | 1 | a0001c0001t0051 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*715T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 715 | chr16 | 85673254 | |||||
| chr16:85673280
|
C | T | 1 | a0001c0001t0068 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*741C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 741 | chr16 | 85673280 | |||||
| chr16:85673347
|
C | A | 1 | a0002c0054t0032 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*808C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 808 | chr16 | 85673347 | |||||
| chr16:85673372
|
TTAACTAT others(5): Show |
T | 1 | a0001c0001t0020 | 2 | HG02630.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*837_*848delCTATTG others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 837 | INFO_REALIGN_3_PRIME | chr16 | 85673372 | ||||
| chr16:85673431
|
GTTTTTCC others(3): Show |
G | 1 | a0004c0007t0052 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*895_*904delTTTCCT others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 895 | INFO_REALIGN_3_PRIME | chr16 | 85673431 | ||||
| chr16:85673443
|
T | C | 1 | a0001c0028t0053 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*904T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 904 | chr16 | 85673443 | |||||
| chr16:85673460
|
G | C | 8 | a0001c0002t0018a0001c0002t0019a0001c0002t0049others(5): Show | 10 | HG01167.hp1 HG01255.hp1 HG02027.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*921G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 921 | chr16 | 85673460 | |||||
| chr16:85673478
|
C | CA | 13 | a0001c0001t0009a0001c0001t0017a0001c0001t0035others(10): Show | 20 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*955dupA | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 956 | INFO_REALIGN_3_PRIME | chr16 | 85673478 | ||||
| chr16:85673478
|
CA | C | 33 | a0001c0001t0003a0001c0001t0011a0001c0001t0015others(30): Show | 59 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*955delA | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 955 | INFO_REALIGN_3_PRIME | chr16 | 85673478 | ||||
| chr16:85673496
|
C | T | 1 | a0005c0047t0065 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*957C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 957 | chr16 | 85673496 | |||||
| chr16:85673531
|
CATTAAAA others(19): Show |
C | 1 | a0001c0001t0043 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*999_*1024delATATT others(21): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 999 | INFO_REALIGN_3_PRIME | chr16 | 85673531 | ||||
| chr16:85673683
|
C | G | 10 | a0001c0001t0004a0001c0001t0035a0001c0001t0039others(7): Show | 24 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1144C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1144 | chr16 | 85673683 | |||||
| chr16:85673720
|
A | G | 1 | a0001c0001t0042 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1181 | chr16 | 85673720 | |||||
| chr16:85673761
|
G | C | 22 | a0001c0001t0002a0001c0001t0009a0001c0001t0022others(19): Show | 74 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1222G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1222 | chr16 | 85673761 | |||||
| chr16:85673826
|
A | G | 1 | a0001c0001t0020 | 2 | HG02630.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1287A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1287 | chr16 | 85673826 | |||||
| chr16:85673845
|
T | C | 2 | a0001c0001t0012a0001c0001t0043 | 4 | HG02055.hp2 HG03486.hp1 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1306T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1306 | chr16 | 85673845 | |||||
| chr16:85673845
|
T | G | 12 | a0001c0001t0020a0001c0001t0046a0001c0021t0033others(9): Show | 17 | HG01257.hp1 HG01258.hp1 HG01943.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1306T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1306 | chr16 | 85673845 | |||||
| chr16:85674022
|
G | GTCT | 10 | a0001c0001t0046a0002c0004t0008a0002c0004t0025others(7): Show | 14 | HG01257.hp1 HG01258.hp1 HG01943.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1486_*1488dupTTC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1489 | INFO_REALIGN_3_PRIME | chr16 | 85674022 | ||||
| chr16:85674027
|
C | T | 1 | a0001c0001t0059 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1488C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1488 | chr16 | 85674027 | |||||
| chr16:85674064
|
T | C | 1 | a0001c0021t0033 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1525T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1525 | chr16 | 85674064 | |||||
| chr16:85674071
|
A | G | 12 | a0001c0002t0019a0001c0002t0049a0001c0021t0033others(9): Show | 15 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1532A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1532 | chr16 | 85674071 | |||||
| chr16:85674115
|
C | T | 1 | a0013c0022t0030 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1576C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1576 | chr16 | 85674115 | |||||
| chr16:85674122
|
T | G | 2 | a0001c0037t0060a0002c0008t0070 | 2 | HG00738.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1583T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1583 | chr16 | 85674122 | |||||
| chr16:85674169
|
C | T | 1 | a0001c0001t0011 | 3 | HG00140.hp2 HG01175.hp2 HG01255.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1630C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1630 | chr16 | 85674169 | |||||
| chr16:85674179
|
G | A | 1 | a0001c0001t0028 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1640G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1640 | chr16 | 85674179 | |||||
| chr16:85674181
|
C | CTGCTCAC others(4): Show |
2 | a0001c0002t0018a0001c0055t0048 | 3 | HG01167.hp1 HG02818.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1643_*1653dupTGCT others(7): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1654 | INFO_REALIGN_3_PRIME | chr16 | 85674181 | ||||
| chr16:85674261
|
T | C | 1 | a0001c0001t0020 | 2 | HG02630.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1722T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1722 | chr16 | 85674261 | |||||
| chr16:85674264
|
C | T | 1 | a0002c0005t0063 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1725C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1725 | chr16 | 85674264 | |||||
| chr16:85674343
|
C | G | 1 | a0001c0001t0022 | 2 | NA19011.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1804C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1804 | chr16 | 85674343 | |||||
| chr16:85674356
|
C | T | 1 | a0001c0001t0058 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1817C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1817 | chr16 | 85674356 | |||||
| chr16:85674436
|
A | AAGAC | 16 | a0001c0001t0004a0001c0001t0012a0001c0001t0017others(13): Show | 33 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1899_*1902dupGACA | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1903 | INFO_REALIGN_3_PRIME | chr16 | 85674436 | ||||
| chr16:85674453
|
G | A | 4 | a0004c0007t0010a0004c0007t0052a0004c0007t0064others(1): Show | 7 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1914G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 1914 | chr16 | 85674453 | |||||
| chr16:85674566
|
A | C | 8 | a0004c0007t0010a0004c0007t0052a0004c0007t0064others(5): Show | 11 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2027A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2027 | chr16 | 85674566 | |||||
| chr16:85674620
|
C | T | 1 | a0002c0045t0047 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2081C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2081 | chr16 | 85674620 | |||||
| chr16:85674807
|
G | A | 9 | a0002c0004t0008a0002c0004t0025a0002c0004t0045others(6): Show | 13 | HG01257.hp1 HG01258.hp1 HG01943.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2268G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2268 | chr16 | 85674807 | |||||
| chr16:85674925
|
G | C | 1 | a0001c0001t0042 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2386G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2386 | chr16 | 85674925 | |||||
| chr16:85675048
|
C | G | 1 | a0025c0033t0038 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2509C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2509 | chr16 | 85675048 | |||||
| chr16:85675059
|
T | A | 2 | a0001c0001t0016a0003c0010t0016 | 2 | HG00639.hp2 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2520T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2520 | chr16 | 85675059 | |||||
| chr16:85675155
|
CTT | C | 4 | a0001c0002t0019a0001c0002t0049a0001c0055t0048others(1): Show | 4 | HG01167.hp1 HG02615.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2617_*2618delTT | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2617 | chr16 | 85675155 | |||||
| chr16:85675156
|
T | TTAAG | 27 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(24): Show | 53 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2619_*2622dupAAGT | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2623 | INFO_REALIGN_3_PRIME | chr16 | 85675156 | ||||
| chr16:85675203
|
C | A | 1 | a0001c0001t0067 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2664C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2664 | chr16 | 85675203 | |||||
| chr16:85675211
|
G | A | 2 | a0004c0007t0052a0004c0007t0064 | 2 | HG02055.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2672G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2672 | chr16 | 85675211 | |||||
| chr16:85675226
|
G | T | 1 | a0007c0012t0034 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2687G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2687 | chr16 | 85675226 | |||||
| chr16:85675232
|
G | C | 1 | a0001c0001t0020 | 2 | HG02630.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2693G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2693 | chr16 | 85675232 | |||||
| chr16:85675240
|
C | A | 24 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(21): Show | 47 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2701C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2701 | chr16 | 85675240 | |||||
| chr16:85675240
|
C | G | 41 | a0001c0001t0004a0001c0001t0012a0001c0001t0017others(38): Show | 68 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2701C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2701 | chr16 | 85675240 | |||||
| chr16:85675257
|
G | A | 1 | a0002c0005t0044 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2718G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2718 | chr16 | 85675257 | |||||
| chr16:85675261
|
C | G | 6 | a0001c0001t0005a0001c0001t0057a0001c0002t0005others(3): Show | 14 | HG00140.hp1 HG00735.hp1 HG01070.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2722C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2722 | chr16 | 85675261 | |||||
| chr16:85675308
|
C | T | 9 | a0002c0004t0008a0002c0004t0025a0002c0004t0045others(6): Show | 13 | HG01257.hp1 HG01258.hp1 HG01943.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2769C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2769 | chr16 | 85675308 | |||||
| chr16:85675346
|
T | C | 1 | a0001c0021t0033 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2807T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2807 | chr16 | 85675346 | |||||
| chr16:85675412
|
T | C | 12 | a0001c0001t0067a0001c0021t0033a0002c0004t0008others(9): Show | 16 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2873T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2873 | chr16 | 85675412 | |||||
| chr16:85675416
|
C | A | 1 | a0001c0001t0056 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2877C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2877 | chr16 | 85675416 | |||||
| chr16:85675448
|
C | T | 1 | a0001c0001t0020 | 2 | HG02630.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2909C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2909 | chr16 | 85675448 | |||||
| chr16:85675536
|
A | G | 9 | a0002c0004t0008a0002c0004t0025a0002c0004t0045others(6): Show | 13 | HG01257.hp1 HG01258.hp1 HG01943.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2997A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 2997 | chr16 | 85675536 | |||||
| chr16:85675700
|
C | T | 9 | a0002c0004t0008a0002c0004t0025a0002c0004t0045others(6): Show | 13 | HG01257.hp1 HG01258.hp1 HG01943.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3161C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 3161 | chr16 | 85675700 | |||||
| chr16:85675710
|
A | G | 67 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(64): Show | 117 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*3171A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 3171 | chr16 | 85675710 | |||||
| chr16:85675906
|
A | C | 1 | a0008c0013t0055 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3367A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 3367 | chr16 | 85675906 | |||||
| chr16:85675938
|
G | C | 14 | a0001c0001t0004a0001c0001t0012a0001c0001t0017others(11): Show | 31 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3399G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 3399 | chr16 | 85675938 | |||||
| chr16:85676004
|
G | A | 61 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(58): Show | 111 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*3465G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 16/16 | 3465 | chr16 | 85676004 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:85613450
|
G | C | 1 | a0002c0004t0004g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7+52G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613450 | ||||||
| chr16:85613461
|
C | T | 1 | a0001c0003t0001g0290 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.7+63C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613461 | ||||||
| chr16:85613568
|
C | T | 1 | a0001c0001t0003g0289 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.7+170C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613568 | ||||||
| chr16:85613621
|
G | C | 2 | a0001c0001t0011g0002a0001c0002t0001g0003 | 2 | HG01175.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.7+223G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613621 | ||||||
| chr16:85613699
|
G | A | 1 | a0001c0001t0003g0004 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.7+301G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613699 | ||||||
| chr16:85613710
|
G | C | 1 | a0001c0001t0003g0005 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.7+312G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613710 | ||||||
| chr16:85613717
|
TG | T | 5 | a0001c0001t0035g0286a0001c0002t0001g0288a0001c0002t0006g0285others(2): Show | 5 | HG01081.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+324delG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85613717 | |||||
| chr16:85613739
|
C | T | 3 | a0001c0002t0006g0281a0001c0002t0018g0283a0006c0011t0019g0282 | 3 | HG02818.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.7+341C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613739 | ||||||
| chr16:85613780
|
G | A | 1 | a0002c0018t0004g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7+382G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613780 | ||||||
| chr16:85613812
|
G | T | 1 | a0023c0031t0002g0280 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.7+414G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613812 | ||||||
| chr16:85613816
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.7+418G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613816 | ||||||
| chr16:85613840
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(7): Show | 10 | HG02738.hp2 HG03486.hp1 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.7+442G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613840 | ||||||
| chr16:85613844
|
G | A | 20 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(17): Show | 20 | HG01081.hp2 HG02145.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.7+446G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613844 | ||||||
| chr16:85613859
|
T | TG | 83 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0094others(80): Show | 83 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.7+473dupG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85613859 | |||||
| chr16:85613859
|
TG | T | 41 | a0001c0001t0004g0009a0001c0001t0009g0262a0001c0001t0011g0269others(38): Show | 41 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.7+473delG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85613859 | |||||
| chr16:85613859
|
TGG | T | 16 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(13): Show | 16 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.7+472_7+473delGG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85613859 | |||||
| chr16:85613862
|
G | T | 3 | a0001c0002t0006g0281a0001c0002t0018g0283a0006c0011t0019g0282 | 3 | HG02818.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.7+464G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613862 | ||||||
| chr16:85613864
|
G | C | 2 | a0001c0001t0003g0020a0002c0004t0002g0019 | 2 | HG01496.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.7+466G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613864 | ||||||
| chr16:85613865
|
G | T | 3 | a0001c0001t0002g0007a0001c0001t0002g0278a0001c0001t0002g0279 | 3 | HG00423.hp1 HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.7+467G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613865 | ||||||
| chr16:85613890
|
C | T | 2 | a0001c0001t0059g0273a0001c0002t0005g0274 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.7+492C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613890 | ||||||
| chr16:85613904
|
C | T | 21 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(18): Show | 21 | HG01081.hp2 HG02145.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.7+506C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613904 | ||||||
| chr16:85613947
|
G | C | 1 | a0001c0001t0022g0021 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.7+549G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613947 | ||||||
| chr16:85613968
|
C | T | 2 | a0001c0001t0035g0286a0008c0013t0021g0284 | 2 | HG01081.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.7+570C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85613968 | ||||||
| chr16:85614044
|
CCT | C | 5 | a0001c0001t0003g0099a0001c0003t0014g0022a0002c0030t0003g0023others(2): Show | 5 | HG00609.hp1 HG00735.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+654_7+655delTC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85614044 | |||||
| chr16:85614081
|
G | GCCCCT | 8 | a0001c0001t0035g0286a0001c0002t0001g0288a0001c0002t0006g0281others(5): Show | 8 | HG01081.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+693_7+697dupTCCC others(1): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85614081 | |||||
| chr16:85614171
|
C | T | 1 | a0018c0043t0003g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7+773C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85614171 | ||||||
| chr16:85614179
|
C | T | 1 | a0001c0001t0004g0240 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+781C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85614179 | ||||||
| chr16:85614182
|
C | T | 1 | a0007c0012t0021g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.7+784C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85614182 | ||||||
| chr16:85614491
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0003g0289a0001c0001t0004g0025others(1): Show | 4 | HG00673.hp2 NA19004.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+1093G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85614491 | ||||||
| chr16:85614570
|
GC | G | 3 | a0001c0001t0035g0286a0001c0002t0001g0288a0008c0013t0021g0284 | 3 | HG01081.hp2 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.7+1175delC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85614570 | |||||
| chr16:85614653
|
C | T | 1 | a0001c0001t0004g0238 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.7+1255C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85614653 | ||||||
| chr16:85615011
|
C | T | 1 | a0001c0002t0001g0288 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.7+1613C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85615011 | ||||||
| chr16:85615034
|
C | G | 1 | a0001c0001t0002g0097 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.7+1636C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85615034 | ||||||
| chr16:85615091
|
C | G | 1 | a0002c0017t0001g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.7+1693C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85615091 | ||||||
| chr16:85615094
|
C | T | 1 | a0001c0001t0002g0236 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.7+1696C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85615094 | ||||||
| chr16:85615102
|
C | T | 3 | a0001c0002t0006g0281a0001c0002t0018g0283a0006c0011t0019g0282 | 3 | HG02818.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.7+1704C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85615102 | ||||||
| chr16:85615202
|
C | T | 1 | a0001c0001t0004g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.7+1804C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85615202 | ||||||
| chr16:85615238
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.7+1840C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85615238 | ||||||
| chr16:85615264
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.7+1866C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85615264 | ||||||
| chr16:85615480
|
GCTGGAGC others(33): Show |
G | 1 | a0001c0002t0001g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7+2091_7+2130delAA others(38): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85615480 | |||||
| chr16:85615521
|
C | T | 1 | a0015c0041t0001g0095 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.7+2123C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85615521 | ||||||
| chr16:85615876
|
G | C | 3 | a0001c0002t0001g0102a0001c0002t0006g0285a0002c0004t0004g0001 | 3 | HG02559.hp1 HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.7+2478G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85615876 | ||||||
| chr16:85615973
|
C | T | 3 | a0001c0002t0006g0281a0001c0002t0018g0283a0006c0011t0019g0282 | 3 | HG02818.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.7+2575C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85615973 | ||||||
| chr16:85616003
|
C | A | 1 | a0001c0055t0048g0241 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.7+2605C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616003 | ||||||
| chr16:85616041
|
T | G | 3 | a0001c0001t0005g0027a0001c0001t0042g0103a0002c0016t0003g0104 | 3 | HG00099.hp1 HG00735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.7+2643T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616041 | ||||||
| chr16:85616064
|
G | A | 1 | a0002c0004t0002g0019 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.7+2666G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616064 | ||||||
| chr16:85616085
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.7+2687A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616085 | ||||||
| chr16:85616153
|
C | G | 1 | a0001c0002t0049g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.7+2755C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616153 | ||||||
| chr16:85616203
|
T | C | 1 | a0001c0020t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7+2805T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616203 | ||||||
| chr16:85616381
|
A | G | 6 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0003g0099others(3): Show | 6 | HG00609.hp1 HG02015.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+2983A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616381 | ||||||
| chr16:85616467
|
C | T | 2 | a0001c0002t0001g0018a0021c0039t0001g0271 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.7+3069C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616467 | ||||||
| chr16:85616488
|
G | A | 1 | a0001c0001t0046g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7+3090G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616488 | ||||||
| chr16:85616518
|
G | A | 1 | a0001c0051t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7+3120G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616518 | ||||||
| chr16:85616550
|
G | A | 2 | a0001c0002t0001g0018a0021c0039t0001g0271 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.7+3152G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616550 | ||||||
| chr16:85616872
|
C | T | 2 | a0006c0011t0013g0230a0006c0011t0013g0270 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.7+3474C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616872 | ||||||
| chr16:85616877
|
G | C | 1 | a0001c0001t0009g0029 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.7+3479G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85616877 | ||||||
| chr16:85617055
|
C | T | 1 | a0001c0001t0022g0021 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.7+3657C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617055 | ||||||
| chr16:85617060
|
C | G | 3 | a0001c0001t0001g0094a0001c0001t0002g0229a0001c0001t0011g0269 | 3 | HG00140.hp2 HG01361.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.7+3662C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617060 | ||||||
| chr16:85617075
|
A | G | 1 | a0002c0004t0008g0093 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.7+3677A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617075 | ||||||
| chr16:85617078
|
T | A | 2 | a0001c0002t0001g0018a0021c0039t0001g0271 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.7+3680T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617078 | ||||||
| chr16:85617102
|
C | T | 2 | a0001c0002t0001g0018a0021c0039t0001g0271 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.7+3704C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617102 | ||||||
| chr16:85617188
|
C | T | 2 | a0001c0002t0001g0018a0021c0039t0001g0271 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.7+3790C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617188 | ||||||
| chr16:85617211
|
C | G | 2 | a0001c0001t0012g0010a0002c0004t0004g0001 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.7+3813C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617211 | ||||||
| chr16:85617218
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0002g0228 | 2 | NA18970.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.7+3820C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617218 | ||||||
| chr16:85617221
|
G | C | 1 | a0001c0001t0002g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.7+3823G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617221 | ||||||
| chr16:85617271
|
G | A | 1 | a0001c0028t0053g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7+3873G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617271 | ||||||
| chr16:85617366
|
G | A | 1 | a0001c0003t0001g0108 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.7+3968G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617366 | ||||||
| chr16:85617560
|
C | T | 1 | a0002c0004t0003g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.7+4162C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617560 | ||||||
| chr16:85617596
|
T | C | 1 | a0003c0009t0002g0109 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7+4198T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617596 | ||||||
| chr16:85617596
|
T | TCCCCCCC others(13): Show |
1 | a0001c0002t0006g0281 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7+4213_7+4214insCC others(18): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85617596 | |||||
| chr16:85617596
|
TC | T | 58 | a0001c0001t0001g0094a0001c0001t0002g0007a0001c0001t0002g0041others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.7+4213delC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85617596 | |||||
| chr16:85617596
|
TCC | T | 160 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0220others(157): Show | 160 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.7+4212_7+4213delCC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85617596 | |||||
| chr16:85617604
|
C | G | 1 | a0001c0001t0004g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.7+4206C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617604 | ||||||
| chr16:85617608
|
C | G | 1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.7+4210C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617608 | ||||||
| chr16:85617608
|
C | T | 2 | a0001c0001t0012g0010a0002c0004t0004g0001 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.7+4210C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617608 | ||||||
| chr16:85617609
|
C | G | 1 | a0001c0001t0002g0224 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.7+4211C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617609 | ||||||
| chr16:85617613
|
T | G | 255 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.7+4215T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617613 | ||||||
| chr16:85617615
|
A | G | 255 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.7+4217A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617615 | ||||||
| chr16:85617744
|
G | C | 1 | a0001c0001t0002g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7+4346G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617744 | ||||||
| chr16:85617811
|
G | T | 1 | a0021c0039t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7+4413G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617811 | ||||||
| chr16:85617899
|
T | C | 2 | a0002c0005t0008g0159a0002c0005t0008g0160 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.7+4501T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617899 | ||||||
| chr16:85617962
|
G | A | 3 | a0001c0001t0035g0286a0001c0002t0001g0288a0008c0013t0021g0284 | 3 | HG01081.hp2 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.7+4564G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85617962 | ||||||
| chr16:85618136
|
C | T | 1 | a0001c0003t0001g0032 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.7+4738C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618136 | ||||||
| chr16:85618312
|
C | T | 1 | a0001c0001t0002g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.7+4914C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618312 | ||||||
| chr16:85618333
|
A | G | 1 | a0007c0012t0021g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.7+4935A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618333 | ||||||
| chr16:85618357
|
A | G | 1 | a0001c0001t0002g0228 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.7+4959A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618357 | ||||||
| chr16:85618385
|
G | A | 1 | a0006c0011t0019g0282 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7+4987G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618385 | ||||||
| chr16:85618427
|
A | G | 11 | a0001c0001t0012g0010a0001c0001t0043g0014a0001c0002t0001g0018others(8): Show | 11 | HG02145.hp1 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.7+5029A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618427 | ||||||
| chr16:85618472
|
G | C | 2 | a0001c0001t0004g0009a0003c0010t0004g0008 | 2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.7+5074G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618472 | ||||||
| chr16:85618587
|
T | G | 1 | a0002c0004t0008g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7+5189T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618587 | ||||||
| chr16:85618812
|
G | A | 4 | a0001c0002t0006g0092a0001c0002t0006g0281a0001c0002t0018g0283others(1): Show | 4 | HG02622.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+5414G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618812 | ||||||
| chr16:85618910
|
C | G | 1 | a0001c0002t0001g0268 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.7+5512C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618910 | ||||||
| chr16:85618921
|
C | T | 1 | a0001c0002t0007g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.7+5523C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618921 | ||||||
| chr16:85618941
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.7+5543G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618941 | ||||||
| chr16:85618998
|
C | T | 3 | a0001c0001t0012g0010a0001c0028t0053g0287a0002c0004t0004g0001 | 3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.7+5600C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85618998 | ||||||
| chr16:85619003
|
C | T | 4 | a0001c0002t0006g0092a0001c0002t0006g0281a0001c0002t0018g0283others(1): Show | 4 | HG02622.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+5605C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619003 | ||||||
| chr16:85619023
|
G | T | 3 | a0001c0001t0035g0286a0001c0002t0001g0288a0008c0013t0021g0284 | 3 | HG01081.hp2 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.7+5625G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619023 | ||||||
| chr16:85619100
|
C | A | 6 | a0001c0001t0012g0010a0001c0001t0043g0014a0001c0028t0053g0287others(3): Show | 6 | HG02145.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+5702C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619100 | ||||||
| chr16:85619101
|
C | G | 4 | a0001c0002t0006g0092a0001c0002t0006g0281a0001c0002t0018g0283others(1): Show | 4 | HG02622.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+5703C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619101 | ||||||
| chr16:85619156
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.7+5758A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619156 | ||||||
| chr16:85619163
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7+5765C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619163 | ||||||
| chr16:85619207
|
C | T | 3 | a0002c0030t0003g0023a0016c0029t0003g0100a0017c0044t0002g0024 | 3 | NA18947.hp2 NA19066.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.7+5809C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619207 | ||||||
| chr16:85619248
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.7+5850C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619248 | ||||||
| chr16:85619249
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0011g0269 | 2 | HG00140.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.7+5851C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619249 | ||||||
| chr16:85619286
|
T | G | 1 | a0001c0002t0001g0268 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.7+5888T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619286 | ||||||
| chr16:85619354
|
A | G | 1 | a0001c0001t0061g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.7+5956A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619354 | ||||||
| chr16:85619374
|
A | G | 1 | a0002c0006t0001g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7+5976A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619374 | ||||||
| chr16:85619484
|
G | C | 1 | a0001c0001t0003g0020 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7+6086G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619484 | ||||||
| chr16:85619501
|
C | T | 2 | a0001c0001t0012g0010a0002c0004t0004g0001 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.7+6103C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619501 | ||||||
| chr16:85619525
|
A | T | 4 | a0001c0002t0006g0092a0001c0002t0006g0281a0001c0002t0018g0283others(1): Show | 4 | HG02622.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+6127A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619525 | ||||||
| chr16:85619644
|
G | C | 1 | a0001c0002t0001g0247 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.7+6246G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619644 | ||||||
| chr16:85619751
|
C | T | 1 | a0001c0001t0020g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7+6353C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85619751 | ||||||
| chr16:85619830
|
AG | A | 3 | a0001c0002t0001g0018a0002c0018t0004g0006a0021c0039t0001g0271 | 3 | HG02258.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7+6436delG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85619830 | |||||
| chr16:85620139
|
G | A | 3 | a0001c0002t0006g0281a0001c0002t0018g0283a0006c0011t0019g0282 | 3 | HG02818.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.7+6741G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85620139 | ||||||
| chr16:85620327
|
A | G | 1 | a0002c0006t0001g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.7+6929A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85620327 | ||||||
| chr16:85620411
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.7+7013T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85620411 | ||||||
| chr16:85620556
|
C | G | 2 | a0001c0001t0001g0120a0001c0001t0022g0031 | 2 | HG00408.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.7+7158C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85620556 | ||||||
| chr16:85620643
|
T | C | 3 | a0001c0002t0006g0281a0001c0002t0018g0283a0006c0011t0019g0282 | 3 | HG02818.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.7+7245T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85620643 | ||||||
| chr16:85620652
|
A | G | 22 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(19): Show | 22 | HG01081.hp2 HG01243.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.7+7254A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85620652 | ||||||
| chr16:85620674
|
T | G | 1 | a0001c0001t0002g0059 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.7+7276T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85620674 | ||||||
| chr16:85620697
|
C | G | 34 | a0001c0001t0001g0220a0001c0001t0012g0210a0001c0001t0012g0212others(31): Show | 34 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.7+7299C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85620697 | ||||||
| chr16:85620754
|
C | T | 8 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0207others(5): Show | 8 | HG01106.hp2 HG01258.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.7+7356C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85620754 | ||||||
| chr16:85620780
|
A | G | 22 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(19): Show | 22 | HG01081.hp2 HG01243.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.7+7382A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85620780 | ||||||
| chr16:85620813
|
T | A | 1 | a0002c0008t0070g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.7+7415T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85620813 | ||||||
| chr16:85621012
|
C | T | 3 | a0001c0002t0006g0281a0001c0002t0018g0283a0006c0011t0019g0282 | 3 | HG02818.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.7+7614C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85621012 | ||||||
| chr16:85621329
|
G | A | 4 | a0001c0002t0002g0248a0001c0002t0002g0250a0003c0009t0002g0109others(1): Show | 4 | HG00738.hp1 HG01123.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+7931G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85621329 | ||||||
| chr16:85621411
|
G | A | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | NA18946.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.7+8013G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85621411 | ||||||
| chr16:85621443
|
G | C | 56 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(53): Show | 56 | HG01081.hp2 HG01109.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.7+8045G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85621443 | ||||||
| chr16:85621467
|
C | T | 4 | a0001c0001t0012g0010a0001c0002t0001g0018a0002c0018t0004g0006others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+8069C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85621467 | ||||||
| chr16:85621877
|
C | G | 1 | a0006c0011t0013g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7+8479C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85621877 | ||||||
| chr16:85621902
|
A | G | 10 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(7): Show | 10 | HG01243.hp1 HG02559.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.7+8504A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85621902 | ||||||
| chr16:85621949
|
G | T | 1 | a0001c0002t0026g0203 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.7+8551G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85621949 | ||||||
| chr16:85621973
|
T | A | 1 | a0020c0042t0008g0042 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7+8575T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85621973 | ||||||
| chr16:85621979
|
CTCCCAAC others(6): Show |
C | 1 | a0020c0042t0008g0042 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7+8582_7+8594delTC others(11): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85621979 | ||||||
| chr16:85622042
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.7+8644G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622042 | ||||||
| chr16:85622071
|
C | T | 1 | a0001c0002t0001g0288 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.7+8673C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622071 | ||||||
| chr16:85622078
|
A | G | 15 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(12): Show | 15 | HG01243.hp1 HG02258.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.7+8680A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622078 | ||||||
| chr16:85622103
|
C | A | 1 | a0001c0001t0051g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.7+8705C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622103 | ||||||
| chr16:85622128
|
C | T | 6 | a0001c0001t0002g0153a0001c0001t0002g0199a0001c0001t0002g0200others(3): Show | 6 | HG01099.hp2 HG01934.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+8730C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622128 | ||||||
| chr16:85622129
|
G | A | 18 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(15): Show | 18 | HG01243.hp1 HG02258.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.7+8731G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622129 | ||||||
| chr16:85622385
|
TC | T | 19 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(16): Show | 19 | HG01243.hp1 HG02258.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.7+8989delC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85622385 | |||||
| chr16:85622386
|
C | A | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.7+8988C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622386 | ||||||
| chr16:85622421
|
T | C | 1 | a0001c0001t0046g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7+9023T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622421 | ||||||
| chr16:85622488
|
G | C | 1 | a0001c0001t0016g0162 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.7+9090G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622488 | ||||||
| chr16:85622501
|
T | C | 1 | a0008c0013t0055g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7+9103T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622501 | ||||||
| chr16:85622559
|
A | G | 1 | a0001c0001t0046g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7+9161A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622559 | ||||||
| chr16:85622569
|
G | A | 1 | a0001c0001t0051g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.7+9171G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622569 | ||||||
| chr16:85622668
|
T | C | 3 | a0001c0001t0043g0014a0001c0002t0018g0283a0006c0011t0019g0282 | 3 | HG02818.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.7+9270T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622668 | ||||||
| chr16:85622682
|
G | A | 1 | a0001c0001t0012g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7+9284G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622682 | ||||||
| chr16:85622744
|
G | A | 2 | a0001c0002t0001g0251a0001c0002t0001g0272 | 2 | HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.7+9346G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622744 | ||||||
| chr16:85622758
|
C | T | 3 | a0001c0002t0001g0018a0002c0018t0004g0006a0021c0039t0001g0271 | 3 | HG02258.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7+9360C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622758 | ||||||
| chr16:85622963
|
G | C | 1 | a0002c0005t0063g0208 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7+9565G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622963 | ||||||
| chr16:85622968
|
C | T | 8 | a0001c0001t0001g0234a0001c0001t0009g0196a0001c0001t0009g0198others(5): Show | 8 | HG00099.hp2 HG01109.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.7+9570C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622968 | ||||||
| chr16:85622970
|
T | C | 2 | a0001c0001t0035g0286a0008c0013t0021g0284 | 2 | HG01081.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.7+9572T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622970 | ||||||
| chr16:85622973
|
G | T | 1 | a0001c0001t0002g0087 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.7+9575G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622973 | ||||||
| chr16:85622984
|
G | T | 1 | a0001c0001t0003g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.7+9586G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85622984 | ||||||
| chr16:85623000
|
C | T | 1 | a0001c0001t0003g0004 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.7+9602C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623000 | ||||||
| chr16:85623100
|
C | G | 1 | a0001c0002t0001g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.7+9702C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623100 | ||||||
| chr16:85623108
|
C | T | 2 | a0001c0002t0018g0283a0006c0011t0019g0282 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.7+9710C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623108 | ||||||
| chr16:85623140
|
G | A | 2 | a0001c0001t0035g0286a0008c0013t0021g0284 | 2 | HG01081.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.7+9742G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623140 | ||||||
| chr16:85623215
|
CT | C | 20 | a0001c0001t0002g0107a0001c0001t0009g0196a0001c0001t0012g0010others(17): Show | 20 | HG00738.hp2 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.7+9834delT | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85623215 | |||||
| chr16:85623340
|
A | T | 3 | a0001c0002t0001g0018a0002c0018t0004g0006a0021c0039t0001g0271 | 3 | HG02258.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7+9942A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623340 | ||||||
| chr16:85623428
|
CTG | C | 3 | a0001c0002t0001g0018a0002c0018t0004g0006a0021c0039t0001g0271 | 3 | HG02258.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7+10031_7+10032del others(2): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623428 | ||||||
| chr16:85623503
|
G | A | 1 | a0001c0001t0003g0141 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.7+10105G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623503 | ||||||
| chr16:85623560
|
G | T | 1 | a0001c0001t0002g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.7+10162G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623560 | ||||||
| chr16:85623573
|
C | T | 4 | a0001c0001t0035g0286a0001c0001t0043g0014a0001c0002t0001g0288others(1): Show | 4 | HG01081.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+10175C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623573 | ||||||
| chr16:85623597
|
A | C | 1 | a0001c0001t0011g0136 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.7+10199A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623597 | ||||||
| chr16:85623641
|
A | C | 4 | a0001c0001t0035g0286a0001c0001t0043g0014a0001c0002t0001g0288others(1): Show | 4 | HG01081.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+10243A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623641 | ||||||
| chr16:85623792
|
C | T | 2 | a0001c0002t0018g0283a0006c0011t0019g0282 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.8-10122C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623792 | ||||||
| chr16:85623890
|
G | A | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.8-10024G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623890 | ||||||
| chr16:85623913
|
T | G | 18 | a0001c0001t0004g0009a0001c0001t0004g0013a0001c0001t0012g0010others(15): Show | 18 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.8-10001T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623913 | ||||||
| chr16:85623994
|
C | G | 3 | a0002c0006t0001g0221a0002c0017t0001g0219a0004c0007t0010g0091 | 3 | HG02970.hp1 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.8-9920C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85623994 | ||||||
| chr16:85624027
|
T | C | 2 | a0002c0018t0004g0006a0021c0039t0001g0271 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.8-9887T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624027 | ||||||
| chr16:85624117
|
C | T | 1 | a0001c0001t0043g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.8-9797C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624117 | ||||||
| chr16:85624137
|
G | A | 21 | a0001c0001t0001g0094a0001c0001t0001g0227a0001c0001t0002g0062others(18): Show | 21 | HG00140.hp2 HG00438.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.8-9777G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624137 | ||||||
| chr16:85624189
|
G | C | 2 | a0001c0001t0035g0286a0008c0013t0021g0284 | 2 | HG01081.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.8-9725G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624189 | ||||||
| chr16:85624326
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.8-9588C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624326 | ||||||
| chr16:85624377
|
T | C | 13 | a0001c0001t0012g0010a0001c0001t0035g0286a0001c0001t0043g0014others(10): Show | 13 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.8-9537T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624377 | ||||||
| chr16:85624380
|
C | T | 1 | a0001c0001t0046g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.8-9534C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624380 | ||||||
| chr16:85624460
|
G | A | 15 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0012others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.8-9454G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624460 | ||||||
| chr16:85624544
|
G | A | 1 | a0001c0001t0069g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.8-9370G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624544 | ||||||
| chr16:85624581
|
C | T | 1 | a0029c0024t0023g0055 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.8-9333C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624581 | ||||||
| chr16:85624711
|
T | C | 1 | a0011c0052t0002g0122 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.8-9203T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624711 | ||||||
| chr16:85624752
|
C | A | 1 | a0004c0007t0010g0265 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.8-9162C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624752 | ||||||
| chr16:85624816
|
C | G | 2 | a0001c0002t0018g0283a0006c0011t0019g0282 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.8-9098C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624816 | ||||||
| chr16:85624844
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.8-9070G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85624844 | ||||||
| chr16:85625059
|
C | T | 2 | a0001c0002t0018g0283a0006c0011t0019g0282 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.8-8855C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625059 | ||||||
| chr16:85625102
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.8-8812C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625102 | ||||||
| chr16:85625117
|
G | A | 1 | a0001c0002t0001g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.8-8797G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625117 | ||||||
| chr16:85625137
|
C | T | 1 | a0001c0028t0053g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.8-8777C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625137 | ||||||
| chr16:85625149
|
G | A | 1 | a0001c0002t0002g0165 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.8-8765G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625149 | ||||||
| chr16:85625263
|
G | A | 2 | a0002c0018t0004g0006a0021c0039t0001g0271 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.8-8651G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625263 | ||||||
| chr16:85625263
|
G | T | 1 | a0001c0001t0002g0097 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.8-8651G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625263 | ||||||
| chr16:85625264
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.8-8650C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625264 | ||||||
| chr16:85625326
|
C | T | 1 | a0010c0015t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.8-8588C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625326 | ||||||
| chr16:85625364
|
C | T | 11 | a0001c0001t0012g0010a0001c0001t0035g0286a0001c0002t0001g0288others(8): Show | 11 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.8-8550C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625364 | ||||||
| chr16:85625368
|
G | A | 1 | a0001c0002t0006g0211 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.8-8546G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625368 | ||||||
| chr16:85625488
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.8-8426C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625488 | ||||||
| chr16:85625548
|
C | G | 4 | a0001c0001t0020g0217a0001c0002t0001g0018a0001c0002t0001g0288others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-8366C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625548 | ||||||
| chr16:85625549
|
C | T | 6 | a0001c0001t0020g0217a0001c0002t0001g0018a0001c0002t0001g0288others(3): Show | 6 | HG02622.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-8365C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625549 | ||||||
| chr16:85625664
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.8-8250G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625664 | ||||||
| chr16:85625881
|
G | C | 1 | a0001c0002t0001g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.8-8033G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625881 | ||||||
| chr16:85625926
|
G | A | 8 | a0001c0001t0012g0010a0001c0002t0018g0283a0002c0004t0004g0001others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-7988G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85625926 | ||||||
| chr16:85626062
|
C | T | 1 | a0001c0002t0006g0281 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.8-7852C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626062 | ||||||
| chr16:85626103
|
G | T | 1 | a0002c0004t0004g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.8-7811G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626103 | ||||||
| chr16:85626135
|
T | G | 23 | a0001c0001t0001g0227a0001c0001t0004g0009a0001c0001t0004g0013others(20): Show | 23 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.8-7779T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626135 | ||||||
| chr16:85626139
|
G | A | 1 | a0001c0001t0016g0162 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.8-7775G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626139 | ||||||
| chr16:85626140
|
A | G | 1 | a0001c0001t0004g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.8-7774A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626140 | ||||||
| chr16:85626259
|
C | G | 23 | a0001c0001t0001g0227a0001c0001t0004g0009a0001c0001t0004g0013others(20): Show | 23 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.8-7655C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626259 | ||||||
| chr16:85626272
|
A | G | 20 | a0001c0001t0001g0227a0001c0001t0004g0009a0001c0001t0004g0013others(17): Show | 20 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.8-7642A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626272 | ||||||
| chr16:85626283
|
A | G | 4 | a0001c0001t0068g0054a0001c0002t0001g0245a0001c0055t0048g0241others(1): Show | 4 | HG01167.hp1 HG02145.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-7631A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626283 | ||||||
| chr16:85626302
|
T | C | 1 | a0001c0001t0002g0087 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.8-7612T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626302 | ||||||
| chr16:85626313
|
C | T | 1 | a0007c0012t0021g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.8-7601C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626313 | ||||||
| chr16:85626354
|
C | T | 1 | a0002c0006t0001g0216 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.8-7560C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626354 | ||||||
| chr16:85626437
|
G | A | 11 | a0001c0001t0012g0010a0001c0001t0035g0286a0001c0002t0001g0288others(8): Show | 11 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.8-7477G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626437 | ||||||
| chr16:85626595
|
G | A | 1 | a0001c0001t0005g0027 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.8-7319G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626595 | ||||||
| chr16:85626765
|
G | T | 8 | a0001c0001t0001g0227a0001c0001t0004g0009a0001c0001t0004g0013others(5): Show | 8 | HG02055.hp2 HG02572.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-7149G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626765 | ||||||
| chr16:85626797
|
A | C | 17 | a0001c0001t0020g0156a0001c0002t0001g0251a0001c0002t0006g0092others(14): Show | 17 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.8-7117A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626797 | ||||||
| chr16:85626801
|
T | C | 3 | a0001c0002t0001g0017a0002c0018t0004g0006a0021c0039t0001g0271 | 3 | HG02258.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.8-7113T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85626801 | ||||||
| chr16:85627044
|
C | CT | 16 | a0001c0001t0002g0037a0001c0001t0002g0097a0001c0001t0002g0123others(13): Show | 16 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-6838dupT | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTT | 10 | a0001c0001t0002g0059a0001c0001t0002g0107a0001c0001t0002g0148others(7): Show | 10 | HG00544.hp2 HG01928.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-6839_8-6838dupTT | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTT | 10 | a0001c0001t0001g0026a0001c0001t0002g0149a0001c0001t0004g0101others(7): Show | 10 | HG00408.hp1 HG00673.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-6840_8-6838dupTT others(1): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTT | 6 | a0001c0001t0003g0004a0001c0001t0003g0141a0001c0002t0006g0285others(3): Show | 6 | HG00323.hp2 HG00738.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-6841_8-6838dupTT others(2): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTT | 9 | a0001c0001t0001g0094a0001c0001t0001g0234a0001c0001t0002g0012others(6): Show | 9 | HG00140.hp2 HG00438.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-6842_8-6838dupTT others(3): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT | 7 | a0001c0001t0002g0073a0001c0001t0004g0071a0001c0002t0005g0197others(4): Show | 7 | HG00544.hp1 HG01358.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-6844_8-6838dupTT others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(1): Show |
15 | a0001c0001t0001g0016a0001c0001t0001g0227a0001c0001t0002g0182others(12): Show | 15 | HG02615.hp2 HG02738.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.8-6845_8-6838dupTT others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(2): Show |
9 | a0001c0003t0001g0075a0001c0003t0001g0290a0001c0020t0001g0028others(6): Show | 9 | HG01978.hp2 HG01981.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-6846_8-6838dupTT others(7): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0057g0185a0001c0001t0058g0051a0007c0012t0021g0239others(1): Show | 4 | HG00639.hp1 HG01106.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-6847_8-6838dupTT others(8): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0007g0135a0001c0001t0007g0186a0001c0001t0027g0063others(2): Show | 5 | HG01069.hp2 HG01081.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-6848_8-6838dupTT others(9): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(5): Show |
7 | a0001c0001t0004g0013a0001c0001t0007g0038a0001c0001t0009g0198others(4): Show | 7 | HG00099.hp2 HG01071.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-6849_8-6838dupTT others(10): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0005g0027a0001c0002t0005g0078a0002c0006t0001g0221others(1): Show | 4 | HG00099.hp1 HG00735.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-6850_8-6838dupTT others(11): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(7): Show |
5 | a0001c0001t0001g0030a0001c0001t0020g0156a0001c0001t0042g0103others(2): Show | 5 | HG01261.hp2 HG01433.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-6851_8-6838dupTT others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(8): Show |
8 | a0001c0001t0002g0151a0001c0001t0003g0187a0001c0001t0017g0090others(5): Show | 8 | HG00597.hp2 HG00741.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-6852_8-6838dupTT others(13): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0004g0053a0001c0002t0007g0267a0020c0042t0008g0042 | 3 | HG00741.hp2 HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.8-6853_8-6838dupTT others(14): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0002g0082a0001c0002t0001g0260a0001c0002t0001g0268 | 3 | HG01993.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.8-6854_8-6838dupTT others(15): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(11): Show |
5 | a0001c0001t0004g0188a0001c0001t0009g0262a0001c0001t0022g0021others(2): Show | 5 | HG02004.hp1 HG02683.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-6855_8-6838dupTT others(16): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0002g0041a0001c0001t0009g0152 | 2 | HG03654.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.8-6856_8-6838dupTT others(17): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(13): Show |
3 | a0001c0002t0001g0018a0001c0002t0005g0079a0001c0002t0006g0281 | 3 | HG00140.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.8-6857_8-6838dupTT others(18): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(14): Show |
6 | a0001c0001t0001g0120a0001c0001t0002g0007a0001c0001t0004g0240others(3): Show | 6 | HG00408.hp2 HG01258.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-6858_8-6838dupTT others(19): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(15): Show |
4 | a0001c0001t0004g0190a0001c0001t0004g0235a0001c0003t0001g0108others(1): Show | 4 | HG01106.hp2 HG01123.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-6859_8-6838dupTT others(20): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(16): Show |
6 | a0001c0001t0002g0087a0001c0001t0017g0243a0001c0003t0001g0206others(3): Show | 6 | HG01928.hp1 HG01993.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-6860_8-6838dupTT others(21): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(17): Show |
3 | a0001c0001t0051g0140a0001c0001t0066g0192a0002c0008t0001g0168 | 3 | HG01891.hp2 HG02895.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.8-6861_8-6838dupTT others(22): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(18): Show |
4 | a0001c0002t0001g0139a0001c0002t0006g0092a0001c0002t0006g0215others(1): Show | 4 | HG00738.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-6862_8-6838dupTT others(23): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(19): Show |
3 | a0001c0001t0022g0031a0001c0002t0001g0263a0002c0005t0007g0080 | 3 | HG01361.hp2 HG02258.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.8-6863_8-6838dupTT others(24): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(20): Show |
2 | a0001c0001t0004g0193a0001c0001t0009g0196 | 2 | HG00673.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.8-6864_8-6838dupTT others(25): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(21): Show |
2 | a0001c0002t0002g0250a0002c0054t0032g0084 | 2 | HG01123.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.8-6865_8-6838dupTT others(26): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0002g0207 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.8-6866_8-6838dupTT others(27): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(23): Show |
3 | a0001c0002t0005g0081a0001c0002t0005g0118a0024c0034t0001g0117 | 3 | HG02735.hp2 HG03831.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.8-6867_8-6838dupTT others(28): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
C | CTTTTTTT others(28): Show |
1 | a0001c0002t0007g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.8-6838_8-6837insTT others(33): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CT | C | 24 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0003g0020others(21): Show | 24 | HG01099.hp1 HG01175.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.8-6838delT | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CTTTT | C | 8 | a0001c0002t0001g0083a0001c0002t0026g0203a0001c0002t0031g0256others(5): Show | 8 | HG00423.hp2 HG01109.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-6841_8-6838delTT others(2): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CTTTTT | C | 8 | a0001c0001t0002g0146a0001c0001t0002g0173a0001c0001t0002g0278others(5): Show | 8 | HG00423.hp1 HG02129.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-6842_8-6838delTT others(3): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CTTTTTT | C | 6 | a0001c0001t0002g0153a0001c0001t0002g0199a0001c0001t0002g0200others(3): Show | 6 | HG01099.hp2 HG01934.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-6843_8-6838delTT others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CTTTTTTT | C | 11 | a0001c0001t0002g0062a0001c0001t0009g0171a0001c0001t0016g0162others(8): Show | 11 | HG00639.hp2 HG01081.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.8-6844_8-6838delTT others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0001g0220a0001c0001t0003g0170a0001c0002t0001g0066others(5): Show | 8 | HG01884.hp1 HG02602.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-6845_8-6838delTT others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CTTTTTTT others(2): Show |
C | 14 | a0001c0001t0012g0210a0001c0002t0001g0017a0001c0002t0002g0165others(11): Show | 14 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.8-6846_8-6838delTT others(7): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.8-6847_8-6838delTT others(8): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0004g0144 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.8-6849_8-6838delTT others(10): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CTTTTTTT others(6): Show |
C | 9 | a0001c0001t0012g0010a0001c0002t0006g0213a0001c0003t0001g0032others(6): Show | 9 | HG00735.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-6850_8-6838delTT others(11): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0002g0231a0002c0004t0008g0015 | 2 | HG02015.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.8-6851_8-6838delTT others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627044
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0040t0001g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.8-6852_8-6838delTT others(13): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627044 | |||||
| chr16:85627076
|
T | A | 3 | a0001c0002t0001g0017a0002c0018t0004g0006a0021c0039t0001g0271 | 3 | HG02258.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.8-6838T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627076 | ||||||
| chr16:85627076
|
T | TTTTTTTT others(3): Show |
3 | a0001c0002t0001g0164a0001c0002t0049g0233a0019c0025t0024g0275 | 3 | HG02109.hp2 HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.8-6838_8-6837insTT others(8): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627076 | ||||||
| chr16:85627076
|
T | TTTTTTTT others(4): Show |
3 | a0001c0002t0006g0184a0002c0004t0003g0276a0004c0007t0052g0076 | 3 | HG02055.hp1 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.8-6838_8-6837insTT others(9): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627076 | ||||||
| chr16:85627077
|
A | T | 1 | a0001c0001t0058g0051 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.8-6837A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627077 | ||||||
| chr16:85627148
|
C | T | 1 | a0001c0001t0002g0011 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.8-6766C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627148 | ||||||
| chr16:85627212
|
C | A | 3 | a0001c0002t0001g0017a0002c0018t0004g0006a0021c0039t0001g0271 | 3 | HG02258.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.8-6702C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627212 | ||||||
| chr16:85627256
|
G | A | 12 | a0001c0001t0012g0010a0001c0001t0035g0286a0001c0002t0001g0017others(9): Show | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-6658G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627256 | ||||||
| chr16:85627267
|
C | A | 12 | a0001c0001t0012g0010a0001c0001t0035g0286a0001c0002t0001g0017others(9): Show | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-6647C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627267 | ||||||
| chr16:85627403
|
T | C | 1 | a0002c0008t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.8-6511T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627403 | ||||||
| chr16:85627497
|
G | T | 1 | a0001c0028t0053g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.8-6417G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627497 | ||||||
| chr16:85627612
|
G | A | 1 | a0002c0004t0004g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.8-6302G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627612 | ||||||
| chr16:85627640
|
A | G | 35 | a0001c0001t0012g0210a0001c0001t0012g0212a0001c0001t0020g0156others(32): Show | 35 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.8-6274A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627640 | ||||||
| chr16:85627665
|
G | GCCCCCGG others(1): Show |
10 | a0001c0001t0001g0120a0001c0001t0003g0004a0001c0001t0004g0009others(7): Show | 10 | HG00099.hp1 HG00408.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-6230_8-6223dupCC others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85627665 | |||||
| chr16:85627682
|
C | G | 3 | a0001c0001t0012g0210a0005c0047t0065g0088a0010c0015t0001g0246 | 3 | HG02055.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.8-6232C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627682 | ||||||
| chr16:85627723
|
G | A | 2 | a0001c0001t0035g0286a0008c0013t0021g0284 | 2 | HG01081.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.8-6191G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627723 | ||||||
| chr16:85627798
|
G | A | 1 | a0001c0001t0003g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.8-6116G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627798 | ||||||
| chr16:85627937
|
G | C | 29 | a0001c0001t0004g0009a0001c0001t0004g0013a0001c0001t0012g0210others(26): Show | 29 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.8-5977G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85627937 | ||||||
| chr16:85628026
|
C | A | 1 | a0010c0015t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.8-5888C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85628026 | ||||||
| chr16:85628084
|
G | A | 1 | a0001c0001t0011g0269 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.8-5830G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85628084 | ||||||
| chr16:85628223
|
T | G | 1 | a0025c0033t0038g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.8-5691T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85628223 | ||||||
| chr16:85628328
|
G | C | 1 | a0001c0001t0058g0051 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.8-5586G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85628328 | ||||||
| chr16:85628386
|
T | C | 1 | a0001c0001t0003g0004 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.8-5528T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85628386 | ||||||
| chr16:85628469
|
G | A | 3 | a0001c0001t0004g0009a0001c0002t0001g0195a0002c0017t0001g0237 | 3 | HG02572.hp2 HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.8-5445G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85628469 | ||||||
| chr16:85628808
|
A | G | 3 | a0001c0001t0002g0069a0009c0014t0005g0176a0009c0014t0054g0257 | 3 | HG01175.hp1 HG01261.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.8-5106A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85628808 | ||||||
| chr16:85628833
|
C | T | 36 | a0001c0001t0001g0227a0001c0001t0004g0009a0001c0001t0012g0210others(33): Show | 36 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.8-5081C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85628833 | ||||||
| chr16:85628859
|
A | G | 7 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0003g0099others(4): Show | 7 | HG00609.hp1 HG02015.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-5055A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85628859 | ||||||
| chr16:85629028
|
G | A | 1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.8-4886G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629028 | ||||||
| chr16:85629142
|
C | A | 5 | a0002c0006t0001g0221a0002c0017t0001g0219a0002c0018t0004g0006others(2): Show | 5 | HG02258.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-4772C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629142 | ||||||
| chr16:85629177
|
A | T | 3 | a0001c0001t0012g0010a0002c0005t0063g0208a0002c0006t0001g0253 | 3 | HG02965.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.8-4737A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629177 | ||||||
| chr16:85629197
|
A | G | 1 | a0001c0001t0066g0192 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.8-4717A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629197 | ||||||
| chr16:85629221
|
A | G | 2 | a0001c0001t0015g0127a0001c0001t0015g0128 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.8-4693A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629221 | ||||||
| chr16:85629304
|
A | G | 3 | a0001c0002t0018g0283a0002c0004t0004g0001a0006c0011t0019g0282 | 3 | HG02559.hp1 HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.8-4610A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629304 | ||||||
| chr16:85629317
|
G | A | 35 | a0001c0001t0001g0094a0001c0001t0002g0037a0001c0001t0002g0039others(32): Show | 35 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.8-4597G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629317 | ||||||
| chr16:85629332
|
C | G | 1 | a0001c0001t0058g0051 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.8-4582C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629332 | ||||||
| chr16:85629374
|
A | C | 1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.8-4540A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629374 | ||||||
| chr16:85629422
|
C | T | 2 | a0002c0018t0004g0006a0021c0039t0001g0271 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.8-4492C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629422 | ||||||
| chr16:85629579
|
G | T | 6 | a0001c0002t0001g0247a0002c0006t0001g0221a0002c0017t0001g0219others(3): Show | 6 | HG02258.hp2 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-4335G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629579 | ||||||
| chr16:85629636
|
G | T | 200 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.8-4278G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629636 | ||||||
| chr16:85629776
|
C | G | 1 | a0001c0001t0005g0027 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.8-4138C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629776 | ||||||
| chr16:85629901
|
C | T | 2 | a0001c0002t0001g0057a0001c0002t0001g0157 | 2 | HG00323.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.8-4013C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629901 | ||||||
| chr16:85629906
|
G | C | 1 | a0022c0038t0013g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-4008G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85629906 | ||||||
| chr16:85630013
|
T | C | 1 | a0001c0001t0022g0031 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.8-3901T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630013 | ||||||
| chr16:85630026
|
C | T | 3 | a0001c0001t0002g0082a0001c0003t0001g0086a0001c0003t0001g0163 | 3 | HG01261.hp2 HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.8-3888C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630026 | ||||||
| chr16:85630146
|
C | G | 1 | a0001c0002t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.8-3768C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630146 | ||||||
| chr16:85630236
|
G | T | 8 | a0001c0001t0035g0286a0001c0002t0001g0247a0002c0006t0001g0221others(5): Show | 8 | HG01081.hp2 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-3678G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630236 | ||||||
| chr16:85630256
|
T | C | 1 | a0001c0001t0012g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.8-3658T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630256 | ||||||
| chr16:85630328
|
G | A | 3 | a0001c0001t0012g0010a0002c0005t0063g0208a0002c0006t0001g0253 | 3 | HG02965.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.8-3586G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630328 | ||||||
| chr16:85630337
|
A | G | 210 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.8-3577A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630337 | ||||||
| chr16:85630402
|
C | T | 1 | a0001c0002t0005g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.8-3512C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630402 | ||||||
| chr16:85630410
|
T | C | 32 | a0001c0001t0001g0227a0001c0001t0004g0009a0001c0001t0012g0210others(29): Show | 32 | HG01167.hp1 HG01167.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.8-3504T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630410 | ||||||
| chr16:85630422
|
G | T | 2 | a0001c0002t0001g0251a0001c0002t0001g0272 | 2 | HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.8-3492G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630422 | ||||||
| chr16:85630469
|
T | C | 1 | a0022c0038t0013g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-3445T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630469 | ||||||
| chr16:85630477
|
C | T | 1 | a0003c0010t0002g0110 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.8-3437C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630477 | ||||||
| chr16:85630511
|
G | A | 1 | a0001c0001t0020g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.8-3403G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630511 | ||||||
| chr16:85630555
|
A | G | 11 | a0001c0001t0012g0210a0001c0001t0035g0286a0001c0002t0001g0247others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.8-3359A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630555 | ||||||
| chr16:85630667
|
C | T | 4 | a0001c0001t0001g0227a0001c0001t0004g0009a0001c0002t0001g0195others(1): Show | 4 | HG02738.hp2 HG04199.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-3247C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630667 | ||||||
| chr16:85630847
|
C | T | 3 | a0002c0004t0008g0068a0002c0005t0001g0077a0022c0038t0013g0089 | 3 | NA19043.hp2 NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.8-3067C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630847 | ||||||
| chr16:85630895
|
G | A | 1 | a0001c0001t0003g0004 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.8-3019G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85630895 | ||||||
| chr16:85631028
|
G | A | 1 | a0001c0002t0014g0204 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.8-2886G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631028 | ||||||
| chr16:85631160
|
T | C | 3 | a0001c0001t0020g0217a0001c0002t0001g0251a0001c0002t0001g0272 | 3 | HG02559.hp2 HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.8-2754T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631160 | ||||||
| chr16:85631304
|
C | T | 4 | a0001c0002t0006g0184a0002c0005t0063g0208a0007c0012t0021g0239others(1): Show | 4 | HG00639.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-2610C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631304 | ||||||
| chr16:85631335
|
C | G | 2 | a0001c0001t0012g0010a0001c0001t0046g0105 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.8-2579C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631335 | ||||||
| chr16:85631373
|
C | T | 7 | a0001c0001t0004g0235a0002c0005t0063g0208a0002c0008t0001g0168others(4): Show | 7 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-2541C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631373 | ||||||
| chr16:85631772
|
G | C | 289 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.8-2142G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631772 | ||||||
| chr16:85631821
|
A | G | 3 | a0001c0001t0046g0105a0001c0001t0067g0111a0022c0038t0013g0089 | 3 | HG01243.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.8-2093A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631821 | ||||||
| chr16:85631835
|
T | G | 1 | a0002c0006t0001g0242 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8-2079T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631835 | ||||||
| chr16:85631853
|
G | A | 1 | a0001c0002t0006g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.8-2061G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631853 | ||||||
| chr16:85631878
|
C | T | 1 | a0001c0003t0001g0032 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.8-2036C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631878 | ||||||
| chr16:85631898
|
G | A | 3 | a0001c0002t0006g0092a0001c0002t0006g0211a0001c0002t0006g0213 | 3 | HG02622.hp1 HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.8-2016G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631898 | ||||||
| chr16:85631925
|
G | A | 1 | a0001c0001t0020g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.8-1989G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631925 | ||||||
| chr16:85631934
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8-1980G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85631934 | ||||||
| chr16:85632037
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.8-1877G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632037 | ||||||
| chr16:85632081
|
C | T | 2 | a0001c0001t0015g0127a0001c0001t0015g0128 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.8-1833C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632081 | ||||||
| chr16:85632113
|
G | A | 4 | a0001c0001t0003g0036a0001c0001t0017g0243a0001c0001t0041g0035others(1): Show | 4 | HG00597.hp1 HG00609.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-1801G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632113 | ||||||
| chr16:85632223
|
C | T | 1 | a0001c0001t0004g0240 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.8-1691C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632223 | ||||||
| chr16:85632330
|
T | C | 46 | a0001c0001t0012g0210a0001c0001t0017g0243a0001c0001t0020g0156others(43): Show | 46 | HG01167.hp1 HG01167.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.8-1584T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632330 | ||||||
| chr16:85632365
|
C | T | 9 | a0001c0021t0033g0225a0001c0036t0006g0112a0002c0006t0001g0113others(6): Show | 9 | HG01255.hp1 HG02109.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-1549C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632365 | ||||||
| chr16:85632483
|
G | A | 153 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.8-1431G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632483 | ||||||
| chr16:85632510
|
C | T | 18 | a0001c0001t0001g0227a0001c0001t0004g0009a0001c0001t0004g0235others(15): Show | 18 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.8-1404C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632510 | ||||||
| chr16:85632520
|
A | G | 31 | a0001c0001t0002g0062a0001c0001t0002g0087a0001c0001t0002g0107others(28): Show | 31 | HG00423.hp2 HG00438.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.8-1394A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632520 | ||||||
| chr16:85632591
|
G | A | 2 | a0001c0001t0020g0217a0007c0012t0021g0239 | 2 | HG00639.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.8-1323G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632591 | ||||||
| chr16:85632717
|
TC | T | 10 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0006g0092others(7): Show | 10 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.8-1196delC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632717 | ||||||
| chr16:85632782
|
C | G | 2 | a0001c0001t0020g0217a0007c0012t0021g0239 | 2 | HG00639.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.8-1132C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632782 | ||||||
| chr16:85632792
|
T | G | 2 | a0001c0001t0007g0186a0031c0019t0002g0249 | 2 | HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.8-1122T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632792 | ||||||
| chr16:85632813
|
G | A | 30 | a0001c0001t0002g0062a0001c0001t0002g0087a0001c0001t0002g0107others(27): Show | 30 | HG00423.hp2 HG00438.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.8-1101G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632813 | ||||||
| chr16:85632855
|
C | A | 1 | a0007c0012t0034g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.8-1059C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632855 | ||||||
| chr16:85632934
|
G | A | 1 | a0007c0012t0021g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.8-980G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85632934 | ||||||
| chr16:85633012
|
G | GTGCCGC | 18 | a0001c0001t0020g0156a0001c0002t0001g0017a0001c0002t0001g0018others(15): Show | 18 | HG01891.hp1 HG02622.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.8-901_8-896dupTGCC others(2): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85633012 | |||||
| chr16:85633013
|
T | TGCCGCC | 201 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.8-889_8-884dupCGCC others(2): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85633013 | |||||
| chr16:85633013
|
T | TGCCGCCG others(2): Show |
4 | a0001c0001t0043g0014a0001c0002t0001g0102a0002c0008t0001g0218others(1): Show | 4 | HG02717.hp2 HG03139.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-892_8-884dupCGCC others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85633013 | |||||
| chr16:85633013
|
TGCC | T | 3 | a0001c0003t0001g0259a0002c0017t0001g0219a0002c0017t0001g0237 | 3 | HG02572.hp2 HG02970.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.8-886_8-884delCGC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 85633013 | |||||
| chr16:85633022
|
C | T | 2 | a0001c0002t0018g0283a0006c0011t0019g0282 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.8-892C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633022 | ||||||
| chr16:85633032
|
G | A | 5 | a0001c0001t0043g0014a0001c0002t0001g0102a0002c0008t0001g0218others(2): Show | 5 | HG00639.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-882G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633032 | ||||||
| chr16:85633032
|
G | C | 1 | a0021c0039t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.8-882G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633032 | ||||||
| chr16:85633175
|
G | A | 3 | a0001c0002t0001g0245a0001c0002t0001g0272a0002c0018t0004g0266 | 3 | HG02145.hp2 HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.8-739G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633175 | ||||||
| chr16:85633335
|
G | A | 1 | a0001c0001t0046g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.8-579G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633335 | ||||||
| chr16:85633408
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.8-506A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633408 | ||||||
| chr16:85633447
|
C | T | 1 | a0022c0038t0013g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-467C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633447 | ||||||
| chr16:85633479
|
G | A | 1 | a0001c0002t0006g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.8-435G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633479 | ||||||
| chr16:85633482
|
G | A | 2 | a0001c0037t0060g0114a0002c0006t0001g0216 | 2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.8-432G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633482 | ||||||
| chr16:85633534
|
G | A | 1 | a0002c0030t0003g0023 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.8-380G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633534 | ||||||
| chr16:85633543
|
G | C | 1 | a0001c0001t0020g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.8-371G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633543 | ||||||
| chr16:85633561
|
T | A | 1 | a0001c0051t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.8-353T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633561 | ||||||
| chr16:85633589
|
C | T | 1 | a0007c0012t0021g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.8-325C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633589 | ||||||
| chr16:85633602
|
C | T | 1 | a0005c0048t0003g0050 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.8-312C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633602 | ||||||
| chr16:85633617
|
G | C | 1 | a0001c0001t0003g0142 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.8-297G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633617 | ||||||
| chr16:85633663
|
G | A | 1 | a0001c0002t0005g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.8-251G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633663 | ||||||
| chr16:85633840
|
C | T | 2 | a0001c0001t0003g0005a0001c0001t0029g0044 | 2 | HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.8-74C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633840 | ||||||
| chr16:85633893
|
G | C | 1 | a0001c0002t0002g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.8-21G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 1/15 | chr16 | 85633893 | ||||||
| chr16:85634195
|
T | C | 3 | a0001c0002t0001g0057a0001c0002t0001g0157a0001c0002t0001g0178 | 3 | HG00323.hp1 HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.226+63T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634195 | ||||||
| chr16:85634198
|
C | T | 7 | a0001c0001t0017g0243a0001c0002t0001g0245a0001c0002t0001g0272others(4): Show | 7 | HG01167.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.226+66C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634198 | ||||||
| chr16:85634204
|
C | T | 3 | a0001c0001t0002g0012a0001c0003t0001g0137a0001c0003t0001g0138 | 3 | HG01243.hp1 NA18946.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.226+72C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634204 | ||||||
| chr16:85634220
|
A | G | 1 | a0002c0004t0008g0093 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.226+88A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634220 | ||||||
| chr16:85634247
|
T | C | 2 | a0002c0017t0001g0219a0002c0017t0001g0237 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.226+115T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634247 | ||||||
| chr16:85634318
|
G | A | 2 | a0001c0002t0001g0247a0002c0008t0036g0277 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.226+186G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634318 | ||||||
| chr16:85634333
|
T | G | 1 | a0001c0001t0043g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.226+201T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634333 | ||||||
| chr16:85634339
|
C | G | 138 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0094others(135): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.226+207C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634339 | ||||||
| chr16:85634389
|
C | T | 1 | a0001c0003t0001g0137 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.226+257C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634389 | ||||||
| chr16:85634398
|
C | G | 1 | a0003c0009t0050g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.226+266C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634398 | ||||||
| chr16:85634493
|
C | G | 7 | a0001c0001t0020g0217a0001c0002t0018g0194a0001c0002t0018g0283others(4): Show | 7 | HG02818.hp2 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.226+361C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634493 | ||||||
| chr16:85634494
|
C | T | 78 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0094others(75): Show | 78 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.226+362C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634494 | ||||||
| chr16:85634542
|
A | G | 1 | a0001c0001t0009g0029 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.226+410A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634542 | ||||||
| chr16:85634562
|
T | A | 1 | a0002c0004t0002g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.226+430T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634562 | ||||||
| chr16:85634596
|
C | G | 1 | a0001c0001t0012g0210 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.226+464C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634596 | ||||||
| chr16:85634628
|
C | G | 51 | a0001c0001t0001g0030a0001c0001t0001g0220a0001c0001t0002g0011others(48): Show | 51 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.226+496C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634628 | ||||||
| chr16:85634758
|
C | T | 3 | a0002c0008t0001g0168a0004c0007t0010g0091a0021c0039t0001g0271 | 3 | HG01891.hp2 HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.226+626C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634758 | ||||||
| chr16:85634831
|
G | T | 12 | a0001c0001t0004g0235a0001c0001t0017g0090a0001c0001t0043g0014others(9): Show | 12 | HG02145.hp2 HG02559.hp2 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.226+699G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634831 | ||||||
| chr16:85634875
|
T | C | 4 | a0001c0001t0002g0201a0001c0003t0001g0163a0001c0003t0014g0022others(1): Show | 4 | HG00735.hp2 HG01975.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+743T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634875 | ||||||
| chr16:85634940
|
G | A | 1 | a0001c0002t0007g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.226+808G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634940 | ||||||
| chr16:85634952
|
C | CG | 25 | a0001c0001t0003g0096a0001c0001t0012g0210a0001c0001t0017g0243others(22): Show | 25 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.226+827dupG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85634952 | |||||
| chr16:85634958
|
G | A | 2 | a0001c0001t0002g0073a0001c0001t0059g0273 | 2 | HG03704.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.226+826G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634958 | ||||||
| chr16:85634958
|
G | C | 1 | a0001c0001t0002g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.226+826G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634958 | ||||||
| chr16:85634988
|
C | T | 36 | a0001c0001t0002g0173a0001c0001t0002g0182a0001c0001t0002g0201others(33): Show | 36 | HG00099.hp1 HG01070.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.226+856C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85634988 | ||||||
| chr16:85635048
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.226+916G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635048 | ||||||
| chr16:85635135
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.226+1003G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635135 | ||||||
| chr16:85635139
|
T | C | 3 | a0001c0002t0019g0145a0002c0018t0004g0006a0019c0025t0024g0275 | 3 | HG02615.hp1 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.226+1007T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635139 | ||||||
| chr16:85635146
|
A | T | 9 | a0001c0001t0002g0201a0001c0001t0003g0187a0001c0001t0041g0035others(6): Show | 9 | HG00597.hp1 HG00741.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.226+1014A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635146 | ||||||
| chr16:85635205
|
G | C | 1 | a0008c0013t0055g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.226+1073G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635205 | ||||||
| chr16:85635210
|
G | C | 2 | a0001c0001t0002g0177a0002c0004t0025g0048 | 2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.226+1078G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635210 | ||||||
| chr16:85635272
|
T | C | 3 | a0001c0001t0003g0020a0001c0001t0028g0129a0002c0008t0070g0060 | 3 | HG00738.hp2 HG01070.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.226+1140T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635272 | ||||||
| chr16:85635288
|
G | A | 2 | a0001c0001t0051g0140a0007c0012t0021g0239 | 2 | HG00639.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.226+1156G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635288 | ||||||
| chr16:85635311
|
G | A | 2 | a0001c0001t0002g0041a0001c0001t0043g0014 | 2 | HG03654.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.226+1179G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635311 | ||||||
| chr16:85635368
|
C | T | 1 | a0005c0047t0065g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.226+1236C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635368 | ||||||
| chr16:85635384
|
C | G | 85 | a0001c0001t0001g0030a0001c0001t0001g0094a0001c0001t0001g0120others(82): Show | 85 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.226+1252C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635384 | ||||||
| chr16:85635441
|
C | G | 2 | a0008c0013t0021g0284a0008c0013t0055g0119 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.226+1309C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635441 | ||||||
| chr16:85635505
|
ACT | A | 47 | a0001c0001t0001g0094a0001c0001t0002g0131a0001c0001t0003g0040others(44): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.226+1378_226+1379d others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85635505 | |||||
| chr16:85635508
|
C | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0037a0001c0001t0002g0133 | 3 | NA18966.hp2 NA18983.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.226+1376C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635508 | ||||||
| chr16:85635508
|
C | T | 1 | a0001c0002t0001g0247 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.226+1376C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635508 | ||||||
| chr16:85635568
|
C | T | 8 | a0001c0001t0002g0201a0001c0001t0004g0240a0001c0001t0009g0029others(5): Show | 8 | HG01975.hp2 HG02258.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+1436C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635568 | ||||||
| chr16:85635594
|
T | C | 16 | a0001c0001t0002g0201a0001c0001t0004g0188a0001c0001t0004g0240others(13): Show | 16 | HG01167.hp2 HG01975.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.226+1462T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635594 | ||||||
| chr16:85635630
|
C | T | 17 | a0001c0001t0002g0201a0001c0001t0004g0240a0001c0001t0009g0029others(14): Show | 17 | HG01167.hp2 HG01891.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.226+1498C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635630 | ||||||
| chr16:85635636
|
C | T | 3 | a0001c0002t0018g0194a0002c0006t0001g0221a0004c0007t0052g0076 | 3 | HG02055.hp1 HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.226+1504C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635636 | ||||||
| chr16:85635696
|
G | A | 21 | a0001c0001t0001g0120a0001c0001t0001g0227a0001c0001t0002g0059others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.226+1564G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635696 | ||||||
| chr16:85635704
|
G | T | 2 | a0002c0006t0001g0222a0002c0006t0001g0255 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.226+1572G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635704 | ||||||
| chr16:85635708
|
G | A | 5 | a0001c0002t0001g0083a0001c0002t0005g0118a0001c0002t0007g0264others(2): Show | 5 | HG01109.hp1 HG02698.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+1576G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635708 | ||||||
| chr16:85635744
|
T | C | 1 | a0001c0003t0001g0259 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.226+1612T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635744 | ||||||
| chr16:85635749
|
T | C | 8 | a0001c0001t0043g0014a0001c0002t0018g0194a0002c0006t0001g0221others(5): Show | 8 | HG01167.hp2 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+1617T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635749 | ||||||
| chr16:85635770
|
C | T | 45 | a0001c0001t0001g0094a0001c0001t0002g0131a0001c0001t0003g0040others(42): Show | 45 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.226+1638C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635770 | ||||||
| chr16:85635798
|
C | T | 1 | a0002c0004t0045g0252 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.226+1666C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635798 | ||||||
| chr16:85635890
|
G | A | 40 | a0001c0001t0002g0012a0001c0001t0002g0041a0001c0001t0002g0123others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.226+1758G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635890 | ||||||
| chr16:85635901
|
C | T | 3 | a0002c0004t0004g0001a0002c0018t0004g0006a0004c0007t0010g0265 | 3 | HG02559.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.226+1769C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635901 | ||||||
| chr16:85635937
|
G | C | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.226+1805G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635937 | ||||||
| chr16:85635941
|
G | GC | 57 | a0001c0001t0002g0012a0001c0001t0002g0041a0001c0001t0002g0123others(54): Show | 57 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.226+1810dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85635941 | |||||
| chr16:85635998
|
T | C | 68 | a0001c0001t0002g0012a0001c0001t0002g0041a0001c0001t0002g0123others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.226+1866T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85635998 | ||||||
| chr16:85636039
|
G | A | 20 | a0001c0001t0001g0227a0001c0001t0002g0059a0001c0001t0002g0097others(17): Show | 20 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.226+1907G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636039 | ||||||
| chr16:85636039
|
G | T | 4 | a0001c0002t0018g0194a0002c0006t0001g0221a0002c0018t0004g0006others(1): Show | 4 | HG02055.hp1 HG02895.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+1907G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636039 | ||||||
| chr16:85636053
|
G | C | 3 | a0001c0001t0002g0011a0001c0001t0002g0037a0001c0001t0002g0133 | 3 | NA18966.hp2 NA18983.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.226+1921G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636053 | ||||||
| chr16:85636110
|
T | G | 141 | a0001c0001t0001g0094a0001c0001t0001g0120a0001c0001t0001g0227others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.226+1978T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636110 | ||||||
| chr16:85636134
|
A | G | 2 | a0001c0001t0012g0212a0018c0043t0003g0098 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.226+2002A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636134 | ||||||
| chr16:85636179
|
A | G | 1 | a0001c0020t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.226+2047A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636179 | ||||||
| chr16:85636236
|
C | T | 3 | a0001c0001t0020g0156a0001c0001t0020g0217a0001c0002t0018g0283 | 3 | HG02630.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.226+2104C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636236 | ||||||
| chr16:85636327
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.226+2195C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636327 | ||||||
| chr16:85636476
|
C | A | 1 | a0001c0001t0003g0004 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.226+2344C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636476 | ||||||
| chr16:85636499
|
G | A | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.226+2367G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636499 | ||||||
| chr16:85636502
|
C | A | 1 | a0001c0001t0009g0196 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.226+2370C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636502 | ||||||
| chr16:85636510
|
C | G | 1 | a0001c0001t0002g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.226+2378C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636510 | ||||||
| chr16:85636569
|
G | A | 2 | a0001c0001t0051g0140a0007c0012t0021g0239 | 2 | HG00639.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.226+2437G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636569 | ||||||
| chr16:85636580
|
C | T | 1 | a0026c0032t0010g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.226+2448C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636580 | ||||||
| chr16:85636592
|
G | A | 2 | a0001c0002t0001g0247a0002c0008t0036g0277 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.226+2460G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636592 | ||||||
| chr16:85636688
|
CG | C | 260 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(257): Show | 260 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.226+2565delG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85636688 | |||||
| chr16:85636696
|
G | C | 1 | a0001c0002t0006g0281 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.226+2564G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636696 | ||||||
| chr16:85636696
|
G | T | 2 | a0001c0002t0001g0247a0002c0008t0036g0277 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.226+2564G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636696 | ||||||
| chr16:85636697
|
G | C | 1 | a0001c0002t0005g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.226+2565G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636697 | ||||||
| chr16:85636698
|
C | T | 1 | a0001c0002t0005g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.226+2566C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636698 | ||||||
| chr16:85636699
|
T | G | 1 | a0001c0002t0005g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.226+2567T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636699 | ||||||
| chr16:85636708
|
C | T | 2 | a0001c0002t0001g0288a0022c0038t0013g0089 | 2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.226+2576C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636708 | ||||||
| chr16:85636740
|
G | A | 3 | a0001c0002t0018g0194a0002c0006t0001g0221a0004c0007t0052g0076 | 3 | HG02055.hp1 HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.226+2608G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636740 | ||||||
| chr16:85636742
|
C | A | 1 | a0001c0001t0002g0201 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.226+2610C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636742 | ||||||
| chr16:85636771
|
A | C | 59 | a0001c0001t0001g0220a0001c0001t0002g0041a0001c0001t0002g0087others(56): Show | 59 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.226+2639A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636771 | ||||||
| chr16:85636776
|
T | C | 57 | a0001c0001t0001g0220a0001c0001t0002g0041a0001c0001t0002g0107others(54): Show | 57 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.226+2644T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636776 | ||||||
| chr16:85636846
|
C | T | 5 | a0001c0001t0067g0111a0002c0008t0001g0168a0004c0007t0010g0045others(2): Show | 5 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+2714C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636846 | ||||||
| chr16:85636858
|
C | G | 1 | a0001c0002t0001g0288 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.226+2726C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636858 | ||||||
| chr16:85636864
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.226+2732G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636864 | ||||||
| chr16:85636903
|
ACCCCCCA others(15): Show |
A | 3 | a0001c0001t0002g0150a0001c0001t0002g0177a0002c0004t0003g0065 | 3 | HG01934.hp2 HG02015.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.226+2785_226+2806d others(24): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85636903 | |||||
| chr16:85636917
|
C | T | 1 | a0002c0005t0044g0169 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.226+2785C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636917 | ||||||
| chr16:85636918
|
T | G | 1 | a0002c0005t0044g0169 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.226+2786T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636918 | ||||||
| chr16:85636925
|
C | T | 1 | a0001c0001t0043g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.226+2793C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636925 | ||||||
| chr16:85636977
|
G | A | 5 | a0001c0001t0020g0156a0001c0001t0020g0217a0001c0002t0001g0247others(2): Show | 5 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+2845G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85636977 | ||||||
| chr16:85637010
|
T | C | 270 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(267): Show | 270 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.226+2878T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637010 | ||||||
| chr16:85637034
|
T | C | 2 | a0001c0002t0001g0288a0025c0033t0038g0209 | 2 | HG01167.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.226+2902T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637034 | ||||||
| chr16:85637075
|
C | T | 1 | a0001c0001t0009g0196 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.226+2943C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637075 | ||||||
| chr16:85637261
|
C | T | 4 | a0001c0001t0001g0026a0001c0002t0001g0172a0001c0002t0014g0204others(1): Show | 4 | HG00673.hp2 NA19056.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+3129C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637261 | ||||||
| chr16:85637330
|
C | T | 31 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0003g0004others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.226+3198C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637330 | ||||||
| chr16:85637342
|
C | T | 1 | a0002c0008t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.226+3210C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637342 | ||||||
| chr16:85637353
|
G | A | 1 | a0012c0023t0001g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.226+3221G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637353 | ||||||
| chr16:85637361
|
T | C | 1 | a0005c0048t0003g0050 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.226+3229T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637361 | ||||||
| chr16:85637463
|
G | GCCCCCTT others(28): Show |
1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.226+3342_226+3376d others(37): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85637463 | |||||
| chr16:85637474
|
T | TGCGGCAG others(28): Show |
1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.226+3344_226+3345i others(37): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85637474 | |||||
| chr16:85637474
|
TGCAGCAG others(28): Show |
T | 3 | a0001c0001t0012g0210a0001c0001t0058g0051a0015c0041t0001g0095 | 3 | HG01099.hp1 HG02055.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.226+3345_226+3379d others(37): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85637474 | |||||
| chr16:85637477
|
A | G | 231 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0094others(228): Show | 231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.226+3345A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637477 | ||||||
| chr16:85637502
|
C | T | 1 | a0001c0002t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.226+3370C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637502 | ||||||
| chr16:85637522
|
A | G | 1 | a0002c0004t0004g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.226+3390A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637522 | ||||||
| chr16:85637528
|
T | C | 24 | a0001c0001t0012g0210a0001c0001t0012g0212a0001c0001t0058g0051others(21): Show | 24 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.226+3396T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637528 | ||||||
| chr16:85637547
|
G | A | 17 | a0001c0001t0002g0201a0001c0001t0009g0029a0001c0001t0020g0156others(14): Show | 17 | HG01243.hp2 HG01891.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.226+3415G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637547 | ||||||
| chr16:85637563
|
C | T | 1 | a0002c0005t0063g0208 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.226+3431C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637563 | ||||||
| chr16:85637591
|
C | T | 2 | a0001c0001t0002g0236a0001c0001t0040g0033 | 2 | NA18981.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.226+3459C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637591 | ||||||
| chr16:85637642
|
C | T | 41 | a0001c0001t0001g0120a0001c0001t0001g0220a0001c0001t0001g0227others(38): Show | 41 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.226+3510C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637642 | ||||||
| chr16:85637687
|
T | C | 135 | a0001c0001t0001g0120a0001c0001t0001g0220a0001c0001t0001g0227others(132): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.226+3555T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637687 | ||||||
| chr16:85637714
|
GACCCCTG others(56): Show |
G | 2 | a0001c0002t0001g0057a0001c0002t0001g0157 | 2 | HG00323.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.226+3585_226+3647d others(65): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85637714 | |||||
| chr16:85637724
|
C | G | 39 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0003g0004others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.226+3592C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637724 | ||||||
| chr16:85637755
|
G | C | 2 | a0001c0001t0051g0140a0007c0012t0021g0239 | 2 | HG00639.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.226+3623G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637755 | ||||||
| chr16:85637852
|
G | A | 8 | a0001c0001t0067g0111a0001c0002t0018g0194a0001c0021t0033g0225others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.226+3720G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637852 | ||||||
| chr16:85637856
|
G | T | 78 | a0001c0001t0001g0220a0001c0001t0001g0227a0001c0001t0002g0059others(75): Show | 78 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.226+3724G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637856 | ||||||
| chr16:85637878
|
G | A | 1 | a0005c0047t0065g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.226+3746G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637878 | ||||||
| chr16:85637900
|
G | A | 1 | a0001c0003t0001g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.226+3768G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637900 | ||||||
| chr16:85637903
|
G | A | 2 | a0008c0013t0021g0284a0008c0013t0055g0119 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.226+3771G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637903 | ||||||
| chr16:85637992
|
G | A | 32 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0003g0004others(29): Show | 32 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.226+3860G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85637992 | ||||||
| chr16:85638027
|
G | A | 4 | a0001c0002t0018g0194a0002c0006t0001g0221a0004c0007t0010g0265others(1): Show | 4 | HG02055.hp1 HG02895.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+3895G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638027 | ||||||
| chr16:85638107
|
A | G | 256 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(253): Show | 256 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.226+3975A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638107 | ||||||
| chr16:85638157
|
A | G | 2 | a0001c0001t0002g0011a0001c0001t0002g0062 | 2 | NA18966.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.226+4025A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638157 | ||||||
| chr16:85638177
|
C | G | 5 | a0001c0001t0028g0129a0001c0002t0001g0083a0001c0002t0005g0118others(2): Show | 5 | HG01070.hp1 HG01109.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+4045C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638177 | ||||||
| chr16:85638443
|
A | T | 1 | a0001c0002t0002g0250 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.226+4311A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638443 | ||||||
| chr16:85638455
|
C | G | 20 | a0001c0001t0001g0227a0001c0001t0002g0059a0001c0001t0002g0236others(17): Show | 20 | HG00544.hp2 HG01069.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.226+4323C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638455 | ||||||
| chr16:85638497
|
C | T | 1 | a0001c0002t0006g0211 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.226+4365C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638497 | ||||||
| chr16:85638514
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.226+4382C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638514 | ||||||
| chr16:85638523
|
G | C | 2 | a0001c0001t0002g0236a0001c0001t0040g0033 | 2 | NA18981.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.226+4391G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638523 | ||||||
| chr16:85638632
|
C | T | 2 | a0001c0001t0003g0096a0001c0001t0003g0170 | 2 | HG01884.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.226+4500C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638632 | ||||||
| chr16:85638696
|
C | G | 34 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0003g0004others(31): Show | 34 | HG00609.hp1 HG00609.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.226+4564C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638696 | ||||||
| chr16:85638738
|
C | G | 1 | a0002c0008t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.226+4606C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638738 | ||||||
| chr16:85638744
|
C | A | 3 | a0001c0001t0002g0279a0001c0001t0004g0240a0001c0001t0022g0021 | 3 | HG02129.hp2 NA19065.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.226+4612C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638744 | ||||||
| chr16:85638786
|
C | T | 28 | a0001c0001t0001g0227a0001c0001t0002g0059a0001c0001t0002g0087others(25): Show | 28 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.226+4654C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638786 | ||||||
| chr16:85638818
|
C | T | 36 | a0001c0001t0001g0227a0001c0001t0002g0059a0001c0001t0002g0087others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.226+4686C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638818 | ||||||
| chr16:85638854
|
C | T | 18 | a0001c0001t0003g0096a0001c0001t0017g0090a0001c0002t0001g0017others(15): Show | 18 | HG00738.hp2 HG01167.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.226+4722C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638854 | ||||||
| chr16:85638862
|
C | T | 24 | a0001c0001t0001g0227a0001c0001t0002g0059a0001c0001t0002g0087others(21): Show | 24 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.226+4730C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638862 | ||||||
| chr16:85638871
|
G | A | 2 | a0001c0001t0003g0005a0001c0028t0053g0287 | 2 | HG02145.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.226+4739G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638871 | ||||||
| chr16:85638883
|
G | A | 1 | a0001c0001t0002g0224 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.226+4751G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638883 | ||||||
| chr16:85638887
|
C | T | 1 | a0001c0001t0020g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.226+4755C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638887 | ||||||
| chr16:85638914
|
C | G | 4 | a0001c0002t0018g0194a0001c0002t0018g0283a0002c0006t0001g0221others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+4782C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638914 | ||||||
| chr16:85638936
|
G | C | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.226+4804G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638936 | ||||||
| chr16:85638964
|
C | G | 23 | a0001c0001t0001g0227a0001c0001t0002g0059a0001c0001t0002g0087others(20): Show | 23 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.226+4832C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638964 | ||||||
| chr16:85638997
|
G | T | 7 | a0001c0001t0020g0217a0001c0002t0001g0288a0001c0002t0018g0194others(4): Show | 7 | HG02615.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.226+4865G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85638997 | ||||||
| chr16:85639003
|
C | T | 3 | a0001c0001t0020g0217a0001c0002t0001g0288a0007c0012t0034g0214 | 3 | HG02615.hp2 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.226+4871C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639003 | ||||||
| chr16:85639039
|
G | A | 4 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0268others(1): Show | 4 | HG02976.hp1 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+4907G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639039 | ||||||
| chr16:85639112
|
A | G | 2 | a0001c0001t0004g0013a0001c0001t0009g0152 | 2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.226+4980A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639112 | ||||||
| chr16:85639203
|
G | A | 2 | a0001c0001t0003g0187a0003c0009t0005g0244 | 2 | HG00741.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.226+5071G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639203 | ||||||
| chr16:85639218
|
C | T | 2 | a0001c0001t0059g0273a0001c0002t0002g0165 | 2 | HG01069.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.226+5086C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639218 | ||||||
| chr16:85639221
|
C | T | 31 | a0001c0001t0002g0069a0001c0001t0002g0223a0001c0001t0003g0004others(28): Show | 31 | HG00609.hp1 HG00609.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.226+5089C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639221 | ||||||
| chr16:85639268
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.226+5136C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639268 | ||||||
| chr16:85639287
|
A | G | 2 | a0001c0037t0060g0114a0002c0008t0070g0060 | 2 | HG00738.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.226+5155A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639287 | ||||||
| chr16:85639305
|
C | T | 2 | a0001c0001t0012g0210a0001c0001t0043g0014 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.226+5173C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639305 | ||||||
| chr16:85639325
|
C | T | 1 | a0002c0004t0045g0252 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.226+5193C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639325 | ||||||
| chr16:85639330
|
C | T | 1 | a0001c0001t0035g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.226+5198C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639330 | ||||||
| chr16:85639384
|
A | T | 4 | a0001c0002t0018g0194a0001c0002t0018g0283a0002c0006t0001g0221others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+5252A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639384 | ||||||
| chr16:85639482
|
C | T | 40 | a0001c0001t0001g0227a0001c0001t0002g0087a0001c0001t0002g0097others(37): Show | 40 | HG00438.hp2 HG00673.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.226+5350C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639482 | ||||||
| chr16:85639484
|
A | G | 141 | a0001c0001t0001g0094a0001c0001t0001g0227a0001c0001t0002g0007others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.226+5352A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639484 | ||||||
| chr16:85639493
|
GGGCGCCA | G | 32 | a0001c0001t0002g0059a0001c0001t0003g0187a0001c0001t0012g0212others(29): Show | 32 | HG00140.hp1 HG00544.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.226+5365_226+5371d others(9): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85639493 | |||||
| chr16:85639504
|
C | T | 32 | a0001c0001t0002g0059a0001c0001t0003g0187a0001c0001t0012g0212others(29): Show | 32 | HG00140.hp1 HG00544.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.226+5372C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639504 | ||||||
| chr16:85639517
|
C | T | 1 | a0002c0006t0001g0216 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.226+5385C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639517 | ||||||
| chr16:85639564
|
G | T | 22 | a0001c0001t0017g0090a0001c0002t0001g0017a0001c0002t0001g0245others(19): Show | 22 | HG00738.hp2 HG01167.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.226+5432G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639564 | ||||||
| chr16:85639611
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.226+5479C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639611 | ||||||
| chr16:85639619
|
C | T | 1 | a0002c0008t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.226+5487C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639619 | ||||||
| chr16:85639736
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.226+5604G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639736 | ||||||
| chr16:85639745
|
C | T | 2 | a0001c0002t0001g0288a0007c0012t0034g0214 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.226+5613C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639745 | ||||||
| chr16:85639772
|
G | T | 1 | a0001c0002t0026g0203 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.226+5640G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639772 | ||||||
| chr16:85639799
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.226+5667C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639799 | ||||||
| chr16:85639842
|
G | A | 1 | a0001c0001t0012g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.226+5710G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639842 | ||||||
| chr16:85639851
|
A | G | 5 | a0001c0002t0018g0194a0001c0002t0018g0283a0002c0004t0004g0001others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+5719A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639851 | ||||||
| chr16:85639861
|
C | T | 18 | a0001c0001t0002g0082a0001c0001t0002g0087a0001c0001t0002g0130others(15): Show | 18 | HG00099.hp2 HG00408.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.226+5729C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639861 | ||||||
| chr16:85639862
|
G | A | 5 | a0001c0002t0001g0263a0001c0002t0002g0165a0001c0002t0031g0256others(2): Show | 5 | HG01069.hp1 HG01361.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+5730G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639862 | ||||||
| chr16:85639886
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.226+5754G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639886 | ||||||
| chr16:85639896
|
G | A | 1 | a0002c0004t0004g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.226+5764G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639896 | ||||||
| chr16:85639897
|
G | C | 5 | a0001c0001t0017g0243a0001c0002t0001g0245a0001c0002t0001g0272others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+5765G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639897 | ||||||
| chr16:85639905
|
T | C | 29 | a0001c0001t0002g0062a0001c0001t0002g0073a0001c0001t0002g0107others(26): Show | 29 | HG00738.hp1 HG01109.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.226+5773T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639905 | ||||||
| chr16:85639921
|
C | T | 1 | a0001c0037t0060g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.226+5789C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639921 | ||||||
| chr16:85639975
|
T | C | 1 | a0001c0001t0046g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.226+5843T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639975 | ||||||
| chr16:85639976
|
T | C | 11 | a0001c0001t0004g0235a0001c0001t0012g0010a0001c0001t0017g0243others(8): Show | 11 | HG02559.hp2 HG02647.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.226+5844T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639976 | ||||||
| chr16:85639983
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.226+5851G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85639983 | ||||||
| chr16:85640068
|
G | A | 1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.226+5936G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640068 | ||||||
| chr16:85640157
|
G | T | 1 | a0001c0002t0001g0247 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.226+6025G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640157 | ||||||
| chr16:85640363
|
T | C | 41 | a0001c0001t0003g0187a0001c0001t0005g0027a0001c0001t0012g0212others(38): Show | 41 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.226+6231T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640363 | ||||||
| chr16:85640387
|
G | A | 1 | a0002c0008t0070g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.226+6255G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640387 | ||||||
| chr16:85640587
|
T | C | 118 | a0001c0001t0001g0094a0001c0001t0002g0069a0001c0001t0002g0097others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.226+6455T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640587 | ||||||
| chr16:85640597
|
G | A | 3 | a0001c0001t0002g0059a0001c0002t0001g0102a0001c0002t0001g0139 | 3 | HG00544.hp2 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.226+6465G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640597 | ||||||
| chr16:85640672
|
C | T | 24 | a0001c0001t0003g0096a0001c0001t0046g0105a0001c0002t0001g0018others(21): Show | 24 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.226+6540C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640672 | ||||||
| chr16:85640715
|
G | A | 2 | a0001c0001t0046g0105a0002c0008t0036g0277 | 2 | HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.226+6583G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640715 | ||||||
| chr16:85640734
|
A | G | 1 | a0001c0002t0062g0167 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.226+6602A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640734 | ||||||
| chr16:85640803
|
G | T | 2 | a0008c0013t0021g0284a0008c0013t0055g0119 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.226+6671G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640803 | ||||||
| chr16:85640823
|
C | T | 2 | a0008c0013t0021g0284a0008c0013t0055g0119 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.226+6691C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640823 | ||||||
| chr16:85640888
|
G | A | 18 | a0001c0001t0004g0009a0001c0001t0004g0025a0001c0001t0004g0101others(15): Show | 18 | HG00408.hp1 HG00673.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.226+6756G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640888 | ||||||
| chr16:85640888
|
G | T | 1 | a0002c0045t0047g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.226+6756G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640888 | ||||||
| chr16:85640910
|
A | G | 22 | a0001c0001t0002g0151a0001c0001t0002g0202a0001c0001t0002g0232others(19): Show | 22 | HG00140.hp1 HG00597.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.226+6778A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640910 | ||||||
| chr16:85640978
|
T | C | 1 | a0001c0002t0006g0211 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.226+6846T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640978 | ||||||
| chr16:85640981
|
C | G | 22 | a0001c0002t0001g0017a0001c0002t0001g0083a0001c0002t0001g0245others(19): Show | 22 | HG01109.hp1 HG01167.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.226+6849C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85640981 | ||||||
| chr16:85641099
|
C | T | 1 | a0001c0001t0067g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.226+6967C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641099 | ||||||
| chr16:85641234
|
C | T | 1 | a0002c0018t0004g0266 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.226+7102C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641234 | ||||||
| chr16:85641238
|
C | T | 13 | a0001c0001t0001g0234a0001c0001t0066g0192a0001c0002t0001g0003others(10): Show | 13 | HG00323.hp1 HG00423.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.226+7106C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641238 | ||||||
| chr16:85641316
|
G | A | 1 | a0001c0002t0005g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.226+7184G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641316 | ||||||
| chr16:85641351
|
C | A | 1 | a0001c0001t0051g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.227-7201C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641351 | ||||||
| chr16:85641410
|
G | A | 251 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.227-7142G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641410 | ||||||
| chr16:85641423
|
G | GC | 24 | a0001c0001t0001g0120a0001c0001t0002g0073a0001c0001t0002g0153others(21): Show | 24 | HG00408.hp2 HG00738.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.227-7120dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85641423 | |||||
| chr16:85641428
|
C | T | 1 | a0002c0006t0001g0242 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.227-7124C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641428 | ||||||
| chr16:85641559
|
G | T | 2 | a0001c0001t0067g0111a0002c0005t0063g0208 | 2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.227-6993G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641559 | ||||||
| chr16:85641565
|
G | A | 14 | a0001c0001t0003g0187a0001c0002t0001g0066a0001c0002t0005g0043others(11): Show | 14 | HG00140.hp1 HG00741.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.227-6987G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641565 | ||||||
| chr16:85641619
|
C | G | 1 | a0002c0008t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.227-6933C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641619 | ||||||
| chr16:85641628
|
C | T | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.227-6924C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641628 | ||||||
| chr16:85641666
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.227-6886G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85641666 | ||||||
| chr16:85642048
|
C | T | 3 | a0001c0001t0051g0140a0002c0008t0070g0060a0022c0038t0013g0089 | 3 | HG00738.hp2 HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.227-6504C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642048 | ||||||
| chr16:85642189
|
A | G | 4 | a0001c0002t0001g0288a0002c0008t0070g0060a0007c0012t0021g0239others(1): Show | 4 | HG00639.hp1 HG00738.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-6363A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642189 | ||||||
| chr16:85642266
|
A | G | 18 | a0001c0001t0002g0146a0001c0001t0003g0187a0001c0001t0011g0269others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.227-6286A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642266 | ||||||
| chr16:85642385
|
C | A | 1 | a0002c0004t0003g0276 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.227-6167C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642385 | ||||||
| chr16:85642461
|
GC | G | 72 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(69): Show | 72 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.227-6090delC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642461 | ||||||
| chr16:85642462
|
C | G | 1 | a0002c0005t0008g0159 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.227-6090C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642462 | ||||||
| chr16:85642479
|
C | T | 1 | a0002c0004t0003g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.227-6073C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642479 | ||||||
| chr16:85642506
|
G | T | 1 | a0027c0027t0003g0181 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.227-6046G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642506 | ||||||
| chr16:85642513
|
G | A | 1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.227-6039G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642513 | ||||||
| chr16:85642514
|
C | A | 15 | a0001c0001t0002g0146a0001c0001t0011g0269a0001c0001t0012g0212others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.227-6038C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642514 | ||||||
| chr16:85642521
|
A | G | 5 | a0001c0001t0017g0243a0001c0001t0051g0140a0002c0004t0004g0001others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-6031A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642521 | ||||||
| chr16:85642556
|
G | A | 1 | a0001c0001t0004g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.227-5996G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642556 | ||||||
| chr16:85642744
|
C | T | 1 | a0001c0035t0004g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.227-5808C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642744 | ||||||
| chr16:85642756
|
T | G | 3 | a0006c0011t0013g0230a0006c0011t0013g0270a0006c0011t0019g0282 | 3 | HG01255.hp1 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.227-5796T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642756 | ||||||
| chr16:85642785
|
G | A | 11 | a0001c0002t0006g0092a0001c0002t0006g0155a0001c0002t0006g0211others(8): Show | 11 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.227-5767G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642785 | ||||||
| chr16:85642861
|
T | C | 15 | a0001c0001t0046g0105a0001c0002t0001g0018a0002c0006t0001g0113others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.227-5691T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642861 | ||||||
| chr16:85642997
|
A | C | 1 | a0001c0002t0002g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.227-5555A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85642997 | ||||||
| chr16:85643006
|
C | T | 8 | a0001c0002t0006g0092a0001c0002t0006g0155a0001c0002t0006g0211others(5): Show | 8 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.227-5546C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643006 | ||||||
| chr16:85643024
|
G | T | 14 | a0001c0001t0002g0146a0001c0001t0011g0269a0001c0002t0001g0066others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.227-5528G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643024 | ||||||
| chr16:85643025
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.227-5527G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643025 | ||||||
| chr16:85643075
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.227-5477C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643075 | ||||||
| chr16:85643121
|
G | C | 12 | a0001c0001t0002g0146a0001c0001t0057g0185a0001c0002t0001g0066others(9): Show | 12 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.227-5431G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643121 | ||||||
| chr16:85643122
|
C | T | 26 | a0001c0001t0046g0105a0001c0002t0001g0018a0001c0002t0006g0092others(23): Show | 26 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.227-5430C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643122 | ||||||
| chr16:85643132
|
C | T | 1 | a0004c0007t0010g0265 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-5420C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643132 | ||||||
| chr16:85643141
|
G | A | 1 | a0001c0001t0056g0179 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.227-5411G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643141 | ||||||
| chr16:85643192
|
C | T | 26 | a0001c0001t0046g0105a0001c0002t0001g0018a0001c0002t0006g0092others(23): Show | 26 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.227-5360C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643192 | ||||||
| chr16:85643405
|
G | A | 1 | a0001c0001t0004g0240 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.227-5147G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643405 | ||||||
| chr16:85643411
|
G | A | 58 | a0001c0001t0001g0227a0001c0001t0002g0231a0001c0001t0002g0279others(55): Show | 58 | HG00408.hp1 HG00673.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.227-5141G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643411 | ||||||
| chr16:85643552
|
T | C | 1 | a0020c0042t0008g0042 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.227-5000T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643552 | ||||||
| chr16:85643720
|
C | T | 1 | a0002c0005t0007g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.227-4832C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643720 | ||||||
| chr16:85643756
|
C | T | 1 | a0018c0043t0003g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.227-4796C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643756 | ||||||
| chr16:85643779
|
C | G | 2 | a0001c0001t0012g0212a0001c0001t0067g0111 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.227-4773C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643779 | ||||||
| chr16:85643794
|
C | T | 2 | a0001c0003t0001g0163a0002c0005t0008g0085 | 2 | HG01975.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.227-4758C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643794 | ||||||
| chr16:85643804
|
C | A | 3 | a0001c0001t0068g0054a0001c0002t0062g0167a0003c0009t0050g0134 | 3 | HG00438.hp1 HG02027.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.227-4748C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643804 | ||||||
| chr16:85643805
|
C | T | 3 | a0001c0001t0068g0054a0001c0002t0062g0167a0003c0009t0050g0134 | 3 | HG00438.hp1 HG02027.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.227-4747C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643805 | ||||||
| chr16:85643860
|
T | G | 5 | a0001c0001t0017g0243a0001c0001t0051g0140a0002c0004t0004g0001others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-4692T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643860 | ||||||
| chr16:85643877
|
C | A | 2 | a0008c0013t0021g0284a0008c0013t0055g0119 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.227-4675C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643877 | ||||||
| chr16:85643905
|
G | A | 3 | a0001c0001t0017g0243a0005c0047t0065g0088a0022c0038t0013g0089 | 3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.227-4647G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643905 | ||||||
| chr16:85643930
|
C | T | 2 | a0002c0004t0002g0124a0002c0004t0003g0226 | 2 | HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.227-4622C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85643930 | ||||||
| chr16:85644008
|
C | T | 2 | a0006c0011t0013g0230a0006c0011t0013g0270 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.227-4544C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85644008 | ||||||
| chr16:85644107
|
C | T | 1 | a0001c0001t0051g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.227-4445C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85644107 | ||||||
| chr16:85644342
|
T | C | 4 | a0001c0001t0012g0210a0001c0001t0012g0212a0001c0001t0067g0111others(1): Show | 4 | HG01243.hp2 HG02055.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-4210T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85644342 | ||||||
| chr16:85644343
|
C | CA | 102 | a0001c0001t0001g0234a0001c0001t0002g0007a0001c0001t0002g0131others(99): Show | 102 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.227-4192dupA | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85644343 | |||||
| chr16:85644343
|
C | CAA | 9 | a0001c0001t0002g0069a0001c0001t0012g0210a0001c0001t0017g0243others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.227-4193_227-4192d others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85644343 | |||||
| chr16:85644379
|
T | C | 1 | a0002c0045t0047g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.227-4173T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85644379 | ||||||
| chr16:85644433
|
G | A | 2 | a0001c0001t0012g0210a0001c0021t0033g0225 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.227-4119G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85644433 | ||||||
| chr16:85644640
|
G | A | 27 | a0001c0001t0001g0234a0001c0001t0004g0235a0001c0001t0066g0192others(24): Show | 27 | HG00323.hp1 HG00423.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.227-3912G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85644640 | ||||||
| chr16:85644766
|
C | T | 1 | a0001c0001t0004g0013 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.227-3786C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85644766 | ||||||
| chr16:85644825
|
C | T | 1 | a0001c0002t0001g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.227-3727C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85644825 | ||||||
| chr16:85644850
|
C | T | 4 | a0001c0001t0002g0153a0001c0001t0002g0199a0001c0001t0002g0200others(1): Show | 4 | HG01099.hp2 HG01934.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-3702C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85644850 | ||||||
| chr16:85644857
|
AT | A | 172 | a0001c0001t0001g0234a0001c0001t0002g0069a0001c0001t0002g0097others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.227-3684delT | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85644857 | |||||
| chr16:85644857
|
ATTTTT | A | 25 | a0001c0001t0001g0094a0001c0001t0002g0131a0001c0001t0007g0049others(22): Show | 25 | HG00099.hp2 HG01069.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.227-3688_227-3684d others(7): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85644857 | |||||
| chr16:85644981
|
C | T | 1 | a0001c0001t0012g0212 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.227-3571C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85644981 | ||||||
| chr16:85644982
|
G | A | 1 | a0001c0002t0005g0274 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.227-3570G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85644982 | ||||||
| chr16:85645016
|
C | CCTGTCCC others(28): Show |
1 | a0001c0050t0002g0180 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.227-3535_227-3501d others(37): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85645016 | |||||
| chr16:85645141
|
C | T | 36 | a0001c0001t0002g0069a0001c0001t0002g0097a0001c0001t0002g0236others(33): Show | 36 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.227-3411C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645141 | ||||||
| chr16:85645174
|
C | T | 25 | a0001c0001t0001g0227a0001c0001t0004g0009a0001c0001t0004g0025others(22): Show | 25 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.227-3378C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645174 | ||||||
| chr16:85645180
|
T | C | 72 | a0001c0001t0001g0094a0001c0001t0001g0234a0001c0001t0002g0131others(69): Show | 72 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.227-3372T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645180 | ||||||
| chr16:85645287
|
G | T | 2 | a0008c0013t0021g0284a0008c0013t0055g0119 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.227-3265G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645287 | ||||||
| chr16:85645312
|
G | A | 4 | a0001c0002t0006g0184a0001c0002t0019g0145a0001c0002t0049g0233others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-3240G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645312 | ||||||
| chr16:85645366
|
G | A | 3 | a0001c0002t0018g0194a0001c0002t0018g0283a0026c0032t0010g0061 | 3 | HG02818.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.227-3186G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645366 | ||||||
| chr16:85645384
|
G | A | 1 | a0001c0037t0060g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.227-3168G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645384 | ||||||
| chr16:85645388
|
G | T | 34 | a0001c0001t0002g0069a0001c0001t0002g0097a0001c0001t0002g0236others(31): Show | 34 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.227-3164G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645388 | ||||||
| chr16:85645466
|
C | T | 2 | a0001c0001t0012g0210a0001c0021t0033g0225 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.227-3086C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645466 | ||||||
| chr16:85645467
|
T | C | 1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.227-3085T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645467 | ||||||
| chr16:85645491
|
C | T | 26 | a0001c0001t0046g0105a0001c0002t0001g0018a0001c0002t0006g0092others(23): Show | 26 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.227-3061C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645491 | ||||||
| chr16:85645498
|
G | C | 17 | a0001c0002t0006g0092a0001c0002t0006g0155a0001c0002t0006g0211others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.227-3054G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645498 | ||||||
| chr16:85645508
|
C | A | 1 | a0001c0001t0002g0228 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.227-3044C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645508 | ||||||
| chr16:85645517
|
A | T | 1 | a0025c0033t0038g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.227-3035A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645517 | ||||||
| chr16:85645537
|
C | G | 15 | a0001c0001t0001g0227a0001c0001t0004g0009a0001c0001t0004g0025others(12): Show | 15 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.227-3015C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645537 | ||||||
| chr16:85645571
|
GC | G | 29 | a0001c0001t0012g0210a0001c0001t0046g0105a0001c0001t0067g0111others(26): Show | 29 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.227-2979delC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85645571 | |||||
| chr16:85645577
|
G | A | 1 | a0001c0003t0001g0259 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.227-2975G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645577 | ||||||
| chr16:85645813
|
C | T | 1 | a0002c0008t0070g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.227-2739C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645813 | ||||||
| chr16:85645843
|
A | G | 1 | a0001c0055t0048g0241 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.227-2709A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645843 | ||||||
| chr16:85645878
|
A | G | 7 | a0001c0001t0012g0212a0001c0001t0017g0243a0001c0001t0043g0014others(4): Show | 7 | HG02559.hp1 HG02895.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.227-2674A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645878 | ||||||
| chr16:85645886
|
A | T | 1 | a0001c0001t0002g0149 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.227-2666A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645886 | ||||||
| chr16:85645886
|
ATTCTACC others(4): Show |
A | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.227-2652_227-2642d others(13): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85645886 | |||||
| chr16:85645891
|
A | C | 27 | a0001c0001t0046g0105a0001c0001t0067g0111a0001c0002t0001g0018others(24): Show | 27 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.227-2661A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645891 | ||||||
| chr16:85645919
|
TGCATTCT others(15): Show |
T | 25 | a0001c0001t0046g0105a0001c0002t0001g0018a0001c0002t0006g0092others(22): Show | 25 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.227-2625_227-2604d others(24): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85645919 | |||||
| chr16:85645927
|
G | A | 4 | a0001c0001t0012g0210a0001c0001t0067g0111a0001c0002t0018g0283others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-2625G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85645927 | ||||||
| chr16:85645927
|
G | GCCTGCTT others(15): Show |
1 | a0001c0001t0002g0039 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.227-2586_227-2565d others(24): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85645927 | |||||
| chr16:85645963
|
CGCATTCT others(63): Show |
C | 1 | a0001c0002t0018g0283 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.227-2536_227-2467d others(72): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85645963 | |||||
| chr16:85645985
|
CGCTTCCT others(41): Show |
C | 25 | a0001c0001t0046g0105a0001c0002t0001g0018a0001c0002t0006g0092others(22): Show | 25 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.227-2564_227-2517d others(50): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85645985 | |||||
| chr16:85646025
|
T | TCTATGCA others(63): Show |
1 | a0001c0001t0002g0133 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.227-2389_227-2320d others(72): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85646025 | |||||
| chr16:85646025
|
TCTATGCA others(28): Show |
T | 37 | a0001c0001t0002g0146a0001c0001t0012g0010a0001c0001t0012g0210others(34): Show | 37 | HG00140.hp1 HG00639.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.227-2354_227-2320d others(37): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85646025 | |||||
| chr16:85646025
|
TCTATGCA others(63): Show |
T | 1 | a0001c0001t0035g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.227-2389_227-2320d others(72): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85646025 | |||||
| chr16:85646076
|
ACCTGCTT others(29): Show |
A | 1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.227-2474_227-2439d others(38): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85646076 | |||||
| chr16:85646086
|
A | C | 26 | a0001c0001t0046g0105a0001c0002t0001g0018a0001c0002t0006g0092others(23): Show | 26 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.227-2466A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646086 | ||||||
| chr16:85646095
|
C | CCTATGCA others(168): Show |
1 | a0001c0001t0004g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.227-2320_227-2319i others(177): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85646095 | |||||
| chr16:85646120
|
T | C | 3 | a0001c0001t0020g0156a0001c0001t0020g0217a0001c0001t0067g0111 | 3 | HG01243.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.227-2432T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646120 | ||||||
| chr16:85646133
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.227-2419A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646133 | ||||||
| chr16:85646141
|
A | C | 1 | a0001c0002t0001g0272 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.227-2411A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646141 | ||||||
| chr16:85646153
|
T | C | 107 | a0001c0001t0001g0094a0001c0001t0001g0234a0001c0001t0002g0131others(104): Show | 107 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.227-2399T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646153 | ||||||
| chr16:85646168
|
A | G | 13 | a0002c0004t0002g0124a0002c0004t0003g0226a0002c0004t0003g0276others(10): Show | 13 | HG02602.hp2 HG02683.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.227-2384A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646168 | ||||||
| chr16:85646172
|
A | G | 31 | a0001c0001t0012g0210a0001c0001t0020g0156a0001c0001t0020g0217others(28): Show | 31 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.227-2380A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646172 | ||||||
| chr16:85646181
|
A | G | 29 | a0001c0001t0020g0156a0001c0001t0020g0217a0001c0001t0046g0105others(26): Show | 29 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.227-2371A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646181 | ||||||
| chr16:85646208
|
TGCATTCT others(15): Show |
T | 5 | a0001c0002t0006g0184a0001c0002t0019g0145a0001c0002t0049g0233others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-2312_227-2291d others(24): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85646208 | |||||
| chr16:85646232
|
C | T | 1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.227-2320C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646232 | ||||||
| chr16:85646241
|
T | G | 5 | a0001c0001t0012g0010a0001c0037t0060g0114a0002c0008t0070g0060others(2): Show | 5 | HG00639.hp1 HG00738.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-2311T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646241 | ||||||
| chr16:85646253
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.227-2299G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646253 | ||||||
| chr16:85646270
|
A | G | 5 | a0001c0002t0006g0184a0001c0002t0019g0145a0001c0002t0049g0233others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-2282A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646270 | ||||||
| chr16:85646282
|
G | A | 4 | a0001c0001t0002g0131a0001c0001t0009g0196a0001c0001t0009g0198others(1): Show | 4 | HG00099.hp2 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-2270G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646282 | ||||||
| chr16:85646326
|
C | A | 31 | a0001c0001t0002g0146a0001c0001t0012g0010a0001c0001t0017g0090others(28): Show | 31 | HG00140.hp1 HG00639.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.227-2226C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646326 | ||||||
| chr16:85646338
|
C | T | 16 | a0001c0001t0012g0010a0001c0037t0060g0114a0002c0004t0003g0276others(13): Show | 16 | HG00639.hp1 HG00738.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.227-2214C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646338 | ||||||
| chr16:85646383
|
G | A | 1 | a0001c0002t0062g0167 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.227-2169G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646383 | ||||||
| chr16:85646386
|
T | G | 41 | a0001c0001t0002g0146a0001c0001t0012g0210a0001c0001t0020g0156others(38): Show | 41 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.227-2166T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646386 | ||||||
| chr16:85646497
|
T | C | 289 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.227-2055T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646497 | ||||||
| chr16:85646696
|
C | T | 15 | a0001c0001t0012g0210a0001c0021t0033g0225a0002c0004t0002g0124others(12): Show | 15 | HG02055.hp2 HG02602.hp2 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.227-1856C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646696 | ||||||
| chr16:85646697
|
G | A | 1 | a0002c0005t0063g0208 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.227-1855G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646697 | ||||||
| chr16:85646718
|
G | A | 2 | a0001c0001t0004g0235a0001c0002t0001g0251 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.227-1834G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646718 | ||||||
| chr16:85646759
|
T | C | 182 | a0001c0001t0001g0094a0001c0001t0001g0234a0001c0001t0002g0041others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.227-1793T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646759 | ||||||
| chr16:85646766
|
G | A | 38 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(35): Show | 38 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.227-1786G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646766 | ||||||
| chr16:85646778
|
C | T | 1 | a0001c0002t0001g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.227-1774C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646778 | ||||||
| chr16:85646785
|
C | A | 2 | a0001c0001t0020g0156a0001c0001t0020g0217 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.227-1767C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646785 | ||||||
| chr16:85646796
|
C | G | 2 | a0008c0013t0021g0284a0008c0013t0055g0119 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.227-1756C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646796 | ||||||
| chr16:85646809
|
A | G | 163 | a0001c0001t0001g0094a0001c0001t0001g0234a0001c0001t0002g0041others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.227-1743A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646809 | ||||||
| chr16:85646892
|
A | AG | 42 | a0001c0001t0002g0041a0001c0001t0002g0059a0001c0001t0002g0069others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.227-1651dupG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85646892 | |||||
| chr16:85646892
|
AG | A | 78 | a0001c0001t0001g0227a0001c0001t0001g0234a0001c0001t0002g0131others(75): Show | 78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-1651delG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 85646892 | |||||
| chr16:85646895
|
G | A | 17 | a0001c0002t0006g0092a0001c0002t0006g0155a0001c0002t0006g0211others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.227-1657G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646895 | ||||||
| chr16:85646898
|
G | T | 8 | a0001c0002t0006g0184a0001c0002t0019g0145a0001c0002t0049g0233others(5): Show | 8 | HG01255.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-1654G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646898 | ||||||
| chr16:85646918
|
G | A | 1 | a0002c0006t0001g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.227-1634G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85646918 | ||||||
| chr16:85647062
|
G | C | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.227-1490G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647062 | ||||||
| chr16:85647116
|
C | T | 1 | a0001c0002t0001g0003 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.227-1436C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647116 | ||||||
| chr16:85647161
|
G | T | 1 | a0002c0004t0004g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.227-1391G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647161 | ||||||
| chr16:85647247
|
C | T | 3 | a0001c0001t0017g0243a0005c0047t0065g0088a0022c0038t0013g0089 | 3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.227-1305C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647247 | ||||||
| chr16:85647336
|
C | G | 4 | a0001c0001t0002g0131a0001c0001t0009g0196a0001c0001t0009g0198others(1): Show | 4 | HG00099.hp2 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-1216C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647336 | ||||||
| chr16:85647356
|
C | T | 1 | a0002c0005t0001g0077 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.227-1196C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647356 | ||||||
| chr16:85647432
|
T | G | 1 | a0001c0001t0002g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.227-1120T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647432 | ||||||
| chr16:85647557
|
G | A | 2 | a0001c0001t0016g0162a0003c0010t0016g0067 | 2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.227-995G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647557 | ||||||
| chr16:85647618
|
C | T | 1 | a0002c0004t0004g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.227-934C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647618 | ||||||
| chr16:85647745
|
C | A | 21 | a0001c0001t0002g0146a0001c0001t0012g0010a0001c0001t0017g0090others(18): Show | 21 | HG00140.hp1 HG00438.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.227-807C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647745 | ||||||
| chr16:85647767
|
A | G | 1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.227-785A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647767 | ||||||
| chr16:85647799
|
A | C | 1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.227-753A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647799 | ||||||
| chr16:85647807
|
G | T | 155 | a0001c0001t0001g0234a0001c0001t0002g0041a0001c0001t0002g0069others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.227-745G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647807 | ||||||
| chr16:85647809
|
A | T | 155 | a0001c0001t0001g0234a0001c0001t0002g0041a0001c0001t0002g0069others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.227-743A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647809 | ||||||
| chr16:85647829
|
T | C | 63 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(60): Show | 63 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.227-723T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647829 | ||||||
| chr16:85647831
|
T | C | 63 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(60): Show | 63 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.227-721T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647831 | ||||||
| chr16:85647844
|
C | G | 37 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(34): Show | 37 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.227-708C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647844 | ||||||
| chr16:85647863
|
G | C | 1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.227-689G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647863 | ||||||
| chr16:85647876
|
C | T | 1 | a0001c0002t0005g0126 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.227-676C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647876 | ||||||
| chr16:85647899
|
C | T | 1 | a0001c0002t0007g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.227-653C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647899 | ||||||
| chr16:85647911
|
C | A | 4 | a0002c0030t0003g0023a0016c0029t0003g0100a0017c0044t0002g0024others(1): Show | 4 | NA18947.hp2 NA19011.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-641C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647911 | ||||||
| chr16:85647911
|
C | T | 1 | a0001c0002t0018g0194 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.227-641C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647911 | ||||||
| chr16:85647918
|
G | A | 2 | a0007c0012t0021g0239a0007c0012t0034g0214 | 2 | HG00639.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.227-634G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647918 | ||||||
| chr16:85647951
|
G | A | 34 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(31): Show | 34 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.227-601G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647951 | ||||||
| chr16:85647958
|
C | T | 1 | a0001c0001t0067g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.227-594C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85647958 | ||||||
| chr16:85648084
|
C | T | 2 | a0001c0001t0012g0210a0001c0021t0033g0225 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.227-468C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85648084 | ||||||
| chr16:85648113
|
G | T | 9 | a0001c0001t0012g0010a0001c0001t0017g0090a0001c0001t0017g0243others(6): Show | 9 | HG00438.hp1 HG01167.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.227-439G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85648113 | ||||||
| chr16:85648158
|
T | G | 1 | a0001c0001t0012g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.227-394T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85648158 | ||||||
| chr16:85648185
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.227-367G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85648185 | ||||||
| chr16:85648203
|
A | C | 17 | a0001c0001t0051g0140a0001c0002t0006g0092a0001c0002t0006g0155others(14): Show | 17 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.227-349A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85648203 | ||||||
| chr16:85648262
|
C | T | 74 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.227-290C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85648262 | ||||||
| chr16:85648316
|
C | T | 1 | a0001c0036t0006g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.227-236C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85648316 | ||||||
| chr16:85648318
|
C | T | 2 | a0001c0001t0002g0123a0001c0001t0002g0232 | 2 | HG03927.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.227-234C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85648318 | ||||||
| chr16:85648371
|
C | T | 2 | a0001c0002t0001g0260a0001c0002t0001g0261 | 2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.227-181C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85648371 | ||||||
| chr16:85648465
|
G | C | 13 | a0001c0001t0011g0269a0001c0001t0057g0185a0001c0002t0001g0066others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.227-87G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 2/15 | chr16 | 85648465 | ||||||
| chr16:85648834
|
C | T | 2 | a0001c0001t0003g0099a0001c0001t0056g0179 | 2 | HG00609.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.426+83C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85648834 | ||||||
| chr16:85648865
|
C | T | 99 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0094others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.426+114C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85648865 | ||||||
| chr16:85648923
|
C | T | 10 | a0001c0003t0001g0032a0001c0003t0001g0075a0001c0003t0001g0086others(7): Show | 10 | HG00735.hp2 HG01106.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.426+172C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85648923 | ||||||
| chr16:85648999
|
G | A | 1 | a0026c0032t0010g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.426+248G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85648999 | ||||||
| chr16:85649012
|
G | A | 97 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(94): Show | 97 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.426+261G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649012 | ||||||
| chr16:85649210
|
C | T | 4 | a0001c0001t0035g0286a0006c0011t0013g0230a0006c0011t0013g0270others(1): Show | 4 | HG01081.hp2 HG01255.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.426+459C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649210 | ||||||
| chr16:85649220
|
G | T | 1 | a0001c0001t0004g0144 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.426+469G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649220 | ||||||
| chr16:85649274
|
C | T | 1 | a0030c0053t0001g0047 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.426+523C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649274 | ||||||
| chr16:85649308
|
G | C | 1 | a0024c0034t0001g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.426+557G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649308 | ||||||
| chr16:85649321
|
T | C | 3 | a0001c0002t0001g0057a0001c0002t0001g0157a0001c0002t0001g0178 | 3 | HG00323.hp1 HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.426+570T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649321 | ||||||
| chr16:85649330
|
G | A | 157 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.426+579G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649330 | ||||||
| chr16:85649349
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.426+598A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649349 | ||||||
| chr16:85649475
|
G | C | 1 | a0002c0045t0047g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.426+724G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649475 | ||||||
| chr16:85649482
|
C | T | 2 | a0001c0002t0001g0172a0001c0002t0026g0203 | 2 | HG00423.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.426+731C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649482 | ||||||
| chr16:85649497
|
G | C | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.426+746G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649497 | ||||||
| chr16:85649513
|
G | C | 2 | a0001c0037t0060g0114a0002c0008t0070g0060 | 2 | HG00738.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.426+762G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649513 | ||||||
| chr16:85649565
|
C | T | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(99): Show | 102 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.426+814C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649565 | ||||||
| chr16:85649599
|
C | T | 148 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.426+848C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649599 | ||||||
| chr16:85649604
|
C | T | 212 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.426+853C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649604 | ||||||
| chr16:85649634
|
G | A | 1 | a0001c0002t0002g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.426+883G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649634 | ||||||
| chr16:85649635
|
G | C | 1 | a0001c0002t0001g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.426+884G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649635 | ||||||
| chr16:85649635
|
G | GC | 31 | a0001c0001t0002g0131a0001c0001t0007g0186a0001c0001t0011g0269others(28): Show | 31 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.426+890dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85649635 | |||||
| chr16:85649641
|
C | T | 20 | a0001c0001t0022g0031a0002c0004t0002g0124a0002c0004t0003g0065others(17): Show | 20 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.426+890C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649641 | ||||||
| chr16:85649663
|
G | A | 6 | a0001c0002t0006g0184a0001c0002t0018g0194a0001c0002t0018g0283others(3): Show | 6 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.426+912G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649663 | ||||||
| chr16:85649802
|
G | T | 96 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(93): Show | 96 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.426+1051G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649802 | ||||||
| chr16:85649912
|
A | G | 1 | a0001c0002t0001g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.426+1161A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649912 | ||||||
| chr16:85649915
|
C | A | 1 | a0002c0016t0003g0104 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.426+1164C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649915 | ||||||
| chr16:85649919
|
A | G | 1 | a0001c0003t0001g0163 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.426+1168A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649919 | ||||||
| chr16:85649970
|
G | T | 2 | a0002c0006t0001g0221a0002c0008t0001g0218 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.426+1219G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85649970 | ||||||
| chr16:85649987
|
A | AC | 8 | a0001c0001t0012g0210a0001c0002t0001g0066a0001c0002t0001g0083others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.426+1241dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85649987 | |||||
| chr16:85650051
|
G | C | 1 | a0001c0002t0005g0197 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.426+1300G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650051 | ||||||
| chr16:85650099
|
G | T | 187 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0094others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.426+1348G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650099 | ||||||
| chr16:85650105
|
T | A | 2 | a0001c0002t0001g0102a0001c0002t0001g0139 | 2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.426+1354T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650105 | ||||||
| chr16:85650282
|
C | G | 1 | a0001c0002t0001g0272 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.426+1531C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650282 | ||||||
| chr16:85650289
|
GC | G | 23 | a0001c0002t0062g0167a0002c0004t0002g0124a0002c0004t0003g0065others(20): Show | 23 | HG00438.hp1 HG01255.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.426+1540delC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85650289 | |||||
| chr16:85650305
|
T | G | 210 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.426+1554T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650305 | ||||||
| chr16:85650339
|
C | G | 1 | a0001c0001t0012g0210 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.426+1588C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650339 | ||||||
| chr16:85650435
|
A | G | 2 | a0001c0001t0016g0162a0003c0010t0016g0067 | 2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.426+1684A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650435 | ||||||
| chr16:85650476
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.426+1725C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650476 | ||||||
| chr16:85650521
|
C | T | 1 | a0018c0043t0003g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.426+1770C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650521 | ||||||
| chr16:85650536
|
C | T | 2 | a0009c0014t0005g0176a0009c0014t0054g0257 | 2 | HG01175.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.426+1785C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650536 | ||||||
| chr16:85650646
|
C | T | 6 | a0004c0007t0010g0045a0004c0007t0010g0091a0004c0007t0010g0116others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.426+1895C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650646 | ||||||
| chr16:85650695
|
C | T | 9 | a0001c0003t0001g0032a0001c0003t0001g0075a0001c0003t0001g0086others(6): Show | 9 | HG00735.hp2 HG01106.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.426+1944C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650695 | ||||||
| chr16:85650729
|
T | C | 110 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(107): Show | 110 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.426+1978T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650729 | ||||||
| chr16:85650779
|
A | G | 269 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.426+2028A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650779 | ||||||
| chr16:85650842
|
G | T | 2 | a0001c0001t0016g0162a0003c0010t0016g0067 | 2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.426+2091G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650842 | ||||||
| chr16:85650862
|
C | T | 1 | a0001c0001t0069g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.426+2111C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650862 | ||||||
| chr16:85650863
|
G | A | 1 | a0001c0001t0022g0021 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.426+2112G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650863 | ||||||
| chr16:85650884
|
CG | C | 3 | a0001c0001t0001g0094a0001c0001t0001g0227a0001c0001t0009g0174 | 3 | HG01257.hp2 HG01515.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.426+2137delG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85650884 | |||||
| chr16:85650888
|
G | A | 1 | a0001c0001t0027g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.426+2137G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650888 | ||||||
| chr16:85650922
|
G | T | 6 | a0004c0007t0010g0045a0004c0007t0010g0091a0004c0007t0010g0116others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.426+2171G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650922 | ||||||
| chr16:85650962
|
C | T | 1 | a0001c0001t0009g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.426+2211C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650962 | ||||||
| chr16:85650971
|
T | G | 47 | a0001c0001t0002g0087a0001c0001t0002g0223a0001c0001t0012g0010others(44): Show | 47 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.426+2220T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650971 | ||||||
| chr16:85650974
|
C | T | 1 | a0002c0008t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.426+2223C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650974 | ||||||
| chr16:85650975
|
G | A | 1 | a0004c0007t0052g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.426+2224G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650975 | ||||||
| chr16:85650978
|
T | C | 1 | a0001c0002t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.426+2227T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85650978 | ||||||
| chr16:85651026
|
G | GCTCCTCC others(17): Show |
1 | a0002c0006t0001g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.426+2291_426+2292i others(26): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85651026 | |||||
| chr16:85651026
|
G | GCTCCTCC others(16): Show |
42 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(39): Show | 42 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.426+2321_426+2343d others(25): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85651026 | |||||
| chr16:85651026
|
G | GCTCCTCC others(39): Show |
3 | a0001c0001t0016g0162a0001c0021t0033g0225a0003c0010t0016g0067 | 3 | HG00639.hp2 HG01358.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.426+2298_426+2343d others(48): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85651026 | |||||
| chr16:85651026
|
G | GCTCTCCC others(16): Show |
1 | a0001c0001t0003g0005 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.426+2278_426+2279i others(25): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85651026 | |||||
| chr16:85651034
|
C | CCCTCCCC others(10): Show |
1 | a0001c0035t0004g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.426+2295_426+2311d others(19): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85651034 | |||||
| chr16:85651052
|
C | CCTCCCCC others(16): Show |
3 | a0002c0004t0002g0019a0011c0052t0002g0122a0014c0049t0037g0125 | 3 | HG02165.hp2 HG02698.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.426+2323_426+2324i others(25): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85651052 | |||||
| chr16:85651069
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.426+2318G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651069 | ||||||
| chr16:85651070
|
C | G | 1 | a0001c0001t0001g0227 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.426+2319C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651070 | ||||||
| chr16:85651077
|
T | TCCCCCTC others(17): Show |
2 | a0001c0001t0011g0002a0003c0010t0002g0110 | 2 | HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.426+2343_426+2344i others(26): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85651077 | |||||
| chr16:85651083
|
T | TCCCCCTC others(40): Show |
1 | a0002c0008t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.426+2343_426+2344i others(49): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85651083 | |||||
| chr16:85651091
|
C | T | 2 | a0001c0001t0002g0059a0022c0038t0013g0089 | 2 | HG00544.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.426+2340C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651091 | ||||||
| chr16:85651107
|
T | C | 1 | a0002c0004t0004g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.426+2356T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651107 | ||||||
| chr16:85651108
|
C | T | 3 | a0002c0004t0004g0001a0002c0018t0004g0006a0002c0018t0004g0266 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.426+2357C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651108 | ||||||
| chr16:85651119
|
C | T | 1 | a0001c0002t0001g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.426+2368C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651119 | ||||||
| chr16:85651156
|
C | G | 3 | a0002c0004t0002g0019a0011c0052t0002g0122a0014c0049t0037g0125 | 3 | HG02165.hp2 HG02698.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.426+2405C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651156 | ||||||
| chr16:85651197
|
G | C | 2 | a0001c0001t0003g0161a0001c0001t0012g0210 | 2 | HG02055.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.426+2446G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651197 | ||||||
| chr16:85651201
|
C | A | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.426+2450C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651201 | ||||||
| chr16:85651204
|
G | T | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.426+2453G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651204 | ||||||
| chr16:85651205
|
C | G | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.426+2454C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651205 | ||||||
| chr16:85651208
|
C | A | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.426+2457C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651208 | ||||||
| chr16:85651209
|
C | T | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.426+2458C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651209 | ||||||
| chr16:85651210
|
G | A | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.426+2459G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651210 | ||||||
| chr16:85651211
|
C | T | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.426+2460C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651211 | ||||||
| chr16:85651252
|
CTTGCCTG others(7): Show |
C | 1 | a0031c0019t0002g0249 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.426+2502_426+2515d others(16): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651252 | ||||||
| chr16:85651276
|
G | T | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.426+2525G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651276 | ||||||
| chr16:85651287
|
C | T | 24 | a0001c0001t0002g0223a0001c0001t0012g0010a0002c0004t0002g0124others(21): Show | 24 | HG01257.hp1 HG01258.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.426+2536C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651287 | ||||||
| chr16:85651348
|
G | A | 1 | a0001c0002t0005g0197 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.426+2597G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651348 | ||||||
| chr16:85651391
|
C | T | 31 | a0001c0001t0002g0223a0001c0001t0012g0010a0001c0001t0069g0121others(28): Show | 31 | HG00639.hp1 HG01257.hp1 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.426+2640C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651391 | ||||||
| chr16:85651418
|
G | A | 1 | a0024c0034t0001g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.426+2667G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651418 | ||||||
| chr16:85651464
|
C | T | 1 | a0001c0002t0001g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.426+2713C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651464 | ||||||
| chr16:85651491
|
A | T | 1 | a0001c0002t0001g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.426+2740A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651491 | ||||||
| chr16:85651514
|
G | A | 31 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(28): Show | 31 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.426+2763G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651514 | ||||||
| chr16:85651595
|
C | T | 3 | a0002c0004t0002g0019a0011c0052t0002g0122a0014c0049t0037g0125 | 3 | HG02165.hp2 HG02698.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.427-2683C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651595 | ||||||
| chr16:85651611
|
G | T | 148 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.427-2667G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651611 | ||||||
| chr16:85651642
|
G | C | 27 | a0001c0001t0012g0010a0002c0004t0002g0124a0002c0004t0003g0065others(24): Show | 27 | HG00639.hp1 HG01257.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.427-2636G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651642 | ||||||
| chr16:85651695
|
C | T | 1 | a0005c0046t0003g0034 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.427-2583C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651695 | ||||||
| chr16:85651761
|
TCCCCACC others(29): Show |
T | 1 | a0007c0012t0034g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427-2516_427-2481d others(38): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651761 | ||||||
| chr16:85651792
|
A | AC | 8 | a0001c0001t0002g0073a0001c0001t0002g0148a0001c0001t0011g0269others(5): Show | 8 | HG00140.hp2 HG01106.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.427-2482dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85651792 | |||||
| chr16:85651820
|
C | G | 29 | a0001c0001t0002g0223a0001c0001t0012g0010a0001c0021t0033g0225others(26): Show | 29 | HG00639.hp1 HG01257.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.427-2458C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651820 | ||||||
| chr16:85651828
|
G | A | 1 | a0008c0013t0021g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.427-2450G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651828 | ||||||
| chr16:85651874
|
C | G | 1 | a0001c0001t0012g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.427-2404C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651874 | ||||||
| chr16:85651888
|
G | T | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.427-2390G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651888 | ||||||
| chr16:85651890
|
G | T | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.427-2388G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651890 | ||||||
| chr16:85651892
|
G | T | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.427-2386G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651892 | ||||||
| chr16:85651893
|
C | T | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.427-2385C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651893 | ||||||
| chr16:85651907
|
G | A | 1 | a0001c0001t0003g0036 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.427-2371G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651907 | ||||||
| chr16:85651911
|
T | C | 38 | a0001c0001t0002g0223a0001c0001t0012g0010a0001c0021t0033g0225others(35): Show | 38 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.427-2367T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651911 | ||||||
| chr16:85651929
|
C | T | 1 | a0002c0008t0036g0277 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.427-2349C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651929 | ||||||
| chr16:85651955
|
C | T | 1 | a0001c0001t0012g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.427-2323C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85651955 | ||||||
| chr16:85652050
|
T | C | 5 | a0001c0001t0002g0223a0002c0004t0002g0019a0003c0010t0002g0110others(2): Show | 5 | HG02165.hp2 HG02698.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.427-2228T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652050 | ||||||
| chr16:85652150
|
T | C | 211 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.427-2128T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652150 | ||||||
| chr16:85652173
|
T | G | 1 | a0007c0012t0034g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427-2105T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652173 | ||||||
| chr16:85652187
|
C | T | 1 | a0001c0001t0012g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.427-2091C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652187 | ||||||
| chr16:85652230
|
G | T | 1 | a0003c0010t0002g0110 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.427-2048G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652230 | ||||||
| chr16:85652288
|
G | C | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.427-1990G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652288 | ||||||
| chr16:85652295
|
C | T | 38 | a0001c0001t0002g0223a0001c0001t0012g0010a0001c0001t0051g0140others(35): Show | 38 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.427-1983C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652295 | ||||||
| chr16:85652312
|
A | C | 1 | a0001c0003t0001g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.427-1966A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652312 | ||||||
| chr16:85652315
|
A | AC | 11 | a0001c0001t0001g0227a0001c0001t0002g0201a0001c0001t0015g0127others(8): Show | 11 | HG01106.hp2 HG01109.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.427-1959dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652315 | |||||
| chr16:85652389
|
G | A | 2 | a0001c0002t0005g0043a0001c0002t0005g0143 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.427-1889G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652389 | ||||||
| chr16:85652404
|
C | T | 3 | a0001c0001t0012g0210a0001c0001t0020g0156a0001c0001t0020g0217 | 3 | HG02055.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.427-1874C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652404 | ||||||
| chr16:85652493
|
C | G | 1 | a0007c0012t0034g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427-1785C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652493 | ||||||
| chr16:85652507
|
C | T | 1 | a0002c0004t0008g0093 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.427-1771C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652507 | ||||||
| chr16:85652539
|
G | A | 33 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(30): Show | 33 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.427-1739G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652539 | ||||||
| chr16:85652545
|
A | AGGC | 106 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0094others(103): Show | 106 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.427-1714_427-1712d others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652545 | |||||
| chr16:85652545
|
A | AGGCGGC | 6 | a0001c0001t0001g0030a0001c0001t0002g0039a0001c0001t0002g0062others(3): Show | 6 | HG01257.hp2 HG01433.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.427-1717_427-1712d others(8): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652545 | |||||
| chr16:85652545
|
A | AGGCGGCG others(5): Show |
15 | a0001c0001t0001g0227a0001c0001t0002g0182a0001c0001t0004g0009others(12): Show | 15 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.427-1723_427-1712d others(14): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652545 | |||||
| chr16:85652545
|
A | AGGCGGCG others(14): Show |
1 | a0001c0001t0004g0144 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.427-1732_427-1712d others(23): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652545 | |||||
| chr16:85652545
|
AGGC | A | 4 | a0001c0001t0004g0115a0001c0028t0053g0287a0002c0008t0001g0168others(1): Show | 4 | HG00408.hp1 HG01891.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.427-1714_427-1712d others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652545 | |||||
| chr16:85652563
|
C | CGGGCGGC others(7): Show |
1 | a0003c0010t0004g0008 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.427-1713_427-1712i others(16): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652563 | |||||
| chr16:85652565
|
G | GCTC | 3 | a0001c0002t0001g0017a0001c0002t0001g0245a0001c0002t0001g0272 | 3 | HG02559.hp2 HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.427-1708_427-1706d others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652565 | |||||
| chr16:85652565
|
G | T | 1 | a0001c0001t0003g0141 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.427-1713G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652565 | ||||||
| chr16:85652633
|
G | A | 1 | a0012c0023t0001g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.427-1645G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652633 | ||||||
| chr16:85652669
|
G | GC | 4 | a0001c0001t0003g0187a0002c0004t0004g0001a0015c0041t0001g0095others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.427-1607dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652669 | |||||
| chr16:85652683
|
T | G | 1 | a0002c0018t0004g0266 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.427-1595T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652683 | ||||||
| chr16:85652723
|
C | T | 1 | a0001c0002t0001g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.427-1555C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652723 | ||||||
| chr16:85652724
|
G | A | 4 | a0001c0001t0003g0020a0001c0001t0011g0002a0001c0001t0011g0136others(1): Show | 4 | HG01070.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-1554G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652724 | ||||||
| chr16:85652748
|
C | A | 1 | a0005c0046t0003g0034 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.427-1530C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652748 | ||||||
| chr16:85652756
|
CA | C | 20 | a0001c0001t0002g0223a0002c0004t0002g0124a0002c0004t0003g0065others(17): Show | 20 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.427-1521delA | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652756 | ||||||
| chr16:85652807
|
C | T | 1 | a0001c0001t0042g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.427-1471C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652807 | ||||||
| chr16:85652819
|
TG | T | 3 | a0001c0001t0009g0174a0001c0002t0001g0083a0004c0007t0010g0116 | 3 | HG01109.hp1 HG01257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.427-1455delG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652819 | |||||
| chr16:85652843
|
G | GT | 3 | a0001c0002t0006g0211a0001c0051t0002g0106a0002c0005t0008g0159 | 3 | HG01257.hp1 HG02896.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.427-1429dupT | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652843 | |||||
| chr16:85652850
|
G | GGGTGTTT others(8): Show |
1 | a0001c0002t0005g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.427-1426_427-1412d others(17): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85652850 | |||||
| chr16:85652884
|
G | T | 6 | a0004c0007t0010g0045a0004c0007t0010g0091a0004c0007t0010g0116others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-1394G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652884 | ||||||
| chr16:85652885
|
C | T | 4 | a0001c0001t0069g0121a0006c0011t0013g0230a0006c0011t0013g0270others(1): Show | 4 | HG01255.hp1 HG02109.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.427-1393C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652885 | ||||||
| chr16:85652898
|
C | T | 1 | a0001c0002t0001g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.427-1380C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652898 | ||||||
| chr16:85652906
|
G | T | 2 | a0007c0012t0021g0239a0007c0012t0034g0214 | 2 | HG00639.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.427-1372G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652906 | ||||||
| chr16:85652916
|
C | A | 1 | a0002c0004t0004g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.427-1362C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652916 | ||||||
| chr16:85652926
|
G | A | 1 | a0001c0001t0009g0262 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.427-1352G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652926 | ||||||
| chr16:85652953
|
C | A | 1 | a0002c0004t0004g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.427-1325C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652953 | ||||||
| chr16:85652974
|
C | T | 12 | a0001c0055t0048g0241a0002c0006t0001g0113a0002c0006t0001g0216others(9): Show | 12 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.427-1304C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85652974 | ||||||
| chr16:85653042
|
A | C | 37 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(34): Show | 37 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.427-1236A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653042 | ||||||
| chr16:85653079
|
G | A | 1 | a0001c0001t0012g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.427-1199G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653079 | ||||||
| chr16:85653119
|
C | T | 1 | a0002c0008t0036g0277 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.427-1159C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653119 | ||||||
| chr16:85653169
|
C | T | 1 | a0017c0044t0002g0024 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.427-1109C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653169 | ||||||
| chr16:85653170
|
GCCCTGAG others(3): Show |
G | 1 | a0025c0033t0038g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.427-1103_427-1094d others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653170 | |||||
| chr16:85653180
|
T | TCCCTCCG others(3): Show |
2 | a0001c0001t0003g0187a0001c0001t0004g0013 | 2 | HG00741.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.427-1091_427-1082d others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653180 | |||||
| chr16:85653187
|
G | GCCCCCCT others(36): Show |
1 | a0002c0004t0002g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(45): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(267): Show |
1 | a0001c0001t0002g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(276): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(432): Show |
1 | a0001c0001t0003g0004 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.427-1082_427-1081i others(441): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(250): Show |
1 | a0001c0001t0015g0127 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(259): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(249): Show |
1 | a0001c0001t0015g0128 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(258): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(217): Show |
1 | a0005c0046t0003g0034 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.427-1082_427-1081i others(226): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(277): Show |
1 | a0001c0001t0003g0036 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.427-1082_427-1081i others(286): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(362): Show |
1 | a0001c0001t0003g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.427-1082_427-1081i others(371): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(258): Show |
1 | a0001c0001t0061g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(267): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(178): Show |
1 | a0001c0001t0004g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(187): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(105): Show |
1 | a0001c0001t0002g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(114): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(115): Show |
1 | a0023c0031t0002g0280 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.427-1082_427-1081i others(124): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(124): Show |
1 | a0001c0050t0002g0180 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.427-1082_427-1081i others(133): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(177): Show |
1 | a0001c0001t0001g0227 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(186): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653187
|
G | GCCCCCCT others(472): Show |
1 | a0001c0001t0003g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.427-1079_427-1078i others(481): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653187 | |||||
| chr16:85653189
|
C | T | 1 | a0001c0001t0004g0190 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.427-1089C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653189 | ||||||
| chr16:85653190
|
C | CCCCTCCG others(112): Show |
1 | a0007c0012t0021g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(121): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653190 | |||||
| chr16:85653191
|
C | CCCCTCCG others(7): Show |
1 | a0001c0001t0002g0073 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.427-1085_427-1084i others(16): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653191 | |||||
| chr16:85653191
|
C | CCCCTCCG others(422): Show |
1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.427-1085_427-1084i others(431): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653191 | |||||
| chr16:85653191
|
C | CCCCTCCG others(210): Show |
1 | a0001c0001t0058g0051 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.427-1085_427-1084i others(219): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653191 | |||||
| chr16:85653191
|
C | CCCCTCCG others(158): Show |
1 | a0001c0001t0022g0021 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.427-1085_427-1084i others(167): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653191 | |||||
| chr16:85653191
|
C | CCCT | 8 | a0001c0001t0003g0289a0001c0001t0004g0013a0001c0001t0068g0054others(5): Show | 8 | HG00438.hp1 HG01255.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.427-1081_427-1079d others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653191 | |||||
| chr16:85653191
|
C | CCCTCCGC others(145): Show |
1 | a0002c0005t0008g0159 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(154): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653191 | |||||
| chr16:85653191
|
C | CCCTCCGC others(141): Show |
1 | a0002c0005t0008g0160 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(150): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653191 | |||||
| chr16:85653191
|
C | CCCTCCGC others(352): Show |
1 | a0001c0001t0056g0179 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.427-1082_427-1081i others(361): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653191 | |||||
| chr16:85653191
|
C | CCCTCCGC others(95): Show |
1 | a0001c0001t0009g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.427-1082_427-1081i others(104): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653191 | |||||
| chr16:85653191
|
C | CCCTCTCT others(309): Show |
1 | a0001c0002t0006g0211 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.427-1083_427-1082i others(318): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653191 | |||||
| chr16:85653191
|
C | CCCTCTGC others(6): Show |
3 | a0002c0004t0004g0001a0002c0018t0004g0006a0002c0018t0004g0266 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.427-1083_427-1082i others(15): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653191 | |||||
| chr16:85653193
|
C | CCTCCGCC others(140): Show |
1 | a0007c0012t0034g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427-1085_427-1084i others(149): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653193 | ||||||
| chr16:85653194
|
T | C | 1 | a0007c0012t0034g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427-1084T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653194 | ||||||
| chr16:85653197
|
T | G | 164 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(161): Show | 164 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.427-1081T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653197 | ||||||
| chr16:85653198
|
C | CCCGCCTC others(365): Show |
1 | a0001c0002t0005g0197 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.427-1078_427-1077i others(374): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653198 | |||||
| chr16:85653198
|
C | CCTCCCCC others(89): Show |
1 | a0025c0033t0038g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.427-1079_427-1078i others(98): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653198 | |||||
| chr16:85653200
|
C | G | 1 | a0002c0008t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427-1078C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653200 | ||||||
| chr16:85653201
|
C | CCCCTCCC others(402): Show |
1 | a0001c0001t0011g0269 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.427-1075_427-1074i others(411): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCCTCCC others(270): Show |
1 | a0002c0040t0001g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.427-1075_427-1074i others(279): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCCTCCC others(292): Show |
1 | a0001c0002t0001g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.427-1075_427-1074i others(301): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCCTCCC others(294): Show |
1 | a0001c0003t0001g0108 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.427-1075_427-1074i others(303): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCCTCCT others(175): Show |
1 | a0001c0001t0002g0201 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.427-1075_427-1074i others(184): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCT | 75 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(72): Show | 75 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.427-1071_427-1069d others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(347): Show |
1 | a0001c0002t0005g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(356): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(349): Show |
1 | a0001c0002t0005g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(358): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(315): Show |
2 | a0001c0002t0005g0043a0001c0002t0005g0143 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.427-1072_427-1071i others(324): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(318): Show |
1 | a0001c0002t0005g0126 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(327): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(226): Show |
1 | a0001c0002t0005g0081 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(235): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(337): Show |
1 | a0001c0002t0005g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(346): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(341): Show |
1 | a0001c0001t0057g0185 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(350): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(281): Show |
1 | a0001c0003t0001g0206 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(290): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(221): Show |
1 | a0004c0007t0010g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(230): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(364): Show |
1 | a0004c0007t0010g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(373): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(228): Show |
1 | a0004c0007t0010g0265 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(237): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(204): Show |
1 | a0004c0007t0010g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(213): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(256): Show |
1 | a0012c0023t0001g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(265): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(459): Show |
1 | a0015c0041t0001g0095 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(468): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(263): Show |
1 | a0001c0002t0001g0263 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(272): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(347): Show |
1 | a0001c0001t0004g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(356): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(392): Show |
1 | a0001c0002t0001g0288 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(401): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(401): Show |
1 | a0024c0034t0001g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(410): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(333): Show |
1 | a0001c0003t0001g0290 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(342): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(368): Show |
1 | a0001c0002t0001g0074 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(377): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(349): Show |
1 | a0001c0002t0001g0003 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(358): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(312): Show |
1 | a0001c0002t0026g0203 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(321): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(373): Show |
1 | a0001c0002t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(382): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(305): Show |
1 | a0001c0002t0014g0204 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(314): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(416): Show |
1 | a0002c0008t0070g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(425): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(505): Show |
1 | a0010c0015t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(514): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(461): Show |
1 | a0001c0002t0001g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(470): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(324): Show |
1 | a0001c0002t0001g0157 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(333): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(323): Show |
1 | a0001c0002t0001g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.427-1072_427-1071i others(332): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCCC others(265): Show |
1 | a0001c0003t0001g0137 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(274): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(171): Show |
1 | a0001c0001t0002g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(180): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(151): Show |
1 | a0001c0001t0009g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(160): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(210): Show |
1 | a0031c0019t0002g0249 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.427-1069_427-1068i others(219): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(224): Show |
1 | a0001c0002t0018g0194 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(233): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(206): Show |
1 | a0001c0001t0022g0031 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(215): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(188): Show |
1 | a0001c0001t0059g0273 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(197): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(207): Show |
1 | a0001c0001t0001g0120 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(216): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(168): Show |
1 | a0001c0001t0066g0192 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.427-1069_427-1068i others(177): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(158): Show |
1 | a0001c0001t0002g0007 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(167): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(162): Show |
1 | a0002c0005t0007g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.427-1069_427-1068i others(171): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(190): Show |
1 | a0001c0002t0002g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.427-1069_427-1068i others(199): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(159): Show |
1 | a0001c0001t0067g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(168): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(145): Show |
1 | a0001c0001t0042g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.427-1069_427-1068i others(154): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | CCCTCCTC others(131): Show |
2 | a0001c0001t0012g0212a0001c0001t0043g0014 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.427-1069_427-1068i others(140): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653201 | |||||
| chr16:85653201
|
C | T | 2 | a0001c0002t0005g0197a0025c0033t0038g0209 | 2 | HG01167.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.427-1077C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653201 | ||||||
| chr16:85653204
|
T | C | 1 | a0002c0008t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427-1074T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653204 | ||||||
| chr16:85653204
|
T | TCCC | 40 | a0001c0001t0001g0234a0001c0002t0001g0017a0001c0002t0001g0083others(37): Show | 40 | HG00735.hp2 HG01109.hp1 HG01258.hp2 others(37): Show |
intron_variant | MODIFIER | c.427-1072_427-1071i others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653204 | |||||
| chr16:85653206
|
C | CCCCTCCC others(358): Show |
1 | a0001c0002t0001g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(367): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653206 | ||||||
| chr16:85653206
|
C | CCCCTCCT others(449): Show |
1 | a0004c0007t0052g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(458): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653206 | ||||||
| chr16:85653206
|
C | CCCCTCCT others(428): Show |
1 | a0004c0007t0064g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(437): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653206 | ||||||
| chr16:85653206
|
C | CCCCTCCT others(518): Show |
1 | a0010c0015t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.427-1072_427-1071i others(527): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653206 | ||||||
| chr16:85653207
|
T | C | 3 | a0001c0002t0001g0066a0002c0008t0001g0218a0010c0015t0001g0246 | 3 | HG02602.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.427-1071T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653207 | ||||||
| chr16:85653207
|
T | G | 18 | a0001c0001t0002g0223a0001c0001t0012g0210a0002c0004t0003g0065others(15): Show | 18 | HG01934.hp2 HG01943.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.427-1071T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653207 | ||||||
| chr16:85653207
|
T | TCCTCC | 17 | a0001c0001t0002g0069a0001c0001t0002g0236a0001c0001t0003g0099others(14): Show | 17 | HG00099.hp1 HG00609.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.427-1069_427-1068i others(7): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653207 | |||||
| chr16:85653208
|
C | A | 1 | a0015c0041t0001g0095 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.427-1070C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653208 | ||||||
| chr16:85653208
|
C | CCTCCCCC others(166): Show |
1 | a0001c0001t0009g0196 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.427-1069_427-1068i others(175): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653208 | |||||
| chr16:85653208
|
C | CCTCCCCC others(182): Show |
1 | a0003c0009t0002g0109 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.427-1069_427-1068i others(191): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653208 | |||||
| chr16:85653208
|
C | CCTCCCCC others(169): Show |
1 | a0001c0001t0002g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.427-1069_427-1068i others(178): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653208 | |||||
| chr16:85653208
|
C | CCTCCCCC others(156): Show |
1 | a0001c0001t0009g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.427-1069_427-1068i others(165): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653208 | |||||
| chr16:85653208
|
C | CCTCCCCC others(166): Show |
1 | a0001c0001t0002g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.427-1069_427-1068i others(175): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653208 | |||||
| chr16:85653208
|
C | CCTCCCCC others(238): Show |
1 | a0001c0001t0002g0039 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(247): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653208 | |||||
| chr16:85653208
|
C | CCTCCCCC others(183): Show |
1 | a0001c0001t0046g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(192): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653208 | |||||
| chr16:85653208
|
C | CCTCCCCC others(177): Show |
1 | a0001c0002t0002g0250 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(186): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653208 | |||||
| chr16:85653208
|
C | CTCTCCCC others(495): Show |
1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.427-1070_427-1069i others(504): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653208 | ||||||
| chr16:85653208
|
C | T | 1 | a0002c0008t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427-1070C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653208 | ||||||
| chr16:85653209
|
C | CTCCCCCC others(325): Show |
1 | a0003c0010t0002g0110 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(334): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653209 | ||||||
| chr16:85653209
|
C | CTCCCCCC others(184): Show |
1 | a0001c0002t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.427-1069_427-1068i others(193): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653209 | ||||||
| chr16:85653210
|
C | G | 9 | a0001c0055t0048g0241a0002c0006t0001g0113a0002c0006t0001g0216others(6): Show | 9 | HG01109.hp2 HG01167.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.427-1068C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653210 | ||||||
| chr16:85653210
|
C | T | 63 | a0001c0001t0001g0227a0001c0001t0001g0234a0001c0001t0002g0062others(60): Show | 63 | HG00438.hp2 HG00735.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.427-1068C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653210 | ||||||
| chr16:85653211
|
C | CCCTCCGC others(270): Show |
1 | a0001c0001t0012g0210 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(279): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653211 | |||||
| chr16:85653211
|
C | T | 30 | a0001c0001t0002g0039a0001c0001t0003g0170a0001c0001t0004g0235others(27): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.427-1067C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653211 | ||||||
| chr16:85653211
|
CCCTCCCC others(2): Show |
C | 6 | a0001c0055t0048g0241a0002c0006t0001g0216a0002c0006t0001g0222others(3): Show | 6 | HG01109.hp2 HG01167.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.427-1061_427-1053d others(11): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653211 | |||||
| chr16:85653212
|
C | T | 2 | a0001c0001t0058g0051a0007c0012t0034g0214 | 2 | HG02056.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.427-1066C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653212 | ||||||
| chr16:85653213
|
C | CCCCCCCT others(589): Show |
1 | a0001c0001t0002g0097 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.427-1065_427-1064i others(598): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653213 | ||||||
| chr16:85653213
|
C | CCCCCCTC others(353): Show |
1 | a0001c0001t0003g0005 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.427-1065_427-1064i others(362): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653213 | ||||||
| chr16:85653213
|
C | CCCCCCTC others(173): Show |
1 | a0001c0001t0069g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.427-1065_427-1064i others(182): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653213 | ||||||
| chr16:85653213
|
C | CCCCCCTC others(330): Show |
1 | a0001c0001t0003g0142 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.427-1065_427-1064i others(339): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653213 | ||||||
| chr16:85653213
|
C | CCCCCTCC others(455): Show |
1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.427-1065_427-1064i others(464): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653213 | ||||||
| chr16:85653213
|
C | T | 6 | a0001c0001t0003g0161a0001c0001t0056g0179a0001c0002t0001g0172others(3): Show | 6 | HG01106.hp2 HG01243.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-1065C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653213 | ||||||
| chr16:85653214
|
T | C | 27 | a0001c0001t0001g0227a0001c0001t0002g0097a0001c0001t0002g0229others(24): Show | 27 | HG00438.hp2 HG01106.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.427-1064T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653214 | ||||||
| chr16:85653214
|
T | G | 1 | a0002c0008t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427-1064T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653214 | ||||||
| chr16:85653214
|
T | TCCGC | 14 | a0002c0004t0003g0065a0002c0004t0003g0226a0002c0004t0003g0276others(11): Show | 14 | HG01934.hp2 HG01943.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.427-1062_427-1061i others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCGCCCC others(145): Show |
1 | a0001c0001t0002g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(154): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTC | 15 | a0001c0001t0002g0041a0001c0001t0003g0004a0001c0001t0003g0036others(12): Show | 15 | HG00099.hp2 HG00609.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.427-1062_427-1061i others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(194): Show |
1 | a0001c0002t0018g0283 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(203): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(169): Show |
1 | a0001c0001t0002g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(178): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(30): Show |
1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(39): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(167): Show |
1 | a0013c0022t0030g0072 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(176): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(176): Show |
3 | a0005c0048t0003g0050a0027c0027t0003g0181a0028c0026t0003g0183 | 3 | HG01978.hp2 HG02300.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.427-1062_427-1061i others(185): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(244): Show |
1 | a0001c0001t0039g0147 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(253): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(237): Show |
1 | a0001c0001t0002g0231 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(246): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(312): Show |
1 | a0006c0011t0019g0282 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(321): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(181): Show |
1 | a0008c0013t0021g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(190): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(475): Show |
1 | a0001c0001t0068g0054 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(484): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(284): Show |
1 | a0006c0011t0013g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(293): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(309): Show |
1 | a0022c0038t0013g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(318): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(156): Show |
1 | a0001c0001t0004g0013 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(165): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(185): Show |
1 | a0001c0001t0003g0289 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(194): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCCC others(176): Show |
1 | a0001c0001t0002g0073 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(185): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(351): Show |
1 | a0002c0017t0001g0219 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(360): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(310): Show |
1 | a0003c0009t0005g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(319): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(156): Show |
1 | a0001c0001t0017g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(165): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(238): Show |
1 | a0001c0056t0014g0189 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(247): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(257): Show |
1 | a0002c0005t0001g0077 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(266): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(339): Show |
1 | a0001c0002t0001g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(348): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(333): Show |
1 | a0001c0002t0001g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(342): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(256): Show |
1 | a0001c0002t0031g0256 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(265): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(296): Show |
1 | a0001c0002t0001g0272 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(305): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(314): Show |
1 | a0002c0017t0001g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(323): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(256): Show |
1 | a0001c0002t0001g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(265): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(307): Show |
5 | a0001c0002t0006g0184a0001c0002t0006g0213a0001c0002t0006g0281others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-1062_427-1061i others(316): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(326): Show |
1 | a0001c0002t0006g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(335): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(327): Show |
1 | a0001c0002t0006g0215 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(336): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(321): Show |
1 | a0001c0002t0001g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(330): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(310): Show |
1 | a0001c0002t0006g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(319): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(298): Show |
1 | a0001c0003t0001g0075 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(307): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(323): Show |
1 | a0002c0016t0003g0046 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(332): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(295): Show |
1 | a0001c0003t0001g0032 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(304): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(293): Show |
1 | a0001c0003t0001g0205 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(302): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(282): Show |
1 | a0001c0003t0001g0259 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(291): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(272): Show |
1 | a0001c0003t0001g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(281): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(291): Show |
1 | a0001c0003t0001g0163 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(300): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(273): Show |
1 | a0001c0003t0014g0022 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(282): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(287): Show |
1 | a0001c0002t0001g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(296): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(471): Show |
1 | a0001c0002t0001g0268 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(480): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(496): Show |
1 | a0001c0002t0001g0261 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(505): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(518): Show |
1 | a0001c0002t0001g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(527): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(568): Show |
1 | a0001c0020t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(577): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653214
|
T | TCCTCCTC others(165): Show |
1 | a0001c0001t0002g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(174): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653214 | |||||
| chr16:85653215
|
C | CCTCCCCC others(177): Show |
1 | a0001c0002t0049g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(186): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653215 | |||||
| chr16:85653215
|
C | CCTCCCCC others(197): Show |
1 | a0016c0029t0003g0100 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(206): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653215 | |||||
| chr16:85653215
|
C | CCTCCCCC others(180): Show |
1 | a0001c0002t0007g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(189): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653215 | |||||
| chr16:85653215
|
C | CCTCCCCC others(197): Show |
1 | a0002c0004t0004g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(206): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653215 | |||||
| chr16:85653215
|
C | CCTCCTCC others(130): Show |
1 | a0002c0004t0025g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(139): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653215 | |||||
| chr16:85653216
|
C | CTCCCCCC others(182): Show |
1 | a0001c0002t0019g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(191): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(161): Show |
1 | a0026c0032t0010g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(170): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(165): Show |
1 | a0001c0001t0020g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(174): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(164): Show |
1 | a0001c0001t0020g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(173): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(192): Show |
1 | a0001c0001t0002g0062 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(201): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(367): Show |
1 | a0001c0001t0004g0115 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(376): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(153): Show |
1 | a0001c0051t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(162): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(202): Show |
1 | a0001c0001t0035g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(211): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(176): Show |
3 | a0001c0001t0002g0012a0001c0001t0002g0224a0001c0001t0009g0262 | 3 | HG02683.hp1 NA18946.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.427-1062_427-1061i others(185): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(178): Show |
1 | a0001c0001t0002g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(187): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(189): Show |
1 | a0001c0001t0002g0182 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(198): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(117): Show |
1 | a0001c0001t0012g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(126): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(258): Show |
1 | a0001c0001t0041g0035 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(267): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(167): Show |
1 | a0001c0001t0002g0200 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(176): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(164): Show |
1 | a0001c0001t0002g0278 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(173): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(196): Show |
1 | a0001c0001t0001g0026 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(205): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(179): Show |
1 | a0001c0001t0002g0279 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(188): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(153): Show |
3 | a0001c0001t0002g0011a0001c0001t0002g0037a0001c0001t0002g0133 | 3 | NA18966.hp2 NA18983.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.427-1062_427-1061i others(162): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(186): Show |
2 | a0001c0001t0002g0151a0001c0001t0002g0202 | 2 | HG00597.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.427-1062_427-1061i others(195): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(176): Show |
3 | a0001c0001t0001g0030a0001c0001t0002g0131a0001c0001t0007g0186 | 3 | HG01081.hp1 HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.427-1062_427-1061i others(185): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(210): Show |
1 | a0001c0001t0007g0049 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(219): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(179): Show |
1 | a0001c0001t0001g0016 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(188): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(191): Show |
4 | a0001c0001t0001g0220a0001c0001t0005g0027a0009c0014t0005g0176others(1): Show | 4 | HG00735.hp1 HG01175.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.427-1062_427-1061i others(200): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(203): Show |
1 | a0001c0001t0002g0228 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(212): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(163): Show |
1 | a0001c0001t0002g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(172): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(166): Show |
5 | a0001c0001t0002g0059a0001c0001t0002g0149a0001c0001t0002g0153others(2): Show | 5 | HG00544.hp2 HG01934.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.427-1062_427-1061i others(175): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(169): Show |
1 | a0001c0001t0002g0087 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(178): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(189): Show |
1 | a0002c0018t0004g0266 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(198): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(166): Show |
1 | a0001c0001t0003g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(175): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(185): Show |
1 | a0032c0057t0003g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(194): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(202): Show |
1 | a0002c0018t0004g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(211): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(178): Show |
4 | a0001c0001t0001g0094a0001c0002t0002g0165a0001c0002t0002g0248others(1): Show | 4 | HG01069.hp1 HG01123.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-1062_427-1061i others(187): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(235): Show |
1 | a0001c0001t0004g0071 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(244): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(232): Show |
1 | a0001c0001t0004g0009 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(241): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(238): Show |
1 | a0001c0001t0004g0188 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(247): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(225): Show |
3 | a0001c0001t0004g0025a0001c0001t0004g0101a0001c0001t0004g0238 | 3 | NA18612.hp1 NA19004.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.427-1062_427-1061i others(234): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(215): Show |
1 | a0001c0001t0004g0190 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(224): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(223): Show |
1 | a0001c0001t0004g0193 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(232): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(230): Show |
1 | a0001c0001t0040g0033 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(239): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(186): Show |
1 | a0001c0001t0002g0177 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(195): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(406): Show |
1 | a0001c0028t0053g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(415): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(196): Show |
1 | a0008c0013t0055g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(205): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(356): Show |
1 | a0014c0049t0037g0125 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(365): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(391): Show |
1 | a0001c0002t0062g0167 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(400): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(493): Show |
1 | a0003c0009t0050g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(502): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(156): Show |
1 | a0001c0001t0002g0148 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(165): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(176): Show |
1 | a0001c0001t0002g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(185): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(136): Show |
1 | a0001c0001t0002g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(145): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCCCCC others(182): Show |
1 | a0001c0001t0002g0207 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(191): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCT | 5 | a0001c0001t0002g0123a0001c0001t0002g0232a0001c0001t0009g0152others(2): Show | 5 | HG01978.hp1 HG03669.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-1062_427-1061i others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCTCCC others(269): Show |
1 | a0001c0003t0001g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(278): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCTCCC others(378): Show |
1 | a0005c0047t0065g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(387): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCTCCC others(385): Show |
1 | a0001c0002t0001g0247 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(394): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCTCCC others(361): Show |
1 | a0001c0002t0001g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(370): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCTCCC others(343): Show |
1 | a0001c0002t0001g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(352): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCTCCC others(377): Show |
1 | a0021c0039t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(386): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCTCCC others(354): Show |
1 | a0001c0002t0001g0139 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.427-1062_427-1061i others(363): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | CTCCTCCC others(397): Show |
1 | a0001c0001t0001g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.427-1062_427-1061i others(406): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653216
|
C | T | 1 | a0001c0001t0003g0161 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.427-1062C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653216 | ||||||
| chr16:85653217
|
C | CTCCTCCC others(205): Show |
1 | a0002c0030t0003g0023 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.427-1061_427-1060i others(214): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653217 | ||||||
| chr16:85653217
|
C | T | 75 | a0001c0001t0001g0120a0001c0001t0001g0227a0001c0001t0002g0007others(72): Show | 75 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.427-1061C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653217 | ||||||
| chr16:85653220
|
T | C | 81 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(78): Show | 81 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.427-1058T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653220 | ||||||
| chr16:85653220
|
T | G | 3 | a0001c0001t0051g0140a0002c0008t0001g0168a0002c0008t0036g0277 | 3 | HG01891.hp2 HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.427-1058T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653220 | ||||||
| chr16:85653220
|
T | TCCTCCCC others(368): Show |
1 | a0001c0001t0007g0038 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.427-1053_427-1052i others(377): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653220 | |||||
| chr16:85653220
|
T | TCCTCCCC others(387): Show |
1 | a0001c0001t0003g0099 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.427-1053_427-1052i others(396): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653220 | |||||
| chr16:85653220
|
T | TCCTCCCC others(512): Show |
1 | a0001c0001t0027g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.427-1053_427-1052i others(521): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653220 | |||||
| chr16:85653220
|
T | TCCTCCCC others(636): Show |
1 | a0017c0044t0002g0024 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.427-1053_427-1052i others(645): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653220 | |||||
| chr16:85653220
|
T | TCCTCCCC others(485): Show |
1 | a0001c0001t0011g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.427-1053_427-1052i others(494): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653220 | |||||
| chr16:85653220
|
T | TCCTCCCC others(483): Show |
1 | a0001c0001t0011g0136 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.427-1053_427-1052i others(492): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653220 | |||||
| chr16:85653220
|
T | TCCTCCCC others(370): Show |
1 | a0001c0001t0029g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.427-1053_427-1052i others(379): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653220 | |||||
| chr16:85653221
|
CCT | C | 4 | a0001c0001t0051g0140a0002c0008t0001g0168a0002c0008t0036g0277others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-1055_427-1054d others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653221 | |||||
| chr16:85653223
|
T | C | 8 | a0001c0001t0002g0229a0001c0055t0048g0241a0002c0004t0002g0019others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.427-1055T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653223 | ||||||
| chr16:85653223
|
T | TC | 8 | a0001c0001t0003g0141a0001c0001t0007g0135a0001c0001t0016g0162others(5): Show | 8 | HG00099.hp1 HG00639.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.427-1053dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653223
|
T | TCCCC | 15 | a0001c0001t0002g0007a0001c0001t0002g0082a0001c0001t0002g0223others(12): Show | 15 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.427-1053_427-1052i others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653223
|
T | TCCCCCCC others(558): Show |
1 | a0001c0001t0003g0020 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.427-1053_427-1052i others(567): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653223
|
T | TCCCCCCT others(414): Show |
1 | a0001c0001t0002g0236 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.427-1053_427-1052i others(423): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653223
|
T | TCCCCCCT others(155): Show |
1 | a0001c0002t0007g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.427-1053_427-1052i others(164): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653223
|
T | TCCCCCCT others(506): Show |
1 | a0001c0001t0028g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.427-1053_427-1052i others(515): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653223
|
T | TCCCCCCT others(41): Show |
1 | a0001c0001t0009g0174 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.427-1053_427-1052i others(50): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653223
|
T | TCCCCCCT others(413): Show |
1 | a0001c0001t0002g0069 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.427-1053_427-1052i others(422): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653223
|
T | TCCCCCCT others(438): Show |
1 | a0001c0037t0060g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.427-1053_427-1052i others(447): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653223
|
T | TCCCCCCT others(330): Show |
1 | a0003c0010t0004g0008 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.427-1053_427-1052i others(339): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653223
|
T | TCCCCCCT others(307): Show |
1 | a0001c0035t0004g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.427-1053_427-1052i others(316): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653223
|
T | TCCTCCCC others(202): Show |
1 | a0006c0011t0013g0270 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.427-1050_427-1049i others(211): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653223 | |||||
| chr16:85653226
|
T | C | 15 | a0001c0001t0003g0141a0001c0001t0007g0135a0001c0001t0009g0198others(12): Show | 15 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.427-1052T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653226 | ||||||
| chr16:85653226
|
T | TCCCC | 16 | a0001c0002t0001g0018a0002c0004t0003g0065a0002c0004t0003g0226others(13): Show | 16 | HG01934.hp2 HG01943.hp1 HG02293.hp2 others(13): Show |
intron_variant | MODIFIER | c.427-1050_427-1049i others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653226 | |||||
| chr16:85653226
|
T | TCCCCCCT others(120): Show |
1 | a0030c0053t0001g0047 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.427-1050_427-1049i others(129): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653226 | |||||
| chr16:85653226
|
T | TCCCCCCT others(109): Show |
1 | a0002c0004t0008g0068 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.427-1050_427-1049i others(118): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653226 | |||||
| chr16:85653230
|
C | CCTCCCCC others(136): Show |
1 | a0001c0001t0009g0174 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.427-1031_427-1030i others(145): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653230 | |||||
| chr16:85653232
|
T | C | 3 | a0001c0001t0002g0173a0001c0001t0022g0021a0004c0007t0010g0091 | 3 | HG03130.hp1 NA19056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.427-1046T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653232 | ||||||
| chr16:85653233
|
C | A | 1 | a0001c0002t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.427-1045C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653233 | ||||||
| chr16:85653233
|
C | CCT | 11 | a0001c0001t0001g0120a0001c0001t0002g0007a0001c0001t0002g0082others(8): Show | 11 | HG00408.hp2 HG00738.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.427-1044_427-1043i others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653233 | |||||
| chr16:85653233
|
C | CCTCCTCC others(33): Show |
1 | a0001c0001t0022g0021 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.427-1044_427-1043i others(42): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653233 | |||||
| chr16:85653234
|
C | T | 1 | a0002c0004t0002g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.427-1044C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653234 | ||||||
| chr16:85653235
|
C | CCCCTCCT others(9): Show |
1 | a0001c0003t0001g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.427-1040_427-1025d others(18): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653235 | |||||
| chr16:85653235
|
C | CCCCTCCT others(6): Show |
1 | a0004c0007t0010g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.427-1032_427-1031i others(15): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653235 | |||||
| chr16:85653235
|
C | T | 29 | a0001c0001t0001g0234a0001c0001t0002g0146a0001c0001t0009g0198others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.427-1043C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653235 | ||||||
| chr16:85653236
|
C | CCCTCCTC others(139): Show |
1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.427-1031_427-1030i others(148): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653236 | |||||
| chr16:85653236
|
C | CCCTCCTC others(5): Show |
1 | a0002c0005t0007g0191 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.427-1032_427-1021d others(14): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653236 | |||||
| chr16:85653236
|
C | CCCTCTTC others(194): Show |
1 | a0001c0001t0002g0229 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.427-1038_427-1037i others(203): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653236 | |||||
| chr16:85653236
|
C | CCCTCTTC others(232): Show |
1 | a0001c0001t0004g0144 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.427-1038_427-1037i others(241): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653236 | |||||
| chr16:85653236
|
C | CCCTCTTC others(229): Show |
1 | a0001c0001t0004g0240 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.427-1038_427-1037i others(238): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653236 | |||||
| chr16:85653236
|
C | CCTCCTCC others(185): Show |
1 | a0002c0004t0002g0019 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.427-1041_427-1040i others(194): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653236 | |||||
| chr16:85653236
|
C | T | 29 | a0001c0001t0001g0120a0001c0001t0002g0007a0001c0001t0002g0082others(26): Show | 29 | HG00408.hp2 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.427-1042C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653236 | ||||||
| chr16:85653238
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.427-1040C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653238 | ||||||
| chr16:85653239
|
T | A | 1 | a0001c0002t0001g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.427-1039T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653239 | ||||||
| chr16:85653239
|
T | C | 12 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0236others(9): Show | 12 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.427-1039T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653239 | ||||||
| chr16:85653242
|
T | C | 1 | a0001c0002t0001g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.427-1036T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653242 | ||||||
| chr16:85653242
|
T | TCCCC | 14 | a0002c0004t0003g0065a0002c0004t0003g0226a0002c0004t0003g0276others(11): Show | 14 | HG01934.hp2 HG01943.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.427-1034_427-1033i others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653242 | |||||
| chr16:85653242
|
T | TCCCCCCC others(408): Show |
1 | a0001c0001t0003g0141 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.427-1034_427-1033i others(417): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653242 | |||||
| chr16:85653242
|
T | TCCCCCCT others(454): Show |
1 | a0003c0010t0016g0067 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.427-1034_427-1033i others(463): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653242 | |||||
| chr16:85653242
|
T | TCCCCCCT others(297): Show |
1 | a0001c0001t0016g0162 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.427-1034_427-1033i others(306): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653242 | |||||
| chr16:85653242
|
T | TCCCCCCT others(544): Show |
1 | a0002c0016t0003g0104 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.427-1034_427-1033i others(553): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653242 | |||||
| chr16:85653242
|
T | TCCCCCCT others(388): Show |
1 | a0001c0001t0007g0135 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.427-1034_427-1033i others(397): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653242 | |||||
| chr16:85653242
|
T | TCCCCCCT others(308): Show |
1 | a0001c0002t0005g0274 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.427-1034_427-1033i others(317): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653242 | |||||
| chr16:85653242
|
T | TCCTCCCC others(331): Show |
1 | a0002c0005t0063g0208 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.427-1031_427-1030i others(340): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653242 | |||||
| chr16:85653242
|
T | TCCTCCTC others(3): Show |
7 | a0001c0002t0006g0092a0001c0002t0006g0155a0001c0002t0006g0211others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.427-1034_427-1025d others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653242 | |||||
| chr16:85653243
|
CCT | C | 9 | a0001c0055t0048g0241a0002c0004t0008g0068a0002c0006t0001g0113others(6): Show | 9 | HG01109.hp2 HG01167.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.427-1033_427-1032d others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653243 | |||||
| chr16:85653245
|
T | C | 4 | a0001c0001t0003g0141a0001c0001t0007g0135a0001c0002t0007g0267others(1): Show | 4 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-1033T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653245 | ||||||
| chr16:85653245
|
T | TCCCCCCC others(20): Show |
1 | a0001c0001t0029g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.427-1031_427-1030i others(29): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653245 | |||||
| chr16:85653245
|
T | TCCCCCCC others(17): Show |
1 | a0001c0001t0007g0038 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.427-1031_427-1030i others(26): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653245 | |||||
| chr16:85653245
|
T | TCCTCCTC others(3): Show |
2 | a0001c0001t0056g0179a0001c0002t0006g0213 | 2 | HG02818.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.427-1025_427-1024i others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653245 | |||||
| chr16:85653245
|
T | TCCTCCTC others(6): Show |
1 | a0003c0009t0050g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.427-1025_427-1024i others(15): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653245 | |||||
| chr16:85653245
|
T | TCCTCCTC others(129): Show |
2 | a0001c0001t0015g0127a0001c0001t0015g0128 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.427-1025_427-1024i others(138): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653245 | |||||
| chr16:85653247
|
C | CCCCA | 5 | a0001c0001t0051g0140a0002c0006t0001g0221a0002c0008t0001g0168others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.427-1031_427-1030i others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653247 | ||||||
| chr16:85653248
|
T | C | 11 | a0001c0001t0001g0120a0001c0055t0048g0241a0002c0004t0002g0124others(8): Show | 11 | HG00408.hp2 HG01109.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.427-1030T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653248 | ||||||
| chr16:85653248
|
T | TC | 11 | a0002c0004t0003g0065a0002c0004t0003g0226a0002c0004t0003g0276others(8): Show | 11 | HG01934.hp2 HG01943.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.427-1028dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653248 | |||||
| chr16:85653248
|
T | TCCC | 5 | a0001c0001t0001g0227a0001c0001t0003g0289a0001c0001t0004g0013others(2): Show | 5 | HG03942.hp1 HG04184.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.427-1028_427-1027i others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653248 | |||||
| chr16:85653248
|
T | TCCCC | 6 | a0001c0001t0012g0010a0001c0001t0012g0210a0002c0004t0025g0048others(3): Show | 6 | HG01167.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-1028_427-1027i others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653248 | |||||
| chr16:85653249
|
C | CCTCCCCC others(4): Show |
1 | a0001c0001t0069g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.427-1025_427-1024i others(13): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653249 | |||||
| chr16:85653251
|
T | C | 12 | a0001c0001t0009g0171a0002c0004t0003g0065a0002c0004t0003g0226others(9): Show | 12 | HG00738.hp1 HG01934.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.427-1027T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653251 | ||||||
| chr16:85653251
|
T | TC | 3 | a0001c0001t0003g0170a0001c0001t0020g0156a0001c0001t0020g0217 | 3 | HG01884.hp1 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.427-1025dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653251 | |||||
| chr16:85653251
|
T | TCTCCCCT others(66): Show |
3 | a0002c0004t0008g0015a0002c0054t0032g0084a0029c0024t0023g0055 | 3 | HG03239.hp2 HG04199.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.427-1026_427-1025i others(75): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653251 | |||||
| chr16:85653253
|
C | T | 1 | a0008c0013t0055g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.427-1025C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653253 | ||||||
| chr16:85653254
|
T | C | 10 | a0001c0001t0002g0069a0001c0001t0002g0236a0001c0001t0003g0036others(7): Show | 10 | HG00609.hp2 HG01884.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.427-1024T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653254 | ||||||
| chr16:85653257
|
T | C | 20 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0236others(17): Show | 20 | HG00609.hp1 HG00609.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.427-1021T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653257 | ||||||
| chr16:85653257
|
T | TCC | 8 | a0001c0001t0001g0220a0001c0001t0002g0059a0001c0001t0002g0150others(5): Show | 8 | HG00544.hp2 HG01261.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.427-1021_427-1020i others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653257 | ||||||
| chr16:85653257
|
TA | T | 81 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(78): Show | 81 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.427-1020delA | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653257 | ||||||
| chr16:85653258
|
A | C | 156 | a0001c0001t0001g0227a0001c0001t0001g0234a0001c0001t0002g0007others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.427-1020A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653258 | ||||||
| chr16:85653258
|
A | T | 16 | a0001c0001t0001g0220a0001c0001t0002g0059a0001c0001t0002g0150others(13): Show | 16 | HG00544.hp2 HG00609.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.427-1020A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653258 | ||||||
| chr16:85653260
|
C | T | 32 | a0001c0002t0001g0017a0001c0002t0001g0083a0001c0002t0001g0102others(29): Show | 32 | HG00738.hp2 HG01109.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.427-1018C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653260 | ||||||
| chr16:85653261
|
C | T | 105 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(102): Show | 105 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.427-1017C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653261 | ||||||
| chr16:85653263
|
C | A | 8 | a0001c0055t0048g0241a0002c0006t0001g0113a0002c0006t0001g0216others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.427-1015C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653263 | ||||||
| chr16:85653264
|
T | C | 36 | a0001c0001t0003g0020a0001c0001t0003g0141a0001c0001t0003g0161others(33): Show | 36 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.427-1014T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653264 | ||||||
| chr16:85653264
|
T | TCCTCCTC others(3): Show |
2 | a0002c0017t0001g0219a0002c0017t0001g0237 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.427-1012_427-1003d others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653264 | |||||
| chr16:85653264
|
T | TCCTCCTC others(6): Show |
1 | a0001c0003t0001g0108 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.427-1003_427-1002i others(15): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653264 | |||||
| chr16:85653264
|
T | TCCTCCTC others(173): Show |
1 | a0004c0007t0010g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.427-1003_427-1002i others(182): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653264 | |||||
| chr16:85653264
|
T | TCCTCCTC others(154): Show |
1 | a0004c0007t0010g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.427-1003_427-1002i others(163): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653264 | |||||
| chr16:85653267
|
T | C | 3 | a0001c0001t0029g0044a0002c0006t0001g0221a0019c0025t0024g0275 | 3 | HG02630.hp2 HG02738.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.427-1011T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653267 | ||||||
| chr16:85653267
|
T | TCCCCCCT others(102): Show |
5 | a0002c0004t0003g0065a0002c0004t0003g0226a0002c0005t0008g0085others(2): Show | 5 | HG01934.hp2 HG02293.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-1009_427-1008i others(111): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653267 | |||||
| chr16:85653267
|
T | TCCTCCCC | 3 | a0002c0004t0008g0015a0002c0054t0032g0084a0029c0024t0023g0055 | 3 | HG03239.hp2 HG04199.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.427-1006_427-1005i others(9): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653267 | |||||
| chr16:85653267
|
T | TCCTCCTC others(72): Show |
1 | a0022c0038t0013g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.427-1000_427-999in others(80): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653267 | |||||
| chr16:85653267
|
T | TCCTCTCC others(115): Show |
1 | a0002c0004t0008g0093 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.427-1007_427-1006i others(124): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653267 | |||||
| chr16:85653267
|
T | TCCTCTCC others(132): Show |
1 | a0002c0045t0047g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.427-1007_427-1006i others(141): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653267 | |||||
| chr16:85653267
|
T | TCCTCTCC others(112): Show |
1 | a0002c0004t0003g0276 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.427-1007_427-1006i others(121): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653267 | |||||
| chr16:85653267
|
T | TCCTCTCC others(92): Show |
1 | a0002c0005t0044g0169 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.427-1007_427-1006i others(101): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653267 | |||||
| chr16:85653267
|
T | TCCTCTCC others(105): Show |
1 | a0002c0004t0045g0252 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.427-1007_427-1006i others(114): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653267 | |||||
| chr16:85653267
|
TCCTCCTC others(34): Show |
T | 3 | a0001c0001t0051g0140a0002c0008t0001g0168a0002c0008t0036g0277 | 3 | HG01891.hp2 HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.427-993_427-953del others(41): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653267 | |||||
| chr16:85653269
|
C | T | 1 | a0008c0013t0021g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.427-1009C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653269 | ||||||
| chr16:85653270
|
T | TC | 5 | a0001c0001t0004g0238a0001c0001t0012g0210a0001c0001t0039g0147others(2): Show | 5 | HG01167.hp2 HG02055.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-1006dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653270 | |||||
| chr16:85653270
|
T | TCCCC | 45 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0002g0059others(42): Show | 45 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.427-1006_427-1005i others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653270 | |||||
| chr16:85653270
|
T | TCCCCCCC others(181): Show |
1 | a0005c0046t0003g0034 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.427-1006_427-1005i others(190): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653270 | |||||
| chr16:85653270
|
T | TCCCCCCC others(159): Show |
1 | a0001c0001t0003g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.427-1006_427-1005i others(168): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653270 | |||||
| chr16:85653270
|
T | TCCCCCCT others(157): Show |
1 | a0001c0001t0003g0142 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.427-1006_427-1005i others(166): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653270 | |||||
| chr16:85653270
|
T | TCCCCCCT others(126): Show |
1 | a0001c0001t0061g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.427-1006_427-1005i others(135): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653270 | |||||
| chr16:85653270
|
T | TCCCCCCT others(177): Show |
1 | a0001c0001t0003g0036 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.427-1006_427-1005i others(186): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653270 | |||||
| chr16:85653270
|
T | TCCTCCCC others(214): Show |
1 | a0001c0001t0002g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.427-1003_427-1002i others(223): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653270 | |||||
| chr16:85653270
|
T | TCCTCCTC others(12): Show |
1 | a0024c0034t0001g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.427-973_427-955dup others(19): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653270 | |||||
| chr16:85653270
|
TCCTCCTC others(12): Show |
T | 2 | a0001c0001t0004g0235a0002c0040t0001g0064 | 2 | HG01496.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.427-973_427-955del others(19): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653270 | |||||
| chr16:85653273
|
T | C | 7 | a0001c0001t0002g0223a0001c0001t0004g0238a0001c0001t0012g0210others(4): Show | 7 | HG01167.hp2 HG01978.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.427-1005T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653273 | ||||||
| chr16:85653273
|
T | TCCCC | 36 | a0001c0001t0001g0094a0001c0001t0001g0227a0001c0001t0002g0011others(33): Show | 36 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.427-1003_427-1002i others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653273 | |||||
| chr16:85653274
|
CCT | C | 8 | a0001c0002t0001g0018a0001c0055t0048g0241a0002c0006t0001g0113others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.427-1002_427-1001d others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653274 | |||||
| chr16:85653274
|
CCTCCTCC others(5): Show |
C | 1 | a0001c0001t0002g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.427-1002_427-991de others(13): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653274 | |||||
| chr16:85653275
|
CTCCTCCT others(4): Show |
C | 1 | a0002c0008t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427-1002_427-992de others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653275 | ||||||
| chr16:85653276
|
T | C | 5 | a0001c0001t0002g0146a0001c0001t0009g0198a0001c0050t0002g0180others(2): Show | 5 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(2): Show |
intron_variant | MODIFIER | c.427-1002T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653276 | ||||||
| chr16:85653276
|
T | TC | 3 | a0001c0001t0003g0170a0007c0012t0021g0239a0010c0015t0001g0246 | 3 | HG00639.hp1 HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.427-1000dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653276 | |||||
| chr16:85653277
|
CCT | C | 11 | a0001c0001t0003g0020a0001c0001t0003g0141a0001c0001t0003g0161others(8): Show | 11 | HG00741.hp2 HG01070.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.427-999_427-998del others(2): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653277 | |||||
| chr16:85653279
|
T | C | 12 | a0001c0001t0003g0170a0001c0002t0001g0018a0001c0003t0001g0290others(9): Show | 12 | HG00639.hp2 HG01109.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.427-999T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653279 | ||||||
| chr16:85653279
|
T | TC | 4 | a0001c0001t0007g0038a0001c0001t0029g0044a0002c0016t0003g0104others(1): Show | 4 | HG00099.hp1 HG01071.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-997dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653279 | |||||
| chr16:85653279
|
T | TCCCCCCT others(170): Show |
1 | a0001c0002t0005g0274 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.427-997_427-996ins others(177): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653279 | |||||
| chr16:85653279
|
T | TCCCCCCT others(105): Show |
1 | a0001c0001t0016g0162 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.427-997_427-996ins others(112): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653279 | |||||
| chr16:85653282
|
T | C | 25 | a0001c0001t0001g0120a0001c0001t0003g0020a0001c0001t0003g0141others(22): Show | 25 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.427-996T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653282 | ||||||
| chr16:85653282
|
T | TACCC | 22 | a0001c0001t0001g0234a0001c0001t0011g0269a0001c0002t0001g0066others(19): Show | 22 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.427-996_427-995ins others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653282 | ||||||
| chr16:85653282
|
T | TCCTCCCC others(182): Show |
1 | a0001c0001t0003g0004 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.427-993_427-992ins others(189): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653282 | |||||
| chr16:85653282
|
T | TCCTCCTC others(2): Show |
7 | a0001c0001t0002g0007a0001c0001t0002g0039a0001c0001t0002g0201others(4): Show | 7 | HG01361.hp1 HG02155.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.427-993_427-992ins others(9): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653282 | |||||
| chr16:85653282
|
TCCTACCC | T | 3 | a0001c0001t0046g0105a0001c0002t0049g0233a0014c0049t0037g0125 | 3 | HG02165.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.427-992_427-986del others(7): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653282 | |||||
| chr16:85653283
|
C | A | 4 | a0001c0001t0057g0185a0001c0020t0001g0028a0002c0016t0003g0046others(1): Show | 4 | HG01106.hp1 HG02027.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-995C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653283 | ||||||
| chr16:85653284
|
CTA | C | 3 | a0001c0002t0001g0057a0001c0002t0001g0157a0004c0007t0010g0265 | 3 | HG00323.hp1 HG03516.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.427-993_427-992del others(2): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653284 | ||||||
| chr16:85653285
|
T | C | 24 | a0001c0001t0007g0135a0001c0001t0012g0210a0001c0001t0056g0179others(21): Show | 24 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.427-993T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653285 | ||||||
| chr16:85653285
|
T | TCC | 69 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0094others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.427-993_427-992ins others(2): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653285 | ||||||
| chr16:85653285
|
T | TCCTCC | 6 | a0001c0001t0004g0240a0005c0048t0003g0050a0013c0022t0030g0072others(3): Show | 6 | HG01978.hp2 HG02300.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-993_427-992ins others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653285 | ||||||
| chr16:85653285
|
T | TCCTCCCC others(124): Show |
1 | a0001c0001t0002g0097 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.427-993_427-992ins others(131): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653285 | ||||||
| chr16:85653285
|
TA | T | 46 | a0001c0001t0001g0026a0001c0001t0002g0062a0001c0001t0002g0073others(43): Show | 46 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.427-992delA | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653285 | ||||||
| chr16:85653285
|
TACCC | T | 3 | a0001c0001t0002g0082a0001c0002t0002g0052a0001c0002t0018g0283 | 3 | HG01993.hp2 HG02818.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.427-992_427-989del others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653285 | ||||||
| chr16:85653286
|
A | C | 105 | a0001c0001t0001g0120a0001c0001t0001g0220a0001c0001t0001g0227others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.427-992A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653286 | ||||||
| chr16:85653286
|
A | T | 81 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0094others(78): Show | 81 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.427-992A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653286 | ||||||
| chr16:85653286
|
ACCCCCTC others(13): Show |
A | 1 | a0004c0007t0064g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.427-987_427-968del others(20): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653286 | |||||
| chr16:85653287
|
CCCCCTCC others(11): Show |
C | 1 | a0004c0007t0052g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.427-986_427-969del others(18): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653287 | |||||
| chr16:85653288
|
C | A | 7 | a0001c0055t0048g0241a0002c0006t0001g0113a0002c0006t0001g0216others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.427-990C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653288 | ||||||
| chr16:85653288
|
C | T | 15 | a0001c0001t0003g0170a0002c0004t0002g0124a0002c0004t0003g0065others(12): Show | 15 | HG01884.hp1 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.427-990C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653288 | ||||||
| chr16:85653289
|
C | CCCCTCCT others(3): Show |
3 | a0001c0002t0001g0083a0001c0003t0001g0108a0002c0008t0070g0060 | 3 | HG00738.hp2 HG01106.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.427-987_427-986ins others(10): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653289 | |||||
| chr16:85653289
|
C | CCCTCCT | 9 | a0001c0002t0006g0092a0001c0002t0006g0155a0001c0002t0006g0184others(6): Show | 9 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.427-979_427-974dup others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653289 | |||||
| chr16:85653289
|
C | CCCTCCTC others(2): Show |
23 | a0001c0002t0001g0017a0001c0002t0001g0102a0001c0002t0001g0139others(20): Show | 23 | HG01358.hp2 HG01433.hp1 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.427-982_427-974dup others(9): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653289 | |||||
| chr16:85653289
|
C | CCCTCCTC others(5): Show |
2 | a0001c0002t0001g0261a0002c0005t0001g0077 | 2 | HG02976.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.427-985_427-974dup others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653289 | |||||
| chr16:85653289
|
C | CCTCCTCC others(222): Show |
1 | a0004c0007t0010g0265 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.427-988_427-987ins others(229): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653289 | |||||
| chr16:85653289
|
C | CCTCCTCC others(26): Show |
2 | a0001c0002t0001g0057a0001c0002t0001g0157 | 2 | HG00323.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.427-988_427-987ins others(33): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653289 | |||||
| chr16:85653289
|
C | CTCCTCCT | 4 | a0001c0001t0057g0185a0001c0002t0026g0203a0001c0020t0001g0028others(1): Show | 4 | HG00423.hp2 HG01106.hp1 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-989_427-988ins others(7): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653289 | ||||||
| chr16:85653289
|
C | T | 134 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.427-989C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653289 | ||||||
| chr16:85653291
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.427-987C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653291 | ||||||
| chr16:85653292
|
T | C | 16 | a0001c0001t0003g0099a0001c0001t0003g0170a0002c0004t0002g0124others(13): Show | 16 | HG00609.hp1 HG01884.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.427-986T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653292 | ||||||
| chr16:85653295
|
T | C | 2 | a0001c0001t0003g0170a0001c0001t0017g0243 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.427-983T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653295 | ||||||
| chr16:85653295
|
T | TCCTCCTC others(131): Show |
1 | a0001c0001t0003g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.427-974_427-973ins others(138): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653295 | |||||
| chr16:85653295
|
TCCTCCTC others(6): Show |
T | 1 | a0002c0008t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427-973_427-961del others(13): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653295 | |||||
| chr16:85653298
|
T | C | 1 | a0001c0051t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.427-980T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653298 | ||||||
| chr16:85653301
|
T | C | 108 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(105): Show | 108 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.427-977T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653301 | ||||||
| chr16:85653301
|
T | TCCCCCCC others(63): Show |
1 | a0001c0050t0002g0180 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.427-975_427-974ins others(70): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653301 | |||||
| chr16:85653301
|
T | TCCCCCCC others(64): Show |
1 | a0001c0001t0001g0227 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.427-975_427-974ins others(71): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653301 | |||||
| chr16:85653301
|
T | TCCCCCCT others(133): Show |
3 | a0001c0001t0004g0013a0001c0001t0004g0053a0001c0002t0001g0195 | 3 | HG03942.hp1 HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.427-975_427-974ins others(140): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653301 | |||||
| chr16:85653301
|
T | TCCCCCCT others(67): Show |
3 | a0001c0001t0002g0146a0001c0001t0009g0198a0023c0031t0002g0280 | 3 | HG00099.hp2 HG00323.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.427-975_427-974ins others(74): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653301 | |||||
| chr16:85653301
|
T | TCCTCCCC others(150): Show |
1 | a0001c0001t0003g0099 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.427-974_427-973ins others(157): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653301 | |||||
| chr16:85653301
|
T | TCCTCCCC others(8): Show |
1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.427-974_427-973ins others(15): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653301 | |||||
| chr16:85653301
|
T | TCCTCCTC others(8): Show |
1 | a0001c0001t0001g0220 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.427-974_427-973ins others(15): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653301 | |||||
| chr16:85653301
|
T | TCCTCCTC others(11): Show |
3 | a0001c0001t0002g0173a0001c0001t0003g0289a0008c0013t0021g0284 | 3 | HG02572.hp1 NA19007.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.427-974_427-973ins others(18): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653301 | |||||
| chr16:85653301
|
T | TCCTCCTC others(14): Show |
1 | a0003c0010t0004g0008 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.427-974_427-973ins others(21): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653301 | |||||
| chr16:85653301
|
T | TCCTCCTC others(17): Show |
1 | a0002c0005t0007g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.427-974_427-973ins others(24): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653301 | |||||
| chr16:85653302
|
C | A | 1 | a0001c0002t0001g0288 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.427-976C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653302 | ||||||
| chr16:85653304
|
T | C | 33 | a0001c0001t0002g0223a0001c0001t0056g0179a0001c0001t0068g0054others(30): Show | 33 | HG00438.hp1 HG01109.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.427-974T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653304 | ||||||
| chr16:85653304
|
T | TC | 4 | a0001c0001t0002g0073a0001c0001t0002g0123a0001c0001t0002g0231others(1): Show | 4 | HG01978.hp1 HG02015.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.427-974_427-973ins others(1): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653304 | ||||||
| chr16:85653304
|
T | TCCCTCCT others(4): Show |
1 | a0007c0012t0034g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427-974_427-973ins others(11): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653304 | ||||||
| chr16:85653304
|
T | TCCTCCTC others(3): Show |
2 | a0002c0017t0001g0219a0004c0007t0010g0091 | 2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.427-974_427-973ins others(10): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653304 | ||||||
| chr16:85653304
|
T | TCCTCCTC others(10): Show |
1 | a0001c0001t0009g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.427-974_427-973ins others(17): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653304 | ||||||
| chr16:85653305
|
A | C | 189 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.427-973A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653305 | ||||||
| chr16:85653305
|
A | T | 12 | a0001c0001t0009g0171a0001c0001t0012g0010a0001c0050t0002g0180others(9): Show | 12 | HG01109.hp2 HG01167.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.427-973A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653305 | ||||||
| chr16:85653307
|
C | CCCCTCCT others(3): Show |
9 | a0001c0002t0006g0092a0001c0002t0006g0155a0001c0002t0006g0184others(6): Show | 9 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.427-968_427-959dup others(10): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653307 | |||||
| chr16:85653307
|
C | T | 1 | a0001c0001t0022g0021 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.427-971C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653307 | ||||||
| chr16:85653308
|
C | CCCTCCTC others(117): Show |
1 | a0003c0010t0002g0110 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.427-956_427-955ins others(124): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653308 | |||||
| chr16:85653308
|
C | CCTCCCCC others(5): Show |
1 | a0001c0001t0002g0039 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.427-969_427-968ins others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653308 | |||||
| chr16:85653308
|
C | T | 35 | a0001c0001t0002g0223a0001c0001t0012g0010a0001c0001t0068g0054others(32): Show | 35 | HG00438.hp1 HG01109.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.427-970C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653308 | ||||||
| chr16:85653317
|
T | TCCTCCTC others(3): Show |
4 | a0001c0001t0068g0054a0001c0002t0062g0167a0006c0011t0019g0282others(1): Show | 4 | HG00438.hp1 HG02155.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.427-952_427-951ins others(10): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653317 | |||||
| chr16:85653317
|
T | TCCTCCTC others(6): Show |
2 | a0003c0009t0050g0134a0006c0011t0013g0230 | 2 | HG02027.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.427-953_427-952ins others(13): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653317 | |||||
| chr16:85653317
|
T | TCCTCCTC others(94): Show |
1 | a0006c0011t0013g0270 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.427-953_427-952ins others(101): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653317 | |||||
| chr16:85653323
|
T | TCCCCCCT others(189): Show |
1 | a0001c0001t0069g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.427-952_427-951ins others(196): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653323 | |||||
| chr16:85653327
|
A | C | 1 | a0001c0001t0069g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.427-951A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653327 | ||||||
| chr16:85653328
|
C | T | 1 | a0001c0002t0001g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.427-950C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653328 | ||||||
| chr16:85653330
|
T | C | 1 | a0001c0001t0069g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.427-948T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653330 | ||||||
| chr16:85653391
|
C | T | 2 | a0001c0001t0002g0012a0001c0001t0002g0224 | 2 | NA18946.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.427-887C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653391 | ||||||
| chr16:85653396
|
C | T | 1 | a0001c0002t0001g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.427-882C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653396 | ||||||
| chr16:85653536
|
C | T | 1 | a0002c0004t0002g0019 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.427-742C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653536 | ||||||
| chr16:85653542
|
A | G | 42 | a0001c0001t0002g0223a0001c0001t0012g0010a0001c0001t0012g0210others(39): Show | 42 | HG00438.hp1 HG01109.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.427-736A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653542 | ||||||
| chr16:85653546
|
C | T | 1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.427-732C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653546 | ||||||
| chr16:85653560
|
C | G | 20 | a0001c0001t0002g0223a0002c0004t0002g0124a0002c0004t0003g0065others(17): Show | 20 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.427-718C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653560 | ||||||
| chr16:85653619
|
C | T | 2 | a0001c0001t0035g0286a0001c0002t0005g0078 | 2 | HG01081.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.427-659C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653619 | ||||||
| chr16:85653630
|
A | G | 1 | a0001c0001t0002g0039 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.427-648A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653630 | ||||||
| chr16:85653638
|
A | AC | 19 | a0001c0001t0001g0227a0001c0001t0002g0073a0001c0001t0002g0149others(16): Show | 19 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.427-636dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 85653638 | |||||
| chr16:85653658
|
G | A | 1 | a0004c0007t0010g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.427-620G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653658 | ||||||
| chr16:85653704
|
C | T | 1 | a0001c0051t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.427-574C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653704 | ||||||
| chr16:85653759
|
C | T | 2 | a0008c0013t0021g0284a0008c0013t0055g0119 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.427-519C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653759 | ||||||
| chr16:85653809
|
G | C | 7 | a0001c0001t0068g0054a0001c0002t0062g0167a0003c0009t0050g0134others(4): Show | 7 | HG00438.hp1 HG01255.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.427-469G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653809 | ||||||
| chr16:85653823
|
G | A | 3 | a0001c0002t0018g0194a0001c0002t0018g0283a0026c0032t0010g0061 | 3 | HG02818.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.427-455G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653823 | ||||||
| chr16:85653846
|
A | C | 1 | a0001c0001t0040g0033 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.427-432A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653846 | ||||||
| chr16:85653858
|
G | A | 2 | a0001c0002t0001g0083a0001c0002t0005g0081 | 2 | HG01109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.427-420G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653858 | ||||||
| chr16:85653863
|
A | G | 1 | a0001c0002t0005g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.427-415A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653863 | ||||||
| chr16:85653896
|
C | G | 20 | a0001c0001t0002g0223a0002c0004t0002g0124a0002c0004t0003g0065others(17): Show | 20 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.427-382C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653896 | ||||||
| chr16:85653909
|
T | C | 1 | a0001c0001t0003g0141 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.427-369T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653909 | ||||||
| chr16:85653923
|
G | A | 2 | a0001c0001t0002g0229a0031c0019t0002g0249 | 2 | HG00738.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.427-355G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653923 | ||||||
| chr16:85653954
|
G | T | 1 | a0001c0001t0066g0192 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.427-324G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653954 | ||||||
| chr16:85653978
|
C | G | 6 | a0004c0007t0010g0045a0004c0007t0010g0091a0004c0007t0010g0116others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-300C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85653978 | ||||||
| chr16:85654117
|
A | C | 1 | a0001c0001t0058g0051 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.427-161A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85654117 | ||||||
| chr16:85654174
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0135 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.427-104G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85654174 | ||||||
| chr16:85654266
|
C | A | 3 | a0006c0011t0013g0230a0006c0011t0013g0270a0006c0011t0019g0282 | 3 | HG01255.hp1 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.427-12C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85654266 | ||||||
| chr16:85654266
|
C | T | 1 | a0001c0001t0009g0174 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.427-12C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 3/15 | chr16 | 85654266 | ||||||
| chr16:85654557
|
C | CT | 4 | a0001c0001t0003g0020a0001c0001t0011g0002a0001c0001t0011g0136others(1): Show | 4 | HG01070.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.599+108dupT | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | 85654557 | |||||
| chr16:85654700
|
C | T | 1 | a0001c0001t0040g0033 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.600-94C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 4/15 | chr16 | 85654700 | ||||||
| chr16:85654735
|
C | T | 18 | a0001c0001t0002g0223a0002c0004t0002g0124a0002c0004t0003g0065others(15): Show | 18 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.600-59C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 4/15 | chr16 | 85654735 | ||||||
| chr16:85654763
|
T | TC | 4 | a0001c0001t0001g0026a0001c0002t0005g0118a0006c0011t0013g0270others(1): Show | 4 | HG00673.hp2 HG01255.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.600-27dupC | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | 85654763 | |||||
| chr16:85654780
|
A | G | 1 | a0002c0006t0001g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.600-14A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 4/15 | chr16 | 85654780 | ||||||
| chr16:85655008
|
G | A | 1 | a0001c0001t0002g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.797+17G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 5/15 | chr16 | 85655008 | ||||||
| chr16:85655065
|
G | A | 1 | a0014c0049t0037g0125 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.797+74G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 5/15 | chr16 | 85655065 | ||||||
| chr16:85655442
|
C | T | 1 | a0002c0045t0047g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.798-284C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 5/15 | chr16 | 85655442 | ||||||
| chr16:85655546
|
G | C | 1 | a0001c0001t0002g0062 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.798-180G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 5/15 | chr16 | 85655546 | ||||||
| chr16:85655547
|
C | A | 1 | a0001c0055t0048g0241 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.798-179C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 5/15 | chr16 | 85655547 | ||||||
| chr16:85655708
|
C | T | 3 | a0001c0001t0003g0036a0001c0001t0061g0158a0005c0046t0003g0034 | 3 | HG00609.hp2 HG02129.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.798-18C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 5/15 | chr16 | 85655708 | ||||||
| chr16:85656047
|
A | G | 115 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.989+130A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 6/15 | chr16 | 85656047 | ||||||
| chr16:85656057
|
A | G | 2 | a0007c0012t0021g0239a0007c0012t0034g0214 | 2 | HG00639.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.989+140A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 6/15 | chr16 | 85656057 | ||||||
| chr16:85656090
|
T | G | 1 | a0016c0029t0003g0100 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.989+173T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 6/15 | chr16 | 85656090 | ||||||
| chr16:85656103
|
G | A | 1 | a0001c0051t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.989+186G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 6/15 | chr16 | 85656103 | ||||||
| chr16:85656115
|
A | T | 1 | a0003c0010t0004g0008 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.989+198A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 6/15 | chr16 | 85656115 | ||||||
| chr16:85656236
|
A | G | 9 | a0001c0002t0001g0066a0001c0002t0005g0043a0001c0002t0005g0078others(6): Show | 9 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.990-107A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 6/15 | chr16 | 85656236 | ||||||
| chr16:85656300
|
T | C | 4 | a0001c0001t0067g0111a0008c0013t0021g0284a0008c0013t0055g0119others(1): Show | 4 | HG01167.hp2 HG01243.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.990-43T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 6/15 | chr16 | 85656300 | ||||||
| chr16:85656329
|
T | C | 3 | a0001c0002t0001g0172a0001c0002t0014g0204a0001c0002t0026g0203 | 3 | HG00423.hp2 NA19056.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.990-14T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 6/15 | chr16 | 85656329 | ||||||
| chr16:85656331
|
C | T | 4 | a0002c0008t0001g0168a0002c0008t0001g0218a0002c0008t0036g0277others(1): Show | 4 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.990-12C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 6/15 | chr16 | 85656331 | ||||||
| chr16:85656714
|
G | A | 1 | a0001c0001t0043g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1312+49G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85656714 | ||||||
| chr16:85656732
|
G | A | 43 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(40): Show | 43 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.1312+67G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85656732 | ||||||
| chr16:85656748
|
G | A | 1 | a0001c0001t0002g0073 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1312+83G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85656748 | ||||||
| chr16:85656789
|
C | G | 12 | a0002c0006t0001g0113a0002c0006t0001g0216a0002c0006t0001g0221others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1312+124C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85656789 | ||||||
| chr16:85656887
|
T | C | 1 | a0003c0009t0050g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1312+222T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85656887 | ||||||
| chr16:85656891
|
C | T | 5 | a0002c0008t0001g0168a0002c0008t0001g0218a0002c0008t0036g0277others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312+226C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85656891 | ||||||
| chr16:85656906
|
G | C | 12 | a0002c0006t0001g0113a0002c0006t0001g0216a0002c0006t0001g0221others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1312+241G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85656906 | ||||||
| chr16:85656920
|
C | G | 2 | a0001c0001t0020g0156a0001c0001t0020g0217 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1312+255C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85656920 | ||||||
| chr16:85657125
|
G | A | 12 | a0002c0006t0001g0113a0002c0006t0001g0216a0002c0006t0001g0221others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1313-152G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85657125 | ||||||
| chr16:85657145
|
C | T | 119 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(116): Show | 119 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1313-132C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85657145 | ||||||
| chr16:85657153
|
T | A | 3 | a0001c0002t0001g0247a0001c0002t0001g0288a0021c0039t0001g0271 | 3 | HG02258.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1313-124T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85657153 | ||||||
| chr16:85657160
|
G | A | 1 | a0002c0004t0008g0093 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1313-117G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85657160 | ||||||
| chr16:85657180
|
G | C | 20 | a0002c0004t0002g0124a0002c0004t0003g0065a0002c0004t0003g0226others(17): Show | 20 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.1313-97G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85657180 | ||||||
| chr16:85657199
|
G | T | 1 | a0007c0012t0034g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1313-78G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | chr16 | 85657199 | ||||||
| chr16:85657272
|
C | CA | 44 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(41): Show | 44 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(41): Show |
splice_region_variant&intron_variant | LOW | c.1313-4dupA | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 85657272 | |||||
| chr16:85657687
|
C | T | 16 | a0002c0004t0003g0065a0002c0004t0003g0276a0002c0004t0008g0015others(13): Show | 16 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1640+83C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85657687 | ||||||
| chr16:85657688
|
A | G | 267 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1640+84A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85657688 | ||||||
| chr16:85657731
|
TCTTTCAT others(13): Show |
T | 1 | a0016c0029t0003g0100 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1640+128_1640+147d others(22): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85657731 | ||||||
| chr16:85657747
|
T | C | 1 | a0001c0002t0006g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1640+143T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85657747 | ||||||
| chr16:85657771
|
G | A | 1 | a0001c0001t0012g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1640+167G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85657771 | ||||||
| chr16:85657836
|
A | G | 6 | a0004c0007t0010g0045a0004c0007t0010g0091a0004c0007t0010g0116others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1640+232A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85657836 | ||||||
| chr16:85657946
|
T | C | 1 | a0029c0024t0023g0055 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1640+342T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85657946 | ||||||
| chr16:85657956
|
C | G | 3 | a0002c0004t0002g0124a0002c0004t0003g0226a0020c0042t0008g0042 | 3 | HG03239.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1640+352C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85657956 | ||||||
| chr16:85658032
|
A | G | 1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1640+428A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658032 | ||||||
| chr16:85658076
|
G | A | 1 | a0001c0001t0035g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1640+472G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658076 | ||||||
| chr16:85658167
|
C | G | 6 | a0002c0006t0001g0113a0002c0006t0001g0216a0002c0006t0001g0222others(3): Show | 6 | HG01109.hp2 HG02970.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1640+563C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658167 | ||||||
| chr16:85658302
|
G | C | 19 | a0002c0004t0002g0124a0002c0004t0003g0065a0002c0004t0003g0226others(16): Show | 19 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1640+698G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658302 | ||||||
| chr16:85658330
|
C | T | 207 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1640+726C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658330 | ||||||
| chr16:85658337
|
C | T | 13 | a0001c0001t0046g0105a0001c0001t0068g0054a0001c0002t0018g0194others(10): Show | 13 | HG00438.hp1 HG01167.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1640+733C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658337 | ||||||
| chr16:85658497
|
C | T | 1 | a0014c0049t0037g0125 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1640+893C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658497 | ||||||
| chr16:85658546
|
G | A | 1 | a0001c0001t0017g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1640+942G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658546 | ||||||
| chr16:85658655
|
G | A | 5 | a0001c0001t0002g0082a0001c0001t0002g0107a0001c0001t0002g0148others(2): Show | 5 | HG01928.hp2 HG01943.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640+1051G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658655 | ||||||
| chr16:85658727
|
A | C | 8 | a0002c0006t0001g0113a0002c0006t0001g0216a0002c0006t0001g0221others(5): Show | 8 | HG01109.hp2 HG02630.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1640+1123A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658727 | ||||||
| chr16:85658757
|
C | G | 1 | a0001c0002t0001g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1640+1153C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658757 | ||||||
| chr16:85658804
|
C | CTTCT | 52 | a0001c0001t0001g0094a0001c0001t0002g0041a0001c0001t0002g0069others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1640+1202_1640+120 others(8): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 85658804 | |||||
| chr16:85658863
|
G | A | 12 | a0002c0006t0001g0113a0002c0006t0001g0216a0002c0006t0001g0221others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1640+1259G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658863 | ||||||
| chr16:85658865
|
C | G | 1 | a0002c0005t0007g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1640+1261C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658865 | ||||||
| chr16:85658992
|
T | C | 216 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1640+1388T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85658992 | ||||||
| chr16:85659120
|
G | T | 6 | a0004c0007t0010g0045a0004c0007t0010g0091a0004c0007t0010g0116others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1640+1516G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85659120 | ||||||
| chr16:85659161
|
G | A | 2 | a0004c0007t0010g0116a0004c0007t0010g0265 | 2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1640+1557G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85659161 | ||||||
| chr16:85659459
|
G | A | 1 | a0001c0001t0017g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1641-1687G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85659459 | ||||||
| chr16:85659511
|
T | C | 13 | a0001c0037t0060g0114a0002c0006t0001g0113a0002c0006t0001g0216others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1641-1635T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85659511 | ||||||
| chr16:85659529
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1641-1617G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85659529 | ||||||
| chr16:85659633
|
G | A | 1 | a0001c0037t0060g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1641-1513G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85659633 | ||||||
| chr16:85659634
|
C | A | 1 | a0001c0001t0058g0051 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1641-1512C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85659634 | ||||||
| chr16:85659642
|
C | T | 4 | a0007c0012t0021g0239a0007c0012t0034g0214a0008c0013t0021g0284others(1): Show | 4 | HG00639.hp1 HG01891.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1641-1504C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85659642 | ||||||
| chr16:85659826
|
C | G | 6 | a0001c0001t0003g0096a0001c0001t0003g0170a0001c0001t0003g0187others(3): Show | 6 | HG00741.hp1 HG01123.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1641-1320C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85659826 | ||||||
| chr16:85660044
|
G | A | 1 | a0001c0003t0001g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1641-1102G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660044 | ||||||
| chr16:85660072
|
G | T | 1 | a0001c0001t0043g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1641-1074G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660072 | ||||||
| chr16:85660087
|
C | T | 1 | a0001c0002t0026g0203 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1641-1059C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660087 | ||||||
| chr16:85660107
|
C | G | 1 | a0001c0001t0035g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1641-1039C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660107 | ||||||
| chr16:85660154
|
C | G | 13 | a0001c0001t0068g0054a0001c0002t0018g0194a0001c0002t0018g0283others(10): Show | 13 | HG00438.hp1 HG01167.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1641-992C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660154 | ||||||
| chr16:85660188
|
C | T | 1 | a0001c0002t0026g0203 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1641-958C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660188 | ||||||
| chr16:85660233
|
A | T | 1 | a0001c0001t0002g0200 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1641-913A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660233 | ||||||
| chr16:85660270
|
G | A | 2 | a0001c0002t0005g0043a0001c0002t0005g0143 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1641-876G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660270 | ||||||
| chr16:85660285
|
T | C | 4 | a0001c0001t0002g0232a0001c0001t0041g0035a0001c0001t0056g0179others(1): Show | 4 | HG00597.hp1 HG02129.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.1641-861T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660285 | ||||||
| chr16:85660319
|
G | T | 1 | a0001c0001t0001g0227 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1641-827G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660319 | ||||||
| chr16:85660341
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1641-805C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660341 | ||||||
| chr16:85660376
|
C | A | 1 | a0023c0031t0002g0280 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1641-770C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660376 | ||||||
| chr16:85660468
|
C | T | 1 | a0001c0001t0012g0212 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1641-678C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660468 | ||||||
| chr16:85660524
|
A | G | 194 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1641-622A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660524 | ||||||
| chr16:85660526
|
C | T | 1 | a0001c0001t0011g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1641-620C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660526 | ||||||
| chr16:85660567
|
A | G | 1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1641-579A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660567 | ||||||
| chr16:85660779
|
C | A | 13 | a0001c0037t0060g0114a0002c0006t0001g0113a0002c0006t0001g0216others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1641-367C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660779 | ||||||
| chr16:85660829
|
A | G | 1 | a0001c0001t0005g0027 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1641-317A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660829 | ||||||
| chr16:85660865
|
T | C | 68 | a0001c0001t0001g0094a0001c0001t0001g0227a0001c0001t0003g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1641-281T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660865 | ||||||
| chr16:85660876
|
C | G | 6 | a0004c0007t0010g0045a0004c0007t0010g0091a0004c0007t0010g0116others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1641-270C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660876 | ||||||
| chr16:85660918
|
C | G | 1 | a0002c0005t0044g0169 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1641-228C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660918 | ||||||
| chr16:85660926
|
G | C | 1 | a0001c0001t0002g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1641-220G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660926 | ||||||
| chr16:85660929
|
C | T | 1 | a0002c0004t0045g0252 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1641-217C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660929 | ||||||
| chr16:85660987
|
G | A | 1 | a0002c0004t0002g0019 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1641-159G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85660987 | ||||||
| chr16:85661069
|
C | T | 1 | a0002c0045t0047g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1641-77C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85661069 | ||||||
| chr16:85661132
|
G | C | 14 | a0001c0001t0051g0140a0001c0037t0060g0114a0002c0006t0001g0113others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1641-14G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 8/15 | chr16 | 85661132 | ||||||
| chr16:85661852
|
C | T | 1 | a0001c0001t0069g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2260+87C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85661852 | ||||||
| chr16:85661895
|
T | G | 4 | a0001c0001t0012g0010a0001c0001t0012g0210a0001c0001t0012g0212others(1): Show | 4 | HG02055.hp2 HG03486.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2260+130T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85661895 | ||||||
| chr16:85661963
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2260+198G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85661963 | ||||||
| chr16:85662051
|
G | A | 1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2260+286G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662051 | ||||||
| chr16:85662081
|
A | C | 1 | a0001c0002t0005g0126 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2260+316A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662081 | ||||||
| chr16:85662128
|
G | T | 1 | a0001c0021t0033g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2260+363G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662128 | ||||||
| chr16:85662192
|
C | T | 1 | a0001c0002t0002g0250 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2260+427C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662192 | ||||||
| chr16:85662250
|
TG | T | 13 | a0001c0037t0060g0114a0002c0006t0001g0113a0002c0006t0001g0216others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2260+490delG | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 85662250 | |||||
| chr16:85662253
|
G | T | 13 | a0001c0037t0060g0114a0002c0006t0001g0113a0002c0006t0001g0216others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2260+488G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662253 | ||||||
| chr16:85662262
|
G | A | 1 | a0001c0001t0004g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2260+497G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662262 | ||||||
| chr16:85662275
|
G | A | 2 | a0002c0005t0008g0085a0008c0013t0055g0119 | 2 | HG01891.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2260+510G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662275 | ||||||
| chr16:85662320
|
CGA | C | 3 | a0001c0002t0001g0102a0001c0002t0001g0139a0005c0047t0065g0088 | 3 | HG02717.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2260+559_2260+560d others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 85662320 | |||||
| chr16:85662321
|
G | A | 1 | a0001c0001t0004g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2260+556G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662321 | ||||||
| chr16:85662351
|
G | A | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2260+586G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662351 | ||||||
| chr16:85662360
|
T | C | 13 | a0001c0037t0060g0114a0002c0006t0001g0113a0002c0006t0001g0216others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2260+595T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662360 | ||||||
| chr16:85662529
|
C | T | 1 | a0001c0001t0046g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2261-452C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662529 | ||||||
| chr16:85662582
|
C | CTG | 19 | a0001c0001t0002g0069a0001c0001t0046g0105a0001c0002t0019g0145others(16): Show | 19 | HG01167.hp1 HG01257.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2261-392_2261-391d others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 85662582 | |||||
| chr16:85662598
|
C | T | 13 | a0001c0037t0060g0114a0002c0006t0001g0113a0002c0006t0001g0216others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2261-383C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662598 | ||||||
| chr16:85662623
|
C | T | 1 | a0001c0002t0001g0263 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2261-358C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662623 | ||||||
| chr16:85662652
|
G | C | 1 | a0002c0004t0003g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2261-329G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662652 | ||||||
| chr16:85662669
|
T | C | 1 | a0001c0001t0046g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2261-312T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662669 | ||||||
| chr16:85662742
|
G | A | 1 | a0001c0003t0001g0290 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2261-239G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662742 | ||||||
| chr16:85662792
|
G | A | 1 | a0002c0045t0047g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2261-189G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662792 | ||||||
| chr16:85662806
|
C | T | 77 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(74): Show | 77 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.2261-175C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662806 | ||||||
| chr16:85662918
|
G | A | 1 | a0025c0033t0038g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2261-63G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 9/15 | chr16 | 85662918 | ||||||
| chr16:85663114
|
C | T | 30 | a0001c0001t0046g0105a0001c0001t0068g0054a0001c0002t0018g0194others(27): Show | 30 | HG00438.hp1 HG00639.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.2373+21C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 10/15 | chr16 | 85663114 | ||||||
| chr16:85663119
|
A | G | 1 | a0001c0001t0016g0162 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2373+26A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 10/15 | chr16 | 85663119 | ||||||
| chr16:85663170
|
C | A | 1 | a0001c0003t0001g0259 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2373+77C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 10/15 | chr16 | 85663170 | ||||||
| chr16:85663272
|
G | A | 1 | a0001c0036t0006g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2374-72G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 10/15 | chr16 | 85663272 | ||||||
| chr16:85663280
|
C | T | 1 | a0002c0004t0025g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2374-64C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 10/15 | chr16 | 85663280 | ||||||
| chr16:85663625
|
G | T | 1 | a0007c0012t0021g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2644+11G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85663625 | ||||||
| chr16:85663652
|
G | A | 6 | a0004c0007t0010g0045a0004c0007t0010g0091a0004c0007t0010g0116others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2644+38G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85663652 | ||||||
| chr16:85663711
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0005g0027 | 2 | HG00735.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2644+97C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85663711 | ||||||
| chr16:85663820
|
A | C | 1 | a0002c0045t0047g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2644+206A>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85663820 | ||||||
| chr16:85663929
|
G | C | 1 | a0001c0003t0001g0108 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2644+315G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85663929 | ||||||
| chr16:85664000
|
T | A | 3 | a0001c0002t0001g0102a0001c0002t0001g0139a0005c0047t0065g0088 | 3 | HG02717.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2644+386T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664000 | ||||||
| chr16:85664128
|
C | A | 1 | a0001c0002t0005g0126 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2644+514C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664128 | ||||||
| chr16:85664164
|
G | A | 1 | a0025c0033t0038g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2644+550G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664164 | ||||||
| chr16:85664239
|
G | T | 1 | a0001c0001t0005g0027 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2644+625G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664239 | ||||||
| chr16:85664296
|
C | G | 1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2644+682C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664296 | ||||||
| chr16:85664416
|
C | G | 1 | a0002c0045t0047g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2645-599C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664416 | ||||||
| chr16:85664419
|
A | G | 15 | a0001c0001t0017g0243a0001c0021t0033g0225a0001c0037t0060g0114others(12): Show | 15 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2645-596A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664419 | ||||||
| chr16:85664432
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2645-583C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664432 | ||||||
| chr16:85664447
|
C | T | 1 | a0002c0016t0003g0046 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2645-568C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664447 | ||||||
| chr16:85664473
|
T | C | 15 | a0001c0021t0033g0225a0001c0037t0060g0114a0002c0006t0001g0113others(12): Show | 15 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2645-542T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664473 | ||||||
| chr16:85664473
|
T | G | 161 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(158): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.2645-542T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664473 | ||||||
| chr16:85664670
|
G | A | 2 | a0002c0017t0001g0219a0002c0017t0001g0237 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2645-345G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664670 | ||||||
| chr16:85664675
|
T | C | 6 | a0004c0007t0010g0045a0004c0007t0010g0091a0004c0007t0010g0116others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2645-340T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664675 | ||||||
| chr16:85664723
|
C | T | 1 | a0001c0001t0058g0051 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2645-292C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664723 | ||||||
| chr16:85664724
|
G | A | 1 | a0001c0001t0020g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2645-291G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664724 | ||||||
| chr16:85664776
|
C | T | 1 | a0001c0001t0004g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2645-239C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664776 | ||||||
| chr16:85664790
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2645-225T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664790 | ||||||
| chr16:85664792
|
T | C | 1 | a0002c0045t0047g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2645-223T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664792 | ||||||
| chr16:85664827
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2645-188C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664827 | ||||||
| chr16:85664965
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2645-50C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 11/15 | chr16 | 85664965 | ||||||
| chr16:85665204
|
G | C | 1 | a0002c0004t0003g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2758+76G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665204 | ||||||
| chr16:85665234
|
T | C | 2 | a0001c0037t0060g0114a0002c0008t0070g0060 | 2 | HG00738.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2758+106T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665234 | ||||||
| chr16:85665269
|
C | T | 15 | a0001c0021t0033g0225a0001c0037t0060g0114a0002c0004t0002g0124others(12): Show | 15 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2758+141C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665269 | ||||||
| chr16:85665295
|
T | C | 1 | a0001c0001t0002g0278 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2758+167T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665295 | ||||||
| chr16:85665296
|
T | G | 14 | a0001c0021t0033g0225a0001c0037t0060g0114a0002c0006t0001g0113others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2758+168T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665296 | ||||||
| chr16:85665304
|
A | G | 1 | a0001c0001t0003g0020 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2758+176A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665304 | ||||||
| chr16:85665326
|
CAG | C | 18 | a0001c0001t0012g0010a0001c0001t0012g0210a0001c0001t0012g0212others(15): Show | 18 | HG00438.hp1 HG01167.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.2758+201_2758+202d others(4): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 85665326 | |||||
| chr16:85665433
|
A | G | 1 | a0001c0001t0002g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2758+305A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665433 | ||||||
| chr16:85665504
|
C | G | 1 | a0001c0037t0060g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2758+376C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665504 | ||||||
| chr16:85665595
|
T | TACA | 118 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(115): Show | 118 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.2759-380_2759-378d others(5): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | 85665595 | |||||
| chr16:85665659
|
C | T | 3 | a0006c0011t0013g0230a0006c0011t0013g0270a0006c0011t0019g0282 | 3 | HG01255.hp1 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2759-317C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665659 | ||||||
| chr16:85665741
|
G | A | 2 | a0001c0002t0007g0267a0014c0049t0037g0125 | 2 | HG00741.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2759-235G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665741 | ||||||
| chr16:85665817
|
T | G | 2 | a0001c0001t0003g0096a0001c0001t0003g0170 | 2 | HG01884.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2759-159T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665817 | ||||||
| chr16:85665833
|
G | A | 4 | a0001c0002t0005g0043a0001c0002t0005g0143a0007c0012t0021g0239others(1): Show | 4 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2759-143G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665833 | ||||||
| chr16:85665859
|
G | C | 10 | a0001c0001t0003g0099a0001c0001t0003g0161a0001c0001t0003g0289others(7): Show | 10 | HG00609.hp1 HG01978.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.2759-117G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665859 | ||||||
| chr16:85665887
|
G | C | 1 | a0001c0001t0012g0210 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2759-89G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665887 | ||||||
| chr16:85665921
|
A | G | 142 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(139): Show | 142 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.2759-55A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 12/15 | chr16 | 85665921 | ||||||
| chr16:85666429
|
C | T | 1 | a0002c0008t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3130+82C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666429 | ||||||
| chr16:85666470
|
A | G | 2 | a0001c0001t0020g0156a0001c0001t0020g0217 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3130+123A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666470 | ||||||
| chr16:85666489
|
A | G | 1 | a0002c0005t0008g0085 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3130+142A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666489 | ||||||
| chr16:85666490
|
T | C | 1 | a0022c0038t0013g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3130+143T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666490 | ||||||
| chr16:85666501
|
C | T | 1 | a0007c0012t0034g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3130+154C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666501 | ||||||
| chr16:85666730
|
T | C | 1 | a0001c0001t0002g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3130+383T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666730 | ||||||
| chr16:85666754
|
G | A | 41 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0020others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.3130+407G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666754 | ||||||
| chr16:85666799
|
A | G | 3 | a0001c0002t0001g0017a0001c0002t0001g0245a0001c0002t0001g0272 | 3 | HG02559.hp2 HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3130+452A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666799 | ||||||
| chr16:85666843
|
T | G | 2 | a0001c0001t0020g0156a0001c0001t0020g0217 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3130+496T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666843 | ||||||
| chr16:85666875
|
G | A | 41 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0020others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.3130+528G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666875 | ||||||
| chr16:85666943
|
T | C | 13 | a0001c0021t0033g0225a0001c0037t0060g0114a0002c0006t0001g0113others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3130+596T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666943 | ||||||
| chr16:85666948
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3130+601T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666948 | ||||||
| chr16:85666985
|
G | A | 7 | a0004c0007t0010g0045a0004c0007t0010g0091a0004c0007t0010g0116others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3130+638G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85666985 | ||||||
| chr16:85667027
|
T | C | 1 | a0007c0012t0034g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3130+680T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667027 | ||||||
| chr16:85667124
|
C | G | 13 | a0001c0021t0033g0225a0001c0037t0060g0114a0002c0006t0001g0113others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3130+777C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667124 | ||||||
| chr16:85667144
|
G | T | 10 | a0001c0001t0003g0099a0001c0001t0003g0161a0001c0001t0003g0289others(7): Show | 10 | HG00609.hp1 HG01978.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.3130+797G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667144 | ||||||
| chr16:85667150
|
C | T | 1 | a0001c0001t0004g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3130+803C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667150 | ||||||
| chr16:85667151
|
G | A | 2 | a0001c0001t0012g0212a0001c0001t0043g0014 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3130+804G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667151 | ||||||
| chr16:85667158
|
C | CAGAATAC others(9): Show |
3 | a0007c0012t0021g0239a0008c0013t0021g0284a0008c0013t0055g0119 | 3 | HG00639.hp1 HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3130+819_3130+820i others(18): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 85667158 | |||||
| chr16:85667163
|
T | A | 4 | a0001c0001t0012g0010a0001c0001t0012g0210a0001c0001t0012g0212others(1): Show | 4 | HG02055.hp2 HG03486.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3130+816T>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667163 | ||||||
| chr16:85667293
|
G | GCCATACC others(1): Show |
13 | a0001c0021t0033g0225a0001c0037t0060g0114a0002c0006t0001g0113others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3131-846_3131-839d others(10): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 85667293 | |||||
| chr16:85667363
|
C | A | 47 | a0001c0001t0004g0009a0001c0001t0004g0013a0001c0001t0004g0025others(44): Show | 47 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.3131-777C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667363 | ||||||
| chr16:85667409
|
C | T | 2 | a0001c0001t0020g0156a0001c0001t0020g0217 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3131-731C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667409 | ||||||
| chr16:85667471
|
G | T | 1 | a0001c0001t0012g0210 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3131-669G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667471 | ||||||
| chr16:85667513
|
G | A | 1 | a0001c0051t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3131-627G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667513 | ||||||
| chr16:85667544
|
T | C | 16 | a0001c0001t0002g0166a0001c0001t0046g0105a0002c0004t0008g0015others(13): Show | 16 | HG01257.hp1 HG01258.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.3131-596T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667544 | ||||||
| chr16:85667549
|
A | G | 1 | a0001c0002t0001g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3131-591A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667549 | ||||||
| chr16:85667614
|
T | G | 1 | a0002c0018t0004g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3131-526T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667614 | ||||||
| chr16:85667680
|
G | A | 3 | a0001c0002t0001g0245a0001c0002t0001g0272a0001c0003t0001g0086 | 3 | HG01261.hp2 HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3131-460G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667680 | ||||||
| chr16:85667806
|
C | T | 3 | a0001c0001t0009g0196a0001c0001t0009g0198a0001c0001t0009g0262 | 3 | HG00099.hp2 HG02683.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.3131-334C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667806 | ||||||
| chr16:85667814
|
C | T | 1 | a0001c0001t0009g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3131-326C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667814 | ||||||
| chr16:85667832
|
T | C | 1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3131-308T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667832 | ||||||
| chr16:85667900
|
G | GGTCCA | 99 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(96): Show | 99 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.3131-239_3131-235d others(7): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 85667900 | |||||
| chr16:85667956
|
G | A | 2 | a0001c0001t0017g0090a0001c0002t0001g0263 | 2 | HG01361.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3131-184G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667956 | ||||||
| chr16:85667966
|
A | ACGCTGGG others(2): Show |
210 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.3131-174_3131-173i others(11): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667966 | ||||||
| chr16:85667967
|
A | T | 210 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.3131-173A>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667967 | ||||||
| chr16:85667979
|
G | A | 2 | a0001c0002t0007g0267a0014c0049t0037g0125 | 2 | HG00741.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.3131-161G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667979 | ||||||
| chr16:85667980
|
C | T | 208 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.3131-160C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85667980 | ||||||
| chr16:85668007
|
C | T | 1 | a0001c0002t0007g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3131-133C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85668007 | ||||||
| chr16:85668047
|
C | T | 3 | a0001c0002t0001g0247a0001c0002t0001g0288a0021c0039t0001g0271 | 3 | HG02258.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3131-93C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85668047 | ||||||
| chr16:85668052
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3131-88C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85668052 | ||||||
| chr16:85668065
|
G | A | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3131-75G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 13/15 | chr16 | 85668065 | ||||||
| chr16:85668446
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3415+22G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85668446 | ||||||
| chr16:85668447
|
G | A | 1 | a0001c0001t0004g0193 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3415+23G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85668447 | ||||||
| chr16:85668500
|
T | G | 1 | a0001c0001t0056g0179 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3415+76T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85668500 | ||||||
| chr16:85668586
|
G | C | 1 | a0001c0001t0042g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3415+162G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85668586 | ||||||
| chr16:85668687
|
G | T | 1 | a0029c0024t0023g0055 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3415+263G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85668687 | ||||||
| chr16:85668750
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3415+326C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85668750 | ||||||
| chr16:85668991
|
G | A | 1 | a0001c0001t0007g0049 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3415+567G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85668991 | ||||||
| chr16:85668994
|
T | C | 1 | a0002c0005t0063g0208 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3415+570T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85668994 | ||||||
| chr16:85669019
|
C | T | 14 | a0001c0021t0033g0225a0001c0037t0060g0114a0002c0004t0004g0001others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.3415+595C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669019 | ||||||
| chr16:85669025
|
C | T | 1 | a0001c0002t0001g0288 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3415+601C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669025 | ||||||
| chr16:85669084
|
T | C | 211 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.3415+660T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669084 | ||||||
| chr16:85669086
|
G | A | 1 | a0001c0037t0060g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3415+662G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669086 | ||||||
| chr16:85669135
|
C | T | 1 | a0001c0002t0001g0288 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3415+711C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669135 | ||||||
| chr16:85669225
|
G | C | 2 | a0001c0002t0001g0245a0001c0002t0001g0272 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3415+801G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669225 | ||||||
| chr16:85669459
|
C | T | 2 | a0001c0001t0020g0156a0001c0001t0020g0217 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3415+1035C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669459 | ||||||
| chr16:85669549
|
C | T | 1 | a0022c0038t0013g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3415+1125C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669549 | ||||||
| chr16:85669725
|
C | T | 1 | a0001c0001t0009g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3416-1270C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669725 | ||||||
| chr16:85669749
|
C | T | 1 | a0001c0002t0062g0167 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3416-1246C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669749 | ||||||
| chr16:85669884
|
G | A | 1 | a0002c0004t0008g0093 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3416-1111G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669884 | ||||||
| chr16:85669993
|
C | T | 1 | a0001c0001t0012g0210 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3416-1002C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85669993 | ||||||
| chr16:85670018
|
C | T | 1 | a0001c0002t0062g0167 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3416-977C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85670018 | ||||||
| chr16:85670021
|
T | G | 121 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(118): Show | 121 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.3416-974T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85670021 | ||||||
| chr16:85670081
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3416-914T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85670081 | ||||||
| chr16:85670118
|
G | A | 1 | a0001c0001t0067g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3416-877G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85670118 | ||||||
| chr16:85670163
|
G | C | 13 | a0001c0001t0068g0054a0001c0002t0018g0194a0001c0002t0018g0283others(10): Show | 13 | HG00438.hp1 HG01167.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.3416-832G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85670163 | ||||||
| chr16:85670577
|
C | G | 1 | a0001c0003t0001g0205 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3416-418C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85670577 | ||||||
| chr16:85670583
|
G | C | 191 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0120others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.3416-412G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85670583 | ||||||
| chr16:85670690
|
AT | A | 112 | a0001c0001t0001g0026a0001c0001t0001g0094a0001c0001t0001g0120others(109): Show | 112 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.3416-292delT | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 85670690 | |||||
| chr16:85670978
|
A | G | 104 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(101): Show | 104 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.3416-17A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 14/15 | chr16 | 85670978 | ||||||
| chr16:85671112
|
G | A | 5 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0097others(2): Show | 5 | HG00438.hp2 HG03654.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.3519+14G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671112 | ||||||
| chr16:85671115
|
T | C | 4 | a0007c0012t0021g0239a0007c0012t0034g0214a0008c0013t0021g0284others(1): Show | 4 | HG00639.hp1 HG01891.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.3519+17T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671115 | ||||||
| chr16:85671236
|
C | G | 1 | a0001c0001t0017g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3519+138C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671236 | ||||||
| chr16:85671301
|
G | A | 1 | a0002c0005t0063g0208 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3519+203G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671301 | ||||||
| chr16:85671370
|
G | A | 1 | a0001c0001t0004g0190 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3519+272G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671370 | ||||||
| chr16:85671388
|
C | T | 2 | a0001c0001t0057g0185a0001c0002t0005g0081 | 2 | HG01106.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3519+290C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671388 | ||||||
| chr16:85671394
|
T | C | 1 | a0001c0001t0012g0210 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3519+296T>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671394 | ||||||
| chr16:85671419
|
G | A | 2 | a0001c0002t0001g0003a0001c0002t0001g0074 | 2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3519+321G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671419 | ||||||
| chr16:85671426
|
C | A | 8 | a0002c0006t0001g0113a0002c0006t0001g0216a0002c0006t0001g0221others(5): Show | 8 | HG01109.hp2 HG02630.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.3519+328C>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671426 | ||||||
| chr16:85671439
|
C | CA | 15 | a0001c0001t0002g0231a0001c0002t0005g0118a0001c0002t0018g0194others(12): Show | 15 | HG01167.hp1 HG01255.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.3519+359dupA | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAA | 27 | a0001c0001t0004g0009a0001c0001t0004g0025a0001c0001t0004g0071others(24): Show | 27 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.3519+356_3519+359d others(6): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAA | 15 | a0001c0001t0004g0013a0001c0001t0012g0010a0001c0001t0012g0210others(12): Show | 15 | HG01258.hp1 HG01943.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3519+355_3519+359d others(7): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAAAA | 8 | a0001c0001t0003g0020a0001c0001t0011g0136a0001c0001t0011g0269others(5): Show | 8 | HG00140.hp2 HG01070.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.3519+353_3519+359d others(9): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAAAA others(1): Show |
26 | a0001c0001t0003g0004a0001c0001t0003g0040a0001c0001t0003g0099others(23): Show | 26 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.3519+352_3519+359d others(10): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAAAA others(2): Show |
13 | a0001c0001t0003g0036a0001c0001t0003g0096a0001c0001t0003g0142others(10): Show | 13 | HG00609.hp2 HG00741.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.3519+351_3519+359d others(11): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAAAA others(3): Show |
56 | a0001c0001t0001g0120a0001c0001t0001g0227a0001c0001t0001g0234others(53): Show | 56 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.3519+350_3519+359d others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAAAA others(4): Show |
34 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(31): Show | 34 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.3519+349_3519+359d others(13): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0002g0182a0001c0001t0009g0152a0001c0050t0002g0180others(1): Show | 4 | HG00738.hp1 HG03669.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.3519+348_3519+359d others(14): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0002g0131a0030c0053t0001g0047 | 2 | HG01975.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.3519+347_3519+359d others(15): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAAAA others(8): Show |
1 | a0002c0006t0001g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3519+345_3519+359d others(17): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAAAA others(9): Show |
1 | a0019c0025t0024g0275 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3519+344_3519+359d others(18): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAAAA others(10): Show |
1 | a0002c0008t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3519+343_3519+359d others(19): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAAAAAAA others(12): Show |
3 | a0007c0012t0021g0239a0008c0013t0021g0284a0008c0013t0055g0119 | 3 | HG00639.hp1 HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3519+359_3519+360i others(21): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671439
|
C | CAGAAAAA others(3): Show |
1 | a0001c0001t0003g0289 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3519+342_3519+343i others(12): Show |
GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 85671439 | |||||
| chr16:85671458
|
G | A | 100 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(97): Show | 100 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.3519+360G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671458 | ||||||
| chr16:85671466
|
T | G | 103 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(100): Show | 103 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.3519+368T>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671466 | ||||||
| chr16:85671525
|
G | C | 32 | a0001c0001t0004g0009a0001c0001t0004g0013a0001c0001t0004g0025others(29): Show | 32 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.3519+427G>C | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671525 | ||||||
| chr16:85671572
|
C | G | 1 | a0002c0045t0047g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3519+474C>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671572 | ||||||
| chr16:85671674
|
C | T | 1 | a0018c0043t0003g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3519+576C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671674 | ||||||
| chr16:85671675
|
C | T | 1 | a0001c0001t0069g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3519+577C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85671675 | ||||||
| chr16:85672005
|
G | T | 84 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0036others(81): Show | 84 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.3520-400G>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85672005 | ||||||
| chr16:85672084
|
C | T | 1 | a0001c0001t0056g0179 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3520-321C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85672084 | ||||||
| chr16:85672090
|
C | T | 1 | a0001c0003t0001g0108 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3520-315C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85672090 | ||||||
| chr16:85672132
|
A | G | 1 | a0001c0001t0068g0054 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3520-273A>G | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85672132 | ||||||
| chr16:85672274
|
C | T | 28 | a0001c0001t0004g0009a0001c0001t0004g0013a0001c0001t0004g0025others(25): Show | 28 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3520-131C>T | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85672274 | ||||||
| chr16:85672291
|
G | A | 1 | a0001c0002t0001g0268 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3520-114G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85672291 | ||||||
| chr16:85672295
|
G | A | 27 | a0001c0001t0004g0009a0001c0001t0004g0013a0001c0001t0004g0025others(24): Show | 27 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.3520-110G>A | GSE1 | ENSG00000131149.19 | transcript | ENST00000253458.12 | protein_coding | 15/15 | chr16 | 85672295 |