Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1103 |
|---|---|
| ensemblid | ENSG00000070748.19 |
| hgncid | 1912 |
| symbol | CHAT |
| name | choline O-acetyltransferase |
| refseq_nuc | NM_020549.5 |
| refseq_prot | NP_065574.4 |
| ensembl_nuc | ENST00000337653.7 |
| ensembl_prot | ENSP00000337103.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 49614037 |
| end | 49667942 |
| strand | + |
| ver | v1.2 |
| region | chr10:49614037-49667942 |
| region5000 | chr10:49609037-49672942 |
| regionname0 | CHAT_chr10_49614037_49667942 |
| regionname5000 | CHAT_chr10_49609037_49672942 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 748 | 261 | 76 | 56 | 82 | 13 | 33 | 63 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002 | 0/0 | 748 | 67 | 0 | 16 | 36 | 4 | 11 | 29 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003 | 0/0 | 748 | 63 | 1 | 4 | 58 | 0 | 0 | 40 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0004 | 1/0 | 748 | 11 | 10 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0005 | 0/0 | 748 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0006 | 0/0 | 748 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0007 | 0/0 | 748 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0008 | 0/0 | 748 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0009 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0010 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0011 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0012 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0013 | 0/0 | 748 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0014 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0015 | 0/0 | 748 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0016 | 0/0 | 748 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0017 | 0/0 | 748 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2247 | 172 | 50 | 40 | 45 | 10 | 26 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0002 | 0/0 | 2247 | 50 | 0 | 15 | 21 | 4 | 10 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0003 | 0/0 | 2247 | 43 | 7 | 13 | 15 | 3 | 5 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0004 | 0/0 | 2247 | 31 | 0 | 3 | 28 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0005 | 0/0 | 2247 | 20 | 0 | 0 | 20 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0006 | 0/0 | 2247 | 17 | 0 | 0 | 17 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0007 | 0/0 | 2247 | 14 | 1 | 1 | 12 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0008 | 0/0 | 2247 | 13 | 0 | 1 | 12 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0009 | 1/0 | 2247 | 9 | 8 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0010 | 0/0 | 2247 | 9 | 8 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0011 | 0/0 | 2247 | 4 | 4 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0012 | 0/0 | 2247 | 3 | 0 | 0 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0013 | 0/0 | 2247 | 3 | 3 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0014 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0015 | 0/0 | 2247 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0016 | 0/0 | 2247 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0017 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0018 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0019 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0020 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0021 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0022 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0023 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0024 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0025 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0026 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0027 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0028 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0029 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0030 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0031 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0032 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0033 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0034 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0035 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0036 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0037 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0038 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| c0039 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3050 | 67 | 12 | 10 | 40 | 1 | 4 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0002 | 0/1 | 3050 | 63 | 1 | 17 | 27 | 5 | 12 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0003 | 0/0 | 3050 | 41 | 28 | 8 | 5 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0004 | 0/0 | 3050 | 36 | 10 | 7 | 13 | 3 | 3 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0005 | 0/0 | 3050 | 36 | 7 | 1 | 28 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0006 | 0/0 | 3050 | 33 | 3 | 11 | 17 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0007 | 0/0 | 3050 | 32 | 2 | 7 | 12 | 4 | 7 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0008 | 0/0 | 3050 | 26 | 3 | 12 | 5 | 2 | 4 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0009 | 0/0 | 3050 | 18 | 1 | 1 | 16 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0010 | 0/0 | 3050 | 18 | 0 | 0 | 13 | 2 | 3 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0011 | 1/0 | 3050 | 7 | 4 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0012 | 0/0 | 3050 | 6 | 0 | 0 | 0 | 0 | 6 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0013 | 0/0 | 3050 | 5 | 4 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0014 | 0/0 | 3050 | 4 | 3 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0015 | 0/0 | 3050 | 3 | 3 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0016 | 0/0 | 3032 | 3 | 3 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0017 | 0/0 | 3050 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0018 | 0/0 | 3050 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0019 | 0/0 | 3050 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0020 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0021 | 0/0 | 3050 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0022 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0023 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0024 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0025 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0026 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0027 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0028 | 0/0 | 3032 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0029 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0030 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0031 | 0/0 | 3050 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0032 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0033 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0034 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0035 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| t0036 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| 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 | 3 | 0 | 2 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0041 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2247 | 172 | 50 | 40 | 45 | 10 | 26 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0003 | 0/0 | 2247 | 43 | 7 | 13 | 15 | 3 | 5 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0005 | 0/0 | 2247 | 20 | 0 | 0 | 20 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0010 | 0/0 | 2247 | 9 | 8 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0011 | 0/0 | 2247 | 4 | 4 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0013 | 0/0 | 2247 | 3 | 3 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0015 | 0/0 | 2247 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0017 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0019 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0026 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0027 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0028 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0030 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0035 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0002 | 0/0 | 2247 | 50 | 0 | 15 | 21 | 4 | 10 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0008 | 0/0 | 2247 | 13 | 0 | 1 | 12 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0012 | 0/0 | 2247 | 3 | 0 | 0 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0020 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0004 | 0/0 | 2247 | 31 | 0 | 3 | 28 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0006 | 0/0 | 2247 | 17 | 0 | 0 | 17 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0007 | 0/0 | 2247 | 14 | 1 | 1 | 12 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0039 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0004c0009 | 1/0 | 2247 | 9 | 8 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0004c0025 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0004c0034 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0005c0016 | 0/0 | 2247 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0006c0014 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0007c0023 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0007c0024 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0008c0038 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0009c0036 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0010c0032 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0011c0033 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0012c0031 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0013c0029 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0014c0037 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0015c0021 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0016c0022 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0017c0018 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5296 | 42 | 12 | 7 | 18 | 1 | 4 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0002 | 0/1 | 5296 | 30 | 1 | 8 | 12 | 2 | 6 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0003 | 0/0 | 5296 | 14 | 11 | 3 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0004 | 0/0 | 5296 | 28 | 8 | 7 | 9 | 2 | 2 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0005 | 0/0 | 5296 | 4 | 3 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0006 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0007 | 0/0 | 5296 | 19 | 1 | 5 | 4 | 3 | 6 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0008 | 0/0 | 5296 | 12 | 0 | 6 | 0 | 2 | 4 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0011 | 0/0 | 5296 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0012 | 0/0 | 5296 | 2 | 0 | 0 | 0 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0013 | 0/0 | 5296 | 4 | 4 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0014 | 0/0 | 5296 | 3 | 2 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0015 | 0/0 | 5296 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0016 | 0/0 | 5278 | 3 | 3 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0018 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0019 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0023 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0026 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0028 | 0/0 | 5278 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0001t0036 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0003t0003 | 0/0 | 5296 | 3 | 2 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0003t0006 | 0/0 | 5296 | 23 | 1 | 11 | 9 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0003t0008 | 0/0 | 5296 | 4 | 2 | 1 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0003t0010 | 0/0 | 5296 | 9 | 0 | 0 | 4 | 2 | 3 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0003t0020 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0003t0021 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0003t0033 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0003t0034 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0005t0005 | 0/0 | 5296 | 10 | 0 | 0 | 10 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0005t0009 | 0/0 | 5296 | 9 | 0 | 0 | 9 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0005t0030 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0010t0003 | 0/0 | 5296 | 8 | 7 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0010t0008 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0011t0003 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0011t0022 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0011t0024 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0011t0029 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0013t0005 | 0/0 | 5296 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0013t0032 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0015t0005 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0015t0009 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0017t0003 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0017t0004 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0019t0002 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0026t0005 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0027t0031 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0028t0005 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0030t0004 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0001c0035t0003 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0002t0002 | 0/0 | 5296 | 30 | 0 | 8 | 14 | 3 | 5 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0002t0007 | 0/0 | 5296 | 11 | 0 | 2 | 7 | 1 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0002t0008 | 0/0 | 5296 | 4 | 0 | 4 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0002t0009 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0002t0012 | 0/0 | 5296 | 3 | 0 | 0 | 0 | 0 | 3 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0002t0017 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0008t0008 | 0/0 | 5296 | 4 | 0 | 1 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0008t0010 | 0/0 | 5296 | 9 | 0 | 0 | 9 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0012t0009 | 0/0 | 5296 | 3 | 0 | 0 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0002c0020t0012 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0004t0001 | 0/0 | 5296 | 25 | 0 | 3 | 22 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0004t0004 | 0/0 | 5296 | 4 | 0 | 0 | 4 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0004t0013 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0004t0027 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0006t0005 | 0/0 | 5296 | 17 | 0 | 0 | 17 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0007t0003 | 0/0 | 5296 | 6 | 0 | 1 | 5 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0007t0006 | 0/0 | 5296 | 8 | 1 | 0 | 7 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0003c0039t0006 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0004c0009t0003 | 0/0 | 5296 | 3 | 3 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0004c0009t0011 | 1/0 | 5296 | 5 | 4 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0004c0009t0014 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0004c0025t0003 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0004c0034t0015 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0005c0016t0008 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0005c0016t0009 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0006c0014t0004 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0006c0014t0007 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0007c0023t0007 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0007c0024t0009 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0008c0038t0004 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0009c0036t0003 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0010c0032t0025 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0011c0033t0009 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0012c0031t0003 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0013c0029t0009 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0014c0037t0035 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0015c0021t0002 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0016c0022t0002 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| a0017c0018t0003 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | copy fasta | chr10 | 49609037 | 49672942 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0006g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0011g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0011g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0012g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0012g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0013g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0013g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0013g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0014g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0014g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0014g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0015g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0016g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0016g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0018g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0019g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0023g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0026g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0028g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0036g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0008g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0008g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0008g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0020g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0021g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0033g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0034g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0030g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0011t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0011t0022g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0011t0024g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0011t0029g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0013t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0013t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0013t0032g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0015t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0015t0009g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0017t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0017t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0019t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0026t0005g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0027t0031g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0028t0005g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0030t0004g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0035t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0008g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0008g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0008g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0008g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0009g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0012g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0012g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0012g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0017g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0008g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0008g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0008g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0008g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0012t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0012t0009g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0012t0009g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0020t0012g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0013g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0027g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0039t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0003g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0011g0041 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0014g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0025t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0034t0015g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0005c0016t0008g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0005c0016t0009g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0006c0014t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0006c0014t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0007c0023t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0007c0024t0009g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0008c0038t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0009c0036t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0010c0032t0025g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0011c0033t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0012c0031t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0013c0029t0009g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0014c0037t0035g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0015c0021t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0016c0022t0002g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0017c0018t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0021 | g0298 | EUR | GBR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0296 | EUR | GBR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | GBR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0036 | EUR | GBR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00280 | hp1 | a0008 | c0038 | t0004 | g0233 | EUR | FIN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00280 | hp2 | a0001 | c0001 | t0008 | g0297 | EUR | FIN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0094 | EUR | FIN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | FIN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00408 | hp1 | a0003 | c0006 | t0005 | g0131 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00408 | hp2 | a0003 | c0004 | t0001 | g0133 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00423 | hp1 | a0003 | c0007 | t0003 | g0145 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00423 | hp2 | a0001 | c0005 | t0005 | g0335 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00438 | hp1 | a0003 | c0006 | t0005 | g0118 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00544 | hp1 | a0001 | c0003 | t0006 | g0049 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00544 | hp2 | a0003 | c0007 | t0003 | g0125 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00597 | hp2 | a0002 | c0012 | t0009 | g0373 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00609 | hp1 | a0001 | c0005 | t0005 | g0350 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00609 | hp2 | a0003 | c0004 | t0004 | g0166 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00621 | hp1 | a0001 | c0005 | t0005 | g0063 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00621 | hp2 | a0001 | c0005 | t0005 | g0307 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0086 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00639 | hp2 | a0001 | c0035 | t0003 | g0235 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00642 | hp1 | a0002 | c0002 | t0009 | g0098 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0266 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00673 | hp1 | a0001 | c0001 | t0026 | g0061 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0078 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00735 | hp1 | a0001 | c0001 | t0011 | g0172 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00738 | hp1 | a0002 | c0008 | t0008 | g0365 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00738 | hp2 | a0001 | c0001 | t0008 | g0033 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00741 | hp1 | a0002 | c0002 | t0008 | g0362 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0236 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0305 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0355 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0003 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0003 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0332 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0299 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01081 | hp2 | a0015 | c0021 | t0002 | g0081 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01106 | hp1 | a0002 | c0002 | t0007 | g0087 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0232 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01109 | hp1 | a0001 | c0001 | t0014 | g0282 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01167 | hp2 | a0001 | c0010 | t0003 | g0258 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0241 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01175 | hp1 | a0001 | c0003 | t0006 | g0055 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01243 | hp1 | a0001 | c0001 | t0011 | g0173 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01255 | hp2 | a0001 | c0003 | t0006 | g0023 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01256 | hp2 | a0002 | c0002 | t0008 | g0361 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01261 | hp2 | a0001 | c0003 | t0006 | g0311 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01358 | hp1 | a0001 | c0003 | t0006 | g0023 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01358 | hp2 | a0002 | c0002 | t0008 | g0089 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0201 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01433 | hp2 | a0002 | c0002 | t0008 | g0088 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01496 | hp2 | a0001 | c0003 | t0006 | g0366 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0011 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01516 | hp1 | a0002 | c0002 | t0007 | g0090 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01516 | hp2 | a0001 | c0003 | t0010 | g0016 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01517 | hp1 | a0001 | c0003 | t0010 | g0016 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0011 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01884 | hp1 | a0001 | c0013 | t0005 | g0294 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01891 | hp1 | a0001 | c0026 | t0005 | g0369 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01891 | hp2 | a0004 | c0009 | t0011 | g0040 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01928 | hp1 | a0003 | c0004 | t0001 | g0167 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01928 | hp2 | a0001 | c0003 | t0006 | g0310 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01934 | hp1 | a0002 | c0002 | t0007 | g0100 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01943 | hp1 | a0003 | c0007 | t0003 | g0112 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01943 | hp2 | a0003 | c0004 | t0001 | g0163 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0028 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01952 | hp2 | a0001 | c0003 | t0008 | g0253 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01975 | hp1 | a0001 | c0003 | t0006 | g0024 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0315 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0244 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01981 | hp1 | a0001 | c0027 | t0031 | g0174 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01981 | hp2 | a0001 | c0003 | t0006 | g0024 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02015 | hp1 | a0003 | c0004 | t0001 | g0132 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02027 | hp1 | a0002 | c0008 | t0010 | g0069 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02055 | hp2 | a0001 | c0001 | t0013 | g0334 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02056 | hp2 | a0003 | c0004 | t0001 | g0160 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02071 | hp1 | a0003 | c0004 | t0001 | g0120 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02071 | hp2 | a0003 | c0004 | t0001 | g0124 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02074 | hp1 | a0001 | c0005 | t0005 | g0064 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02074 | hp2 | a0003 | c0004 | t0027 | g0113 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02083 | hp1 | a0003 | c0007 | t0003 | g0135 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02132 | hp1 | a0001 | c0003 | t0008 | g0183 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02132 | hp2 | a0003 | c0004 | t0001 | g0119 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02135 | hp1 | a0003 | c0007 | t0003 | g0122 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02145 | hp1 | a0001 | c0028 | t0005 | g0370 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02148 | hp1 | a0001 | c0003 | t0006 | g0322 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02148 | hp2 | a0003 | c0004 | t0001 | g0129 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02155 | hp1 | a0001 | c0005 | t0005 | g0026 | EAS | CDX | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02155 | hp2 | a0002 | c0002 | t0007 | g0381 | EAS | CDX | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02165 | hp1 | a0003 | c0004 | t0001 | g0046 | EAS | CDX | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CDX | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02257 | hp2 | a0001 | c0010 | t0003 | g0045 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02258 | hp2 | a0001 | c0011 | t0024 | g0283 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0331 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02273 | hp2 | a0001 | c0003 | t0006 | g0360 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02280 | hp1 | a0003 | c0007 | t0006 | g0159 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02280 | hp2 | a0004 | c0009 | t0011 | g0038 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02293 | hp1 | a0001 | c0003 | t0006 | g0308 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0095 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02300 | hp2 | a0001 | c0003 | t0003 | g0314 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02451 | hp2 | a0001 | c0010 | t0003 | g0259 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02523 | hp1 | a0003 | c0004 | t0001 | g0142 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02572 | hp1 | a0001 | c0001 | t0013 | g0225 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02572 | hp2 | a0001 | c0013 | t0032 | g0384 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0074 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02602 | hp2 | a0001 | c0019 | t0002 | g0171 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02622 | hp1 | a0001 | c0001 | t0023 | g0284 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0207 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0051 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0195 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02698 | hp2 | a0001 | c0030 | t0004 | g0316 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02717 | hp1 | a0010 | c0032 | t0025 | g0056 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02723 | hp2 | a0004 | c0009 | t0003 | g0275 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0179 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0180 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02738 | hp2 | a0001 | c0003 | t0010 | g0034 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02818 | hp1 | a0001 | c0010 | t0003 | g0257 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02886 | hp1 | a0001 | c0011 | t0003 | g0214 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02886 | hp2 | a0001 | c0001 | t0036 | g0300 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02895 | hp2 | a0001 | c0003 | t0008 | g0015 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02896 | hp1 | a0001 | c0017 | t0004 | g0228 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02896 | hp2 | a0001 | c0001 | t0015 | g0020 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02897 | hp1 | a0001 | c0001 | t0015 | g0020 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02897 | hp2 | a0001 | c0003 | t0008 | g0015 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0306 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02970 | hp1 | a0012 | c0031 | t0003 | g0222 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02970 | hp2 | a0004 | c0009 | t0003 | g0383 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0219 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02976 | hp2 | a0001 | c0001 | t0013 | g0018 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03041 | hp1 | a0001 | c0010 | t0008 | g0268 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0291 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03098 | hp1 | a0009 | c0036 | t0003 | g0337 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03098 | hp2 | a0004 | c0034 | t0015 | g0278 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03130 | hp1 | a0004 | c0009 | t0011 | g0043 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0288 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03195 | hp1 | a0001 | c0010 | t0003 | g0044 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03195 | hp2 | a0014 | c0037 | t0035 | g0301 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0292 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03209 | hp2 | a0001 | c0010 | t0003 | g0223 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03225 | hp1 | a0001 | c0003 | t0034 | g0368 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03225 | hp2 | a0004 | c0009 | t0003 | g0276 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0075 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0234 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03453 | hp1 | a0001 | c0017 | t0003 | g0256 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03453 | hp2 | a0001 | c0010 | t0003 | g0262 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03486 | hp2 | a0001 | c0011 | t0029 | g0216 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03491 | hp2 | a0001 | c0003 | t0006 | g0352 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03492 | hp1 | a0001 | c0001 | t0019 | g0245 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0356 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03540 | hp1 | a0001 | c0010 | t0003 | g0260 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0342 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0080 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03654 | hp2 | a0001 | c0003 | t0010 | g0243 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0035 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03669 | hp2 | a0001 | c0003 | t0006 | g0323 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0083 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03688 | hp2 | a0001 | c0001 | t0007 | g0003 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03704 | hp1 | a0001 | c0001 | t0018 | g0213 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03704 | hp2 | a0002 | c0002 | t0007 | g0108 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0211 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03834 | hp1 | a0001 | c0001 | t0012 | g0192 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03927 | hp2 | a0002 | c0020 | t0012 | g0085 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0202 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04115 | hp1 | a0002 | c0002 | t0012 | g0076 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04115 | hp2 | a0001 | c0003 | t0010 | g0170 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04184 | hp1 | a0002 | c0002 | t0012 | g0099 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04184 | hp2 | a0002 | c0002 | t0017 | g0084 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04199 | hp2 | a0002 | c0002 | t0012 | g0096 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0210 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04228 | hp2 | a0001 | c0001 | t0012 | g0188 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0182 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18522 | hp2 | a0006 | c0014 | t0007 | g0178 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18612 | hp1 | a0003 | c0004 | t0001 | g0144 | EAS | CHB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18612 | hp2 | a0003 | c0039 | t0006 | g0151 | EAS | CHB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | CHB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18747 | hp2 | a0001 | c0005 | t0005 | g0026 | EAS | CHB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18939 | hp1 | a0003 | c0004 | t0001 | g0143 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18943 | hp1 | a0001 | c0001 | t0007 | g0358 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18944 | hp1 | a0001 | c0003 | t0006 | g0004 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18944 | hp2 | a0003 | c0006 | t0005 | g0140 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18946 | hp1 | a0003 | c0004 | t0013 | g0153 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18946 | hp2 | a0007 | c0024 | t0009 | g0101 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18947 | hp2 | a0001 | c0005 | t0009 | g0252 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18948 | hp1 | a0005 | c0016 | t0009 | g0271 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18948 | hp2 | a0003 | c0007 | t0006 | g0165 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18949 | hp1 | a0001 | c0001 | t0007 | g0240 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18949 | hp2 | a0003 | c0004 | t0001 | g0147 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18952 | hp2 | a0002 | c0008 | t0010 | g0068 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18953 | hp1 | a0001 | c0005 | t0005 | g0326 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0367 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18954 | hp1 | a0001 | c0003 | t0010 | g0238 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18954 | hp2 | a0002 | c0002 | t0007 | g0375 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18957 | hp2 | a0003 | c0006 | t0005 | g0116 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18959 | hp1 | a0002 | c0008 | t0010 | g0010 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18960 | hp1 | a0001 | c0005 | t0009 | g0265 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18960 | hp2 | a0003 | c0004 | t0001 | g0014 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18962 | hp1 | a0003 | c0007 | t0006 | g0150 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18962 | hp2 | a0005 | c0016 | t0008 | g0269 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18964 | hp1 | a0002 | c0008 | t0010 | g0382 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18964 | hp2 | a0002 | c0008 | t0008 | g0377 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18965 | hp1 | a0003 | c0006 | t0005 | g0149 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18965 | hp2 | a0001 | c0003 | t0006 | g0004 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18966 | hp1 | a0003 | c0006 | t0005 | g0134 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18966 | hp2 | a0001 | c0001 | t0007 | g0247 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18968 | hp1 | a0002 | c0002 | t0007 | g0091 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18969 | hp1 | a0003 | c0007 | t0006 | g0162 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18969 | hp2 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18970 | hp1 | a0003 | c0004 | t0001 | g0139 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18971 | hp2 | a0002 | c0002 | t0007 | g0372 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18973 | hp1 | a0002 | c0002 | t0007 | g0070 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18973 | hp2 | a0001 | c0005 | t0030 | g0341 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18974 | hp2 | a0001 | c0003 | t0010 | g0208 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18975 | hp2 | a0002 | c0008 | t0008 | g0378 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18979 | hp1 | a0003 | c0004 | t0004 | g0126 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18979 | hp2 | a0003 | c0004 | t0001 | g0121 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18982 | hp1 | a0001 | c0003 | t0006 | g0319 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18983 | hp2 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18984 | hp1 | a0003 | c0006 | t0005 | g0123 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18984 | hp2 | a0003 | c0004 | t0004 | g0156 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18985 | hp2 | a0003 | c0004 | t0004 | g0128 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18986 | hp2 | a0001 | c0005 | t0009 | g0190 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18988 | hp1 | a0001 | c0005 | t0009 | g0249 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18988 | hp2 | a0001 | c0003 | t0010 | g0209 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18990 | hp1 | a0003 | c0007 | t0006 | g0136 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18993 | hp1 | a0001 | c0003 | t0010 | g0187 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18993 | hp2 | a0001 | c0005 | t0009 | g0239 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18994 | hp1 | a0002 | c0008 | t0010 | g0093 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18994 | hp2 | a0003 | c0006 | t0005 | g0161 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18995 | hp1 | a0001 | c0003 | t0006 | g0351 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18995 | hp2 | a0002 | c0002 | t0007 | g0106 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18997 | hp1 | a0003 | c0007 | t0006 | g0114 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18997 | hp2 | a0016 | c0022 | t0002 | g0376 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18998 | hp1 | a0002 | c0002 | t0007 | g0363 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18999 | hp2 | a0001 | c0005 | t0009 | g0272 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19000 | hp2 | a0003 | c0006 | t0005 | g0148 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19002 | hp2 | a0001 | c0005 | t0009 | g0186 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19005 | hp1 | a0003 | c0006 | t0005 | g0012 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19007 | hp1 | a0003 | c0006 | t0005 | g0157 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19007 | hp2 | a0002 | c0008 | t0010 | g0010 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0379 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19009 | hp2 | a0003 | c0007 | t0003 | g0158 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0343 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19012 | hp2 | a0003 | c0006 | t0005 | g0012 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0281 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19030 | hp2 | a0006 | c0014 | t0004 | g0287 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19043 | hp1 | a0004 | c0009 | t0011 | g0039 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19043 | hp2 | a0001 | c0001 | t0013 | g0018 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0345 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19054 | hp2 | a0003 | c0006 | t0005 | g0141 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19057 | hp1 | a0003 | c0004 | t0001 | g0130 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19058 | hp1 | a0003 | c0004 | t0001 | g0137 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19058 | hp2 | a0001 | c0005 | t0009 | g0250 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19060 | hp1 | a0003 | c0006 | t0005 | g0152 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19062 | hp1 | a0001 | c0003 | t0020 | g0067 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0270 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19063 | hp1 | a0001 | c0015 | t0009 | g0248 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19063 | hp2 | a0003 | c0007 | t0006 | g0164 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19065 | hp1 | a0003 | c0007 | t0006 | g0127 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19065 | hp2 | a0002 | c0012 | t0009 | g0371 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19068 | hp1 | a0013 | c0029 | t0009 | g0251 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19068 | hp2 | a0003 | c0004 | t0001 | g0154 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19070 | hp1 | a0003 | c0004 | t0001 | g0138 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19070 | hp2 | a0001 | c0005 | t0005 | g0304 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19074 | hp2 | a0001 | c0003 | t0006 | g0303 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19076 | hp2 | a0002 | c0008 | t0008 | g0374 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19078 | hp1 | a0007 | c0023 | t0007 | g0102 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19079 | hp2 | a0003 | c0006 | t0005 | g0155 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19080 | hp1 | a0003 | c0004 | t0001 | g0014 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19080 | hp2 | a0001 | c0003 | t0006 | g0004 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19081 | hp1 | a0001 | c0005 | t0009 | g0193 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19081 | hp2 | a0001 | c0001 | t0028 | g0347 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19083 | hp1 | a0001 | c0003 | t0006 | g0328 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19083 | hp2 | a0002 | c0008 | t0010 | g0092 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19084 | hp1 | a0002 | c0012 | t0009 | g0077 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19085 | hp2 | a0003 | c0004 | t0001 | g0115 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19087 | hp1 | a0002 | c0008 | t0010 | g0380 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19088 | hp2 | a0003 | c0006 | t0005 | g0117 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19090 | hp1 | a0003 | c0006 | t0005 | g0146 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19090 | hp2 | a0002 | c0008 | t0010 | g0364 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19091 | hp1 | a0001 | c0015 | t0005 | g0312 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19091 | hp2 | a0001 | c0003 | t0006 | g0336 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19240 | hp1 | a0001 | c0003 | t0003 | g0293 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | ASW | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | ASW | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0242 | EUR | TSI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0047 | EUR | TSI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20805 | hp1 | a0001 | c0001 | t0008 | g0001 | EUR | TSI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0181 | EUR | TSI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01123 | hp1 | a0017 | c0018 | t0003 | g0330 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02109 | hp2 | a0001 | c0003 | t0033 | g0042 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02486 | hp1 | a0004 | c0009 | t0014 | g0280 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0022 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0279 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02559 | hp2 | a0001 | c0011 | t0022 | g0286 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03471 | hp1 | a0001 | c0013 | t0005 | g0217 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0267 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0353 | AFR | USA | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG06807 | hp2 | a0001 | c0001 | t0016 | g0022 | AFR | USA | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18955 | hp1 | a0001 | c0005 | t0005 | g0168 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | USA | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20300 | hp2 | a0001 | c0003 | t0006 | g0309 | AFR | USA | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA21309 | hp1 | a0004 | c0025 | t0003 | g0357 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA21309 | hp2 | a0011 | c0033 | t0009 | g0177 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0199 | REF | REF | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| homoSapiens_grch38 | hp1 | a0004 | c0009 | t0011 | g0041 | REF | REF | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49614245
|
G | C | 1 | a0017 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.56G>C | p.Arg19Thr | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 209/5296 | 56/2247 | 19/748 | chr10 | 49614245 | ||
| chr10:49614330
|
C | G | 1 | a0003 | 63 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
missense_variant | MODERATE | c.141C>G | p.Asp47Glu | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 294/5296 | 141/2247 | 47/748 | chr10 | 49614330 | ||
| chr10:49616573
|
G | A | 4 | a0002a0007a0015others(1): Show | 71 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(68): Show |
missense_variant | MODERATE | c.358G>A | p.Ala120Thr | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/15 | 511/5296 | 358/2247 | 120/748 | chr10 | 49616573 | ||
| chr10:49622109
|
C | G | 1 | a0007 | 2 | NA18946.hp2 NA19078.hp1 |
missense_variant | MODERATE | c.711C>G | p.Ser237Arg | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/15 | 864/5296 | 711/2247 | 237/748 | chr10 | 49622109 | ||
| chr10:49622125
|
C | T | 1 | a0008 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.727C>T | p.Leu243Phe | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/15 | 880/5296 | 727/2247 | 243/748 | chr10 | 49622125 | ||
| chr10:49622138
|
C | T | 1 | a0014 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.740C>T | p.Ala247Val | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/15 | 893/5296 | 740/2247 | 247/748 | chr10 | 49622138 | ||
| chr10:49625616
|
C | T | 2 | a0009a0017 | 2 | HG01123.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.896C>T | p.Pro299Leu | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/15 | 1049/5296 | 896/2247 | 299/748 | chr10 | 49625616 | ||
| chr10:49627707
|
G | A | 1 | a0013 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.1033G>A | p.Glu345Lys | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/15 | 1186/5296 | 1033/2247 | 345/748 | chr10 | 49627707 | ||
| chr10:49627743
|
G | A | 1 | a0012 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.1069G>A | p.Gly357Arg | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/15 | 1222/5296 | 1069/2247 | 357/748 | chr10 | 49627743 | ||
| chr10:49646528
|
G | C | 1 | a0006 | 2 | NA18522.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.1135G>C | p.Asp379His | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/15 | 1288/5296 | 1135/2247 | 379/748 | chr10 | 49646528 | ||
| chr10:49648606
|
G | A | 14 | a0001a0002a0003others(11): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
missense_variant&splice_region_variant | MODERATE | c.1381G>A | p.Val461Met | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/15 | 1534/5296 | 1381/2247 | 461/748 | chr10 | 49648606 | ||
| chr10:49655142
|
G | A | 1 | a0015 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.1682G>A | p.Arg561Gln | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 12/15 | 1835/5296 | 1682/2247 | 561/748 | chr10 | 49655142 | ||
| chr10:49655178
|
C | A | 1 | a0016 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.1718C>A | p.Ala573Asp | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 12/15 | 1871/5296 | 1718/2247 | 573/748 | chr10 | 49655178 | ||
| chr10:49655210
|
G | A | 1 | a0010 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1750G>A | p.Val584Met | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 12/15 | 1903/5296 | 1750/2247 | 584/748 | chr10 | 49655210 | ||
| chr10:49664982
|
C | T | 2 | a0005a0013 | 3 | NA18948.hp1 NA18962.hp2 NA19068.hp1 |
missense_variant | MODERATE | c.2183C>T | p.Thr728Ile | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2336/5296 | 2183/2247 | 728/748 | chr10 | 49664982 | ||
| chr10:49665021
|
G | A | 1 | a0011 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2222G>A | p.Arg741Lys | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2375/5296 | 2222/2247 | 741/748 | chr10 | 49665021 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49616542
|
G | A | 1 | a0001c0019 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.327G>A | p.Thr109Thr | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/15 | 480/5296 | 327/2247 | 109/748 | chr10 | 49616542 | ||
| chr10:49625509
|
G | A | 1 | a0004c0025 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.789G>A | p.Leu263Leu | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/15 | 942/5296 | 789/2247 | 263/748 | chr10 | 49625509 | ||
| chr10:49625623
|
T | C | 4 | a0001c0011a0001c0026a0001c0027others(1): Show | 7 | HG01891.hp1 HG01981.hp1 HG02145.hp1 others(4): Show |
synonymous_variant | LOW | c.903T>C | p.Pro301Pro | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/15 | 1056/5296 | 903/2247 | 301/748 | chr10 | 49625623 | ||
| chr10:49625629
|
C | T | 1 | a0001c0035 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.909C>T | p.His303His | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/15 | 1062/5296 | 909/2247 | 303/748 | chr10 | 49625629 | ||
| chr10:49627736
|
G | A | 1 | a0001c0030 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.1062G>A | p.Thr354Thr | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/15 | 1215/5296 | 1062/2247 | 354/748 | chr10 | 49627736 | ||
| chr10:49646515
|
C | T | 3 | a0001c0010a0001c0017a0001c0028 | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
synonymous_variant | LOW | c.1122C>T | p.Asn374Asn | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/15 | 1275/5296 | 1122/2247 | 374/748 | chr10 | 49646515 | ||
| chr10:49646524
|
G | A | 3 | a0001c0010a0001c0017a0001c0028 | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
synonymous_variant | LOW | c.1131G>A | p.Ser377Ser | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/15 | 1284/5296 | 1131/2247 | 377/748 | chr10 | 49646524 | ||
| chr10:49646566
|
C | T | 1 | a0001c0027 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.1173C>T | p.Asp391Asp | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/15 | 1326/5296 | 1173/2247 | 391/748 | chr10 | 49646566 | ||
| chr10:49646641
|
C | T | 1 | a0003c0039 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.1248C>T | p.Asn416Asn | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/15 | 1401/5296 | 1248/2247 | 416/748 | chr10 | 49646641 | ||
| chr10:49649533
|
C | A | 1 | a0002c0020 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.1408C>A | p.Arg470Arg | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/15 | 1561/5296 | 1408/2247 | 470/748 | chr10 | 49649533 | ||
| chr10:49655101
|
T | C | 27 | a0001c0001a0001c0005a0001c0011others(24): Show | 321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
synonymous_variant | LOW | c.1641T>C | p.His547His | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 12/15 | 1794/5296 | 1641/2247 | 547/748 | chr10 | 49655101 | ||
| chr10:49655134
|
C | T | 4 | a0001c0010a0001c0013a0001c0026others(1): Show | 14 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
synonymous_variant | LOW | c.1674C>T | p.Ser558Ser | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 12/15 | 1827/5296 | 1674/2247 | 558/748 | chr10 | 49655134 | ||
| chr10:49662687
|
C | A | 1 | a0001c0015 | 2 | NA19063.hp1 NA19091.hp1 |
synonymous_variant | LOW | c.1882C>A | p.Arg628Arg | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/15 | 2035/5296 | 1882/2247 | 628/748 | chr10 | 49662687 | ||
| chr10:49664866
|
C | T | 7 | a0001c0005a0001c0015a0002c0012others(4): Show | 46 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
synonymous_variant | LOW | c.2067C>T | p.Ile689Ile | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2220/5296 | 2067/2247 | 689/748 | chr10 | 49664866 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49614087
|
C | G | 2 | a0001c0001t0036a0014c0037t0035 | 2 | HG02886.hp2 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-103C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 103 | chr10 | 49614087 | |||||
| chr10:49614134
|
C | T | 1 | a0001c0003t0034 | 1 | HG03225.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-56C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | chr10 | 49614134 | ||||||
| chr10:49614146
|
G | C | 33 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(30): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
5_prime_UTR_variant | MODIFIER | c.-44G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 44 | chr10 | 49614146 | |||||
| chr10:49614173
|
G | A | 7 | a0001c0001t0014a0001c0001t0015a0001c0001t0023others(4): Show | 10 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-17G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 17 | chr10 | 49614173 | |||||
| chr10:49614180
|
T | G | 84 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(81): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
5_prime_UTR_variant | MODIFIER | c.-10T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 10 | chr10 | 49614180 | |||||
| chr10:49665257
|
T | A | 1 | a0001c0011t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 211 | chr10 | 49665257 | |||||
| chr10:49665439
|
C | T | 1 | a0001c0011t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 393 | chr10 | 49665439 | |||||
| chr10:49665577
|
G | A | 1 | a0010c0032t0025 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*531G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 531 | chr10 | 49665577 | |||||
| chr10:49665982
|
T | C | 13 | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(10): Show | 137 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*936T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 936 | chr10 | 49665982 | |||||
| chr10:49666237
|
CCCAGCCC others(11): Show |
C | 2 | a0001c0001t0016a0001c0001t0028 | 4 | HG02486.hp2 HG02976.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1233_*1250delCCCA others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1233 | INFO_REALIGN_3_PRIME | chr10 | 49666237 | ||||
| chr10:49666300
|
G | A | 1 | a0001c0001t0019 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1254G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1254 | chr10 | 49666300 | |||||
| chr10:49666327
|
G | C | 1 | a0001c0001t0026 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1281G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1281 | chr10 | 49666327 | |||||
| chr10:49666392
|
C | T | 3 | a0001c0001t0012a0002c0002t0012a0002c0020t0012 | 6 | HG03834.hp1 HG03927.hp2 HG04115.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1346C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1346 | chr10 | 49666392 | |||||
| chr10:49666503
|
C | A | 16 | a0001c0001t0004a0001c0001t0007a0001c0001t0013others(13): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1457C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1457 | chr10 | 49666503 | |||||
| chr10:49666514
|
C | G | 16 | a0001c0001t0004a0001c0001t0007a0001c0001t0013others(13): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1468C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1468 | chr10 | 49666514 | |||||
| chr10:49666752
|
C | T | 1 | a0001c0027t0031 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1706C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1706 | chr10 | 49666752 | |||||
| chr10:49666855
|
G | T | 1 | a0001c0005t0030 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1809G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1809 | chr10 | 49666855 | |||||
| chr10:49667004
|
C | G | 1 | a0001c0003t0021 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1958C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1958 | chr10 | 49667004 | |||||
| chr10:49667028
|
G | A | 1 | a0001c0003t0020 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1982G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1982 | chr10 | 49667028 | |||||
| chr10:49667071
|
T | C | 1 | a0001c0011t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2025T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2025 | chr10 | 49667071 | |||||
| chr10:49667253
|
C | T | 9 | a0001c0001t0006a0001c0003t0006a0001c0003t0010others(6): Show | 54 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2207C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2207 | chr10 | 49667253 | |||||
| chr10:49667355
|
C | T | 1 | a0003c0004t0027 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2309C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2309 | chr10 | 49667355 | |||||
| chr10:49667377
|
A | G | 1 | a0001c0001t0018 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2331A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2331 | chr10 | 49667377 | |||||
| chr10:49667456
|
T | C | 33 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(30): Show | 201 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*2410T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2410 | chr10 | 49667456 | |||||
| chr10:49667602
|
C | G | 3 | a0001c0003t0034a0001c0011t0024a0001c0011t0029 | 3 | HG02258.hp2 HG03225.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2556C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2556 | chr10 | 49667602 | |||||
| chr10:49667624
|
G | C | 1 | a0002c0002t0017 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2578G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2578 | chr10 | 49667624 | |||||
| chr10:49667882
|
A | T | 1 | a0010c0032t0025 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2836 | chr10 | 49667882 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49614513
|
T | C | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.286+38T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614513 | ||||||
| chr10:49614519
|
G | T | 1 | a0001c0013t0032g0384 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.286+44G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614519 | ||||||
| chr10:49614716
|
C | T | 1 | a0004c0009t0003g0383 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.286+241C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614716 | ||||||
| chr10:49614734
|
A | G | 13 | a0002c0002t0002g0030a0002c0002t0002g0379a0002c0002t0007g0372others(10): Show | 14 | HG00597.hp2 HG02155.hp2 HG03710.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+259A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614734 | ||||||
| chr10:49614889
|
A | G | 3 | a0001c0003t0034g0368a0001c0026t0005g0369a0001c0028t0005g0370 | 3 | HG01891.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.286+414A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614889 | ||||||
| chr10:49614939
|
G | A | 5 | a0001c0001t0007g0035a0001c0001t0007g0036a0001c0001t0008g0001others(2): Show | 7 | HG00140.hp2 HG00738.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+464G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614939 | ||||||
| chr10:49614992
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.286+517G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614992 | ||||||
| chr10:49615001
|
C | CACAG | 377 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(374): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.286+529_286+530ins others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 49615001 | |||||
| chr10:49615158
|
G | C | 2 | a0001c0010t0003g0044a0001c0010t0003g0045 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.286+683G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615158 | ||||||
| chr10:49615166
|
G | C | 1 | a0003c0004t0001g0046 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.286+691G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615166 | ||||||
| chr10:49615166
|
G | T | 1 | a0001c0001t0002g0367 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.286+691G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615166 | ||||||
| chr10:49615397
|
G | A | 1 | a0001c0001t0007g0047 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.286+922G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615397 | ||||||
| chr10:49615465
|
A | G | 1 | a0001c0001t0001g0029 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.286+990A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615465 | ||||||
| chr10:49615706
|
A | G | 1 | a0001c0003t0006g0366 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287-796A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615706 | ||||||
| chr10:49615784
|
G | A | 22 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(19): Show | 25 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-718G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615784 | ||||||
| chr10:49615796
|
C | T | 2 | a0002c0008t0008g0365a0002c0008t0010g0364 | 2 | HG00738.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.287-706C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615796 | ||||||
| chr10:49615838
|
A | G | 1 | a0002c0002t0007g0363 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.287-664A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615838 | ||||||
| chr10:49615880
|
G | A | 1 | a0002c0012t0009g0371 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.287-622G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615880 | ||||||
| chr10:49615922
|
C | A | 1 | a0001c0003t0020g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.287-580C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615922 | ||||||
| chr10:49615935
|
C | T | 22 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(19): Show | 25 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-567C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615935 | ||||||
| chr10:49615939
|
A | G | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.287-563A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615939 | ||||||
| chr10:49615992
|
C | T | 24 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(21): Show | 27 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.287-510C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615992 | ||||||
| chr10:49616018
|
C | T | 1 | a0001c0003t0006g0360 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.287-484C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49616018 | ||||||
| chr10:49616060
|
C | T | 1 | a0001c0001t0001g0359 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.287-442C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49616060 | ||||||
| chr10:49616071
|
G | A | 64 | a0002c0002t0002g0002a0002c0002t0002g0008a0002c0002t0002g0009others(61): Show | 71 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.287-431G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49616071 | ||||||
| chr10:49616198
|
C | A | 22 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(19): Show | 25 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-304C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49616198 | ||||||
| chr10:49616433
|
G | C | 1 | a0001c0001t0004g0109 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.287-69G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49616433 | ||||||
| chr10:49616702
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.387+100T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49616702 | ||||||
| chr10:49616980
|
C | T | 1 | a0001c0001t0007g0358 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.387+378C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49616980 | ||||||
| chr10:49617020
|
A | G | 2 | a0001c0001t0006g0356a0004c0025t0003g0357 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.387+418A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617020 | ||||||
| chr10:49617055
|
C | T | 2 | a0001c0001t0001g0354a0001c0001t0004g0355 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.387+453C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617055 | ||||||
| chr10:49617116
|
C | T | 288 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(285): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.387+514C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617116 | ||||||
| chr10:49617139
|
C | G | 1 | a0001c0001t0003g0353 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.387+537C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617139 | ||||||
| chr10:49617145
|
C | T | 66 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0302others(63): Show | 74 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.387+543C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617145 | ||||||
| chr10:49617170
|
TCTTCCCC | T | 4 | a0001c0001t0002g0296a0001c0001t0008g0297a0001c0001t0008g0299others(1): Show | 4 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+583_387+589del others(7): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 49617170 | |||||
| chr10:49617272
|
T | C | 209 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0169others(206): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.387+670T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617272 | ||||||
| chr10:49617607
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.387+1005G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617607 | ||||||
| chr10:49617730
|
A | G | 1 | a0001c0003t0006g0352 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.387+1128A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617730 | ||||||
| chr10:49617735
|
C | G | 22 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(19): Show | 25 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.387+1133C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617735 | ||||||
| chr10:49617749
|
G | T | 3 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0017t0004g0228 | 3 | HG02896.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.387+1147G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617749 | ||||||
| chr10:49617776
|
G | T | 2 | a0001c0003t0006g0351a0001c0005t0005g0350 | 2 | HG00609.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.387+1174G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617776 | ||||||
| chr10:49617885
|
C | G | 170 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(167): Show | 185 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.387+1283C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617885 | ||||||
| chr10:49617999
|
C | G | 1 | a0002c0002t0007g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.387+1397C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617999 | ||||||
| chr10:49618000
|
A | C | 373 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(370): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.387+1398A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618000 | ||||||
| chr10:49618051
|
A | G | 2 | a0001c0001t0002g0212a0001c0001t0018g0213 | 2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.387+1449A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618051 | ||||||
| chr10:49618117
|
A | G | 366 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(363): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.387+1515A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618117 | ||||||
| chr10:49618231
|
A | G | 1 | a0004c0009t0011g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.388-1494A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618231 | ||||||
| chr10:49618361
|
C | T | 1 | a0004c0009t0003g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.388-1364C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618361 | ||||||
| chr10:49618552
|
A | G | 69 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0169others(66): Show | 78 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.388-1173A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618552 | ||||||
| chr10:49618652
|
T | C | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG02055.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.388-1073T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618652 | ||||||
| chr10:49618684
|
C | G | 1 | a0001c0001t0001g0349 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.388-1041C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618684 | ||||||
| chr10:49618816
|
C | G | 163 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(160): Show | 178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.388-909C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618816 | ||||||
| chr10:49618839
|
G | A | 1 | a0001c0001t0006g0356 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.388-886G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618839 | ||||||
| chr10:49619143
|
C | G | 1 | a0001c0001t0001g0066 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.388-582C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49619143 | ||||||
| chr10:49619144
|
A | C | 1 | a0001c0001t0001g0066 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.388-581A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49619144 | ||||||
| chr10:49619657
|
G | C | 10 | a0001c0001t0001g0285a0001c0001t0014g0279a0001c0001t0014g0281others(7): Show | 11 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.388-68G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49619657 | ||||||
| chr10:49619675
|
C | T | 63 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0317others(60): Show | 71 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.388-50C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49619675 | ||||||
| chr10:49619953
|
C | T | 1 | a0001c0001t0006g0356 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.579+37C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49619953 | ||||||
| chr10:49620018
|
A | C | 23 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(20): Show | 26 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.579+102A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620018 | ||||||
| chr10:49620156
|
T | A | 3 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0017t0004g0228 | 3 | HG02896.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.579+240T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620156 | ||||||
| chr10:49620212
|
G | T | 1 | a0002c0002t0002g0107 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.580-283G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620212 | ||||||
| chr10:49620247
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.580-248G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620247 | ||||||
| chr10:49620430
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.580-65T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620430 | ||||||
| chr10:49620431
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.580-64C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620431 | ||||||
| chr10:49620460
|
G | A | 373 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(370): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.580-35G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620460 | ||||||
| chr10:49620629
|
T | C | 1 | a0003c0007t0003g0112 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.698+16T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620629 | ||||||
| chr10:49620673
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.698+60C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620673 | ||||||
| chr10:49620750
|
C | T | 1 | a0001c0003t0033g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.698+137C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620750 | ||||||
| chr10:49620809
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0016g0022 | 3 | HG02258.hp1 HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.698+196A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620809 | ||||||
| chr10:49620912
|
G | A | 2 | a0001c0003t0010g0170a0001c0019t0002g0171 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.698+299G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620912 | ||||||
| chr10:49620916
|
C | A | 1 | a0001c0001t0008g0001 | 3 | HG01167.hp1 HG01169.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.698+303C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620916 | ||||||
| chr10:49621029
|
G | C | 1 | a0006c0014t0004g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.698+416G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621029 | ||||||
| chr10:49621068
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.698+455G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621068 | ||||||
| chr10:49621173
|
A | T | 106 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(103): Show | 117 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.698+560A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621173 | ||||||
| chr10:49621201
|
G | A | 1 | a0001c0011t0003g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.698+588G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621201 | ||||||
| chr10:49621218
|
C | T | 44 | a0001c0001t0001g0169a0001c0001t0001g0215a0001c0001t0001g0302others(41): Show | 45 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.698+605C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621218 | ||||||
| chr10:49621256
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.698+643A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621256 | ||||||
| chr10:49621384
|
T | A | 4 | a0001c0001t0001g0029a0001c0001t0002g0175a0001c0001t0004g0232others(1): Show | 5 | HG00735.hp2 HG01106.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.699-713T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621384 | ||||||
| chr10:49621434
|
G | A | 169 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(166): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.699-663G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621434 | ||||||
| chr10:49621439
|
A | T | 65 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0224others(62): Show | 72 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.699-658A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621439 | ||||||
| chr10:49621550
|
G | A | 1 | a0001c0013t0032g0384 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.699-547G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621550 | ||||||
| chr10:49621567
|
G | A | 33 | a0001c0001t0001g0025a0001c0001t0001g0317a0001c0001t0001g0318others(30): Show | 37 | HG00609.hp2 HG00621.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.699-530G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621567 | ||||||
| chr10:49621674
|
C | T | 1 | a0001c0001t0008g0211 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.699-423C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621674 | ||||||
| chr10:49621717
|
G | A | 3 | a0001c0001t0001g0048a0001c0027t0031g0174a0001c0035t0003g0235 | 3 | HG00639.hp2 HG01981.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.699-380G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621717 | ||||||
| chr10:49621749
|
T | A | 5 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(2): Show | 5 | HG02055.hp1 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.699-348T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621749 | ||||||
| chr10:49621782
|
A | G | 376 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(373): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.699-315A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621782 | ||||||
| chr10:49621847
|
G | T | 88 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0229others(85): Show | 97 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.699-250G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621847 | ||||||
| chr10:49621857
|
GGCAAGAA others(15): Show |
G | 1 | a0001c0001t0015g0020 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.699-236_699-215del others(22): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621857 | |||||
| chr10:49621861
|
A | AGAACCAC others(15): Show |
2 | a0002c0002t0007g0106a0002c0002t0007g0363 | 2 | NA18995.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.699-214_699-193dup others(22): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621861 | |||||
| chr10:49621861
|
AGAACCAC others(15): Show |
A | 11 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0295others(8): Show | 13 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.699-214_699-193del others(22): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621861 | |||||
| chr10:49621907
|
C | T | 6 | a0001c0003t0006g0351a0001c0011t0003g0214a0001c0011t0022g0286others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.699-190C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621907 | ||||||
| chr10:49621928
|
G | A | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.699-169G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621928 | ||||||
| chr10:49621928
|
G | T | 3 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0017t0004g0228 | 3 | HG02896.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.699-169G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621928 | ||||||
| chr10:49621964
|
G | GAGGGAGG others(59): Show |
330 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(327): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.699-122_699-57dupA others(65): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621964 | |||||
| chr10:49621964
|
G | GAGGGAGG others(125): Show |
32 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0054others(29): Show | 34 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.699-57_699-56insAA others(130): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621964 | |||||
| chr10:49621964
|
G | GAGGGAGG others(191): Show |
1 | a0001c0001t0002g0176 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.699-57_699-56insAA others(196): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621964 | |||||
| chr10:49621964
|
G | GAGGGAGG others(455): Show |
1 | a0001c0001t0002g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.699-57_699-56insAA others(460): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621964 | |||||
| chr10:49621972
|
G | GAGAAGGG others(48): Show |
1 | a0002c0002t0007g0070 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.699-112_699-58dupA others(54): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621972 | |||||
| chr10:49622009
|
G | GGAAGGAG others(59): Show |
1 | a0001c0001t0016g0219 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.699-57_699-56insAA others(64): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49622009 | |||||
| chr10:49622022
|
G | GAGCGGCC others(87): Show |
1 | a0001c0001t0004g0329 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.699-75_699-74insAG others(92): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49622022 | ||||||
| chr10:49622038
|
G | C | 1 | a0001c0001t0004g0329 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.699-59G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49622038 | ||||||
| chr10:49622039
|
A | G | 1 | a0001c0001t0004g0329 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.699-58A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49622039 | ||||||
| chr10:49622041
|
G | T | 3 | a0001c0001t0004g0329a0001c0005t0005g0063a0001c0005t0005g0064 | 3 | HG00621.hp1 HG02074.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.699-56G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49622041 | ||||||
| chr10:49622205
|
T | A | 6 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.752+55T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622205 | ||||||
| chr10:49622272
|
T | C | 2 | a0001c0003t0006g0351a0001c0005t0005g0350 | 2 | HG00609.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.752+122T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622272 | ||||||
| chr10:49622287
|
C | T | 3 | a0002c0002t0002g0071a0002c0002t0002g0072a0002c0002t0002g0073 | 3 | HG02015.hp2 HG02083.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.752+137C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622287 | ||||||
| chr10:49622531
|
G | A | 1 | a0001c0005t0005g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.752+381G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622531 | ||||||
| chr10:49622533
|
G | C | 1 | a0002c0008t0010g0380 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.752+383G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622533 | ||||||
| chr10:49622602
|
C | T | 1 | a0002c0002t0007g0381 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.752+452C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622602 | ||||||
| chr10:49622652
|
C | A | 31 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0229others(28): Show | 34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.752+502C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622652 | ||||||
| chr10:49622703
|
G | T | 11 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0295others(8): Show | 13 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.752+553G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622703 | ||||||
| chr10:49623001
|
G | A | 1 | a0001c0001t0007g0236 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.752+851G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623001 | ||||||
| chr10:49623010
|
C | G | 26 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0295others(23): Show | 29 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.752+860C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623010 | ||||||
| chr10:49623069
|
C | T | 1 | a0001c0027t0031g0174 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.752+919C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623069 | ||||||
| chr10:49623117
|
T | TTGTCTCC others(8): Show |
1 | a0003c0004t0001g0130 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.752+973_752+987dup others(15): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49623117 | |||||
| chr10:49623155
|
C | G | 1 | a0003c0007t0006g0162 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.752+1005C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623155 | ||||||
| chr10:49623156
|
G | A | 1 | a0001c0001t0016g0219 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.752+1006G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623156 | ||||||
| chr10:49623202
|
C | T | 3 | a0001c0001t0001g0048a0001c0003t0034g0368a0001c0035t0003g0235 | 3 | HG00639.hp2 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.752+1052C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623202 | ||||||
| chr10:49623203
|
G | A | 1 | a0001c0001t0008g0033 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.752+1053G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623203 | ||||||
| chr10:49623283
|
C | CTT | 31 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0229others(28): Show | 34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.752+1133_752+1134i others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623283 | ||||||
| chr10:49623462
|
C | T | 1 | a0001c0001t0016g0219 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.752+1312C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623462 | ||||||
| chr10:49623498
|
A | G | 1 | a0001c0001t0007g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.752+1348A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623498 | ||||||
| chr10:49623531
|
T | C | 1 | a0002c0002t0002g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.752+1381T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623531 | ||||||
| chr10:49623605
|
G | A | 11 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0295others(8): Show | 13 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.752+1455G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623605 | ||||||
| chr10:49623632
|
C | T | 1 | a0001c0001t0006g0356 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.752+1482C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623632 | ||||||
| chr10:49623781
|
T | A | 31 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0229others(28): Show | 34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.752+1631T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623781 | ||||||
| chr10:49623798
|
C | G | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.752+1648C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623798 | ||||||
| chr10:49623808
|
T | C | 31 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0229others(28): Show | 34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.752+1658T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623808 | ||||||
| chr10:49623865
|
G | T | 2 | a0001c0001t0001g0344a0001c0001t0004g0343 | 2 | NA19012.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.753-1608G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623865 | ||||||
| chr10:49624020
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0016g0022 | 3 | HG02258.hp1 HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.753-1453G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624020 | ||||||
| chr10:49624050
|
A | T | 2 | a0001c0005t0009g0272a0005c0016t0009g0271 | 2 | NA18948.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.753-1423A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624050 | ||||||
| chr10:49624055
|
G | A | 26 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0273others(23): Show | 31 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.753-1418G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624055 | ||||||
| chr10:49624056
|
A | C | 26 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0273others(23): Show | 31 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.753-1417A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624056 | ||||||
| chr10:49624063
|
C | T | 63 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0029others(60): Show | 70 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.753-1410C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624063 | ||||||
| chr10:49624204
|
C | G | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.753-1269C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624204 | ||||||
| chr10:49624231
|
T | C | 148 | a0001c0001t0001g0050a0001c0001t0001g0169a0001c0001t0001g0254others(145): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.753-1242T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624231 | ||||||
| chr10:49624570
|
T | C | 31 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0229others(28): Show | 34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.753-903T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624570 | ||||||
| chr10:49624639
|
C | T | 5 | a0001c0001t0007g0358a0001c0003t0006g0004a0001c0003t0006g0303others(2): Show | 7 | NA18943.hp1 NA18944.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.753-834C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624639 | ||||||
| chr10:49624706
|
TGGAA | T | 4 | a0001c0001t0001g0021a0001c0001t0003g0289a0001c0001t0003g0290others(1): Show | 5 | HG01069.hp2 HG01071.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.753-755_753-752del others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624706 | |||||
| chr10:49624718
|
A | T | 7 | a0001c0001t0001g0218a0001c0001t0001g0295a0001c0001t0003g0292others(4): Show | 8 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.753-755A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624718 | ||||||
| chr10:49624718
|
AGGATGGA others(5): Show |
A | 146 | a0001c0001t0001g0050a0001c0001t0001g0169a0001c0001t0001g0254others(143): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.753-743_753-732del others(12): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624718 | |||||
| chr10:49624722
|
TGGATGGA others(1): Show |
T | 9 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0001t0014g0281others(6): Show | 10 | HG01109.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.753-743_753-736del others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624722 | |||||
| chr10:49624726
|
TGGAC | T | 8 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(5): Show | 8 | HG01981.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.753-743_753-740del others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624726 | |||||
| chr10:49624730
|
C | T | 14 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0295others(11): Show | 16 | HG01069.hp2 HG01071.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.753-743C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624730 | ||||||
| chr10:49624730
|
CGGAT | C | 3 | a0001c0001t0001g0354a0001c0001t0004g0355a0003c0004t0027g0113 | 3 | HG01070.hp1 HG01074.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.753-719_753-716del others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624730 | |||||
| chr10:49624730
|
CGGATGGA others(5): Show |
C | 4 | a0001c0001t0002g0273a0001c0001t0007g0240a0001c0003t0010g0238others(1): Show | 4 | NA18949.hp1 NA18954.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.753-727_753-716del others(12): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624730 | |||||
| chr10:49624909
|
G | T | 1 | a0001c0001t0002g0367 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.753-564G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624909 | ||||||
| chr10:49625015
|
A | G | 31 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0229others(28): Show | 34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.753-458A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625015 | ||||||
| chr10:49625024
|
T | C | 6 | a0001c0011t0003g0214a0001c0011t0022g0286a0001c0011t0024g0283others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.753-449T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625024 | ||||||
| chr10:49625035
|
C | T | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.753-438C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625035 | ||||||
| chr10:49625038
|
G | A | 1 | a0001c0001t0004g0051 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.753-435G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625038 | ||||||
| chr10:49625069
|
A | G | 31 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0229others(28): Show | 34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.753-404A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625069 | ||||||
| chr10:49625274
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.753-199G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625274 | ||||||
| chr10:49625310
|
C | T | 1 | a0001c0003t0010g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.753-163C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625310 | ||||||
| chr10:49625338
|
A | C | 31 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0229others(28): Show | 34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.753-135A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625338 | ||||||
| chr10:49625447
|
C | T | 31 | a0001c0001t0001g0021a0001c0001t0001g0218a0001c0001t0001g0229others(28): Show | 34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.753-26C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625447 | ||||||
| chr10:49625457
|
C | T | 1 | a0001c0028t0005g0370 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.753-16C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625457 | ||||||
| chr10:49625793
|
G | A | 26 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0273others(23): Show | 31 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.933+140G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49625793 | ||||||
| chr10:49625848
|
G | A | 6 | a0001c0001t0011g0172a0001c0001t0011g0173a0001c0013t0005g0217others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.933+195G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49625848 | ||||||
| chr10:49625850
|
G | A | 2 | a0001c0011t0024g0283a0001c0011t0029g0216 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.933+197G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49625850 | ||||||
| chr10:49625954
|
C | A | 1 | a0004c0025t0003g0357 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.933+301C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49625954 | ||||||
| chr10:49626010
|
A | C | 1 | a0001c0005t0005g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.933+357A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626010 | ||||||
| chr10:49626011
|
C | A | 3 | a0001c0001t0001g0048a0001c0003t0034g0368a0001c0035t0003g0235 | 3 | HG00639.hp2 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.933+358C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626011 | ||||||
| chr10:49626065
|
T | A | 7 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.933+412T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626065 | ||||||
| chr10:49626099
|
G | T | 2 | a0001c0001t0001g0285a0001c0001t0023g0284 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.933+446G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626099 | ||||||
| chr10:49626189
|
C | T | 2 | a0001c0001t0001g0285a0001c0001t0023g0284 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.933+536C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626189 | ||||||
| chr10:49626319
|
C | G | 1 | a0004c0025t0003g0357 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.933+666C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626319 | ||||||
| chr10:49626328
|
A | G | 1 | a0004c0025t0003g0357 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.933+675A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626328 | ||||||
| chr10:49626382
|
T | C | 1 | a0001c0013t0005g0217 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.933+729T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626382 | ||||||
| chr10:49626425
|
C | G | 1 | a0001c0003t0006g0311 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.933+772C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626425 | ||||||
| chr10:49626568
|
G | A | 19 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(16): Show | 20 | HG01109.hp1 HG01243.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.933+915G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626568 | ||||||
| chr10:49626600
|
G | A | 3 | a0001c0011t0022g0286a0001c0026t0005g0369a0001c0028t0005g0370 | 3 | HG01891.hp1 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.933+947G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626600 | ||||||
| chr10:49626604
|
G | A | 12 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0004g0226others(9): Show | 13 | HG01109.hp1 HG01243.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+951G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626604 | ||||||
| chr10:49626608
|
C | T | 12 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0004g0226others(9): Show | 13 | HG01109.hp1 HG01243.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+955C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626608 | ||||||
| chr10:49626879
|
C | T | 1 | a0001c0010t0008g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.934-729C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626879 | ||||||
| chr10:49626932
|
A | G | 132 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0054others(129): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.934-676A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626932 | ||||||
| chr10:49626990
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.934-618G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626990 | ||||||
| chr10:49627194
|
G | A | 2 | a0001c0001t0002g0274a0003c0004t0004g0166 | 2 | HG00609.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.934-414G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627194 | ||||||
| chr10:49627217
|
C | T | 1 | a0004c0009t0003g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.934-391C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627217 | ||||||
| chr10:49627218
|
G | A | 54 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0054others(51): Show | 62 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.934-390G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627218 | ||||||
| chr10:49627417
|
T | C | 1 | a0002c0002t0002g0075 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.934-191T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627417 | ||||||
| chr10:49627427
|
C | T | 1 | a0001c0001t0016g0219 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.934-181C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627427 | ||||||
| chr10:49627452
|
C | T | 1 | a0001c0001t0016g0219 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.934-156C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627452 | ||||||
| chr10:49627561
|
C | T | 1 | a0002c0002t0012g0099 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.934-47C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627561 | ||||||
| chr10:49627565
|
G | A | 6 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0015g0020others(3): Show | 7 | HG01243.hp2 HG01981.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.934-43G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627565 | ||||||
| chr10:49627793
|
G | A | 1 | a0001c0001t0005g0221 | 1 | HG02922.hp2 | splice_region_variant&intron_variant | LOW | c.1111+8G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49627793 | ||||||
| chr10:49627830
|
G | A | 17 | a0001c0001t0001g0254a0001c0001t0003g0019a0001c0001t0003g0037others(14): Show | 18 | HG01167.hp2 HG01192.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1111+45G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49627830 | ||||||
| chr10:49627921
|
C | A | 276 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0054others(273): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1111+136C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49627921 | ||||||
| chr10:49628044
|
C | T | 2 | a0002c0002t0007g0100a0002c0002t0007g0108 | 2 | HG01934.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1111+259C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628044 | ||||||
| chr10:49628102
|
G | T | 1 | a0001c0001t0003g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1111+317G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628102 | ||||||
| chr10:49628126
|
G | C | 2 | a0001c0003t0010g0170a0001c0019t0002g0171 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1111+341G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628126 | ||||||
| chr10:49628350
|
G | C | 1 | a0004c0009t0003g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1111+565G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628350 | ||||||
| chr10:49628356
|
C | G | 1 | a0002c0002t0009g0098 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1111+571C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628356 | ||||||
| chr10:49628378
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0003g0289a0001c0001t0003g0290 | 4 | HG01069.hp2 HG01071.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+593T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628378 | ||||||
| chr10:49628420
|
C | T | 273 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0054others(270): Show | 297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1111+635C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628420 | ||||||
| chr10:49628572
|
T | C | 12 | a0001c0001t0001g0224a0001c0001t0003g0353a0001c0001t0013g0018others(9): Show | 13 | HG01891.hp1 HG01981.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1111+787T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628572 | ||||||
| chr10:49628686
|
G | C | 139 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0057others(136): Show | 152 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1111+901G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628686 | ||||||
| chr10:49628728
|
G | A | 1 | a0002c0002t0012g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1111+943G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628728 | ||||||
| chr10:49628778
|
G | T | 2 | a0001c0001t0002g0204a0001c0001t0002g0205 | 2 | HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1111+993G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628778 | ||||||
| chr10:49628788
|
C | G | 20 | a0001c0001t0001g0048a0001c0001t0001g0224a0001c0001t0001g0229others(17): Show | 23 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1111+1003C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628788 | ||||||
| chr10:49628868
|
T | C | 379 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(376): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.1111+1083T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628868 | ||||||
| chr10:49628896
|
G | A | 1 | a0003c0004t0004g0156 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1111+1111G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628896 | ||||||
| chr10:49628945
|
C | G | 1 | a0001c0001t0003g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1111+1160C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628945 | ||||||
| chr10:49628987
|
C | T | 10 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0066others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.1111+1202C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628987 | ||||||
| chr10:49628988
|
G | A | 1 | a0001c0011t0022g0286 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1111+1203G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628988 | ||||||
| chr10:49629043
|
C | T | 1 | a0001c0013t0005g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1111+1258C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629043 | ||||||
| chr10:49629125
|
A | C | 1 | a0003c0004t0013g0153 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1111+1340A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629125 | ||||||
| chr10:49629150
|
C | G | 1 | a0002c0002t0002g0379 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1111+1365C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629150 | ||||||
| chr10:49629363
|
G | C | 1 | a0002c0012t0009g0371 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1111+1578G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629363 | ||||||
| chr10:49629533
|
T | C | 4 | a0001c0001t0001g0317a0001c0005t0005g0307a0003c0004t0004g0156others(1): Show | 4 | HG00621.hp2 NA18984.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111+1748T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629533 | ||||||
| chr10:49629711
|
C | T | 1 | a0001c0001t0013g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1111+1926C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629711 | ||||||
| chr10:49629733
|
G | T | 1 | a0004c0009t0003g0275 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1111+1948G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629733 | ||||||
| chr10:49629795
|
G | T | 1 | a0001c0001t0008g0001 | 3 | HG01167.hp1 HG01169.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1111+2010G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629795 | ||||||
| chr10:49629826
|
A | C | 1 | a0001c0010t0003g0262 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1111+2041A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629826 | ||||||
| chr10:49629829
|
G | A | 1 | a0001c0001t0003g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1111+2044G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629829 | ||||||
| chr10:49629946
|
C | G | 41 | a0001c0001t0001g0048a0001c0001t0001g0224a0001c0001t0001g0229others(38): Show | 45 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.1111+2161C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629946 | ||||||
| chr10:49629949
|
C | T | 1 | a0001c0001t0007g0234 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1111+2164C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629949 | ||||||
| chr10:49629956
|
A | G | 3 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0017t0004g0228 | 3 | HG02896.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1111+2171A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629956 | ||||||
| chr10:49629995
|
C | A | 3 | a0002c0002t0002g0002a0002c0002t0002g0103a0002c0012t0009g0077 | 5 | NA18955.hp2 NA18983.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+2210C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629995 | ||||||
| chr10:49630040
|
G | A | 3 | a0001c0001t0004g0288a0001c0001t0007g0182a0006c0014t0007g0178 | 3 | HG03139.hp2 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1111+2255G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49630040 | ||||||
| chr10:49630106
|
G | C | 3 | a0001c0001t0001g0021a0001c0001t0003g0289a0001c0001t0003g0290 | 4 | HG01069.hp2 HG01071.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+2321G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49630106 | ||||||
| chr10:49630155
|
TCAGTA | T | 3 | a0001c0001t0001g0254a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG01243.hp2 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1111+2374_1111+237 others(9): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49630155 | |||||
| chr10:49630212
|
G | A | 2 | a0001c0003t0034g0368a0001c0035t0003g0235 | 2 | HG00639.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111+2427G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49630212 | ||||||
| chr10:49630583
|
C | T | 376 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(373): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.1111+2798C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49630583 | ||||||
| chr10:49630828
|
A | G | 247 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0029others(244): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1111+3043A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49630828 | ||||||
| chr10:49631138
|
T | C | 5 | a0001c0001t0001g0354a0001c0001t0004g0355a0001c0001t0007g0035others(2): Show | 5 | HG00140.hp2 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+3353T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631138 | ||||||
| chr10:49631166
|
A | T | 1 | a0001c0003t0006g0328 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1111+3381A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631166 | ||||||
| chr10:49631357
|
G | A | 94 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0318others(91): Show | 107 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1111+3572G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631357 | ||||||
| chr10:49631521
|
C | T | 65 | a0001c0001t0001g0318a0001c0001t0002g0017a0001c0001t0002g0263others(62): Show | 70 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1111+3736C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631521 | ||||||
| chr10:49631598
|
G | C | 2 | a0001c0010t0003g0262a0001c0010t0008g0268 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1111+3813G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631598 | ||||||
| chr10:49631600
|
G | T | 1 | a0011c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111+3815G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631600 | ||||||
| chr10:49631836
|
G | A | 2 | a0001c0001t0003g0220a0004c0025t0003g0357 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1111+4051G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631836 | ||||||
| chr10:49631851
|
A | G | 1 | a0004c0025t0003g0357 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1111+4066A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631851 | ||||||
| chr10:49632044
|
T | C | 1 | a0002c0002t0007g0381 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1111+4259T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632044 | ||||||
| chr10:49632151
|
C | T | 4 | a0001c0001t0003g0353a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG01109.hp1 HG06807.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+4366C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632151 | ||||||
| chr10:49632292
|
G | A | 2 | a0001c0026t0005g0369a0001c0028t0005g0370 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1111+4507G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632292 | ||||||
| chr10:49632615
|
A | C | 376 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(373): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.1111+4830A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632615 | ||||||
| chr10:49632640
|
C | T | 1 | a0001c0001t0014g0282 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1111+4855C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632640 | ||||||
| chr10:49632641
|
G | A | 3 | a0002c0002t0002g0079a0002c0002t0002g0105a0003c0004t0001g0132 | 3 | HG00673.hp2 HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1111+4856G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632641 | ||||||
| chr10:49632652
|
T | C | 9 | a0001c0001t0001g0215a0001c0001t0001g0224a0001c0001t0001g0295others(6): Show | 10 | HG01884.hp1 HG01981.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1111+4867T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632652 | ||||||
| chr10:49632690
|
G | A | 271 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(268): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1111+4905G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632690 | ||||||
| chr10:49632740
|
T | C | 376 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(373): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.1111+4955T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632740 | ||||||
| chr10:49632851
|
G | C | 1 | a0001c0001t0003g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1111+5066G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632851 | ||||||
| chr10:49632868
|
C | T | 351 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(348): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.1111+5083C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632868 | ||||||
| chr10:49633420
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1111+5635G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633420 | ||||||
| chr10:49633530
|
C | T | 1 | a0001c0001t0002g0274 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1111+5745C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633530 | ||||||
| chr10:49633604
|
T | C | 6 | a0001c0001t0001g0224a0001c0001t0001g0295a0001c0001t0003g0220others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111+5819T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633604 | ||||||
| chr10:49633658
|
C | T | 290 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0029others(287): Show | 311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1111+5873C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633658 | ||||||
| chr10:49633681
|
A | G | 1 | a0002c0002t0002g0379 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1111+5896A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633681 | ||||||
| chr10:49633685
|
C | T | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1111+5900C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633685 | ||||||
| chr10:49633745
|
GC | G | 9 | a0001c0001t0004g0005a0001c0001t0004g0051a0001c0001t0005g0267others(6): Show | 10 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1111+5966delC | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49633745 | |||||
| chr10:49633978
|
C | T | 194 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0060others(191): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1111+6193C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633978 | ||||||
| chr10:49634139
|
A | C | 39 | a0001c0001t0001g0057a0001c0001t0001g0354a0001c0001t0002g0194others(36): Show | 43 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.1111+6354A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634139 | ||||||
| chr10:49634218
|
A | G | 47 | a0001c0001t0001g0169a0001c0001t0001g0346a0001c0001t0002g0176others(44): Show | 50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1111+6433A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634218 | ||||||
| chr10:49634270
|
G | T | 1 | a0001c0010t0003g0260 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1111+6485G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634270 | ||||||
| chr10:49634288
|
G | A | 1 | a0011c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111+6503G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634288 | ||||||
| chr10:49634298
|
A | G | 2 | a0003c0004t0001g0143a0003c0004t0001g0144 | 2 | NA18612.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1111+6513A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634298 | ||||||
| chr10:49634310
|
G | A | 5 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0262others(2): Show | 5 | HG02257.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111+6525G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634310 | ||||||
| chr10:49634329
|
C | T | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1111+6544C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634329 | ||||||
| chr10:49634391
|
G | T | 3 | a0001c0001t0003g0353a0001c0001t0014g0282a0001c0027t0031g0174 | 3 | HG01109.hp1 HG01981.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1111+6606G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634391 | ||||||
| chr10:49634462
|
T | C | 10 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0004g0005others(7): Show | 11 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111+6677T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634462 | ||||||
| chr10:49634537
|
T | C | 125 | a0001c0001t0001g0025a0001c0001t0001g0318a0001c0001t0001g0346others(122): Show | 136 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1111+6752T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634537 | ||||||
| chr10:49634538
|
G | C | 124 | a0001c0001t0001g0025a0001c0001t0001g0318a0001c0001t0001g0346others(121): Show | 135 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1111+6753G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634538 | ||||||
| chr10:49634610
|
T | C | 2 | a0001c0010t0003g0223a0001c0028t0005g0370 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1111+6825T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634610 | ||||||
| chr10:49634657
|
T | G | 2 | a0001c0001t0006g0356a0001c0011t0022g0286 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1111+6872T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634657 | ||||||
| chr10:49634766
|
C | T | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111+6981C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634766 | ||||||
| chr10:49634842
|
A | G | 372 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(369): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.1111+7057A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634842 | ||||||
| chr10:49634990
|
C | T | 109 | a0001c0001t0001g0025a0001c0001t0001g0346a0001c0001t0002g0176others(106): Show | 118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1111+7205C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634990 | ||||||
| chr10:49634995
|
T | C | 2 | a0001c0003t0003g0291a0001c0003t0003g0293 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111+7210T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634995 | ||||||
| chr10:49635062
|
T | A | 129 | a0001c0001t0001g0025a0001c0001t0001g0318a0001c0001t0001g0346others(126): Show | 140 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1111+7277T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635062 | ||||||
| chr10:49635080
|
C | T | 1 | a0001c0001t0007g0234 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1111+7295C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635080 | ||||||
| chr10:49635133
|
A | G | 6 | a0001c0001t0003g0019a0001c0001t0003g0037a0001c0001t0003g0255others(3): Show | 7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111+7348A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635133 | ||||||
| chr10:49635221
|
T | G | 1 | a0003c0007t0006g0164 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1111+7436T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635221 | ||||||
| chr10:49635543
|
G | A | 44 | a0001c0001t0001g0346a0001c0001t0002g0176a0001c0001t0002g0184others(41): Show | 46 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1111+7758G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635543 | ||||||
| chr10:49635598
|
G | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111+7813G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635598 | ||||||
| chr10:49635683
|
G | A | 98 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(95): Show | 110 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1111+7898G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635683 | ||||||
| chr10:49635730
|
C | G | 12 | a0001c0001t0001g0318a0001c0001t0003g0353a0001c0001t0004g0109others(9): Show | 13 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1111+7945C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635730 | ||||||
| chr10:49635811
|
T | C | 100 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(97): Show | 112 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1111+8026T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635811 | ||||||
| chr10:49636093
|
C | T | 10 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0004g0005others(7): Show | 11 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111+8308C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636093 | ||||||
| chr10:49636106
|
A | G | 1 | a0001c0026t0005g0369 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1111+8321A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636106 | ||||||
| chr10:49636119
|
G | A | 1 | a0003c0006t0005g0152 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1111+8334G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636119 | ||||||
| chr10:49636161
|
C | T | 3 | a0001c0001t0007g0047a0001c0003t0010g0016a0001c0003t0010g0243 | 4 | HG01516.hp2 HG01517.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+8376C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636161 | ||||||
| chr10:49636310
|
A | G | 1 | a0001c0001t0005g0221 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1111+8525A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636310 | ||||||
| chr10:49636372
|
G | A | 2 | a0001c0003t0003g0291a0001c0003t0003g0293 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111+8587G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636372 | ||||||
| chr10:49636519
|
G | T | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111+8734G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636519 | ||||||
| chr10:49636560
|
C | G | 11 | a0001c0001t0001g0224a0001c0001t0003g0289a0001c0001t0003g0290others(8): Show | 12 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1111+8775C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636560 | ||||||
| chr10:49636582
|
G | A | 6 | a0001c0001t0003g0019a0001c0001t0003g0037a0001c0001t0003g0255others(3): Show | 7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111+8797G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636582 | ||||||
| chr10:49636662
|
T | C | 371 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(368): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1111+8877T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636662 | ||||||
| chr10:49636692
|
C | G | 4 | a0001c0001t0005g0221a0001c0013t0005g0217a0001c0013t0005g0294others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+8907C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636692 | ||||||
| chr10:49636729
|
C | T | 1 | a0001c0030t0004g0316 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1111+8944C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636729 | ||||||
| chr10:49636942
|
T | C | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111+9157T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636942 | ||||||
| chr10:49636957
|
CTTA | C | 6 | a0001c0001t0003g0019a0001c0001t0003g0037a0001c0001t0003g0255others(3): Show | 7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111+9177_1111+917 others(7): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49636957 | |||||
| chr10:49636974
|
G | A | 1 | a0003c0006t0005g0152 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1111+9189G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636974 | ||||||
| chr10:49636981
|
G | T | 2 | a0001c0003t0003g0291a0001c0003t0003g0293 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111+9196G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636981 | ||||||
| chr10:49637011
|
G | A | 109 | a0001c0001t0001g0025a0001c0001t0001g0346a0001c0001t0002g0176others(106): Show | 118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1111+9226G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637011 | ||||||
| chr10:49637040
|
C | CT | 30 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(27): Show | 33 | HG00735.hp1 HG00738.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1111+9266dupT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49637040 | |||||
| chr10:49637071
|
T | C | 1 | a0001c0001t0004g0051 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1111+9286T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637071 | ||||||
| chr10:49637094
|
C | T | 10 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0004g0005others(7): Show | 11 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111+9309C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637094 | ||||||
| chr10:49637153
|
A | G | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-9352A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637153 | ||||||
| chr10:49637250
|
C | A | 2 | a0001c0003t0003g0291a0001c0003t0003g0293 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1112-9255C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637250 | ||||||
| chr10:49637291
|
A | G | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-9214A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637291 | ||||||
| chr10:49637371
|
T | A | 9 | a0001c0003t0006g0004a0001c0003t0006g0303a0001c0003t0006g0336others(6): Show | 11 | NA18944.hp1 NA18952.hp2 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1112-9134T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637371 | ||||||
| chr10:49637549
|
C | G | 2 | a0001c0001t0001g0029a0001c0001t0002g0264 | 3 | HG02615.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1112-8956C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637549 | ||||||
| chr10:49638149
|
GTCT | G | 4 | a0001c0001t0007g0181a0001c0001t0008g0299a0001c0030t0004g0316others(1): Show | 4 | HG01081.hp1 HG01358.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112-8351_1112-834 others(7): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49638149 | |||||
| chr10:49638221
|
A | C | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-8284A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638221 | ||||||
| chr10:49638226
|
G | A | 1 | a0001c0005t0005g0063 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1112-8279G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638226 | ||||||
| chr10:49638230
|
T | C | 8 | a0001c0001t0005g0305a0001c0001t0005g0306a0001c0001t0007g0179others(5): Show | 8 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1112-8275T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638230 | ||||||
| chr10:49638291
|
T | G | 1 | a0003c0007t0006g0165 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1112-8214T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638291 | ||||||
| chr10:49638520
|
C | T | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-7985C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638520 | ||||||
| chr10:49638836
|
A | C | 63 | a0001c0001t0001g0025a0001c0001t0003g0220a0001c0001t0004g0051others(60): Show | 70 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(67): Show |
intron_variant | MODIFIER | c.1112-7669A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638836 | ||||||
| chr10:49638935
|
T | TA | 13 | a0001c0003t0034g0368a0001c0010t0003g0044a0001c0010t0003g0045others(10): Show | 13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1112-7562dupA | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49638935 | |||||
| chr10:49638953
|
G | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-7552G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638953 | ||||||
| chr10:49638990
|
C | T | 4 | a0001c0001t0005g0221a0001c0013t0005g0217a0001c0013t0005g0294others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112-7515C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638990 | ||||||
| chr10:49638996
|
G | A | 2 | a0001c0003t0003g0291a0001c0003t0003g0293 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1112-7509G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638996 | ||||||
| chr10:49639016
|
G | A | 109 | a0001c0001t0001g0025a0001c0001t0001g0346a0001c0001t0002g0176others(106): Show | 118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1112-7489G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639016 | ||||||
| chr10:49639096
|
G | A | 1 | a0017c0018t0003g0330 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1112-7409G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639096 | ||||||
| chr10:49639182
|
C | A | 7 | a0001c0001t0005g0305a0001c0001t0005g0306a0001c0001t0007g0179others(4): Show | 7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-7323C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639182 | ||||||
| chr10:49639282
|
G | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-7223G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639282 | ||||||
| chr10:49639475
|
GA | G | 371 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(368): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1112-7020delA | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639475 | |||||
| chr10:49639538
|
TATAC | T | 4 | a0001c0001t0005g0221a0001c0013t0005g0217a0001c0013t0005g0294others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112-6965_1112-696 others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639538 | |||||
| chr10:49639540
|
TAC | T | 3 | a0001c0001t0001g0048a0001c0001t0013g0225a0002c0008t0010g0092 | 3 | HG02145.hp2 HG02572.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1112-6937_1112-693 others(6): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639540 | |||||
| chr10:49639540
|
TACAC | T | 74 | a0001c0001t0001g0025a0001c0001t0001g0285a0001c0001t0001g0295others(71): Show | 82 | HG00099.hp1 HG00544.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.1112-6939_1112-693 others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639540 | |||||
| chr10:49639540
|
TACACAC | T | 199 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(196): Show | 218 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.1112-6941_1112-693 others(10): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639540 | |||||
| chr10:49639540
|
TACACACA others(1): Show |
T | 83 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0060others(80): Show | 90 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1112-6943_1112-693 others(12): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639540 | |||||
| chr10:49639542
|
C | T | 8 | a0001c0001t0005g0305a0001c0001t0005g0306a0001c0001t0007g0179others(5): Show | 8 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1112-6963C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639542 | ||||||
| chr10:49639546
|
C | T | 3 | a0001c0001t0003g0353a0001c0001t0014g0282a0001c0003t0034g0368 | 3 | HG01109.hp1 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1112-6959C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639546 | ||||||
| chr10:49639565
|
ACACATAT others(3): Show |
A | 7 | a0001c0001t0005g0305a0001c0001t0005g0306a0001c0001t0007g0179others(4): Show | 7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-6939_1112-693 others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639565 | ||||||
| chr10:49639578
|
T | G | 7 | a0001c0001t0005g0305a0001c0001t0005g0306a0001c0001t0007g0179others(4): Show | 7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-6927T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639578 | ||||||
| chr10:49639790
|
T | G | 8 | a0001c0001t0005g0305a0001c0001t0005g0306a0001c0001t0007g0179others(5): Show | 8 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1112-6715T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639790 | ||||||
| chr10:49639855
|
C | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-6650C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639855 | ||||||
| chr10:49639906
|
C | A | 5 | a0001c0001t0001g0317a0003c0004t0001g0137a0003c0004t0001g0138others(2): Show | 5 | NA18970.hp1 NA18985.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.1112-6599C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639906 | ||||||
| chr10:49639951
|
C | T | 109 | a0001c0001t0001g0025a0001c0001t0001g0346a0001c0001t0002g0176others(106): Show | 118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1112-6554C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639951 | ||||||
| chr10:49639980
|
C | T | 2 | a0001c0003t0008g0015a0003c0004t0004g0128 | 3 | HG02895.hp2 HG02897.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1112-6525C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639980 | ||||||
| chr10:49640017
|
C | A | 34 | a0001c0001t0001g0057a0001c0001t0001g0354a0001c0001t0002g0194others(31): Show | 38 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1112-6488C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640017 | ||||||
| chr10:49640334
|
T | A | 10 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0004g0005others(7): Show | 11 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1112-6171T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640334 | ||||||
| chr10:49640468
|
C | A | 1 | a0002c0008t0010g0382 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1112-6037C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640468 | ||||||
| chr10:49640501
|
T | TG | 87 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0060others(84): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1112-5998dupG | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49640501 | |||||
| chr10:49640708
|
G | A | 3 | a0001c0001t0004g0261a0001c0001t0004g0288a0001c0001t0007g0182 | 3 | HG03139.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1112-5797G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640708 | ||||||
| chr10:49640709
|
G | T | 1 | a0014c0037t0035g0301 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1112-5796G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640709 | ||||||
| chr10:49640719
|
A | C | 3 | a0001c0011t0024g0283a0001c0011t0029g0216a0001c0027t0031g0174 | 3 | HG01981.hp1 HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1112-5786A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640719 | ||||||
| chr10:49640808
|
T | G | 1 | a0001c0001t0003g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1112-5697T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640808 | ||||||
| chr10:49640822
|
G | A | 4 | a0001c0001t0005g0221a0001c0013t0005g0217a0001c0013t0005g0294others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112-5683G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640822 | ||||||
| chr10:49641007
|
AACAG | A | 6 | a0001c0001t0003g0019a0001c0001t0003g0037a0001c0001t0003g0255others(3): Show | 7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-5494_1112-549 others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49641007 | |||||
| chr10:49641153
|
G | C | 6 | a0001c0001t0003g0019a0001c0001t0003g0037a0001c0001t0003g0255others(3): Show | 7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-5352G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641153 | ||||||
| chr10:49641204
|
G | T | 1 | a0001c0026t0005g0369 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1112-5301G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641204 | ||||||
| chr10:49641296
|
T | G | 98 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(95): Show | 110 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1112-5209T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641296 | ||||||
| chr10:49641341
|
CCTTCCTC others(7): Show |
C | 4 | a0001c0001t0005g0221a0001c0013t0005g0217a0001c0013t0005g0294others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112-5160_1112-514 others(18): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49641341 | |||||
| chr10:49641355
|
T | C | 6 | a0001c0005t0009g0249a0001c0005t0009g0250a0001c0005t0030g0341others(3): Show | 6 | HG00408.hp1 NA18973.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.1112-5150T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641355 | ||||||
| chr10:49641488
|
A | G | 10 | a0001c0001t0003g0053a0001c0001t0003g0065a0001c0001t0008g0001others(7): Show | 12 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-5017A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641488 | ||||||
| chr10:49641503
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1112-5002T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641503 | ||||||
| chr10:49641559
|
A | T | 2 | a0001c0003t0003g0291a0001c0003t0003g0293 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1112-4946A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641559 | ||||||
| chr10:49641574
|
C | A | 1 | a0001c0010t0003g0257 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1112-4931C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641574 | ||||||
| chr10:49641667
|
G | A | 1 | a0001c0001t0001g0354 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1112-4838G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641667 | ||||||
| chr10:49641950
|
T | C | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-4555T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641950 | ||||||
| chr10:49642004
|
G | A | 7 | a0001c0001t0005g0305a0001c0001t0005g0306a0001c0001t0007g0179others(4): Show | 7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-4501G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642004 | ||||||
| chr10:49642008
|
C | T | 3 | a0001c0001t0004g0261a0001c0001t0004g0288a0001c0001t0007g0182 | 3 | HG03139.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1112-4497C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642008 | ||||||
| chr10:49642024
|
A | G | 1 | a0001c0001t0018g0213 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1112-4481A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642024 | ||||||
| chr10:49642117
|
G | A | 97 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(94): Show | 109 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1112-4388G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642117 | ||||||
| chr10:49642194
|
T | C | 7 | a0001c0001t0005g0305a0001c0001t0005g0306a0001c0001t0007g0179others(4): Show | 7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-4311T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642194 | ||||||
| chr10:49642228
|
A | G | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-4277A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642228 | ||||||
| chr10:49642299
|
T | C | 371 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(368): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1112-4206T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642299 | ||||||
| chr10:49642306
|
C | T | 1 | a0001c0003t0006g0310 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1112-4199C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642306 | ||||||
| chr10:49642332
|
C | T | 11 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0004g0005others(8): Show | 12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1112-4173C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642332 | ||||||
| chr10:49642481
|
G | T | 1 | a0001c0001t0002g0242 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1112-4024G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642481 | ||||||
| chr10:49642598
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1112-3907C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642598 | ||||||
| chr10:49642673
|
G | C | 10 | a0001c0001t0003g0053a0001c0001t0003g0065a0001c0001t0008g0001others(7): Show | 12 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-3832G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642673 | ||||||
| chr10:49642708
|
C | A | 115 | a0001c0001t0001g0025a0001c0001t0001g0346a0001c0001t0002g0176others(112): Show | 124 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1112-3797C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642708 | ||||||
| chr10:49642735
|
G | A | 108 | a0001c0001t0001g0025a0001c0001t0001g0346a0001c0001t0002g0176others(105): Show | 117 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1112-3770G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642735 | ||||||
| chr10:49642768
|
C | T | 1 | a0001c0001t0004g0051 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1112-3737C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642768 | ||||||
| chr10:49642814
|
T | C | 7 | a0001c0001t0005g0305a0001c0001t0005g0306a0001c0001t0007g0179others(4): Show | 7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-3691T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642814 | ||||||
| chr10:49642875
|
A | G | 24 | a0001c0001t0001g0285a0001c0001t0001g0295a0001c0001t0003g0053others(21): Show | 27 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112-3630A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642875 | ||||||
| chr10:49643058
|
T | C | 10 | a0001c0001t0003g0053a0001c0001t0003g0065a0001c0001t0008g0001others(7): Show | 12 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-3447T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643058 | ||||||
| chr10:49643098
|
G | A | 3 | a0001c0011t0024g0283a0001c0011t0029g0216a0001c0027t0031g0174 | 3 | HG01981.hp1 HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1112-3407G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643098 | ||||||
| chr10:49643100
|
C | G | 1 | a0001c0005t0005g0350 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1112-3405C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643100 | ||||||
| chr10:49643228
|
A | G | 1 | a0012c0031t0003g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1112-3277A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643228 | ||||||
| chr10:49643304
|
G | A | 1 | a0003c0004t0001g0142 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1112-3201G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643304 | ||||||
| chr10:49643562
|
C | T | 1 | a0001c0003t0006g0323 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1112-2943C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643562 | ||||||
| chr10:49643601
|
G | A | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-2904G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643601 | ||||||
| chr10:49643712
|
C | G | 1 | a0001c0003t0010g0238 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1112-2793C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643712 | ||||||
| chr10:49643788
|
T | C | 377 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(374): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.1112-2717T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643788 | ||||||
| chr10:49643827
|
C | G | 1 | a0001c0001t0002g0199 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1112-2678C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643827 | ||||||
| chr10:49643865
|
C | A | 62 | a0001c0001t0001g0025a0001c0001t0003g0220a0001c0001t0004g0051others(59): Show | 69 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(66): Show |
intron_variant | MODIFIER | c.1112-2640C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643865 | ||||||
| chr10:49643947
|
G | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-2558G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643947 | ||||||
| chr10:49644009
|
G | A | 1 | a0001c0003t0006g0323 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1112-2496G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644009 | ||||||
| chr10:49644082
|
A | T | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-2423A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644082 | ||||||
| chr10:49644103
|
A | T | 371 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(368): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1112-2402A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644103 | ||||||
| chr10:49644106
|
G | A | 3 | a0001c0010t0003g0262a0001c0010t0008g0268a0001c0017t0003g0256 | 3 | HG03041.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1112-2399G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644106 | ||||||
| chr10:49644137
|
C | T | 120 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0060others(117): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1112-2368C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644137 | ||||||
| chr10:49644211
|
C | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-2294C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644211 | ||||||
| chr10:49644215
|
G | A | 2 | a0001c0003t0003g0291a0001c0003t0003g0293 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1112-2290G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644215 | ||||||
| chr10:49644278
|
C | G | 44 | a0001c0001t0001g0346a0001c0001t0002g0176a0001c0001t0002g0184others(41): Show | 46 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1112-2227C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644278 | ||||||
| chr10:49644280
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0002g0264 | 3 | HG02615.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1112-2225C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644280 | ||||||
| chr10:49644481
|
G | C | 38 | a0001c0001t0001g0057a0001c0001t0001g0354a0001c0001t0002g0194others(35): Show | 42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.1112-2024G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644481 | ||||||
| chr10:49644499
|
T | G | 1 | a0001c0001t0004g0331 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1112-2006T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644499 | ||||||
| chr10:49644548
|
G | A | 6 | a0001c0001t0003g0019a0001c0001t0003g0037a0001c0001t0003g0255others(3): Show | 7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-1957G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644548 | ||||||
| chr10:49644573
|
G | C | 24 | a0001c0001t0001g0318a0001c0001t0003g0353a0001c0001t0004g0109others(21): Show | 25 | HG00738.hp1 HG01109.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1112-1932G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644573 | ||||||
| chr10:49644660
|
CAGAGT | C | 11 | a0001c0001t0001g0318a0001c0001t0003g0353a0001c0001t0004g0109others(8): Show | 12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1112-1841_1112-183 others(9): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49644660 | |||||
| chr10:49644707
|
C | T | 11 | a0001c0001t0001g0318a0001c0001t0003g0353a0001c0001t0004g0109others(8): Show | 12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1112-1798C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644707 | ||||||
| chr10:49644718
|
G | A | 371 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(368): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1112-1787G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644718 | ||||||
| chr10:49644736
|
G | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-1769G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644736 | ||||||
| chr10:49644786
|
C | T | 371 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(368): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1112-1719C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644786 | ||||||
| chr10:49644954
|
T | C | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1551T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644954 | ||||||
| chr10:49645039
|
G | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-1466G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645039 | ||||||
| chr10:49645087
|
C | T | 1 | a0002c0002t0002g0078 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1112-1418C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645087 | ||||||
| chr10:49645144
|
T | A | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1361T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645144 | ||||||
| chr10:49645146
|
T | C | 109 | a0001c0001t0001g0025a0001c0001t0001g0346a0001c0001t0002g0176others(106): Show | 118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1112-1359T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645146 | ||||||
| chr10:49645297
|
C | T | 86 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0060others(83): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1112-1208C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645297 | ||||||
| chr10:49645304
|
C | T | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1201C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645304 | ||||||
| chr10:49645348
|
C | T | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1157C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645348 | ||||||
| chr10:49645352
|
G | A | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1153G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645352 | ||||||
| chr10:49645458
|
T | G | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1047T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645458 | ||||||
| chr10:49645480
|
T | C | 263 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(260): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1112-1025T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645480 | ||||||
| chr10:49645500
|
G | A | 2 | a0009c0036t0003g0337a0017c0018t0003g0330 | 2 | HG01123.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1112-1005G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645500 | ||||||
| chr10:49645539
|
C | T | 13 | a0001c0001t0004g0315a0001c0010t0003g0044a0001c0010t0003g0045others(10): Show | 13 | HG01167.hp2 HG01978.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1112-966C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645539 | ||||||
| chr10:49645579
|
G | A | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-926G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645579 | ||||||
| chr10:49645775
|
C | T | 2 | a0001c0001t0002g0263a0001c0005t0009g0252 | 2 | NA18943.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1112-730C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645775 | ||||||
| chr10:49646041
|
A | AT | 11 | a0001c0001t0001g0318a0001c0001t0003g0353a0001c0001t0004g0109others(8): Show | 12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1112-462dupT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49646041 | |||||
| chr10:49646087
|
T | C | 1 | a0011c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1112-418T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646087 | ||||||
| chr10:49646136
|
G | A | 1 | a0004c0034t0015g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1112-369G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646136 | ||||||
| chr10:49646151
|
G | A | 111 | a0001c0001t0001g0025a0001c0001t0001g0346a0001c0001t0002g0176others(108): Show | 120 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1112-354G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646151 | ||||||
| chr10:49646155
|
C | G | 1 | a0001c0001t0003g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1112-350C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646155 | ||||||
| chr10:49646347
|
C | T | 1 | a0001c0030t0004g0316 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1112-158C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646347 | ||||||
| chr10:49646395
|
C | T | 46 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0062others(43): Show | 49 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1112-110C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646395 | ||||||
| chr10:49646422
|
G | T | 11 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0004g0005others(8): Show | 12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1112-83G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646422 | ||||||
| chr10:49646437
|
G | A | 61 | a0001c0001t0001g0025a0001c0001t0002g0204a0001c0001t0003g0220others(58): Show | 67 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.1112-68G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646437 | ||||||
| chr10:49646451
|
G | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-54G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646451 | ||||||
| chr10:49646690
|
G | A | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1281+16G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646690 | ||||||
| chr10:49646721
|
G | A | 45 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0062others(42): Show | 48 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1281+47G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646721 | ||||||
| chr10:49646756
|
C | T | 1 | a0001c0001t0004g0232 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1281+82C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646756 | ||||||
| chr10:49646761
|
G | A | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1281+87G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646761 | ||||||
| chr10:49646765
|
G | A | 5 | a0001c0003t0010g0208a0001c0003t0010g0209a0003c0007t0006g0114others(2): Show | 5 | NA18974.hp2 NA18988.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.1281+91G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646765 | ||||||
| chr10:49646856
|
T | A | 1 | a0001c0001t0004g0232 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1281+182T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646856 | ||||||
| chr10:49647016
|
G | C | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1281+342G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647016 | ||||||
| chr10:49647021
|
C | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1281+347C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647021 | ||||||
| chr10:49647104
|
A | G | 11 | a0001c0001t0001g0318a0001c0001t0003g0353a0001c0001t0004g0109others(8): Show | 12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1281+430A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647104 | ||||||
| chr10:49647115
|
T | G | 11 | a0001c0001t0001g0318a0001c0001t0003g0353a0001c0001t0004g0109others(8): Show | 12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1281+441T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647115 | ||||||
| chr10:49647321
|
C | T | 1 | a0001c0001t0001g0354 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1281+647C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647321 | ||||||
| chr10:49647322
|
C | G | 118 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0060others(115): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1281+648C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647322 | ||||||
| chr10:49647366
|
C | G | 1 | a0002c0002t0002g0009 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1281+692C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647366 | ||||||
| chr10:49647453
|
A | G | 13 | a0001c0003t0034g0368a0001c0010t0003g0044a0001c0010t0003g0045others(10): Show | 13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1281+779A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647453 | ||||||
| chr10:49647593
|
C | T | 13 | a0001c0003t0034g0368a0001c0010t0003g0044a0001c0010t0003g0045others(10): Show | 13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1282-914C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647593 | ||||||
| chr10:49647622
|
A | G | 1 | a0001c0011t0003g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1282-885A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647622 | ||||||
| chr10:49647734
|
C | T | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1282-773C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647734 | ||||||
| chr10:49647738
|
GCTTTCCT others(14): Show |
G | 1 | a0001c0005t0005g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1282-765_1282-745d others(23): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647738 | |||||
| chr10:49647740
|
T | TTTCC | 10 | a0001c0001t0003g0019a0001c0003t0003g0314a0001c0003t0006g0328others(7): Show | 11 | HG01192.hp1 HG02083.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1282-700_1282-697d others(6): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | |||||
| chr10:49647740
|
T | TTTCCTTC others(5): Show |
1 | a0003c0007t0003g0112 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1282-708_1282-697d others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | |||||
| chr10:49647740
|
TTTCC | T | 25 | a0001c0001t0001g0318a0001c0001t0003g0290a0001c0001t0004g0321others(22): Show | 27 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1282-700_1282-697d others(6): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | |||||
| chr10:49647740
|
TTTCCTTC others(1): Show |
T | 34 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0215others(31): Show | 38 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1282-704_1282-697d others(10): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | |||||
| chr10:49647740
|
TTTCCTTC others(5): Show |
T | 23 | a0001c0001t0001g0218a0001c0001t0003g0031a0001c0001t0003g0032others(20): Show | 25 | HG01243.hp2 HG01978.hp1 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.1282-708_1282-697d others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | |||||
| chr10:49647740
|
TTTCCTTC others(9): Show |
T | 30 | a0001c0001t0001g0060a0001c0001t0001g0169a0001c0001t0001g0229others(27): Show | 30 | HG00099.hp1 HG00621.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1282-712_1282-697d others(18): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | |||||
| chr10:49647740
|
TTTCCTTC others(13): Show |
T | 126 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0050others(123): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1282-716_1282-697d others(22): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | |||||
| chr10:49647740
|
TTTCCTTC others(17): Show |
T | 61 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0062others(58): Show | 68 | HG00280.hp1 HG00544.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1282-720_1282-697d others(26): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | |||||
| chr10:49647740
|
TTTCCTTC others(21): Show |
T | 38 | a0001c0001t0001g0346a0001c0001t0001g0354a0001c0001t0002g0176others(35): Show | 42 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1282-724_1282-697d others(30): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | |||||
| chr10:49647740
|
TTTCCTTC others(25): Show |
T | 7 | a0001c0001t0001g0285a0001c0001t0001g0295a0001c0001t0013g0018others(4): Show | 8 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-728_1282-697d others(34): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | |||||
| chr10:49647740
|
TTTCCTTC others(33): Show |
T | 1 | a0001c0001t0023g0284 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1282-736_1282-697d others(42): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | |||||
| chr10:49647787
|
C | T | 2 | a0001c0003t0006g0055a0001c0003t0010g0034 | 2 | HG01175.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1282-720C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647787 | ||||||
| chr10:49647787
|
CCTTCCTT others(17): Show |
C | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1282-719_1282-696d others(26): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647787 | ||||||
| chr10:49647799
|
C | G | 1 | a0001c0003t0006g0309 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1282-708C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647799 | ||||||
| chr10:49647877
|
G | T | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1282-630G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647877 | ||||||
| chr10:49647968
|
T | G | 1 | a0001c0003t0008g0183 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1282-539T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647968 | ||||||
| chr10:49648092
|
G | T | 96 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(93): Show | 107 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1282-415G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49648092 | ||||||
| chr10:49648145
|
G | A | 2 | a0006c0014t0004g0287a0006c0014t0007g0178 | 2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1282-362G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49648145 | ||||||
| chr10:49648185
|
C | G | 1 | a0001c0001t0002g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1282-322C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49648185 | ||||||
| chr10:49648482
|
G | A | 12 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(9): Show | 12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1282-25G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49648482 | ||||||
| chr10:49648709
|
G | GA | 6 | a0001c0001t0003g0019a0001c0001t0003g0037a0001c0001t0003g0255others(3): Show | 7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1382+109dupA | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648709 | |||||
| chr10:49648726
|
T | TAC | 5 | a0002c0002t0002g0009a0004c0009t0003g0275a0004c0009t0011g0038others(2): Show | 6 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1382+150_1382+151d others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | |||||
| chr10:49648726
|
T | TACAC | 45 | a0001c0001t0002g0176a0001c0001t0002g0184a0001c0001t0002g0185others(42): Show | 49 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1382+148_1382+151d others(6): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | |||||
| chr10:49648726
|
T | TACACAC | 5 | a0001c0001t0016g0219a0001c0003t0034g0368a0003c0004t0001g0046others(2): Show | 5 | HG02165.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1382+146_1382+151d others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | |||||
| chr10:49648726
|
T | TACACACA others(3): Show |
1 | a0001c0001t0014g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1382+142_1382+151d others(12): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | |||||
| chr10:49648726
|
T | TACACACA others(5): Show |
2 | a0001c0001t0003g0277a0010c0032t0025g0056 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1382+140_1382+151d others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | |||||
| chr10:49648726
|
T | TACACACA others(9): Show |
6 | a0001c0001t0003g0019a0001c0001t0003g0037a0001c0001t0003g0255others(3): Show | 7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1382+136_1382+151d others(18): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | |||||
| chr10:49648726
|
T | TACACACA others(11): Show |
1 | a0001c0011t0003g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1382+134_1382+151d others(20): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | |||||
| chr10:49648726
|
T | TACACACA others(13): Show |
1 | a0001c0001t0003g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1382+132_1382+151d others(22): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | |||||
| chr10:49648726
|
TAC | T | 259 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0029others(256): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1382+150_1382+151d others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | |||||
| chr10:49648726
|
TACACAC | T | 14 | a0001c0003t0003g0291a0001c0003t0003g0293a0001c0010t0003g0044others(11): Show | 14 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1382+146_1382+151d others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | |||||
| chr10:49648726
|
TACACACA others(1): Show |
T | 11 | a0001c0001t0001g0318a0001c0001t0003g0353a0001c0001t0004g0109others(8): Show | 12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1382+144_1382+151d others(10): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | |||||
| chr10:49648856
|
A | AGGAATTC others(4): Show |
1 | a0003c0006t0005g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1382+251_1382+261d others(13): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648856 | |||||
| chr10:49649033
|
G | A | 1 | a0003c0004t0001g0046 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1382+426G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649033 | ||||||
| chr10:49649034
|
C | T | 1 | a0001c0001t0007g0036 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1382+427C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649034 | ||||||
| chr10:49649036
|
C | T | 13 | a0001c0003t0034g0368a0001c0010t0003g0044a0001c0010t0003g0045others(10): Show | 13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1382+429C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649036 | ||||||
| chr10:49649060
|
T | C | 13 | a0001c0003t0034g0368a0001c0010t0003g0044a0001c0010t0003g0045others(10): Show | 13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1383-448T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649060 | ||||||
| chr10:49649068
|
A | G | 10 | a0001c0001t0003g0053a0001c0001t0003g0065a0001c0001t0008g0001others(7): Show | 12 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1383-440A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649068 | ||||||
| chr10:49649256
|
C | G | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1383-252C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649256 | ||||||
| chr10:49649303
|
G | A | 13 | a0001c0003t0034g0368a0001c0010t0003g0044a0001c0010t0003g0045others(10): Show | 13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1383-205G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649303 | ||||||
| chr10:49649422
|
C | T | 1 | a0014c0037t0035g0301 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1383-86C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649422 | ||||||
| chr10:49649466
|
G | C | 25 | a0001c0001t0001g0021a0001c0001t0001g0215a0001c0001t0001g0218others(22): Show | 28 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1383-42G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649466 | ||||||
| chr10:49649789
|
T | C | 117 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(114): Show | 130 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1511+153T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649789 | ||||||
| chr10:49649803
|
C | T | 314 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(311): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1511+167C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649803 | ||||||
| chr10:49649822
|
T | C | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1511+186T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649822 | ||||||
| chr10:49649844
|
T | C | 377 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(374): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.1511+208T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649844 | ||||||
| chr10:49649866
|
AT | A | 55 | a0001c0001t0001g0285a0001c0001t0001g0295a0001c0001t0003g0053others(52): Show | 61 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1511+258delT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | |||||
| chr10:49649866
|
ATT | A | 133 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0224others(130): Show | 143 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1511+257_1511+258d others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | |||||
| chr10:49649866
|
ATTT | A | 50 | a0001c0001t0003g0353a0001c0001t0004g0006a0001c0001t0004g0007others(47): Show | 55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1511+256_1511+258d others(5): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | |||||
| chr10:49649866
|
ATTTTTTT others(4): Show |
A | 11 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(8): Show | 11 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511+248_1511+258d others(13): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | |||||
| chr10:49649866
|
ATTTTTTT others(5): Show |
A | 6 | a0001c0001t0001g0349a0001c0001t0014g0279a0001c0005t0005g0350others(3): Show | 6 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.1511+247_1511+258d others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | |||||
| chr10:49649866
|
ATTTTTTT others(6): Show |
A | 110 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(107): Show | 122 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1511+246_1511+258d others(15): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | |||||
| chr10:49649873
|
T | A | 13 | a0001c0001t0003g0053a0001c0001t0003g0065a0001c0001t0008g0001others(10): Show | 15 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1511+237T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649873 | ||||||
| chr10:49649880
|
T | A | 13 | a0001c0001t0003g0053a0001c0001t0003g0065a0001c0001t0008g0001others(10): Show | 15 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1511+244T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649880 | ||||||
| chr10:49649894
|
T | C | 1 | a0001c0001t0011g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1511+258T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649894 | ||||||
| chr10:49649926
|
G | A | 1 | a0003c0007t0003g0125 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1511+290G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649926 | ||||||
| chr10:49649931
|
A | G | 116 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(113): Show | 128 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1511+295A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649931 | ||||||
| chr10:49649946
|
A | AG | 116 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(113): Show | 128 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1511+315dupG | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649946 | |||||
| chr10:49649999
|
A | C | 116 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(113): Show | 128 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1511+363A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649999 | ||||||
| chr10:49650000
|
A | C | 116 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(113): Show | 128 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1511+364A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650000 | ||||||
| chr10:49650012
|
T | C | 3 | a0001c0003t0003g0291a0001c0003t0003g0293a0011c0033t0009g0177 | 3 | HG03041.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1511+376T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650012 | ||||||
| chr10:49650076
|
G | T | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1511+440G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650076 | ||||||
| chr10:49650140
|
C | T | 111 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(108): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1511+504C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650140 | ||||||
| chr10:49650185
|
G | T | 1 | a0001c0001t0001g0021 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1511+549G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650185 | ||||||
| chr10:49650288
|
T | C | 1 | a0001c0001t0001g0021 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1511+652T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650288 | ||||||
| chr10:49650300
|
T | C | 112 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(109): Show | 124 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1511+664T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650300 | ||||||
| chr10:49650345
|
A | G | 365 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(362): Show | 398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.1511+709A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650345 | ||||||
| chr10:49650383
|
C | T | 5 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0004g0005others(2): Show | 6 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1511+747C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650383 | ||||||
| chr10:49650459
|
G | C | 4 | a0001c0001t0001g0346a0002c0002t0007g0070a0005c0016t0009g0271others(1): Show | 4 | NA18948.hp1 NA18973.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1511+823G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650459 | ||||||
| chr10:49650487
|
T | G | 2 | a0001c0001t0004g0343a0007c0023t0007g0102 | 2 | NA19012.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1511+851T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650487 | ||||||
| chr10:49650494
|
A | G | 11 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(8): Show | 11 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511+858A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650494 | ||||||
| chr10:49650593
|
G | T | 5 | a0001c0001t0003g0019a0001c0001t0003g0037a0001c0001t0003g0255others(2): Show | 6 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1511+957G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650593 | ||||||
| chr10:49650641
|
C | T | 2 | a0001c0001t0007g0035a0001c0001t0007g0036 | 2 | HG00140.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1511+1005C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650641 | ||||||
| chr10:49650658
|
C | A | 1 | a0001c0003t0008g0015 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1511+1022C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650658 | ||||||
| chr10:49650808
|
T | G | 370 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(367): Show | 404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1512-1076T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650808 | ||||||
| chr10:49650931
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1512-953G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650931 | ||||||
| chr10:49651000
|
C | A | 6 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0004g0005others(3): Show | 7 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1512-884C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651000 | ||||||
| chr10:49651057
|
A | C | 111 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(108): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1512-827A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651057 | ||||||
| chr10:49651084
|
G | A | 1 | a0011c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1512-800G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651084 | ||||||
| chr10:49651100
|
G | A | 1 | a0001c0017t0004g0228 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1512-784G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651100 | ||||||
| chr10:49651110
|
G | A | 2 | a0001c0001t0003g0277a0001c0001t0014g0281 | 2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1512-774G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651110 | ||||||
| chr10:49651199
|
A | G | 122 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(119): Show | 134 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1512-685A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651199 | ||||||
| chr10:49651203
|
A | G | 111 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(108): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1512-681A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651203 | ||||||
| chr10:49651227
|
C | T | 1 | a0001c0027t0031g0174 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1512-657C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651227 | ||||||
| chr10:49651361
|
G | T | 1 | a0001c0003t0006g0352 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1512-523G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651361 | ||||||
| chr10:49651379
|
C | T | 6 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0004g0005others(3): Show | 7 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1512-505C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651379 | ||||||
| chr10:49651438
|
T | C | 111 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(108): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1512-446T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651438 | ||||||
| chr10:49651447
|
A | G | 2 | a0001c0001t0003g0353a0001c0001t0014g0282 | 2 | HG01109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1512-437A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651447 | ||||||
| chr10:49651560
|
G | A | 2 | a0001c0001t0001g0338a0001c0001t0016g0022 | 3 | HG02486.hp2 HG06807.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1512-324G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651560 | ||||||
| chr10:49651583
|
T | G | 248 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0224others(245): Show | 270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1512-301T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651583 | ||||||
| chr10:49651816
|
G | A | 1 | a0003c0006t0005g0123 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1512-68G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651816 | ||||||
| chr10:49652183
|
C | G | 141 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0285others(138): Show | 152 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1634+177C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652183 | ||||||
| chr10:49652189
|
A | G | 130 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(127): Show | 144 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1634+183A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652189 | ||||||
| chr10:49652337
|
T | C | 370 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(367): Show | 404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1634+331T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652337 | ||||||
| chr10:49652579
|
G | T | 1 | a0001c0001t0003g0032 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1634+573G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652579 | ||||||
| chr10:49652584
|
C | T | 1 | a0002c0002t0002g0079 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1634+578C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652584 | ||||||
| chr10:49652647
|
C | CT | 16 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0004g0005others(13): Show | 17 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1634+644dupT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr10 | 49652647 | |||||
| chr10:49652698
|
C | T | 109 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(106): Show | 122 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1634+692C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652698 | ||||||
| chr10:49652758
|
C | A | 12 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0066others(9): Show | 14 | HG00438.hp2 HG02015.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1634+752C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652758 | ||||||
| chr10:49652857
|
G | A | 4 | a0001c0001t0005g0221a0001c0013t0005g0217a0001c0013t0005g0294others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634+851G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652857 | ||||||
| chr10:49652865
|
C | T | 1 | a0001c0001t0007g0358 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1634+859C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652865 | ||||||
| chr10:49652913
|
C | G | 1 | a0001c0003t0006g0308 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1634+907C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652913 | ||||||
| chr10:49653007
|
A | G | 1 | a0001c0003t0010g0238 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1634+1001A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653007 | ||||||
| chr10:49653062
|
A | G | 11 | a0001c0001t0001g0285a0001c0001t0004g0058a0001c0001t0004g0226others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1634+1056A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653062 | ||||||
| chr10:49653076
|
C | T | 1 | a0001c0003t0008g0015 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1634+1070C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653076 | ||||||
| chr10:49653212
|
C | G | 1 | a0001c0001t0019g0245 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1634+1206C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653212 | ||||||
| chr10:49653307
|
G | A | 1 | a0001c0005t0009g0186 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1634+1301G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653307 | ||||||
| chr10:49653408
|
G | A | 1 | a0004c0009t0011g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1634+1402G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653408 | ||||||
| chr10:49653427
|
AC | A | 120 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(117): Show | 134 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1634+1423delC | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr10 | 49653427 | |||||
| chr10:49653437
|
A | G | 1 | a0002c0002t0002g0011 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1634+1431A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653437 | ||||||
| chr10:49653520
|
C | T | 7 | a0001c0001t0003g0019a0001c0001t0003g0037a0001c0001t0003g0220others(4): Show | 9 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1634+1514C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653520 | ||||||
| chr10:49653544
|
C | T | 2 | a0002c0002t0002g0079a0003c0004t0001g0132 | 2 | HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1634+1538C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653544 | ||||||
| chr10:49653550
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0254a0004c0034t0015g0278 | 3 | HG02145.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1634+1544C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653550 | ||||||
| chr10:49653664
|
T | G | 1 | a0003c0007t0003g0122 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1635-1431T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653664 | ||||||
| chr10:49653704
|
G | A | 4 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0036g0300others(1): Show | 4 | HG00639.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635-1391G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653704 | ||||||
| chr10:49653798
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0002g0194 | 2 | HG01515.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1635-1297C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653798 | ||||||
| chr10:49653889
|
C | T | 5 | a0001c0005t0009g0252a0001c0005t0009g0272a0005c0016t0008g0269others(2): Show | 5 | NA18947.hp2 NA18948.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1635-1206C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653889 | ||||||
| chr10:49653974
|
C | T | 1 | a0001c0001t0006g0356 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1635-1121C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653974 | ||||||
| chr10:49653986
|
G | A | 1 | a0001c0011t0029g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1635-1109G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653986 | ||||||
| chr10:49654219
|
T | C | 12 | a0001c0001t0003g0353a0001c0001t0014g0282a0001c0010t0003g0044others(9): Show | 12 | HG01109.hp1 HG01167.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1635-876T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654219 | ||||||
| chr10:49654289
|
G | C | 205 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(202): Show | 222 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1635-806G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654289 | ||||||
| chr10:49654358
|
T | C | 205 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(202): Show | 222 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1635-737T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654358 | ||||||
| chr10:49654407
|
A | G | 11 | a0001c0003t0003g0314a0001c0003t0008g0183a0001c0003t0008g0253others(8): Show | 11 | HG00423.hp1 HG00544.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1635-688A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654407 | ||||||
| chr10:49654724
|
G | T | 201 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(198): Show | 218 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.1635-371G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654724 | ||||||
| chr10:49654824
|
AT | A | 294 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(291): Show | 321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1635-263delT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr10 | 49654824 | |||||
| chr10:49654907
|
C | T | 4 | a0001c0013t0005g0217a0001c0013t0005g0294a0001c0013t0032g0384others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635-188C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654907 | ||||||
| chr10:49655037
|
A | C | 186 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(183): Show | 203 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1635-58A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49655037 | ||||||
| chr10:49655065
|
C | T | 1 | a0003c0004t0001g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1635-30C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49655065 | ||||||
| chr10:49655511
|
G | C | 1 | a0002c0008t0010g0092 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1839+63G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49655511 | ||||||
| chr10:49655519
|
C | T | 297 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(294): Show | 324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.1839+71C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49655519 | ||||||
| chr10:49655540
|
G | A | 1 | a0001c0003t0006g0319 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1839+92G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49655540 | ||||||
| chr10:49655577
|
A | G | 118 | a0001c0001t0003g0019a0001c0001t0003g0031a0001c0001t0003g0032others(115): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1839+129A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49655577 | ||||||
| chr10:49655997
|
T | A | 297 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(294): Show | 324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.1839+549T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49655997 | ||||||
| chr10:49656002
|
T | C | 1 | a0011c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1839+554T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656002 | ||||||
| chr10:49656060
|
C | G | 2 | a0001c0001t0003g0353a0001c0001t0014g0282 | 2 | HG01109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1839+612C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656060 | ||||||
| chr10:49656198
|
C | T | 2 | a0001c0001t0002g0198a0002c0002t0002g0009 | 3 | HG01255.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1839+750C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656198 | ||||||
| chr10:49656242
|
C | T | 1 | a0001c0011t0022g0286 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1839+794C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656242 | ||||||
| chr10:49656283
|
GT | G | 34 | a0001c0003t0003g0291a0001c0003t0003g0293a0001c0003t0003g0314others(31): Show | 35 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1839+862delT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | |||||
| chr10:49656283
|
GTT | G | 36 | a0001c0003t0006g0004a0001c0003t0006g0023a0001c0003t0006g0024others(33): Show | 42 | HG00099.hp1 HG01167.hp2 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.1839+861_1839+862d others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | |||||
| chr10:49656283
|
GTTTTTTT others(1): Show |
G | 13 | a0001c0001t0001g0320a0001c0001t0002g0185a0001c0001t0002g0198others(10): Show | 14 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1839+855_1839+862d others(10): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | |||||
| chr10:49656283
|
GTTTTTTT others(2): Show |
G | 127 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(124): Show | 141 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1839+854_1839+862d others(11): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | |||||
| chr10:49656283
|
GTTTTTTT others(3): Show |
G | 143 | a0001c0001t0003g0019a0001c0001t0003g0031a0001c0001t0003g0032others(140): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1839+853_1839+862d others(12): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | |||||
| chr10:49656283
|
GTTTTTTT others(4): Show |
G | 14 | a0001c0001t0004g0005a0001c0001t0004g0261a0001c0001t0004g0288others(11): Show | 15 | HG00741.hp2 HG01168.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1839+852_1839+862d others(13): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | |||||
| chr10:49656283
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0011t0022g0286 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1839+848_1839+862d others(17): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | |||||
| chr10:49656421
|
C | T | 1 | a0001c0010t0003g0259 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1839+973C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656421 | ||||||
| chr10:49656441
|
T | C | 3 | a0001c0001t0013g0018a0001c0001t0013g0225a0001c0001t0013g0334 | 4 | HG02055.hp2 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1839+993T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656441 | ||||||
| chr10:49656646
|
G | A | 190 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(187): Show | 207 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1839+1198G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656646 | ||||||
| chr10:49656857
|
G | A | 189 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(186): Show | 206 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1839+1409G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656857 | ||||||
| chr10:49656869
|
A | C | 1 | a0001c0005t0009g0249 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1839+1421A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656869 | ||||||
| chr10:49657115
|
A | T | 1 | a0011c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1839+1667A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657115 | ||||||
| chr10:49657181
|
G | T | 116 | a0001c0001t0003g0019a0001c0001t0003g0031a0001c0001t0003g0032others(113): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1839+1733G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657181 | ||||||
| chr10:49657185
|
A | G | 191 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(188): Show | 208 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1839+1737A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657185 | ||||||
| chr10:49657187
|
T | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1839+1739T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657187 | ||||||
| chr10:49657305
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1839+1857T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657305 | ||||||
| chr10:49657379
|
C | G | 4 | a0001c0001t0016g0022a0001c0001t0016g0219a0001c0011t0024g0283others(1): Show | 5 | HG02258.hp2 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1839+1931C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657379 | ||||||
| chr10:49657411
|
T | C | 10 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(7): Show | 10 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1839+1963T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657411 | ||||||
| chr10:49657427
|
C | A | 1 | a0001c0003t0006g0319 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1839+1979C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657427 | ||||||
| chr10:49657525
|
A | G | 191 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(188): Show | 208 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1839+2077A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657525 | ||||||
| chr10:49657627
|
A | C | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1839+2179A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657627 | ||||||
| chr10:49657704
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1839+2256G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657704 | ||||||
| chr10:49657766
|
T | C | 1 | a0002c0002t0007g0381 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1839+2318T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657766 | ||||||
| chr10:49657929
|
G | A | 27 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0053others(24): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1839+2481G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657929 | ||||||
| chr10:49658018
|
T | C | 1 | a0001c0003t0008g0015 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1839+2570T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658018 | ||||||
| chr10:49658263
|
C | A | 2 | a0001c0003t0006g0328a0002c0008t0010g0382 | 2 | NA18964.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1839+2815C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658263 | ||||||
| chr10:49658296
|
A | G | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1839+2848A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658296 | ||||||
| chr10:49658378
|
G | A | 2 | a0003c0006t0005g0149a0010c0032t0025g0056 | 2 | HG02717.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.1839+2930G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658378 | ||||||
| chr10:49658385
|
C | T | 1 | a0001c0011t0022g0286 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1839+2937C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658385 | ||||||
| chr10:49658386
|
A | G | 359 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(356): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.1839+2938A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658386 | ||||||
| chr10:49658443
|
G | A | 2 | a0001c0011t0024g0283a0001c0011t0029g0216 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1839+2995G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658443 | ||||||
| chr10:49658551
|
C | A | 381 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(378): Show | 415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.1839+3103C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658551 | ||||||
| chr10:49658577
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1839+3129C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658577 | ||||||
| chr10:49658640
|
C | T | 9 | a0001c0001t0005g0305a0001c0001t0005g0306a0001c0001t0012g0188others(6): Show | 9 | HG00642.hp1 HG01069.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1839+3192C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658640 | ||||||
| chr10:49658649
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1839+3201C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658649 | ||||||
| chr10:49658755
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1839+3307A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658755 | ||||||
| chr10:49659162
|
G | A | 1 | a0001c0001t0012g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1840-3483G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659162 | ||||||
| chr10:49659398
|
A | C | 192 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(189): Show | 209 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1840-3247A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659398 | ||||||
| chr10:49659436
|
C | T | 10 | a0001c0010t0003g0044a0001c0010t0003g0045a0001c0010t0003g0223others(7): Show | 10 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1840-3209C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659436 | ||||||
| chr10:49659519
|
G | A | 50 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0028others(47): Show | 55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1840-3126G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659519 | ||||||
| chr10:49659779
|
A | T | 309 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(306): Show | 336 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.1840-2866A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659779 | ||||||
| chr10:49659811
|
G | A | 50 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0028others(47): Show | 55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1840-2834G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659811 | ||||||
| chr10:49660076
|
C | T | 1 | a0001c0011t0029g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1840-2569C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660076 | ||||||
| chr10:49660137
|
G | A | 1 | a0001c0001t0001g0359 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1840-2508G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660137 | ||||||
| chr10:49660157
|
T | A | 2 | a0001c0003t0003g0291a0001c0003t0003g0293 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1840-2488T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660157 | ||||||
| chr10:49660396
|
C | T | 1 | a0001c0001t0001g0338 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1840-2249C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660396 | ||||||
| chr10:49660397
|
G | A | 25 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0053others(22): Show | 27 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1840-2248G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660397 | ||||||
| chr10:49660398
|
C | T | 9 | a0001c0001t0004g0005a0001c0001t0004g0261a0001c0001t0004g0288others(6): Show | 10 | HG00741.hp2 HG01168.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1840-2247C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660398 | ||||||
| chr10:49660399
|
G | A | 1 | a0001c0001t0016g0022 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1840-2246G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660399 | ||||||
| chr10:49660443
|
GA | G | 281 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(278): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1840-2189delA | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49660443 | |||||
| chr10:49660460
|
C | G | 1 | a0001c0001t0003g0031 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1840-2185C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660460 | ||||||
| chr10:49660612
|
G | A | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1840-2033G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660612 | ||||||
| chr10:49660615
|
C | T | 1 | a0001c0001t0026g0061 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1840-2030C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660615 | ||||||
| chr10:49660679
|
A | C | 25 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0053others(22): Show | 27 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1840-1966A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660679 | ||||||
| chr10:49660686
|
T | G | 2 | a0001c0001t0003g0353a0001c0001t0014g0282 | 2 | HG01109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1840-1959T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660686 | ||||||
| chr10:49660865
|
G | A | 44 | a0001c0005t0005g0026a0001c0005t0005g0063a0001c0005t0005g0064others(41): Show | 46 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1840-1780G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660865 | ||||||
| chr10:49661114
|
C | T | 1 | a0001c0001t0005g0267 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1840-1531C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661114 | ||||||
| chr10:49661116
|
C | T | 47 | a0001c0003t0006g0004a0001c0003t0006g0023a0001c0003t0006g0024others(44): Show | 53 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.1840-1529C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661116 | ||||||
| chr10:49661381
|
T | C | 1 | a0001c0001t0001g0338 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1840-1264T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661381 | ||||||
| chr10:49661402
|
C | T | 2 | a0001c0001t0003g0353a0001c0001t0014g0282 | 2 | HG01109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1840-1243C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661402 | ||||||
| chr10:49661479
|
G | A | 44 | a0001c0005t0005g0026a0001c0005t0005g0063a0001c0005t0005g0064others(41): Show | 46 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1840-1166G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661479 | ||||||
| chr10:49661537
|
C | A | 190 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(187): Show | 207 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1840-1108C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661537 | ||||||
| chr10:49661827
|
A | T | 1 | a0001c0011t0022g0286 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1840-818A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661827 | ||||||
| chr10:49661830
|
C | T | 1 | a0001c0005t0005g0063 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1840-815C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661830 | ||||||
| chr10:49662025
|
A | G | 191 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(188): Show | 208 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1840-620A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662025 | ||||||
| chr10:49662054
|
T | G | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1840-591T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662054 | ||||||
| chr10:49662297
|
G | A | 1 | a0011c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1840-348G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662297 | ||||||
| chr10:49662339
|
C | A | 2 | a0001c0027t0031g0174a0010c0032t0025g0056 | 2 | HG01981.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1840-306C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662339 | ||||||
| chr10:49662453
|
C | G | 1 | a0001c0003t0034g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1840-192C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662453 | ||||||
| chr10:49662453
|
C | T | 1 | a0001c0011t0022g0286 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1840-192C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662453 | ||||||
| chr10:49662454
|
G | A | 106 | a0001c0001t0003g0019a0001c0001t0003g0031a0001c0001t0003g0032others(103): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1840-191G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662454 | ||||||
| chr10:49662473
|
T | C | 190 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(187): Show | 207 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1840-172T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662473 | ||||||
| chr10:49662487
|
C | T | 3 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0011t0003g0214 | 3 | HG01243.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1840-158C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662487 | ||||||
| chr10:49662839
|
A | T | 2 | a0001c0001t0001g0346a0002c0002t0002g0107 | 2 | NA18952.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1977+57A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49662839 | ||||||
| chr10:49662881
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1977+99G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49662881 | ||||||
| chr10:49663011
|
T | C | 1 | a0001c0001t0018g0213 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1977+229T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663011 | ||||||
| chr10:49663101
|
G | A | 29 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0066others(26): Show | 32 | HG00438.hp2 HG02015.hp2 HG02027.hp2 others(29): Show |
intron_variant | MODIFIER | c.1977+319G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663101 | ||||||
| chr10:49663143
|
T | C | 191 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(188): Show | 208 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1977+361T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663143 | ||||||
| chr10:49663420
|
T | A | 124 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(121): Show | 138 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1977+638T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663420 | ||||||
| chr10:49663420
|
T | C | 1 | a0001c0003t0008g0183 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1977+638T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663420 | ||||||
| chr10:49663475
|
A | G | 2 | a0001c0001t0002g0197a0001c0001t0002g0199 | 2 | HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1977+693A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663475 | ||||||
| chr10:49663500
|
A | G | 5 | a0001c0001t0002g0200a0001c0001t0002g0367a0003c0004t0001g0013others(2): Show | 6 | HG02071.hp2 NA18953.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1977+718A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663500 | ||||||
| chr10:49663578
|
G | A | 1 | a0003c0004t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1977+796G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663578 | ||||||
| chr10:49663635
|
C | T | 1 | a0001c0010t0003g0258 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1977+853C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663635 | ||||||
| chr10:49663670
|
A | G | 28 | a0001c0001t0004g0028a0001c0001t0004g0109a0001c0001t0004g0313others(25): Show | 29 | HG00609.hp2 HG01074.hp1 HG01952.hp1 others(26): Show |
intron_variant | MODIFIER | c.1977+888A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663670 | ||||||
| chr10:49663795
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1978-982C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663795 | ||||||
| chr10:49664200
|
A | G | 308 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(305): Show | 335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.1978-577A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664200 | ||||||
| chr10:49664306
|
G | C | 2 | a0001c0001t0001g0359a0015c0021t0002g0081 | 2 | HG01081.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1978-471G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664306 | ||||||
| chr10:49664356
|
C | G | 191 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(188): Show | 208 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1978-421C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664356 | ||||||
| chr10:49664365
|
G | A | 1 | a0002c0002t0002g0094 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1978-412G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664365 | ||||||
| chr10:49664401
|
G | A | 1 | a0010c0032t0025g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1978-376G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664401 | ||||||
| chr10:49664450
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1978-327C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664450 | ||||||
| chr10:49664526
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1978-251G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664526 | ||||||
| chr10:49664615
|
G | A | 2 | a0001c0027t0031g0174a0010c0032t0025g0056 | 2 | HG01981.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1978-162G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664615 | ||||||
| chr10:49664753
|
C | G | 2 | a0001c0003t0003g0291a0001c0003t0003g0293 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1978-24C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664753 | ||||||
| chr10:49664755
|
C | A | 1 | a0011c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1978-22C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664755 |