| geneid | 3356 |
|---|---|
| ensemblid | ENSG00000102468.11 |
| hgncid | 5293 |
| symbol | HTR2A |
| name | 5-hydroxytryptamine receptor 2A |
| refseq_nuc | NM_000621.5 |
| refseq_prot | NP_000612.1 |
| ensembl_nuc | ENST00000542664.4 |
| ensembl_prot | ENSP00000437737.1 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 46831546 |
| end | 46897053 |
| strand | - |
| ver | v1.2 |
| region | chr13:46831546-46897053 |
| region5000 | chr13:46826546-46902053 |
| regionname0 | HTR2A_chr13_46831546_46897053 |
| regionname5000 | HTR2A_chr13_46826546_46902053 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 471 | 311 | 73 | 57 | 139 | 11 | 29 | 110 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0002 | 0/0 | 471 | 18 | 7 | 3 | 1 | 2 | 5 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0003 | 0/0 | 471 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0004 | 0/0 | 471 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0005 | 0/0 | 471 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0006 | 0/0 | 471 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1416 | 183 | 35 | 41 | 79 | 6 | 20 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0002 | 0/0 | 1416 | 119 | 32 | 14 | 60 | 5 | 8 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0003 | 0/0 | 1416 | 10 | 7 | 2 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0004 | 0/0 | 1416 | 8 | 0 | 1 | 1 | 2 | 4 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0005 | 0/0 | 1416 | 6 | 6 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0006 | 0/0 | 1416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0007 | 0/0 | 1416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0008 | 0/0 | 1416 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0009 | 0/0 | 1416 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0010 | 0/0 | 1416 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0011 | 0/0 | 1416 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0012 | 0/0 | 1416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| c0013 | 0/0 | 1416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 4000 | 188 | 19 | 42 | 98 | 10 | 18 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0002 | 0/0 | 4001 | 44 | 4 | 2 | 33 | 0 | 5 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0003 | 0/0 | 4002 | 14 | 5 | 1 | 1 | 2 | 5 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0004 | 1/0 | 4000 | 10 | 3 | 5 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0005 | 0/0 | 4001 | 8 | 8 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0006 | 0/0 | 4001 | 5 | 3 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0007 | 0/0 | 4001 | 4 | 4 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0008 | 0/0 | 4000 | 3 | 2 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0009 | 0/0 | 4001 | 3 | 0 | 2 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0010 | 0/0 | 4001 | 3 | 2 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0011 | 0/0 | 4000 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0012 | 0/0 | 4001 | 2 | 1 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0013 | 0/0 | 4001 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0014 | 0/0 | 4000 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0015 | 0/0 | 4000 | 2 | 1 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0016 | 0/0 | 4001 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0017 | 0/0 | 4000 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0018 | 0/0 | 4001 | 2 | 0 | 0 | 0 | 1 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0019 | 0/0 | 4002 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0020 | 0/0 | 4001 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0021 | 0/0 | 4001 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0022 | 0/0 | 4000 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0023 | 0/0 | 4000 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0024 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0025 | 0/0 | 4000 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0026 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0027 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0028 | 0/0 | 4001 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0029 | 0/0 | 4002 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0030 | 0/0 | 4001 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0031 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0032 | 0/0 | 4001 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0033 | 0/0 | 4000 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0034 | 0/0 | 4000 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0035 | 0/0 | 4000 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0036 | 0/0 | 4000 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0037 | 0/0 | 4000 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0038 | 0/0 | 4000 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0039 | 0/0 | 4000 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0040 | 0/0 | 4000 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0041 | 0/0 | 4000 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0042 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0043 | 0/0 | 4000 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0044 | 0/0 | 4000 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0045 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0046 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0047 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0048 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0049 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0050 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0051 | 0/0 | 4001 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| t0052 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| 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 | 0 | 3 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0034 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1416 | 183 | 35 | 41 | 79 | 6 | 20 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002 | 0/0 | 1416 | 119 | 32 | 14 | 60 | 5 | 8 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0005 | 0/0 | 1416 | 6 | 6 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0010 | 0/0 | 1416 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0012 | 0/0 | 1416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0013 | 0/0 | 1416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0002c0003 | 0/0 | 1416 | 10 | 7 | 2 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0002c0004 | 0/0 | 1416 | 8 | 0 | 1 | 1 | 2 | 4 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0003c0006 | 0/0 | 1416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0003c0007 | 0/0 | 1416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0004c0008 | 0/0 | 1416 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0005c0009 | 0/0 | 1416 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0006c0011 | 0/0 | 1416 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5415 | 107 | 3 | 28 | 58 | 5 | 12 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0002 | 0/0 | 5416 | 23 | 0 | 2 | 18 | 0 | 3 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0004 | 1/0 | 5415 | 10 | 3 | 5 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0005 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0006 | 0/0 | 5416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0008 | 0/0 | 5415 | 3 | 2 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0009 | 0/0 | 5416 | 3 | 0 | 2 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0010 | 0/0 | 5416 | 3 | 2 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0011 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0012 | 0/0 | 5416 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0014 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0015 | 0/0 | 5415 | 2 | 1 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0017 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0018 | 0/0 | 5416 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0020 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0021 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0022 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0024 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0025 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0026 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0035 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0038 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0042 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0043 | 0/0 | 5415 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0044 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0045 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0046 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0047 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0048 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0050 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0051 | 0/0 | 5416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0001t0052 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0001 | 0/0 | 5415 | 77 | 14 | 13 | 40 | 5 | 5 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0002 | 0/0 | 5416 | 20 | 4 | 0 | 15 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0005 | 0/0 | 5416 | 6 | 6 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0006 | 0/0 | 5416 | 4 | 3 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0012 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0023 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0028 | 0/0 | 5416 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0029 | 0/0 | 5417 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0030 | 0/0 | 5416 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0031 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0033 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0034 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0037 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0039 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0040 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0002t0041 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0005t0007 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0005t0016 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0005t0027 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0005t0049 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0010t0036 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0012t0032 | 0/0 | 5416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0001c0013t0001 | 0/0 | 5415 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0002c0003t0003 | 0/0 | 5417 | 7 | 5 | 1 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0002c0003t0013 | 0/0 | 5416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0002c0003t0019 | 0/0 | 5417 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0002c0004t0003 | 0/0 | 5417 | 7 | 0 | 0 | 1 | 2 | 4 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0002c0004t0013 | 0/0 | 5416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0003c0006t0001 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0003c0007t0007 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0004c0008t0001 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0005c0009t0018 | 0/0 | 5416 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| a0006c0011t0002 | 0/0 | 5416 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | copy fasta | chr13 | 46826546 | 46902053 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0034 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0004g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0008g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0008g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0009g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0010g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0011g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0012g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0014g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0014g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0015g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0017g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0017g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0018g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0020g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0020g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0021g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0021g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0022g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0022g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0024g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0025g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0026g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0035g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0038g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0042g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0043g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0044g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0045g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0046g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0047g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0048g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0050g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0051g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0001t0052g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0023g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0028g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0029g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0030g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0031g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0033g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0034g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0037g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0039g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0040g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0002t0041g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0005t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0005t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0005t0016g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0005t0027g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0005t0049g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0010t0036g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0012t0032g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0001c0013t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0003t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0003t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0003t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0003t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0003t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0003t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0003t0013g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0003t0019g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0003t0019g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0004t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0004t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0004t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0004t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0004t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0004t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0004t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0002c0004t0013g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0003c0006t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0003c0006t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0003c0007t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0003c0007t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0004c0008t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0005c0009t0018g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| a0006c0011t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0192 | EUR | GBR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00099 | hp2 | a0005 | c0009 | t0018 | g0298 | EUR | GBR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0308 | EUR | GBR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00140 | hp2 | a0002 | c0004 | t0003 | g0191 | EUR | GBR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00280 | hp2 | a0002 | c0004 | t0003 | g0174 | EUR | FIN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00639 | hp2 | a0001 | c0001 | t0043 | g0290 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0208 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00738 | hp2 | a0002 | c0003 | t0003 | g0153 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01070 | hp1 | a0001 | c0012 | t0032 | g0244 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0163 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01081 | hp2 | a0002 | c0003 | t0013 | g0138 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01109 | hp1 | a0001 | c0002 | t0006 | g0187 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01109 | hp2 | a0001 | c0001 | t0010 | g0125 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01175 | hp1 | a0002 | c0004 | t0013 | g0199 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0264 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0302 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01256 | hp1 | a0001 | c0001 | t0009 | g0010 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01258 | hp2 | a0001 | c0001 | t0009 | g0010 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0246 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0306 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01496 | hp2 | a0001 | c0013 | t0001 | g0276 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0210 | EUR | IBS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0249 | EUR | IBS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01884 | hp2 | a0001 | c0002 | t0012 | g0268 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0271 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0145 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0216 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01975 | hp2 | a0001 | c0001 | t0051 | g0320 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0307 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0300 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02015 | hp1 | a0001 | c0002 | t0030 | g0180 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02055 | hp1 | a0001 | c0002 | t0005 | g0266 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02055 | hp2 | a0001 | c0001 | t0015 | g0053 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02056 | hp1 | a0002 | c0004 | t0003 | g0248 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0279 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | CDX | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | CDX | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | CDX | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0299 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02280 | hp2 | a0001 | c0002 | t0034 | g0281 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02451 | hp1 | a0001 | c0001 | t0048 | g0317 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02451 | hp2 | a0001 | c0002 | t0005 | g0267 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02572 | hp1 | a0001 | c0002 | t0006 | g0286 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02572 | hp2 | a0001 | c0001 | t0045 | g0293 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02602 | hp1 | a0002 | c0004 | t0003 | g0201 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02602 | hp2 | a0004 | c0008 | t0001 | g0023 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02615 | hp1 | a0001 | c0001 | t0022 | g0312 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02630 | hp1 | a0001 | c0001 | t0022 | g0304 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02630 | hp2 | a0001 | c0001 | t0014 | g0136 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02647 | hp1 | a0001 | c0001 | t0020 | g0319 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0188 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02683 | hp1 | a0002 | c0004 | t0003 | g0247 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02683 | hp2 | a0002 | c0004 | t0003 | g0209 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02698 | hp2 | a0001 | c0010 | t0036 | g0110 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02717 | hp1 | a0003 | c0007 | t0007 | g0149 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0129 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02723 | hp1 | a0003 | c0007 | t0007 | g0150 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02723 | hp2 | a0001 | c0001 | t0047 | g0296 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02809 | hp1 | a0001 | c0001 | t0020 | g0310 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0282 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02886 | hp2 | a0003 | c0006 | t0001 | g0148 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02896 | hp1 | a0001 | c0002 | t0005 | g0284 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0273 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0272 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02922 | hp1 | a0001 | c0001 | t0017 | g0292 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0311 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02965 | hp1 | a0001 | c0002 | t0005 | g0265 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0270 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0257 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02970 | hp2 | a0001 | c0001 | t0026 | g0018 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02976 | hp1 | a0003 | c0006 | t0001 | g0147 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02976 | hp2 | a0001 | c0001 | t0024 | g0015 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03041 | hp1 | a0001 | c0001 | t0050 | g0305 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03041 | hp2 | a0001 | c0002 | t0006 | g0260 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03098 | hp1 | a0001 | c0001 | t0021 | g0322 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03098 | hp2 | a0001 | c0005 | t0007 | g0133 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0131 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03139 | hp1 | a0001 | c0001 | t0021 | g0313 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03139 | hp2 | a0001 | c0005 | t0016 | g0013 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03225 | hp1 | a0001 | c0002 | t0006 | g0269 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03225 | hp2 | a0001 | c0002 | t0039 | g0189 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03239 | hp2 | a0001 | c0002 | t0040 | g0287 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03453 | hp1 | a0001 | c0001 | t0044 | g0291 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0262 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0280 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0080 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0016 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03492 | hp1 | a0001 | c0001 | t0025 | g0017 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03516 | hp1 | a0001 | c0005 | t0016 | g0013 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03579 | hp1 | a0001 | c0005 | t0027 | g0019 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03579 | hp2 | a0002 | c0003 | t0019 | g0318 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0158 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03704 | hp1 | a0001 | c0002 | t0023 | g0014 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03710 | hp1 | a0001 | c0001 | t0015 | g0102 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0214 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03831 | hp1 | a0002 | c0004 | t0003 | g0190 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03834 | hp2 | a0001 | c0001 | t0018 | g0309 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG04115 | hp1 | a0002 | c0003 | t0003 | g0155 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG04115 | hp2 | a0006 | c0011 | t0002 | g0204 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0194 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0213 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0220 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18522 | hp1 | a0001 | c0001 | t0042 | g0289 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0315 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | CHB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18952 | hp1 | a0001 | c0002 | t0041 | g0288 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18967 | hp1 | a0001 | c0001 | t0038 | g0126 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18978 | hp2 | a0001 | c0002 | t0029 | g0170 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19004 | hp2 | a0001 | c0002 | t0028 | g0254 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19010 | hp1 | a0001 | c0002 | t0037 | g0253 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19030 | hp1 | a0002 | c0003 | t0003 | g0049 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19030 | hp2 | a0001 | c0001 | t0017 | g0294 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19043 | hp1 | a0002 | c0003 | t0003 | g0048 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19043 | hp2 | a0002 | c0003 | t0003 | g0146 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19076 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19078 | hp2 | a0001 | c0001 | t0012 | g0101 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19084 | hp1 | a0001 | c0001 | t0035 | g0079 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19240 | hp1 | a0001 | c0005 | t0049 | g0303 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | ASW | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA20129 | hp2 | a0001 | c0005 | t0007 | g0134 | AFR | ASW | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0200 | EUR | TSI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0224 | EUR | TSI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02109 | hp1 | a0002 | c0003 | t0019 | g0314 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02486 | hp1 | a0001 | c0002 | t0005 | g0021 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03471 | hp1 | a0002 | c0003 | t0003 | g0046 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG03471 | hp2 | a0001 | c0001 | t0046 | g0295 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | USA | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| HG06807 | hp2 | a0001 | c0002 | t0033 | g0176 | AFR | USA | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA21309 | hp1 | a0001 | c0001 | t0052 | g0316 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| NA21309 | hp2 | a0001 | c0002 | t0031 | g0186 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0034 | REF | REF | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0321 | REF | REF | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:46834895
|
G | A | 1 | a0006 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1358C>T | p.Ser453Phe | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2066/5415 | 1358/1416 | 453/471 | chr13 | 46834895 | ||
| chr13:46834899
|
G | A | 1 | a0002 | 18 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(15): Show |
missense_variant | MODERATE | c.1354C>T | p.His452Tyr | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2062/5415 | 1354/1416 | 452/471 | chr13 | 46834899 | ||
| chr13:46892414
|
T | C | 1 | a0003 | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
missense_variant | MODERATE | c.589A>G | p.Ile197Val | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/4 | 1297/5415 | 589/1416 | 197/471 | chr13 | 46892414 | ||
| chr13:46895833
|
G | T | 1 | a0005 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.74C>A | p.Thr25Asn | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 782/5415 | 74/1416 | 25/471 | chr13 | 46895833 | ||
| chr13:46895872
|
C | T | 1 | a0004 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.35G>A | p.Ser12Asn | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 743/5415 | 35/1416 | 12/471 | chr13 | 46895872 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:46835014
|
T | A | 3 | a0001c0005a0001c0012a0003c0007 | 9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
synonymous_variant | LOW | c.1239A>T | p.Thr413Thr | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1947/5415 | 1239/1416 | 413/471 | chr13 | 46835014 | ||
| chr13:46835359
|
C | T | 1 | a0001c0010 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.894G>A | p.Ser298Ser | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1602/5415 | 894/1416 | 298/471 | chr13 | 46835359 | ||
| chr13:46892487
|
G | A | 1 | a0001c0013 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.516C>T | p.Asp172Asp | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/4 | 1224/5415 | 516/1416 | 172/471 | chr13 | 46892487 | ||
| chr13:46895805
|
G | A | 6 | a0001c0002a0001c0012a0001c0013others(3): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
synonymous_variant | LOW | c.102C>T | p.Ser34Ser | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 810/5415 | 102/1416 | 34/471 | chr13 | 46895805 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:46831587
|
C | G | 1 | a0001c0002t0033 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3250G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 3250 | chr13 | 46831587 | |||||
| chr13:46831601
|
G | A | 2 | a0001c0001t0018a0005c0009t0018 | 2 | HG00099.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3236C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 3236 | chr13 | 46831601 | |||||
| chr13:46831605
|
C | T | 1 | a0001c0002t0033 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3232G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 3232 | chr13 | 46831605 | |||||
| chr13:46831699
|
T | A | 3 | a0001c0001t0006a0001c0001t0051a0001c0002t0006 | 6 | HG01074.hp1 HG01109.hp1 HG01975.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3138A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 3138 | chr13 | 46831699 | |||||
| chr13:46831840
|
T | C | 1 | a0001c0010t0036 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2997A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2997 | chr13 | 46831840 | |||||
| chr13:46832277
|
A | C | 1 | a0001c0012t0032 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2560T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2560 | chr13 | 46832277 | |||||
| chr13:46832277
|
A | G | 5 | a0001c0005t0007a0001c0005t0016a0001c0005t0027others(2): Show | 8 | HG02717.hp1 HG02723.hp1 HG03098.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2560T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2560 | chr13 | 46832277 | |||||
| chr13:46832493
|
A | T | 9 | a0001c0001t0046a0001c0001t0048a0001c0002t0031others(6): Show | 22 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2344T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2344 | chr13 | 46832493 | |||||
| chr13:46832596
|
T | C | 9 | a0001c0001t0046a0001c0001t0048a0001c0002t0031others(6): Show | 22 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2241A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2241 | chr13 | 46832596 | |||||
| chr13:46832644
|
T | C | 4 | a0001c0001t0046a0001c0001t0048a0001c0002t0031others(1): Show | 4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2193A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2193 | chr13 | 46832644 | |||||
| chr13:46832701
|
T | C | 1 | a0001c0001t0035 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2136A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2136 | chr13 | 46832701 | |||||
| chr13:46832710
|
C | T | 25 | a0001c0001t0002a0001c0001t0009a0001c0001t0018others(22): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2127G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2127 | chr13 | 46832710 | |||||
| chr13:46832821
|
C | T | 9 | a0001c0001t0046a0001c0001t0048a0001c0002t0031others(6): Show | 22 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2016G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2016 | chr13 | 46832821 | |||||
| chr13:46832900
|
T | C | 4 | a0001c0001t0046a0001c0001t0048a0001c0002t0031others(1): Show | 4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1937A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1937 | chr13 | 46832900 | |||||
| chr13:46833066
|
G | A | 4 | a0001c0001t0046a0001c0001t0048a0001c0002t0031others(1): Show | 4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1771C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1771 | chr13 | 46833066 | |||||
| chr13:46833295
|
T | G | 10 | a0001c0001t0021a0001c0001t0046a0001c0001t0048others(7): Show | 24 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1542A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1542 | chr13 | 46833295 | |||||
| chr13:46833327
|
G | T | 6 | a0001c0005t0007a0001c0005t0016a0001c0005t0027others(3): Show | 9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1510C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1510 | chr13 | 46833327 | |||||
| chr13:46833329
|
C | G | 2 | a0001c0001t0011a0001c0001t0014 | 4 | HG01891.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1508G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1508 | chr13 | 46833329 | |||||
| chr13:46833357
|
T | C | 2 | a0001c0001t0015a0001c0010t0036 | 3 | HG02055.hp2 HG02698.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1480A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1480 | chr13 | 46833357 | |||||
| chr13:46833368
|
C | CT | 8 | a0001c0001t0010a0001c0001t0024a0001c0001t0047others(5): Show | 23 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1468dupA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1468 | chr13 | 46833368 | |||||
| chr13:46833597
|
C | A | 1 | a0001c0002t0037 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1240G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1240 | chr13 | 46833597 | |||||
| chr13:46833623
|
C | T | 1 | a0001c0002t0034 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1214G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1214 | chr13 | 46833623 | |||||
| chr13:46833648
|
G | A | 1 | a0001c0002t0033 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1189C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1189 | chr13 | 46833648 | |||||
| chr13:46833799
|
T | C | 1 | a0001c0001t0038 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1038A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1038 | chr13 | 46833799 | |||||
| chr13:46833806
|
C | T | 1 | a0001c0001t0009 | 3 | HG01256.hp1 HG01258.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1031G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1031 | chr13 | 46833806 | |||||
| chr13:46833807
|
G | A | 1 | a0001c0002t0033 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1030C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1030 | chr13 | 46833807 | |||||
| chr13:46834042
|
A | G | 4 | a0001c0001t0046a0001c0001t0048a0001c0002t0031others(1): Show | 4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*795T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 795 | chr13 | 46834042 | |||||
| chr13:46834091
|
G | A | 4 | a0001c0001t0046a0001c0001t0048a0001c0002t0031others(1): Show | 4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*746C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 746 | chr13 | 46834091 | |||||
| chr13:46834114
|
C | G | 1 | a0001c0002t0028 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*723G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 723 | chr13 | 46834114 | |||||
| chr13:46834215
|
T | C | 4 | a0001c0001t0046a0001c0001t0048a0001c0002t0031others(1): Show | 4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*622A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 622 | chr13 | 46834215 | |||||
| chr13:46834406
|
C | T | 4 | a0001c0001t0046a0001c0001t0048a0001c0002t0031others(1): Show | 4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*431G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 431 | chr13 | 46834406 | |||||
| chr13:46834435
|
T | G | 21 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(18): Show | 76 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*402A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 402 | chr13 | 46834435 | |||||
| chr13:46834716
|
C | G | 11 | a0001c0001t0002a0001c0001t0009a0001c0001t0018others(8): Show | 54 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*121G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 121 | chr13 | 46834716 | |||||
| chr13:46834767
|
A | AT | 36 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(33): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*69dupA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 69 | chr13 | 46834767 | |||||
| chr13:46895924
|
T | C | 1 | a0001c0002t0040 | 1 | HG03239.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-18A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | chr13 | 46895924 | ||||||
| chr13:46895936
|
T | A | 1 | a0001c0002t0041 | 1 | NA18952.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 30 | chr13 | 46895936 | |||||
| chr13:46896131
|
T | C | 1 | a0001c0001t0044 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-225A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 225 | chr13 | 46896131 | |||||
| chr13:46896157
|
C | G | 5 | a0001c0001t0017a0001c0001t0045a0001c0001t0046others(2): Show | 7 | HG02572.hp2 HG02723.hp2 HG02922.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-251G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 251 | chr13 | 46896157 | |||||
| chr13:46896158
|
C | A | 3 | a0001c0001t0042a0001c0001t0043a0001c0001t0044 | 3 | HG00639.hp2 HG03453.hp1 NA18522.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-252G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | chr13 | 46896158 | ||||||
| chr13:46896217
|
C | T | 44 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(41): Show | 297 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
5_prime_UTR_variant | MODIFIER | c.-311G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 311 | chr13 | 46896217 | |||||
| chr13:46896689
|
C | T | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(46): Show | 304 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
5_prime_UTR_variant | MODIFIER | c.-344G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | 783 | chr13 | 46896689 | |||||
| chr13:46896789
|
A | G | 2 | a0001c0001t0011a0001c0005t0027 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-444T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | 883 | chr13 | 46896789 | |||||
| chr13:46896888
|
C | G | 1 | a0001c0001t0026 | 1 | HG02970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-543G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | chr13 | 46896888 | ||||||
| chr13:46896912
|
C | G | 1 | a0001c0001t0025 | 1 | HG03492.hp1 | 5_prime_UTR_variant | MODIFIER | c.-567G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | 1006 | chr13 | 46896912 | |||||
| chr13:46896949
|
C | T | 2 | a0001c0001t0008a0001c0001t0024 | 4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-604G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | 1043 | chr13 | 46896949 | |||||
| chr13:46897032
|
C | T | 1 | a0001c0002t0023 | 1 | HG03704.hp1 | 5_prime_UTR_variant | MODIFIER | c.-687G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | 1126 | chr13 | 46897032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:46835968
|
T | A | 137 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0032others(134): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.614-329A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46835968 | ||||||
| chr13:46836190
|
TA | T | 58 | a0001c0001t0002g0031a0001c0001t0002g0044a0001c0001t0002g0051others(55): Show | 59 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.614-552delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836190 | ||||||
| chr13:46836480
|
A | G | 1 | a0001c0002t0034g0281 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.614-841T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836480 | ||||||
| chr13:46836563
|
A | T | 1 | a0001c0002t0034g0281 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.614-924T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836563 | ||||||
| chr13:46836703
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.614-1064G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836703 | ||||||
| chr13:46836831
|
T | C | 8 | a0001c0005t0007g0133a0001c0005t0007g0134a0001c0005t0016g0013others(5): Show | 9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-1192A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836831 | ||||||
| chr13:46836907
|
A | C | 1 | a0001c0001t0017g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.614-1268T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836907 | ||||||
| chr13:46837022
|
C | G | 1 | a0001c0005t0027g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.614-1383G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837022 | ||||||
| chr13:46837035
|
G | T | 6 | a0001c0001t0010g0080a0001c0001t0010g0125a0001c0001t0010g0129others(3): Show | 6 | HG01109.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-1396C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837035 | ||||||
| chr13:46837072
|
G | T | 6 | a0001c0001t0010g0080a0001c0001t0010g0125a0001c0001t0010g0129others(3): Show | 6 | HG01109.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-1433C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837072 | ||||||
| chr13:46837078
|
G | A | 1 | a0001c0002t0005g0284 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.614-1439C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837078 | ||||||
| chr13:46837432
|
G | A | 4 | a0001c0001t0004g0311a0001c0001t0008g0002a0001c0002t0001g0263others(1): Show | 5 | HG02280.hp1 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-1793C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837432 | ||||||
| chr13:46837470
|
A | G | 1 | a0001c0002t0001g0225 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.614-1831T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837470 | ||||||
| chr13:46837526
|
C | T | 84 | a0001c0001t0002g0031a0001c0001t0002g0044a0001c0001t0002g0051others(81): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.614-1887G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837526 | ||||||
| chr13:46837556
|
G | A | 6 | a0001c0001t0010g0080a0001c0001t0010g0125a0001c0001t0010g0129others(3): Show | 6 | HG01109.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-1917C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837556 | ||||||
| chr13:46837850
|
A | G | 254 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(251): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.614-2211T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837850 | ||||||
| chr13:46837940
|
T | C | 53 | a0001c0001t0002g0031a0001c0001t0002g0044a0001c0001t0002g0051others(50): Show | 54 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.614-2301A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837940 | ||||||
| chr13:46838111
|
G | C | 6 | a0001c0001t0010g0080a0001c0001t0010g0125a0001c0001t0010g0129others(3): Show | 6 | HG01109.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-2472C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838111 | ||||||
| chr13:46838317
|
G | A | 1 | a0001c0002t0001g0283 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.614-2678C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838317 | ||||||
| chr13:46838606
|
G | A | 90 | a0001c0001t0002g0031a0001c0001t0002g0044a0001c0001t0002g0051others(87): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.614-2967C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838606 | ||||||
| chr13:46838734
|
C | A | 1 | a0001c0002t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.614-3095G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838734 | ||||||
| chr13:46838977
|
T | C | 7 | a0001c0005t0007g0133a0001c0005t0007g0134a0001c0005t0016g0013others(4): Show | 8 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-3338A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | ||||||
| chr13:46838977
|
T | TAAACACA others(3): Show |
1 | a0001c0001t0001g0095 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.614-3339_614-3338i others(12): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | ||||||
| chr13:46838977
|
T | TAC | 6 | a0001c0001t0005g0081a0001c0001t0020g0319a0001c0001t0046g0295others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.614-3340_614-3339d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | ||||||
| chr13:46838977
|
T | TACAC | 23 | a0001c0001t0004g0311a0001c0001t0004g0315a0001c0001t0005g0152others(20): Show | 24 | HG01074.hp1 HG01109.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.614-3342_614-3339d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | ||||||
| chr13:46838977
|
T | TACACAC | 4 | a0001c0001t0022g0304a0001c0002t0006g0269a0001c0002t0039g0189others(1): Show | 4 | HG02630.hp1 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-3344_614-3339d others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | ||||||
| chr13:46838977
|
TAC | T | 118 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.614-3340_614-3339d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | ||||||
| chr13:46838977
|
TACAC | T | 5 | a0001c0001t0002g0044a0001c0001t0010g0080a0001c0001t0010g0129others(2): Show | 5 | HG02300.hp1 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-3342_614-3339d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | ||||||
| chr13:46839008
|
A | C | 19 | a0001c0001t0010g0080a0001c0001t0010g0129a0001c0001t0024g0015others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.614-3369T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839008 | ||||||
| chr13:46839011
|
C | T | 1 | a0001c0002t0041g0288 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.614-3372G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839011 | ||||||
| chr13:46839236
|
T | C | 3 | a0001c0001t0001g0078a0001c0002t0001g0203a0001c0002t0030g0180 | 3 | HG02015.hp1 NA18961.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.614-3597A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839236 | ||||||
| chr13:46839423
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.614-3784C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839423 | ||||||
| chr13:46839751
|
C | A | 1 | a0001c0001t0045g0293 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.614-4112G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839751 | ||||||
| chr13:46839823
|
A | G | 1 | a0001c0002t0001g0182 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.614-4184T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839823 | ||||||
| chr13:46839830
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.614-4191A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839830 | ||||||
| chr13:46840819
|
T | C | 3 | a0001c0001t0046g0295a0001c0001t0048g0317a0001c0002t0031g0186 | 3 | HG02451.hp1 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.614-5180A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46840819 | ||||||
| chr13:46840827
|
G | A | 1 | a0005c0009t0018g0298 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.614-5188C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46840827 | ||||||
| chr13:46840866
|
A | C | 158 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0032others(155): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.614-5227T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46840866 | ||||||
| chr13:46840985
|
G | A | 8 | a0001c0005t0007g0133a0001c0005t0007g0134a0001c0005t0016g0013others(5): Show | 9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-5346C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46840985 | ||||||
| chr13:46841027
|
C | T | 8 | a0001c0005t0007g0133a0001c0005t0007g0134a0001c0005t0016g0013others(5): Show | 9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-5388G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841027 | ||||||
| chr13:46841141
|
A | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0032others(31): Show | 35 | HG00099.hp1 HG00438.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.614-5502T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841141 | ||||||
| chr13:46841248
|
C | T | 52 | a0001c0001t0002g0031a0001c0001t0002g0044a0001c0001t0002g0051others(49): Show | 53 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.614-5609G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841248 | ||||||
| chr13:46841371
|
T | C | 1 | a0001c0001t0001g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.614-5732A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841371 | ||||||
| chr13:46841492
|
A | G | 1 | a0001c0002t0001g0280 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.614-5853T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841492 | ||||||
| chr13:46841566
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0004g0300a0001c0002t0001g0246 | 3 | HG00735.hp2 HG01261.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.614-5927G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841566 | ||||||
| chr13:46841852
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.614-6213T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841852 | ||||||
| chr13:46841907
|
C | G | 53 | a0001c0001t0002g0031a0001c0001t0002g0044a0001c0001t0002g0051others(50): Show | 54 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.614-6268G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841907 | ||||||
| chr13:46842048
|
C | T | 1 | a0001c0001t0005g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.614-6409G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842048 | ||||||
| chr13:46842059
|
T | A | 1 | a0001c0001t0048g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-6420A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842059 | ||||||
| chr13:46842132
|
T | G | 2 | a0001c0001t0001g0154a0001c0001t0004g0306 | 2 | HG01358.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.614-6493A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842132 | ||||||
| chr13:46842213
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.614-6574G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842213 | ||||||
| chr13:46842251
|
C | T | 85 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0020others(82): Show | 87 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.614-6612G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842251 | ||||||
| chr13:46842325
|
T | C | 1 | a0001c0001t0035g0079 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.614-6686A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842325 | ||||||
| chr13:46842495
|
G | A | 1 | a0001c0001t0004g0302 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.614-6856C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842495 | ||||||
| chr13:46842541
|
C | T | 9 | a0001c0001t0010g0125a0001c0005t0007g0133a0001c0005t0007g0134others(6): Show | 10 | HG01070.hp1 HG01109.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.614-6902G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842541 | ||||||
| chr13:46842549
|
T | C | 1 | a0001c0002t0033g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.614-6910A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842549 | ||||||
| chr13:46842577
|
A | G | 35 | a0001c0001t0002g0031a0001c0001t0002g0044a0001c0001t0002g0051others(32): Show | 35 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.614-6938T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842577 | ||||||
| chr13:46842752
|
G | A | 1 | a0001c0001t0017g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.614-7113C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842752 | ||||||
| chr13:46842903
|
C | T | 2 | a0002c0003t0013g0138a0002c0004t0013g0199 | 2 | HG01081.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.614-7264G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842903 | ||||||
| chr13:46843014
|
T | C | 1 | a0001c0002t0023g0014 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.614-7375A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46843014 | ||||||
| chr13:46843147
|
G | T | 1 | a0003c0007t0007g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.614-7508C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46843147 | ||||||
| chr13:46843742
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.614-8103A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46843742 | ||||||
| chr13:46843809
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | NA19060.hp2 NA19067.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.614-8170C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46843809 | ||||||
| chr13:46844001
|
C | T | 2 | a0002c0004t0003g0174a0002c0004t0003g0191 | 2 | HG00140.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.614-8362G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844001 | ||||||
| chr13:46844051
|
CCTT | C | 3 | a0001c0001t0010g0125a0001c0001t0011g0003a0001c0001t0014g0136 | 4 | HG01109.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-8415_614-8413d others(5): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844051 | ||||||
| chr13:46844144
|
T | C | 13 | a0001c0001t0010g0080a0001c0001t0010g0129a0001c0001t0024g0015others(10): Show | 14 | HG01070.hp1 HG02717.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.614-8505A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844144 | ||||||
| chr13:46844248
|
G | A | 18 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0047others(15): Show | 18 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.614-8609C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844248 | ||||||
| chr13:46844311
|
A | G | 1 | a0001c0002t0001g0283 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.614-8672T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844311 | ||||||
| chr13:46844408
|
T | C | 24 | a0001c0001t0005g0081a0001c0001t0005g0152a0001c0001t0006g0163others(21): Show | 24 | HG01074.hp1 HG01109.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.614-8769A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844408 | ||||||
| chr13:46844509
|
C | T | 1 | a0001c0002t0033g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.614-8870G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844509 | ||||||
| chr13:46844593
|
C | A | 1 | a0001c0002t0001g0239 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.614-8954G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844593 | ||||||
| chr13:46844694
|
G | T | 1 | a0001c0001t0001g0113 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.614-9055C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844694 | ||||||
| chr13:46844834
|
G | C | 9 | a0001c0002t0001g0280a0001c0005t0007g0133a0001c0005t0007g0134others(6): Show | 10 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.614-9195C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844834 | ||||||
| chr13:46845011
|
CT | C | 86 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0020others(83): Show | 88 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.614-9373delA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845011 | ||||||
| chr13:46845069
|
A | G | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0020others(81): Show | 86 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.614-9430T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845069 | ||||||
| chr13:46845147
|
A | G | 9 | a0001c0002t0001g0280a0001c0005t0007g0133a0001c0005t0007g0134others(6): Show | 10 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.614-9508T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845147 | ||||||
| chr13:46845442
|
A | G | 105 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0020others(102): Show | 107 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.614-9803T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845442 | ||||||
| chr13:46845577
|
G | A | 1 | a0001c0001t0052g0316 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.614-9938C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845577 | ||||||
| chr13:46845643
|
C | CA | 84 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0082others(81): Show | 87 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.614-10005dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845643 | ||||||
| chr13:46845643
|
C | CAA | 9 | a0001c0001t0001g0047a0001c0001t0009g0158a0001c0001t0017g0294others(6): Show | 9 | HG00738.hp2 HG02165.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-10006_614-1000 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845643 | ||||||
| chr13:46845643
|
CA | C | 88 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0020others(85): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.614-10005delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845643 | ||||||
| chr13:46845643
|
CAA | C | 7 | a0001c0001t0001g0066a0001c0001t0001g0075a0001c0001t0001g0122others(4): Show | 7 | HG00621.hp1 NA18939.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-10006_614-1000 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845643 | ||||||
| chr13:46845685
|
G | T | 77 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0032others(74): Show | 80 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.614-10046C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845685 | ||||||
| chr13:46846111
|
A | G | 1 | a0001c0002t0001g0283 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.614-10472T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846111 | ||||||
| chr13:46846177
|
T | C | 197 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.614-10538A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846177 | ||||||
| chr13:46846277
|
A | C | 82 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0020others(79): Show | 84 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.614-10638T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846277 | ||||||
| chr13:46846289
|
C | G | 3 | a0001c0001t0001g0056a0001c0001t0004g0300a0001c0002t0001g0246 | 3 | HG00735.hp2 HG01261.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.614-10650G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846289 | ||||||
| chr13:46846293
|
A | G | 21 | a0001c0001t0001g0036a0001c0001t0005g0081a0001c0001t0005g0152others(18): Show | 21 | HG00280.hp1 HG01074.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.614-10654T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846293 | ||||||
| chr13:46846329
|
T | C | 1 | a0001c0002t0002g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.614-10690A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846329 | ||||||
| chr13:46846650
|
G | C | 1 | a0001c0001t0052g0316 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.614-11011C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846650 | ||||||
| chr13:46846718
|
G | A | 1 | a0001c0002t0001g0225 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.614-11079C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846718 | ||||||
| chr13:46846848
|
G | A | 81 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0020others(78): Show | 83 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.614-11209C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846848 | ||||||
| chr13:46847088
|
G | A | 85 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0020others(82): Show | 88 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.614-11449C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46847088 | ||||||
| chr13:46847131
|
C | T | 170 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(167): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.614-11492G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46847131 | ||||||
| chr13:46847159
|
A | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0004g0299others(7): Show | 10 | HG00738.hp2 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.614-11520T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46847159 | ||||||
| chr13:46847701
|
C | T | 79 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0020others(76): Show | 81 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.614-12062G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46847701 | ||||||
| chr13:46847822
|
G | A | 1 | a0001c0002t0001g0252 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.614-12183C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46847822 | ||||||
| chr13:46848180
|
A | G | 1 | a0001c0001t0048g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-12541T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848180 | ||||||
| chr13:46848321
|
A | G | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.614-12682T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848321 | ||||||
| chr13:46848330
|
A | G | 21 | a0001c0001t0005g0081a0001c0001t0005g0152a0001c0001t0006g0163others(18): Show | 21 | HG01074.hp1 HG01109.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.614-12691T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848330 | ||||||
| chr13:46848499
|
A | C | 8 | a0001c0005t0007g0133a0001c0005t0007g0134a0001c0005t0016g0013others(5): Show | 9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-12860T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848499 | ||||||
| chr13:46848862
|
A | G | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.614-13223T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848862 | ||||||
| chr13:46848907
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0042others(1): Show | 5 | HG01255.hp2 HG01256.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.614-13268A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848907 | ||||||
| chr13:46848951
|
T | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0032others(93): Show | 98 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.614-13312A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848951 | ||||||
| chr13:46848987
|
T | C | 2 | a0001c0002t0001g0283a0001c0002t0034g0281 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.614-13348A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848987 | ||||||
| chr13:46849100
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.614-13461G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849100 | ||||||
| chr13:46849156
|
C | T | 207 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(204): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.614-13517G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849156 | ||||||
| chr13:46849198
|
T | C | 3 | a0001c0001t0017g0292a0001c0002t0001g0272a0001c0002t0001g0273 | 3 | HG02896.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.614-13559A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849198 | ||||||
| chr13:46849256
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.614-13617G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849256 | ||||||
| chr13:46849430
|
A | T | 90 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0032others(87): Show | 93 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.614-13791T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849430 | ||||||
| chr13:46849457
|
C | T | 90 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0032others(87): Show | 93 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.614-13818G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849457 | ||||||
| chr13:46849721
|
A | G | 1 | a0001c0001t0004g0315 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.614-14082T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849721 | ||||||
| chr13:46849744
|
C | T | 5 | a0001c0005t0007g0133a0001c0005t0016g0013a0001c0005t0049g0303others(2): Show | 6 | HG01070.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-14105G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849744 | ||||||
| chr13:46849983
|
A | G | 32 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0086others(29): Show | 33 | HG00423.hp2 HG01074.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.614-14344T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849983 | ||||||
| chr13:46849989
|
G | A | 25 | a0001c0001t0004g0315a0001c0001t0005g0081a0001c0001t0014g0136others(22): Show | 26 | HG01070.hp1 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.614-14350C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849989 | ||||||
| chr13:46850158
|
G | C | 161 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(158): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.614-14519C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850158 | ||||||
| chr13:46850208
|
C | A | 1 | a0001c0002t0001g0184 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.614-14569G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850208 | ||||||
| chr13:46850243
|
T | C | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-14604A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850243 | ||||||
| chr13:46850250
|
A | G | 208 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(205): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.614-14611T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850250 | ||||||
| chr13:46850630
|
A | G | 1 | a0001c0002t0001g0270 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.614-14991T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850630 | ||||||
| chr13:46850635
|
C | T | 1 | a0001c0001t0048g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-14996G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850635 | ||||||
| chr13:46850636
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.614-14997C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850636 | ||||||
| chr13:46850674
|
T | C | 7 | a0001c0001t0026g0018a0001c0005t0007g0133a0001c0005t0016g0013others(4): Show | 8 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-15035A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850674 | ||||||
| chr13:46850677
|
C | T | 205 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(202): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.614-15038G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850677 | ||||||
| chr13:46850714
|
G | T | 1 | a0001c0002t0001g0280 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.614-15075C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850714 | ||||||
| chr13:46850761
|
G | A | 7 | a0001c0001t0026g0018a0001c0005t0007g0133a0001c0005t0016g0013others(4): Show | 8 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-15122C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850761 | ||||||
| chr13:46850809
|
C | G | 160 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(157): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.614-15170G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850809 | ||||||
| chr13:46850859
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.614-15220A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850859 | ||||||
| chr13:46850912
|
A | T | 1 | a0001c0001t0052g0316 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.614-15273T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850912 | ||||||
| chr13:46850940
|
C | G | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-15301G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850940 | ||||||
| chr13:46851110
|
A | G | 22 | a0001c0001t0001g0154a0001c0001t0004g0315a0001c0001t0005g0081others(19): Show | 22 | HG00738.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.614-15471T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851110 | ||||||
| chr13:46851115
|
T | C | 1 | a0001c0002t0034g0281 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.614-15476A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851115 | ||||||
| chr13:46851715
|
C | T | 1 | a0001c0002t0002g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.614-16076G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851715 | ||||||
| chr13:46851806
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0045 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.614-16167T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851806 | ||||||
| chr13:46851812
|
C | T | 1 | a0001c0005t0007g0133 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.614-16173G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851812 | ||||||
| chr13:46851908
|
A | G | 3 | a0001c0001t0010g0125a0001c0001t0011g0003a0001c0005t0027g0019 | 4 | HG01109.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-16269T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851908 | ||||||
| chr13:46851912
|
A | T | 1 | a0001c0002t0001g0184 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.614-16273T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851912 | ||||||
| chr13:46852018
|
T | TGATTCAA others(9): Show |
7 | a0001c0001t0026g0018a0001c0005t0007g0133a0001c0005t0016g0013others(4): Show | 8 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-16395_614-1638 others(20): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852018 | ||||||
| chr13:46852130
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(124): Show | 134 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.614-16491T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852130 | ||||||
| chr13:46852176
|
C | G | 1 | a0001c0002t0034g0281 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.614-16537G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852176 | ||||||
| chr13:46852331
|
T | G | 1 | a0001c0001t0048g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-16692A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852331 | ||||||
| chr13:46852373
|
G | T | 2 | a0001c0002t0001g0197a0001c0002t0041g0288 | 2 | NA18952.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.614-16734C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852373 | ||||||
| chr13:46852417
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.614-16778C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852417 | ||||||
| chr13:46852527
|
C | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0117a0001c0001t0001g0119 | 3 | HG00438.hp1 NA18941.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.614-16888G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852527 | ||||||
| chr13:46852587
|
A | G | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(154): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.614-16948T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852587 | ||||||
| chr13:46852846
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0045 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.614-17207T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852846 | ||||||
| chr13:46852864
|
T | C | 313 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(310): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.614-17225A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852864 | ||||||
| chr13:46852891
|
A | C | 1 | a0001c0001t0001g0116 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.614-17252T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852891 | ||||||
| chr13:46852910
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.614-17271A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852910 | ||||||
| chr13:46852968
|
G | GT | 124 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 131 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.614-17330_614-1732 others(5): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852968 | ||||||
| chr13:46852968
|
GC | G | 3 | a0001c0001t0001g0127a0001c0002t0001g0179a0001c0002t0001g0198 | 3 | HG02165.hp2 NA18943.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.614-17330delG | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852968 | ||||||
| chr13:46852969
|
C | T | 310 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(307): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.614-17330G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852969 | ||||||
| chr13:46852998
|
ATTC | A | 12 | a0001c0001t0001g0130a0001c0001t0005g0152a0001c0001t0017g0294others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.614-17362_614-1736 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852998 | ||||||
| chr13:46853175
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.614-17536C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853175 | ||||||
| chr13:46853209
|
T | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.614-17570A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853209 | ||||||
| chr13:46853377
|
T | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.614-17738A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853377 | ||||||
| chr13:46853491
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.614-17852T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853491 | ||||||
| chr13:46853501
|
T | C | 1 | a0001c0002t0001g0280 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.614-17862A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853501 | ||||||
| chr13:46853541
|
T | C | 313 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(310): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.614-17902A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853541 | ||||||
| chr13:46853547
|
G | C | 1 | a0001c0001t0002g0118 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.614-17908C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853547 | ||||||
| chr13:46853634
|
C | G | 1 | a0001c0002t0001g0280 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.614-17995G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853634 | ||||||
| chr13:46853656
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.614-18017T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853656 | ||||||
| chr13:46853785
|
A | C | 22 | a0001c0001t0001g0154a0001c0001t0004g0315a0001c0001t0005g0081others(19): Show | 22 | HG00738.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.614-18146T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853785 | ||||||
| chr13:46853799
|
C | A | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-18160G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853799 | ||||||
| chr13:46854046
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.614-18407A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854046 | ||||||
| chr13:46854061
|
G | A | 1 | a0001c0001t0017g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.614-18422C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854061 | ||||||
| chr13:46854065
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 128 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.614-18426G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854065 | ||||||
| chr13:46854113
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.614-18474T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854113 | ||||||
| chr13:46854252
|
C | T | 1 | a0001c0002t0001g0280 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.614-18613G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854252 | ||||||
| chr13:46854336
|
A | C | 189 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(186): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.614-18697T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854336 | ||||||
| chr13:46854476
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.614-18837A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854476 | ||||||
| chr13:46854616
|
G | T | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-18977C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854616 | ||||||
| chr13:46854728
|
A | G | 1 | a0001c0002t0034g0281 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.614-19089T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854728 | ||||||
| chr13:46854936
|
C | A | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-19297G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854936 | ||||||
| chr13:46854948
|
T | C | 3 | a0001c0001t0001g0151a0001c0001t0004g0301a0001c0002t0001g0222 | 3 | HG00639.hp1 HG01074.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.614-19309A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854948 | ||||||
| chr13:46855019
|
T | C | 4 | a0001c0001t0021g0313a0001c0001t0021g0322a0001c0002t0002g0022others(1): Show | 4 | HG02970.hp1 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-19380A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855019 | ||||||
| chr13:46855092
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.614-19453T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855092 | ||||||
| chr13:46855093
|
A | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0020others(106): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.614-19454T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855093 | ||||||
| chr13:46855162
|
C | T | 3 | a0001c0001t0001g0036a0001c0002t0001g0249a0002c0003t0013g0138 | 3 | HG00280.hp1 HG01081.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.614-19523G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855162 | ||||||
| chr13:46855163
|
G | A | 1 | a0002c0003t0019g0318 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.614-19524C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855163 | ||||||
| chr13:46855293
|
G | A | 3 | a0001c0001t0014g0136a0001c0002t0001g0280a0001c0002t0034g0281 | 3 | HG02280.hp2 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.614-19654C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855293 | ||||||
| chr13:46855311
|
T | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0047others(42): Show | 47 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.614-19672A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855311 | ||||||
| chr13:46855348
|
A | G | 2 | a0001c0002t0001g0272a0001c0002t0001g0273 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.614-19709T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855348 | ||||||
| chr13:46855410
|
T | C | 5 | a0001c0001t0021g0322a0001c0002t0001g0185a0001c0002t0001g0285others(2): Show | 5 | HG02109.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-19771A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855410 | ||||||
| chr13:46855436
|
T | C | 1 | a0001c0010t0036g0110 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.614-19797A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855436 | ||||||
| chr13:46855516
|
G | C | 1 | a0001c0002t0002g0278 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.614-19877C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855516 | ||||||
| chr13:46855542
|
A | C | 3 | a0001c0001t0001g0058a0001c0001t0004g0306a0001c0002t0001g0200 | 3 | HG00741.hp2 HG01358.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.614-19903T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855542 | ||||||
| chr13:46855634
|
TA | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0058others(4): Show | 7 | HG00741.hp2 HG01192.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.614-19996delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855634 | ||||||
| chr13:46855635
|
A | T | 1 | a0001c0001t0014g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.614-19996T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855635 | ||||||
| chr13:46855657
|
G | A | 1 | a0001c0005t0027g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.614-20018C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855657 | ||||||
| chr13:46855732
|
C | A | 1 | a0001c0002t0001g0221 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.614-20093G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855732 | ||||||
| chr13:46855742
|
A | G | 1 | a0001c0001t0002g0077 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.614-20103T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855742 | ||||||
| chr13:46855837
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.614-20198C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855837 | ||||||
| chr13:46856128
|
C | G | 71 | a0001c0001t0001g0011a0001c0001t0001g0065a0001c0001t0001g0078others(68): Show | 72 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.614-20489G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856128 | ||||||
| chr13:46856128
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.614-20489G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856128 | ||||||
| chr13:46856141
|
C | G | 86 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0028others(83): Show | 89 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.614-20502G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856141 | ||||||
| chr13:46856177
|
T | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0045 | 3 | HG01346.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.614-20538A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856177 | ||||||
| chr13:46856180
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.614-20541T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856180 | ||||||
| chr13:46856231
|
G | A | 314 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(311): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.614-20592C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856231 | ||||||
| chr13:46856344
|
A | G | 149 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(146): Show | 155 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.614-20705T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856344 | ||||||
| chr13:46856383
|
T | C | 1 | a0001c0001t0001g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.614-20744A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856383 | ||||||
| chr13:46856394
|
A | G | 6 | a0001c0001t0004g0302a0001c0001t0021g0313a0001c0001t0044g0291others(3): Show | 6 | HG01243.hp2 HG02615.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.614-20755T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856394 | ||||||
| chr13:46856467
|
T | C | 19 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(16): Show | 19 | HG00099.hp2 HG01169.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.614-20828A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856467 | ||||||
| chr13:46856471
|
G | A | 4 | a0001c0002t0001g0262a0001c0002t0001g0263a0001c0002t0002g0188others(1): Show | 4 | HG01109.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-20832C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856471 | ||||||
| chr13:46856594
|
T | TA | 18 | a0001c0001t0001g0135a0001c0001t0004g0311a0001c0001t0006g0163others(15): Show | 19 | HG01074.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.614-20956dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856594 | ||||||
| chr13:46856594
|
TA | T | 7 | a0001c0001t0001g0084a0001c0001t0005g0081a0001c0001t0010g0080others(4): Show | 7 | HG02155.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.614-20956delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856594 | ||||||
| chr13:46856625
|
T | C | 1 | a0001c0002t0040g0287 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.614-20986A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856625 | ||||||
| chr13:46856653
|
G | A | 11 | a0001c0001t0004g0299a0001c0001t0004g0302a0001c0001t0020g0310others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.614-21014C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856653 | ||||||
| chr13:46856666
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.614-21027A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856666 | ||||||
| chr13:46856755
|
C | G | 1 | a0001c0001t0015g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.614-21116G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856755 | ||||||
| chr13:46856849
|
C | G | 1 | a0001c0001t0008g0016 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.614-21210G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856849 | ||||||
| chr13:46856973
|
G | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0033others(31): Show | 38 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.614-21334C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856973 | ||||||
| chr13:46856986
|
C | T | 6 | a0001c0002t0001g0197a0001c0002t0001g0226a0001c0002t0002g0202others(3): Show | 6 | NA18965.hp2 NA18969.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-21347G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856986 | ||||||
| chr13:46857100
|
G | C | 4 | a0001c0002t0001g0262a0001c0002t0001g0263a0001c0002t0002g0188others(1): Show | 4 | HG01109.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-21461C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857100 | ||||||
| chr13:46857179
|
A | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0047others(17): Show | 21 | HG01070.hp1 HG01099.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.614-21540T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857179 | ||||||
| chr13:46857228
|
G | A | 108 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0067others(105): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.614-21589C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857228 | ||||||
| chr13:46857248
|
G | C | 1 | a0001c0001t0015g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.614-21609C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857248 | ||||||
| chr13:46857297
|
T | TA | 31 | a0001c0001t0001g0073a0001c0001t0001g0098a0001c0001t0002g0112others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.614-21659dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857297 | ||||||
| chr13:46857297
|
T | TAA | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0033others(36): Show | 43 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.614-21660_614-2165 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857297 | ||||||
| chr13:46857297
|
TA | T | 8 | a0001c0001t0001g0093a0001c0002t0001g0215a0001c0002t0001g0256others(5): Show | 8 | HG02129.hp1 HG02717.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.614-21659delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857297 | ||||||
| chr13:46857336
|
G | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0033others(37): Show | 44 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.614-21697C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857336 | ||||||
| chr13:46857374
|
T | C | 32 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.614-21735A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857374 | ||||||
| chr13:46857441
|
A | G | 8 | a0001c0001t0005g0081a0001c0001t0010g0080a0001c0001t0017g0292others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.614-21802T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857441 | ||||||
| chr13:46857558
|
T | C | 5 | a0001c0001t0014g0145a0001c0002t0001g0283a0001c0002t0005g0284others(2): Show | 5 | HG01884.hp1 HG01891.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.614-21919A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857558 | ||||||
| chr13:46857565
|
T | C | 1 | a0001c0001t0043g0290 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.614-21926A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857565 | ||||||
| chr13:46857815
|
G | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0033others(38): Show | 45 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.614-22176C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857815 | ||||||
| chr13:46857909
|
C | G | 2 | a0001c0001t0001g0297a0001c0001t0002g0106 | 2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.614-22270G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857909 | ||||||
| chr13:46858019
|
T | G | 189 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(186): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.614-22380A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858019 | ||||||
| chr13:46858240
|
T | C | 1 | a0001c0012t0032g0244 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.614-22601A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858240 | ||||||
| chr13:46858261
|
A | C | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.614-22622T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858261 | ||||||
| chr13:46858291
|
T | A | 319 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.614-22652A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858291 | ||||||
| chr13:46858357
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.614-22718A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858357 | ||||||
| chr13:46858475
|
T | G | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(184): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.614-22836A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858475 | ||||||
| chr13:46858661
|
G | T | 1 | a0001c0002t0001g0234 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.614-23022C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858661 | ||||||
| chr13:46858793
|
T | G | 22 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.614-23154A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858793 | ||||||
| chr13:46858827
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0141a0001c0001t0001g0144others(1): Show | 5 | HG02040.hp2 NA18952.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.614-23188A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858827 | ||||||
| chr13:46858946
|
T | C | 2 | a0001c0002t0002g0274a0001c0002t0040g0287 | 2 | HG03239.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.614-23307A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858946 | ||||||
| chr13:46859078
|
A | G | 1 | a0001c0002t0002g0245 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.614-23439T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859078 | ||||||
| chr13:46859175
|
A | G | 2 | a0001c0001t0001g0047a0002c0003t0003g0046 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.614-23536T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859175 | ||||||
| chr13:46859212
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.614-23573A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859212 | ||||||
| chr13:46859220
|
C | G | 122 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(119): Show | 126 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.614-23581G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859220 | ||||||
| chr13:46859362
|
G | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.614-23723C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859362 | ||||||
| chr13:46859379
|
A | G | 1 | a0001c0001t0046g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.614-23740T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859379 | ||||||
| chr13:46859690
|
A | G | 4 | a0001c0002t0001g0208a0001c0002t0001g0211a0001c0002t0001g0231others(1): Show | 4 | HG00735.hp1 HG01358.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-24051T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859690 | ||||||
| chr13:46859699
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0002g0109 | 2 | HG00438.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.614-24060G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859699 | ||||||
| chr13:46859709
|
C | G | 67 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(64): Show | 73 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.614-24070G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859709 | ||||||
| chr13:46859753
|
C | T | 2 | a0001c0001t0017g0292a0001c0001t0046g0295 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.614-24114G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859753 | ||||||
| chr13:46859799
|
T | C | 1 | a0001c0001t0006g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.614-24160A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859799 | ||||||
| chr13:46859803
|
C | T | 8 | a0001c0001t0001g0067a0001c0001t0001g0154a0001c0001t0001g0156others(5): Show | 8 | HG00738.hp2 HG01175.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-24164G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859803 | ||||||
| chr13:46859818
|
G | A | 3 | a0001c0001t0008g0002a0001c0001t0008g0016a0001c0001t0024g0015 | 4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-24179C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859818 | ||||||
| chr13:46860114
|
T | C | 2 | a0001c0001t0044g0291a0001c0002t0006g0269 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.614-24475A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860114 | ||||||
| chr13:46860192
|
G | A | 35 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0086others(32): Show | 36 | HG00438.hp2 HG00597.hp1 HG01981.hp1 others(33): Show |
intron_variant | MODIFIER | c.614-24553C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860192 | ||||||
| chr13:46860336
|
A | G | 1 | a0001c0002t0002g0238 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.614-24697T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860336 | ||||||
| chr13:46860487
|
T | A | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.614-24848A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860487 | ||||||
| chr13:46860598
|
C | T | 16 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(13): Show | 19 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.614-24959G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860598 | ||||||
| chr13:46860723
|
A | G | 1 | a0001c0001t0020g0310 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.614-25084T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860723 | ||||||
| chr13:46860971
|
C | G | 29 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(26): Show | 30 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.614-25332G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860971 | ||||||
| chr13:46861148
|
G | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 307 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.614-25509C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861148 | ||||||
| chr13:46861200
|
A | G | 3 | a0001c0001t0008g0002a0001c0001t0008g0016a0001c0001t0024g0015 | 4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-25561T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861200 | ||||||
| chr13:46861208
|
A | C | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-25569T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861208 | ||||||
| chr13:46861251
|
A | C | 3 | a0001c0002t0002g0022a0001c0002t0005g0021a0001c0002t0033g0176 | 3 | HG02486.hp1 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.614-25612T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861251 | ||||||
| chr13:46861325
|
C | G | 3 | a0001c0012t0032g0244a0002c0003t0003g0048a0002c0003t0003g0049 | 3 | HG01070.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.614-25686G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861325 | ||||||
| chr13:46861448
|
G | T | 2 | a0001c0001t0004g0315a0001c0001t0052g0316 | 2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.614-25809C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861448 | ||||||
| chr13:46861469
|
G | A | 2 | a0001c0001t0010g0125a0001c0001t0010g0129 | 2 | HG01109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.614-25830C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861469 | ||||||
| chr13:46861475
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.614-25836T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861475 | ||||||
| chr13:46861476
|
A | C | 1 | a0001c0002t0005g0021 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.614-25837T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861476 | ||||||
| chr13:46861657
|
G | A | 5 | a0001c0001t0001g0065a0001c0001t0002g0060a0001c0001t0002g0063others(2): Show | 5 | NA18612.hp2 NA18982.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-26018C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861657 | ||||||
| chr13:46861729
|
G | C | 3 | a0001c0001t0008g0002a0001c0001t0008g0016a0001c0001t0024g0015 | 4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-26090C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861729 | ||||||
| chr13:46861978
|
A | C | 1 | a0001c0001t0006g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.614-26339T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861978 | ||||||
| chr13:46862031
|
G | A | 1 | a0001c0002t0001g0223 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.614-26392C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862031 | ||||||
| chr13:46862191
|
C | A | 3 | a0001c0001t0001g0105a0001c0001t0002g0096a0001c0001t0002g0112 | 3 | NA18954.hp1 NA18965.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.614-26552G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862191 | ||||||
| chr13:46862214
|
T | C | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-26575A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862214 | ||||||
| chr13:46862228
|
G | A | 1 | a0001c0001t0006g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.614-26589C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862228 | ||||||
| chr13:46862385
|
G | T | 1 | a0001c0001t0006g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.614-26746C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862385 | ||||||
| chr13:46862558
|
G | A | 1 | a0001c0002t0001g0179 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.614-26919C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862558 | ||||||
| chr13:46862582
|
A | C | 1 | a0001c0001t0001g0066 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.614-26943T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862582 | ||||||
| chr13:46862618
|
G | A | 2 | a0001c0001t0010g0125a0001c0001t0010g0129 | 2 | HG01109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.614-26979C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862618 | ||||||
| chr13:46862672
|
T | A | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.614-27033A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862672 | ||||||
| chr13:46862672
|
T | C | 1 | a0001c0001t0047g0296 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.614-27033A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862672 | ||||||
| chr13:46862794
|
A | G | 12 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(9): Show | 14 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.614-27155T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862794 | ||||||
| chr13:46862961
|
T | C | 2 | a0001c0002t0001g0192a0002c0004t0003g0191 | 2 | HG00099.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.614-27322A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862961 | ||||||
| chr13:46862968
|
G | C | 52 | a0001c0001t0001g0011a0001c0001t0001g0135a0001c0001t0001g0139others(49): Show | 57 | HG00099.hp2 HG00140.hp1 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.614-27329C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862968 | ||||||
| chr13:46862976
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0056others(5): Show | 9 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-27337G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862976 | ||||||
| chr13:46863045
|
T | C | 13 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.614-27406A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863045 | ||||||
| chr13:46863081
|
G | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.614-27442C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863081 | ||||||
| chr13:46863247
|
G | C | 49 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(46): Show | 54 | HG00099.hp2 HG00140.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.614-27608C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863247 | ||||||
| chr13:46863290
|
G | T | 1 | a0001c0001t0006g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.614-27651C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863290 | ||||||
| chr13:46863298
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.614-27659C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863298 | ||||||
| chr13:46863410
|
C | T | 15 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.614-27771G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863410 | ||||||
| chr13:46863483
|
C | A | 1 | a0001c0001t0042g0289 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.614-27844G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863483 | ||||||
| chr13:46863517
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(298): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.614-27878T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863517 | ||||||
| chr13:46863630
|
GA | G | 29 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(26): Show | 30 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.614-27992delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863630 | ||||||
| chr13:46863645
|
A | AAAAG | 254 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 263 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.614-28007_614-2800 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863645 | ||||||
| chr13:46863650
|
G | A | 262 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(259): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.614-28011C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863650 | ||||||
| chr13:46863657
|
A | AAAAAG | 8 | a0001c0001t0001g0047a0001c0001t0001g0159a0001c0001t0002g0114others(5): Show | 8 | HG01175.hp2 HG02135.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.614-28019_614-2801 others(9): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863657 | ||||||
| chr13:46863657
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(259): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.614-28018T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863657 | ||||||
| chr13:46863968
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.614-28329T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863968 | ||||||
| chr13:46863982
|
G | T | 2 | a0001c0002t0001g0262a0001c0002t0001g0263 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.614-28343C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863982 | ||||||
| chr13:46864000
|
G | A | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(265): Show | 277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.614-28361C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864000 | ||||||
| chr13:46864011
|
A | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.614-28372T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864011 | ||||||
| chr13:46864065
|
T | C | 2 | a0001c0001t0045g0293a0001c0005t0016g0013 | 3 | HG02572.hp2 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.613+28325A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864065 | ||||||
| chr13:46864081
|
G | A | 27 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.613+28309C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864081 | ||||||
| chr13:46864280
|
G | A | 3 | a0001c0001t0001g0135a0001c0005t0007g0133a0001c0005t0007g0134 | 3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+28110C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864280 | ||||||
| chr13:46864369
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.613+28021T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864369 | ||||||
| chr13:46864414
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.613+27976A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864414 | ||||||
| chr13:46864439
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.613+27951A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864439 | ||||||
| chr13:46864447
|
T | C | 2 | a0001c0001t0005g0081a0001c0001t0010g0080 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.613+27943A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864447 | ||||||
| chr13:46864533
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(10): Show | 15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+27857C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864533 | ||||||
| chr13:46864559
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.613+27831G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864559 | ||||||
| chr13:46864587
|
A | G | 1 | a0001c0002t0001g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.613+27803T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864587 | ||||||
| chr13:46864603
|
C | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.613+27787G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864603 | ||||||
| chr13:46864621
|
C | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(6): Show | 10 | HG01081.hp2 HG01099.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+27769G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864621 | ||||||
| chr13:46864670
|
C | T | 1 | a0001c0001t0048g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.613+27720G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864670 | ||||||
| chr13:46864733
|
G | A | 1 | a0001c0005t0027g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.613+27657C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864733 | ||||||
| chr13:46864772
|
AGTT | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0085others(133): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.613+27615_613+2761 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864772 | ||||||
| chr13:46864839
|
C | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(97): Show | 103 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.613+27551G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864839 | ||||||
| chr13:46864931
|
T | C | 3 | a0001c0001t0001g0135a0001c0005t0007g0133a0001c0005t0007g0134 | 3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+27459A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864931 | ||||||
| chr13:46864944
|
GT | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.613+27445delA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864944 | ||||||
| chr13:46864957
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(262): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.613+27433A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864957 | ||||||
| chr13:46865081
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.613+27309T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865081 | ||||||
| chr13:46865084
|
G | A | 2 | a0001c0002t0001g0164a0001c0002t0001g0228 | 2 | NA18941.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.613+27306C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865084 | ||||||
| chr13:46865105
|
C | T | 1 | a0001c0002t0002g0171 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.613+27285G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865105 | ||||||
| chr13:46865236
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0085others(104): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.613+27154T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865236 | ||||||
| chr13:46865441
|
G | GAAGT | 303 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.613+26948_613+2694 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865441 | ||||||
| chr13:46865533
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.613+26857A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865533 | ||||||
| chr13:46865595
|
G | T | 23 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.613+26795C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865595 | ||||||
| chr13:46865641
|
A | T | 67 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(64): Show | 69 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.613+26749T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865641 | ||||||
| chr13:46865658
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(265): Show | 278 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.613+26732A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865658 | ||||||
| chr13:46865664
|
G | T | 1 | a0001c0002t0001g0258 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.613+26726C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865664 | ||||||
| chr13:46865685
|
T | C | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+26705A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865685 | ||||||
| chr13:46865741
|
C | A | 5 | a0001c0001t0017g0292a0001c0001t0017g0294a0001c0001t0045g0293others(2): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+26649G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865741 | ||||||
| chr13:46865819
|
G | A | 2 | a0001c0001t0002g0137a0001c0001t0021g0322 | 2 | HG03098.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.613+26571C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865819 | ||||||
| chr13:46865820
|
C | A | 1 | a0001c0002t0001g0225 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.613+26570G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865820 | ||||||
| chr13:46865820
|
C | T | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+26570G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865820 | ||||||
| chr13:46865841
|
C | T | 67 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(64): Show | 69 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.613+26549G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865841 | ||||||
| chr13:46865935
|
C | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(95): Show | 101 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.613+26455G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865935 | ||||||
| chr13:46865990
|
G | A | 1 | a0001c0001t0005g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.613+26400C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865990 | ||||||
| chr13:46866140
|
T | C | 1 | a0001c0002t0029g0170 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.613+26250A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866140 | ||||||
| chr13:46866284
|
C | G | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+26106G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866284 | ||||||
| chr13:46866323
|
G | C | 26 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(23): Show | 27 | HG00423.hp2 HG02015.hp2 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.613+26067C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866323 | ||||||
| chr13:46866372
|
C | T | 1 | a0001c0001t0042g0289 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.613+26018G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866372 | ||||||
| chr13:46866425
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.613+25965G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866425 | ||||||
| chr13:46866622
|
C | G | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+25768G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866622 | ||||||
| chr13:46866665
|
T | C | 68 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(65): Show | 70 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.613+25725A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866665 | ||||||
| chr13:46866666
|
G | A | 4 | a0003c0006t0001g0147a0003c0006t0001g0148a0003c0007t0007g0149others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+25724C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866666 | ||||||
| chr13:46866693
|
T | G | 4 | a0001c0001t0042g0289a0001c0001t0044g0291a0001c0002t0006g0269others(1): Show | 4 | HG03225.hp1 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+25697A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866693 | ||||||
| chr13:46866735
|
G | T | 1 | a0001c0001t0006g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.613+25655C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866735 | ||||||
| chr13:46866769
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.613+25621C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866769 | ||||||
| chr13:46866844
|
T | C | 1 | a0002c0004t0003g0174 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.613+25546A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866844 | ||||||
| chr13:46866853
|
A | G | 1 | a0002c0004t0003g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.613+25537T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866853 | ||||||
| chr13:46866900
|
G | A | 1 | a0001c0002t0006g0269 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.613+25490C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866900 | ||||||
| chr13:46866924
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.613+25466T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866924 | ||||||
| chr13:46867122
|
C | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0132a0001c0002t0001g0181others(6): Show | 11 | HG02165.hp2 NA18939.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+25268G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867122 | ||||||
| chr13:46867288
|
A | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0056others(5): Show | 9 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.613+25102T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867288 | ||||||
| chr13:46867326
|
T | C | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+25064A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867326 | ||||||
| chr13:46867375
|
A | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 244 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.613+25015T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867375 | ||||||
| chr13:46867399
|
G | A | 1 | a0001c0001t0050g0305 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.613+24991C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867399 | ||||||
| chr13:46867474
|
G | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.613+24916C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867474 | ||||||
| chr13:46867481
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.613+24909C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867481 | ||||||
| chr13:46867546
|
C | T | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+24844G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867546 | ||||||
| chr13:46867572
|
T | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.613+24818A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867572 | ||||||
| chr13:46867912
|
AT | A | 58 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(55): Show | 60 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.613+24477delA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867912 | ||||||
| chr13:46868029
|
G | GTTAATTC | 68 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(65): Show | 70 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.613+24360_613+2436 others(11): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868029 | ||||||
| chr13:46868160
|
C | T | 1 | a0001c0001t0017g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.613+24230G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868160 | ||||||
| chr13:46868193
|
A | G | 2 | a0001c0005t0007g0133a0001c0005t0007g0134 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+24197T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868193 | ||||||
| chr13:46868378
|
G | A | 2 | a0001c0001t0044g0291a0001c0002t0006g0269 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.613+24012C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868378 | ||||||
| chr13:46868577
|
A | T | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+23813T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868577 | ||||||
| chr13:46868590
|
C | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0085others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.613+23800G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868590 | ||||||
| chr13:46868633
|
T | A | 2 | a0001c0001t0008g0002a0001c0001t0024g0015 | 3 | HG02280.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.613+23757A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868633 | ||||||
| chr13:46869366
|
C | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(230): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.613+23024G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869366 | ||||||
| chr13:46869393
|
C | T | 11 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0306others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+22997G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869393 | ||||||
| chr13:46869475
|
G | A | 1 | a0003c0006t0001g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.613+22915C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869475 | ||||||
| chr13:46869668
|
T | C | 23 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(20): Show | 24 | HG00423.hp2 HG02015.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.613+22722A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869668 | ||||||
| chr13:46869733
|
G | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(317): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.613+22657C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869733 | ||||||
| chr13:46869754
|
A | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 31 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.613+22636T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869754 | ||||||
| chr13:46869918
|
T | C | 37 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(34): Show | 40 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.613+22472A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869918 | ||||||
| chr13:46870129
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0002g0031 | 2 | NA19055.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.613+22261A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46870129 | ||||||
| chr13:46870405
|
C | T | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+21985G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46870405 | ||||||
| chr13:46870414
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0005g0081a0001c0001t0010g0080 | 3 | HG01192.hp2 HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.613+21976T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46870414 | ||||||
| chr13:46870875
|
A | G | 5 | a0001c0001t0017g0292a0001c0001t0017g0294a0001c0001t0045g0293others(2): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+21515T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46870875 | ||||||
| chr13:46871051
|
C | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(23): Show | 29 | HG00558.hp2 HG01255.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.613+21339G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871051 | ||||||
| chr13:46871092
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.613+21298C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871092 | ||||||
| chr13:46871094
|
G | A | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+21296C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871094 | ||||||
| chr13:46871449
|
T | G | 1 | a0001c0005t0027g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.613+20941A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871449 | ||||||
| chr13:46871514
|
A | G | 1 | a0001c0001t0004g0315 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.613+20876T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871514 | ||||||
| chr13:46871568
|
G | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(67): Show | 72 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.613+20822C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871568 | ||||||
| chr13:46871602
|
C | A | 3 | a0001c0001t0042g0289a0001c0001t0044g0291a0001c0002t0006g0269 | 3 | HG03225.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.613+20788G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871602 | ||||||
| chr13:46871620
|
A | T | 29 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(26): Show | 29 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.613+20770T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871620 | ||||||
| chr13:46871703
|
G | GTT | 70 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(67): Show | 72 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.613+20685_613+2068 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871703 | ||||||
| chr13:46871742
|
C | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(95): Show | 101 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.613+20648G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871742 | ||||||
| chr13:46871758
|
G | A | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+20632C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871758 | ||||||
| chr13:46871759
|
G | C | 1 | a0001c0001t0006g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.613+20631C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871759 | ||||||
| chr13:46871789
|
T | C | 3 | a0001c0001t0042g0289a0001c0001t0044g0291a0001c0002t0006g0269 | 3 | HG03225.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.613+20601A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871789 | ||||||
| chr13:46871832
|
A | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(67): Show | 72 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.613+20558T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871832 | ||||||
| chr13:46871859
|
A | G | 36 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(33): Show | 39 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.613+20531T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871859 | ||||||
| chr13:46871867
|
A | G | 2 | a0001c0002t0001g0232a0001c0002t0001g0235 | 2 | HG02135.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.613+20523T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871867 | ||||||
| chr13:46872071
|
A | G | 27 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(24): Show | 30 | HG00558.hp2 HG01255.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.613+20319T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872071 | ||||||
| chr13:46872269
|
A | G | 5 | a0001c0001t0017g0292a0001c0001t0017g0294a0001c0001t0045g0293others(2): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+20121T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872269 | ||||||
| chr13:46872330
|
AT | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(25): Show | 29 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.613+20059delA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872330 | ||||||
| chr13:46872349
|
T | G | 1 | a0001c0002t0039g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.613+20041A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872349 | ||||||
| chr13:46872363
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(28): Show | 33 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.613+20027G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872363 | ||||||
| chr13:46872477
|
CTTTA | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.613+19909_613+1991 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872477 | ||||||
| chr13:46872530
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(230): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.613+19860G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872530 | ||||||
| chr13:46872662
|
C | T | 1 | a0001c0001t0044g0291 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.613+19728G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872662 | ||||||
| chr13:46872687
|
C | T | 1 | a0001c0001t0004g0306 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.613+19703G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872687 | ||||||
| chr13:46872712
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(230): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.613+19678G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872712 | ||||||
| chr13:46872781
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(25): Show | 29 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.613+19609G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872781 | ||||||
| chr13:46872828
|
C | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0056a0001c0001t0001g0059 | 4 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+19562G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872828 | ||||||
| chr13:46872898
|
T | A | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.613+19492A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872898 | ||||||
| chr13:46872952
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.613+19438C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872952 | ||||||
| chr13:46873101
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(172): Show | 181 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.613+19289C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873101 | ||||||
| chr13:46873152
|
CT | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.613+19237delA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873152 | ||||||
| chr13:46873247
|
AG | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(56): Show | 62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.613+19142delC | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873247 | ||||||
| chr13:46873405
|
C | CATT | 238 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(235): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.613+18982_613+1898 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873405 | ||||||
| chr13:46873427
|
T | TTTA | 18 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0032others(15): Show | 18 | HG00558.hp2 HG00639.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.613+18960_613+1896 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | ||||||
| chr13:46873427
|
T | TTTATTA | 63 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0024others(60): Show | 66 | HG00280.hp1 HG00423.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.613+18957_613+1896 others(10): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | ||||||
| chr13:46873427
|
T | TTTATTAT others(2): Show |
6 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0111others(3): Show | 6 | HG00438.hp2 HG00597.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+18954_613+1896 others(13): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | ||||||
| chr13:46873427
|
T | TTTATTAT others(5): Show |
4 | a0001c0001t0001g0130a0001c0001t0017g0294a0001c0001t0044g0291others(1): Show | 4 | HG01081.hp2 HG01192.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+18951_613+1896 others(16): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | ||||||
| chr13:46873427
|
TTTA | T | 52 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0054others(49): Show | 56 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.613+18960_613+1896 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | ||||||
| chr13:46873427
|
TTTATTA | T | 10 | a0001c0001t0017g0292a0001c0001t0045g0293a0001c0001t0046g0295others(7): Show | 11 | HG01070.hp1 HG02572.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.613+18957_613+1896 others(10): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | ||||||
| chr13:46873427
|
TTTATTAT others(2): Show |
T | 5 | a0001c0001t0001g0058a0001c0002t0001g0185a0001c0002t0001g0285others(2): Show | 5 | HG00741.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+18954_613+1896 others(13): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | ||||||
| chr13:46873427
|
TTTATTAT others(5): Show |
T | 109 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0085others(106): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.613+18951_613+1896 others(16): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | ||||||
| chr13:46873427
|
TTTATTAT others(11): Show |
T | 1 | a0001c0002t0001g0241 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.613+18945_613+1896 others(22): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | ||||||
| chr13:46873505
|
G | A | 3 | a0001c0001t0001g0135a0001c0005t0007g0133a0001c0005t0007g0134 | 3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+18885C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873505 | ||||||
| chr13:46873517
|
T | C | 1 | a0001c0001t0015g0053 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.613+18873A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873517 | ||||||
| chr13:46873575
|
T | C | 52 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(49): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.613+18815A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873575 | ||||||
| chr13:46873598
|
C | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(173): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.613+18792G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873598 | ||||||
| chr13:46873653
|
G | T | 2 | a0001c0001t0002g0114a0001c0001t0002g0115 | 2 | HG02135.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.613+18737C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873653 | ||||||
| chr13:46873925
|
C | A | 5 | a0001c0001t0017g0292a0001c0001t0017g0294a0001c0001t0045g0293others(2): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+18465G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873925 | ||||||
| chr13:46873925
|
C | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0085others(149): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.613+18465G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873925 | ||||||
| chr13:46874196
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.613+18194C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874196 | ||||||
| chr13:46874235
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.613+18155T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874235 | ||||||
| chr13:46874337
|
A | G | 1 | a0001c0001t0009g0010 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.613+18053T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874337 | ||||||
| chr13:46874512
|
G | A | 3 | a0001c0002t0001g0230a0001c0002t0002g0229a0001c0002t0028g0254 | 3 | HG00423.hp1 HG00621.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.613+17878C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874512 | ||||||
| chr13:46874526
|
T | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(174): Show | 181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.613+17864A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874526 | ||||||
| chr13:46874767
|
G | C | 2 | a0001c0002t0001g0285a0001c0002t0006g0286 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.613+17623C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874767 | ||||||
| chr13:46875011
|
G | C | 1 | a0001c0001t0015g0053 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.613+17379C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875011 | ||||||
| chr13:46875029
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(171): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.613+17361A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875029 | ||||||
| chr13:46875063
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.613+17327G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875063 | ||||||
| chr13:46875172
|
T | C | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+17218A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875172 | ||||||
| chr13:46875191
|
T | C | 5 | a0001c0001t0017g0292a0001c0001t0017g0294a0001c0001t0045g0293others(2): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+17199A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875191 | ||||||
| chr13:46875306
|
T | C | 3 | a0001c0001t0001g0135a0001c0005t0007g0133a0001c0005t0007g0134 | 3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+17084A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875306 | ||||||
| chr13:46875394
|
T | G | 2 | a0001c0001t0015g0102a0001c0010t0036g0110 | 2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.613+16996A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875394 | ||||||
| chr13:46875400
|
A | C | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+16990T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875400 | ||||||
| chr13:46875430
|
G | T | 31 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(28): Show | 33 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.613+16960C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875430 | ||||||
| chr13:46875566
|
T | G | 1 | a0001c0001t0009g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.613+16824A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875566 | ||||||
| chr13:46875622
|
A | G | 3 | a0001c0001t0001g0135a0001c0005t0007g0133a0001c0005t0007g0134 | 3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+16768T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875622 | ||||||
| chr13:46875703
|
C | G | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+16687G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875703 | ||||||
| chr13:46875726
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0085others(135): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.613+16664C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875726 | ||||||
| chr13:46875905
|
T | G | 1 | a0001c0002t0001g0234 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.613+16485A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875905 | ||||||
| chr13:46875989
|
G | T | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+16401C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875989 | ||||||
| chr13:46876081
|
C | A | 55 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(52): Show | 57 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.613+16309G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876081 | ||||||
| chr13:46876143
|
C | G | 12 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(9): Show | 14 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.613+16247G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876143 | ||||||
| chr13:46876300
|
T | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(233): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.613+16090A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876300 | ||||||
| chr13:46876385
|
C | CATAT | 4 | a0001c0001t0001g0111a0001c0001t0002g0114a0001c0001t0008g0002others(1): Show | 5 | HG00438.hp2 HG02135.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+16001_613+1600 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | ||||||
| chr13:46876385
|
C | CATATAT | 24 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0056others(21): Show | 25 | HG00423.hp2 HG00597.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.613+15999_613+1600 others(10): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | ||||||
| chr13:46876385
|
C | CATATATA others(1): Show |
3 | a0001c0001t0001g0050a0001c0001t0001g0297a0001c0001t0002g0051 | 3 | HG01981.hp1 HG01993.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.613+15997_613+1600 others(12): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | ||||||
| chr13:46876385
|
C | CATATATA others(3): Show |
3 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0094 | 3 | NA18747.hp2 NA19005.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.613+15995_613+1600 others(14): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | ||||||
| chr13:46876385
|
CAT | C | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+16003_613+1600 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | ||||||
| chr13:46876385
|
CATAT | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0085a0001c0001t0001g0119others(96): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.613+16001_613+1600 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | ||||||
| chr13:46876385
|
CATATAT | C | 5 | a0001c0001t0044g0291a0001c0002t0001g0239a0001c0002t0002g0238others(2): Show | 5 | HG00597.hp2 HG02896.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+15999_613+1600 others(10): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | ||||||
| chr13:46876394
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.613+15996T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876394 | ||||||
| chr13:46876396
|
A | G | 9 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.613+15994T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876396 | ||||||
| chr13:46876399
|
TATA | T | 13 | a0001c0001t0001g0083a0001c0002t0001g0164a0001c0002t0001g0197others(10): Show | 13 | HG00735.hp1 HG01109.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.613+15988_613+1599 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876399 | ||||||
| chr13:46876399
|
TATATA | T | 16 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0162others(13): Show | 16 | HG00621.hp2 HG01099.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.613+15986_613+1599 others(9): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876399 | ||||||
| chr13:46876401
|
TATA | T | 3 | a0001c0002t0001g0231a0001c0002t0001g0249a0001c0002t0001g0259 | 3 | HG01358.hp1 HG01517.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.613+15986_613+1598 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876401 | ||||||
| chr13:46876404
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0091a0001c0001t0002g0092 | 2 | NA18946.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.613+15985_613+1598 others(15): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | ||||||
| chr13:46876404
|
A | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0132others(87): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.613+15986T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | ||||||
| chr13:46876404
|
ATTT | A | 6 | a0001c0001t0006g0163a0001c0002t0039g0189a0003c0006t0001g0147others(3): Show | 6 | HG01074.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+15983_613+1598 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | ||||||
| chr13:46876404
|
ATTTT | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0011g0003others(7): Show | 12 | HG01070.hp1 HG02895.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.613+15982_613+1598 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | ||||||
| chr13:46876404
|
ATTTTT | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(18): Show | 22 | HG00280.hp1 HG01167.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.613+15981_613+1598 others(9): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | ||||||
| chr13:46876404
|
ATTTTTT | A | 10 | a0001c0001t0001g0045a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 11 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.613+15980_613+1598 others(10): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | ||||||
| chr13:46876404
|
ATTTTTTT | A | 19 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(16): Show | 19 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.613+15979_613+1598 others(11): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | ||||||
| chr13:46876405
|
T | TA | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 20 | HG00558.hp2 HG01255.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.613+15984_613+1598 others(5): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876405 | ||||||
| chr13:46876405
|
T | TATA | 10 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0074others(7): Show | 10 | HG00639.hp2 HG01109.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+15984_613+1598 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876405 | ||||||
| chr13:46876405
|
T | TATATA | 8 | a0001c0001t0001g0058a0001c0001t0001g0086a0001c0001t0001g0103others(5): Show | 8 | HG00741.hp2 HG03490.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.613+15984_613+1598 others(9): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876405 | ||||||
| chr13:46876405
|
T | TATATATA | 7 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0059others(4): Show | 8 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.613+15984_613+1598 others(11): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876405 | ||||||
| chr13:46876405
|
T | TATATATA others(4): Show |
1 | a0001c0001t0010g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.613+15984_613+1598 others(15): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876405 | ||||||
| chr13:46876406
|
T | A | 36 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0054others(33): Show | 38 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.613+15984A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876406 | ||||||
| chr13:46876407
|
T | A | 39 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(36): Show | 42 | HG00558.hp2 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.613+15983A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876407 | ||||||
| chr13:46876408
|
T | A | 18 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0073others(15): Show | 18 | HG00438.hp2 HG00597.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.613+15982A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876408 | ||||||
| chr13:46876409
|
T | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0002g0112others(6): Show | 9 | HG02257.hp2 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.613+15981A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876409 | ||||||
| chr13:46876410
|
T | A | 8 | a0001c0001t0001g0043a0001c0001t0001g0113a0001c0001t0001g0297others(5): Show | 10 | HG01081.hp1 HG02300.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+15980A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876410 | ||||||
| chr13:46876411
|
T | A | 9 | a0001c0001t0005g0081a0001c0001t0017g0292a0001c0001t0017g0294others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.613+15979A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876411 | ||||||
| chr13:46876412
|
T | A | 3 | a0001c0001t0014g0136a0001c0001t0046g0295a0001c0005t0016g0013 | 4 | HG02630.hp2 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+15978A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876412 | ||||||
| chr13:46876413
|
T | A | 3 | a0001c0001t0017g0292a0001c0001t0021g0313a0001c0001t0045g0293 | 3 | HG02572.hp2 HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.613+15977A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876413 | ||||||
| chr13:46876414
|
T | A | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.613+15976A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876414 | ||||||
| chr13:46876434
|
G | C | 1 | a0001c0001t0021g0313 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.613+15956C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876434 | ||||||
| chr13:46876449
|
G | C | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+15941C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876449 | ||||||
| chr13:46876471
|
G | A | 1 | a0001c0002t0001g0241 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.613+15919C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876471 | ||||||
| chr13:46876474
|
A | G | 1 | a0001c0002t0039g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.613+15916T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876474 | ||||||
| chr13:46876502
|
C | T | 2 | a0001c0001t0042g0289a0001c0001t0044g0291 | 2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.613+15888G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876502 | ||||||
| chr13:46876503
|
G | A | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+15887C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876503 | ||||||
| chr13:46876534
|
T | G | 1 | a0001c0001t0025g0017 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.613+15856A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876534 | ||||||
| chr13:46876552
|
A | G | 3 | a0001c0001t0001g0135a0001c0005t0007g0133a0001c0005t0007g0134 | 3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+15838T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876552 | ||||||
| chr13:46876575
|
AATTTTCT others(6812): Show |
A | 1 | a0001c0001t0025g0017 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.613+8996_613+15814 others(3): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876575 | ||||||
| chr13:46876619
|
T | C | 9 | a0001c0001t0001g0135a0001c0001t0011g0003a0001c0005t0007g0133others(6): Show | 10 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+15771A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876619 | ||||||
| chr13:46876651
|
T | C | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+15739A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876651 | ||||||
| chr13:46876774
|
A | C | 1 | a0001c0001t0002g0114 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.613+15616T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876774 | ||||||
| chr13:46876799
|
C | T | 1 | a0001c0002t0001g0206 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.613+15591G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876799 | ||||||
| chr13:46877066
|
G | C | 1 | a0001c0001t0005g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.613+15324C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877066 | ||||||
| chr13:46877123
|
T | C | 1 | a0001c0002t0039g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.613+15267A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877123 | ||||||
| chr13:46877151
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(233): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.613+15239A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877151 | ||||||
| chr13:46877185
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(169): Show | 176 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.613+15205T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877185 | ||||||
| chr13:46877229
|
C | T | 3 | a0001c0002t0001g0243a0001c0002t0002g0205a0006c0011t0002g0204 | 3 | HG04115.hp2 NA18947.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.613+15161G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877229 | ||||||
| chr13:46877509
|
C | T | 5 | a0001c0001t0017g0292a0001c0001t0017g0294a0001c0001t0045g0293others(2): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+14881G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877509 | ||||||
| chr13:46877644
|
C | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(9): Show | 14 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.613+14746G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877644 | ||||||
| chr13:46877713
|
G | A | 1 | a0001c0001t0006g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.613+14677C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877713 | ||||||
| chr13:46877810
|
T | G | 3 | a0001c0001t0008g0002a0001c0001t0008g0016a0001c0001t0024g0015 | 4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+14580A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877810 | ||||||
| chr13:46877869
|
G | A | 4 | a0003c0006t0001g0147a0003c0006t0001g0148a0003c0007t0007g0149others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+14521C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877869 | ||||||
| chr13:46877903
|
A | C | 57 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(54): Show | 59 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.613+14487T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877903 | ||||||
| chr13:46877998
|
G | A | 57 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(54): Show | 59 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.613+14392C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877998 | ||||||
| chr13:46878022
|
A | C | 1 | a0001c0002t0001g0285 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.613+14368T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878022 | ||||||
| chr13:46878034
|
T | C | 1 | a0005c0009t0018g0298 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.613+14356A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878034 | ||||||
| chr13:46878204
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.613+14186T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878204 | ||||||
| chr13:46878207
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.613+14183A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878207 | ||||||
| chr13:46878309
|
G | C | 2 | a0001c0001t0002g0114a0001c0001t0002g0115 | 2 | HG02135.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.613+14081C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878309 | ||||||
| chr13:46878414
|
G | A | 53 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(50): Show | 55 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.613+13976C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878414 | ||||||
| chr13:46878461
|
G | A | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+13929C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878461 | ||||||
| chr13:46878592
|
G | C | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+13798C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878592 | ||||||
| chr13:46878659
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.613+13731C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878659 | ||||||
| chr13:46878752
|
C | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.613+13638G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878752 | ||||||
| chr13:46878770
|
A | G | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+13620T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878770 | ||||||
| chr13:46878836
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(229): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.613+13554A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878836 | ||||||
| chr13:46878878
|
T | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0056others(5): Show | 9 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.613+13512A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878878 | ||||||
| chr13:46879051
|
G | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(285): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.613+13339C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879051 | ||||||
| chr13:46879062
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0085others(136): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.613+13328T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879062 | ||||||
| chr13:46879177
|
T | C | 4 | a0003c0006t0001g0147a0003c0006t0001g0148a0003c0007t0007g0149others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+13213A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879177 | ||||||
| chr13:46879258
|
C | A | 1 | a0001c0001t0006g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.613+13132G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879258 | ||||||
| chr13:46879308
|
T | C | 3 | a0001c0002t0001g0250a0001c0002t0001g0255a0001c0002t0001g0256 | 3 | NA18948.hp2 NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.613+13082A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879308 | ||||||
| chr13:46879435
|
C | T | 4 | a0001c0002t0001g0185a0001c0002t0001g0285a0001c0002t0006g0286others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+12955G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879435 | ||||||
| chr13:46879500
|
A | G | 53 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(50): Show | 55 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.613+12890T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879500 | ||||||
| chr13:46879538
|
G | A | 2 | a0002c0004t0003g0247a0002c0004t0003g0248 | 2 | HG02056.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.613+12852C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879538 | ||||||
| chr13:46879585
|
T | C | 1 | a0001c0002t0001g0175 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.613+12805A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879585 | ||||||
| chr13:46879595
|
G | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.613+12795C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879595 | ||||||
| chr13:46879666
|
A | G | 27 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.613+12724T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879666 | ||||||
| chr13:46879804
|
A | G | 1 | a0001c0002t0002g0202 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.613+12586T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879804 | ||||||
| chr13:46879826
|
G | GAAAGCCC | 3 | a0001c0001t0001g0135a0001c0005t0007g0133a0001c0005t0007g0134 | 3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+12557_613+1256 others(11): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879826 | ||||||
| chr13:46880010
|
C | CA | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(229): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.613+12379dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880010 | ||||||
| chr13:46880117
|
T | G | 1 | a0001c0002t0001g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.613+12273A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880117 | ||||||
| chr13:46880305
|
G | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(26): Show | 30 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.613+12085C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880305 | ||||||
| chr13:46880362
|
C | T | 5 | a0001c0002t0001g0200a0002c0004t0003g0201a0002c0004t0003g0247others(2): Show | 5 | HG01175.hp1 HG02056.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+12028G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880362 | ||||||
| chr13:46880446
|
T | A | 1 | a0001c0002t0001g0243 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.613+11944A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880446 | ||||||
| chr13:46880449
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.613+11941G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880449 | ||||||
| chr13:46880465
|
T | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.613+11925A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880465 | ||||||
| chr13:46880551
|
A | T | 4 | a0003c0006t0001g0147a0003c0006t0001g0148a0003c0007t0007g0149others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+11839T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880551 | ||||||
| chr13:46880570
|
G | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.613+11820C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880570 | ||||||
| chr13:46880708
|
G | A | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+11682C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880708 | ||||||
| chr13:46880849
|
G | GA | 55 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.613+11540dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880849 | ||||||
| chr13:46880890
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.613+11500G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880890 | ||||||
| chr13:46881012
|
A | G | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+11378T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881012 | ||||||
| chr13:46881081
|
C | T | 2 | a0001c0001t0002g0060a0001c0002t0001g0198 | 2 | HG02165.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.613+11309G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881081 | ||||||
| chr13:46881144
|
G | A | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+11246C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881144 | ||||||
| chr13:46881230
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(182): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.613+11160G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881230 | ||||||
| chr13:46881240
|
C | T | 1 | a0001c0002t0001g0197 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.613+11150G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881240 | ||||||
| chr13:46881265
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.613+11125C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881265 | ||||||
| chr13:46881301
|
C | T | 3 | a0001c0001t0001g0135a0001c0005t0007g0133a0001c0005t0007g0134 | 3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+11089G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881301 | ||||||
| chr13:46881323
|
G | A | 2 | a0001c0001t0010g0125a0001c0001t0010g0129 | 2 | HG01109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.613+11067C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881323 | ||||||
| chr13:46881349
|
T | C | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+11041A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881349 | ||||||
| chr13:46881478
|
G | T | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+10912C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881478 | ||||||
| chr13:46881488
|
A | C | 5 | a0001c0002t0001g0012a0001c0002t0001g0179a0001c0002t0001g0182others(2): Show | 6 | HG00558.hp1 NA18943.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+10902T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881488 | ||||||
| chr13:46881508
|
G | A | 4 | a0001c0001t0017g0292a0001c0001t0045g0293a0001c0001t0046g0295others(1): Show | 5 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+10882C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881508 | ||||||
| chr13:46881590
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(171): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.613+10800C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881590 | ||||||
| chr13:46881622
|
T | C | 1 | a0001c0001t0017g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.613+10768A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881622 | ||||||
| chr13:46881625
|
T | C | 2 | a0003c0006t0001g0147a0003c0006t0001g0148 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.613+10765A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881625 | ||||||
| chr13:46881728
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(166): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.613+10662T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881728 | ||||||
| chr13:46881751
|
A | G | 2 | a0001c0001t0048g0317a0002c0003t0019g0318 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.613+10639T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881751 | ||||||
| chr13:46881790
|
T | C | 1 | a0001c0002t0002g0245 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.613+10600A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881790 | ||||||
| chr13:46881916
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(218): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.613+10474C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881916 | ||||||
| chr13:46881957
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.613+10433G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881957 | ||||||
| chr13:46881958
|
C | A | 1 | a0002c0003t0019g0314 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.613+10432G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881958 | ||||||
| chr13:46882039
|
A | G | 1 | a0001c0002t0001g0194 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.613+10351T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882039 | ||||||
| chr13:46882055
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(228): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.613+10335A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882055 | ||||||
| chr13:46882057
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(225): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.613+10333G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882057 | ||||||
| chr13:46882229
|
T | TA | 19 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0090others(16): Show | 21 | HG01081.hp2 HG01099.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.613+10160dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882229 | ||||||
| chr13:46882229
|
T | TAA | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.613+10159_613+1016 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882229 | ||||||
| chr13:46882229
|
T | TAAA | 7 | a0001c0001t0001g0047a0001c0001t0017g0292a0001c0001t0045g0293others(4): Show | 8 | HG02572.hp2 HG02895.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.613+10158_613+1016 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882229 | ||||||
| chr13:46882290
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(229): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.613+10100A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882290 | ||||||
| chr13:46882304
|
T | A | 2 | a0001c0002t0001g0270a0001c0002t0005g0271 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.613+10086A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882304 | ||||||
| chr13:46882340
|
A | G | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+10050T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882340 | ||||||
| chr13:46882413
|
A | G | 58 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(55): Show | 60 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.613+9977T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882413 | ||||||
| chr13:46882450
|
G | A | 1 | a0001c0002t0001g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.613+9940C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882450 | ||||||
| chr13:46882549
|
C | T | 4 | a0003c0006t0001g0147a0003c0006t0001g0148a0003c0007t0007g0149others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+9841G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882549 | ||||||
| chr13:46882637
|
A | C | 2 | a0001c0001t0001g0089a0001c0001t0002g0088 | 2 | NA19009.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.613+9753T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882637 | ||||||
| chr13:46882722
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.613+9668C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882722 | ||||||
| chr13:46882805
|
T | A | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+9585A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882805 | ||||||
| chr13:46882837
|
T | C | 1 | a0001c0001t0004g0301 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.613+9553A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882837 | ||||||
| chr13:46882839
|
T | A | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+9551A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882839 | ||||||
| chr13:46882864
|
A | G | 14 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.613+9526T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882864 | ||||||
| chr13:46882893
|
A | C | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+9497T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882893 | ||||||
| chr13:46883081
|
G | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(317): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.613+9309C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883081 | ||||||
| chr13:46883106
|
A | T | 3 | a0001c0001t0042g0289a0001c0001t0043g0290a0001c0001t0044g0291 | 3 | HG00639.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.613+9284T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883106 | ||||||
| chr13:46883159
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.613+9231T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883159 | ||||||
| chr13:46883223
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.613+9167G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883223 | ||||||
| chr13:46883264
|
A | AAGGTTAG others(16): Show |
70 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(67): Show | 72 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.613+9125_613+9126i others(25): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883264 | ||||||
| chr13:46883455
|
CTGAAATG others(5688): Show |
C | 1 | a0001c0001t0025g0017 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.613+3240_613+8934d others(2): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883455 | ||||||
| chr13:46883491
|
T | C | 1 | a0001c0001t0017g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.613+8899A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883491 | ||||||
| chr13:46883506
|
C | T | 4 | a0003c0006t0001g0147a0003c0006t0001g0148a0003c0007t0007g0149others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+8884G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883506 | ||||||
| chr13:46883520
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.613+8870C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883520 | ||||||
| chr13:46883558
|
T | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0056others(4): Show | 8 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.613+8832A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883558 | ||||||
| chr13:46883724
|
A | G | 4 | a0003c0006t0001g0147a0003c0006t0001g0148a0003c0007t0007g0149others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+8666T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883724 | ||||||
| chr13:46883784
|
C | T | 70 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0050others(67): Show | 72 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.613+8606G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883784 | ||||||
| chr13:46883793
|
G | A | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+8597C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883793 | ||||||
| chr13:46883913
|
C | A | 1 | a0001c0001t0001g0087 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.613+8477G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883913 | ||||||
| chr13:46883917
|
C | A | 2 | a0002c0004t0003g0247a0002c0004t0003g0248 | 2 | HG02056.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.613+8473G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883917 | ||||||
| chr13:46883917
|
C | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(286): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.613+8473G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883917 | ||||||
| chr13:46883959
|
G | C | 3 | a0001c0002t0001g0279a0001c0002t0001g0280a0001c0002t0034g0281 | 3 | HG02145.hp1 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.613+8431C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883959 | ||||||
| chr13:46884026
|
G | A | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+8364C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884026 | ||||||
| chr13:46884123
|
A | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.613+8267T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884123 | ||||||
| chr13:46884168
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.613+8222G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884168 | ||||||
| chr13:46884182
|
C | T | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+8208G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884182 | ||||||
| chr13:46884257
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.613+8133C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884257 | ||||||
| chr13:46884281
|
A | C | 13 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(10): Show | 15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+8109T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884281 | ||||||
| chr13:46884446
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.613+7944G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884446 | ||||||
| chr13:46884457
|
C | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(220): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.613+7933G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884457 | ||||||
| chr13:46884535
|
A | G | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 107 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.613+7855T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884535 | ||||||
| chr13:46884580
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.613+7810G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884580 | ||||||
| chr13:46884596
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.613+7794C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884596 | ||||||
| chr13:46884603
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0002g0051 | 2 | HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.613+7787C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884603 | ||||||
| chr13:46884675
|
A | G | 12 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(9): Show | 14 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.613+7715T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884675 | ||||||
| chr13:46884705
|
C | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.613+7685G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884705 | ||||||
| chr13:46884739
|
C | T | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 98 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.613+7651G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884739 | ||||||
| chr13:46884798
|
TTGTG | T | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.613+7588_613+7591d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884798 | ||||||
| chr13:46884820
|
A | T | 3 | a0001c0002t0001g0192a0002c0004t0003g0190a0002c0004t0003g0191 | 3 | HG00099.hp1 HG00140.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.613+7570T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884820 | ||||||
| chr13:46884827
|
C | CAT | 112 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0024others(109): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.613+7561_613+7562d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884827 | ||||||
| chr13:46884827
|
C | CATAT | 5 | a0001c0001t0017g0292a0001c0001t0046g0295a0001c0002t0002g0022others(2): Show | 6 | HG02486.hp1 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+7559_613+7562d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884827 | ||||||
| chr13:46885069
|
G | A | 3 | a0001c0001t0008g0002a0001c0001t0008g0016a0001c0001t0024g0015 | 4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+7321C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885069 | ||||||
| chr13:46885071
|
G | A | 4 | a0001c0001t0017g0292a0001c0001t0045g0293a0001c0001t0046g0295others(1): Show | 5 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+7319C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885071 | ||||||
| chr13:46885324
|
T | C | 1 | a0001c0002t0001g0250 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.613+7066A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885324 | ||||||
| chr13:46885385
|
T | C | 6 | a0001c0001t0004g0315a0001c0001t0052g0316a0003c0006t0001g0147others(3): Show | 6 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+7005A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885385 | ||||||
| chr13:46885448
|
T | A | 1 | a0001c0001t0002g0076 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.613+6942A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885448 | ||||||
| chr13:46885451
|
T | C | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+6939A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885451 | ||||||
| chr13:46885572
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.613+6818G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885572 | ||||||
| chr13:46885713
|
G | C | 1 | a0001c0002t0041g0288 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.613+6677C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885713 | ||||||
| chr13:46885937
|
C | T | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.613+6453G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885937 | ||||||
| chr13:46886009
|
A | G | 4 | a0003c0006t0001g0147a0003c0006t0001g0148a0003c0007t0007g0149others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+6381T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886009 | ||||||
| chr13:46886048
|
G | A | 1 | a0001c0001t0042g0289 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.613+6342C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886048 | ||||||
| chr13:46886054
|
A | G | 24 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.613+6336T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886054 | ||||||
| chr13:46886070
|
T | C | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+6320A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886070 | ||||||
| chr13:46886277
|
G | T | 1 | a0001c0002t0001g0184 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.613+6113C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886277 | ||||||
| chr13:46886307
|
G | T | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+6083C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886307 | ||||||
| chr13:46886330
|
T | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.613+6060A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886330 | ||||||
| chr13:46886345
|
T | TAAATG | 313 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(310): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.613+6044_613+6045i others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886345 | ||||||
| chr13:46886378
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.613+6012T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886378 | ||||||
| chr13:46886479
|
A | G | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.613+5911T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886479 | ||||||
| chr13:46886490
|
CAT | C | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.613+5898_613+5899d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886490 | ||||||
| chr13:46886605
|
C | T | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+5785G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886605 | ||||||
| chr13:46886609
|
A | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(283): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.613+5781T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886609 | ||||||
| chr13:46886696
|
G | A | 1 | a0001c0005t0016g0013 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.613+5694C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886696 | ||||||
| chr13:46886755
|
G | A | 2 | a0001c0001t0014g0145a0002c0003t0003g0146 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.613+5635C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886755 | ||||||
| chr13:46886885
|
G | A | 3 | a0001c0002t0001g0283a0001c0002t0002g0282a0001c0002t0005g0284 | 3 | HG01884.hp1 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.613+5505C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886885 | ||||||
| chr13:46886967
|
A | T | 1 | a0001c0002t0001g0183 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.613+5423T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886967 | ||||||
| chr13:46887085
|
A | G | 1 | a0001c0002t0001g0258 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.613+5305T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887085 | ||||||
| chr13:46887145
|
C | T | 2 | a0001c0002t0001g0179a0001c0002t0001g0182 | 2 | NA18943.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.613+5245G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887145 | ||||||
| chr13:46887191
|
G | A | 4 | a0003c0006t0001g0147a0003c0006t0001g0148a0003c0007t0007g0149others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+5199C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887191 | ||||||
| chr13:46887295
|
C | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(10): Show | 15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+5095G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887295 | ||||||
| chr13:46887295
|
C | T | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+5095G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887295 | ||||||
| chr13:46887410
|
G | A | 2 | a0001c0001t0005g0081a0001c0001t0010g0080 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.613+4980C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887410 | ||||||
| chr13:46887422
|
C | CA | 8 | a0001c0001t0001g0135a0001c0001t0026g0018a0001c0002t0001g0165others(5): Show | 8 | HG01167.hp1 HG02015.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.613+4967dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887422 | ||||||
| chr13:46887422
|
C | CAA | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.613+4966_613+4967d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887422 | ||||||
| chr13:46887422
|
C | CAAA | 16 | a0001c0001t0001g0124a0001c0001t0010g0125a0001c0001t0010g0129others(13): Show | 16 | HG01109.hp2 HG02630.hp2 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.613+4965_613+4967d others(5): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887422 | ||||||
| chr13:46887422
|
C | CAAAA | 33 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(30): Show | 34 | HG00099.hp2 HG00280.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.613+4964_613+4967d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887422 | ||||||
| chr13:46887422
|
C | CAAAAA | 20 | a0001c0001t0004g0302a0001c0001t0004g0306a0001c0001t0004g0307others(17): Show | 21 | HG00140.hp1 HG01243.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.613+4963_613+4967d others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887422 | ||||||
| chr13:46887480
|
G | A | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+4910C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887480 | ||||||
| chr13:46887503
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(10): Show | 15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+4887C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887503 | ||||||
| chr13:46887599
|
A | G | 10 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+4791T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887599 | ||||||
| chr13:46887615
|
T | A | 54 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0083others(51): Show | 55 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.613+4775A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887615 | ||||||
| chr13:46887792
|
A | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.613+4598T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887792 | ||||||
| chr13:46888086
|
C | CA | 246 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(243): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.613+4303dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888086 | ||||||
| chr13:46888086
|
C | CAA | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(40): Show | 47 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.613+4302_613+4303d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888086 | ||||||
| chr13:46888086
|
C | CAAAA | 10 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(7): Show | 12 | HG01099.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.613+4300_613+4303d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888086 | ||||||
| chr13:46888189
|
C | T | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+4201G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888189 | ||||||
| chr13:46888355
|
G | A | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+4035C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888355 | ||||||
| chr13:46888356
|
C | A | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+4034G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888356 | ||||||
| chr13:46888470
|
G | GA | 176 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(173): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.613+3919dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888470 | ||||||
| chr13:46888470
|
GA | G | 29 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(26): Show | 30 | HG00280.hp1 HG01081.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.613+3919delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888470 | ||||||
| chr13:46888600
|
T | G | 2 | a0001c0001t0001g0078a0001c0001t0002g0077 | 2 | NA18946.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.613+3790A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888600 | ||||||
| chr13:46888601
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0002g0077 | 2 | NA18946.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.613+3789A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888601 | ||||||
| chr13:46888665
|
A | G | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.613+3725T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888665 | ||||||
| chr13:46888802
|
G | A | 5 | a0001c0001t0017g0292a0001c0001t0017g0294a0001c0001t0045g0293others(2): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+3588C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888802 | ||||||
| chr13:46889038
|
G | A | 2 | a0001c0001t0048g0317a0002c0003t0019g0318 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.613+3352C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889038 | ||||||
| chr13:46889057
|
C | T | 1 | a0003c0007t0007g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.613+3333G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889057 | ||||||
| chr13:46889063
|
A | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(10): Show | 15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+3327T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889063 | ||||||
| chr13:46889320
|
T | C | 13 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(10): Show | 15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+3070A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889320 | ||||||
| chr13:46889345
|
A | C | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.613+3045T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889345 | ||||||
| chr13:46889364
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(10): Show | 15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+3026G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889364 | ||||||
| chr13:46889488
|
A | G | 12 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(9): Show | 13 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.613+2902T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889488 | ||||||
| chr13:46889511
|
G | T | 1 | a0001c0002t0033g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.613+2879C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889511 | ||||||
| chr13:46889684
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(285): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.613+2706T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889684 | ||||||
| chr13:46889855
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(25): Show | 29 | HG00280.hp1 HG01081.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.613+2535G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889855 | ||||||
| chr13:46889877
|
C | T | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.613+2513G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889877 | ||||||
| chr13:46889984
|
T | C | 1 | a0001c0001t0035g0079 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.613+2406A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889984 | ||||||
| chr13:46890036
|
T | A | 2 | a0003c0006t0001g0147a0003c0006t0001g0148 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.613+2354A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890036 | ||||||
| chr13:46890133
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0132a0001c0001t0006g0163others(139): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.613+2257G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890133 | ||||||
| chr13:46890179
|
A | G | 12 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(9): Show | 13 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.613+2211T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890179 | ||||||
| chr13:46890203
|
C | T | 4 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0175others(1): Show | 4 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+2187G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890203 | ||||||
| chr13:46890204
|
G | A | 1 | a0001c0002t0002g0257 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.613+2186C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890204 | ||||||
| chr13:46890283
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.613+2107G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890283 | ||||||
| chr13:46890330
|
C | T | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+2060G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890330 | ||||||
| chr13:46890593
|
G | C | 2 | a0001c0002t0001g0258a0001c0002t0001g0259 | 2 | HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.613+1797C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890593 | ||||||
| chr13:46890722
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0132a0001c0002t0001g0012others(113): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.613+1668T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890722 | ||||||
| chr13:46890757
|
A | G | 2 | a0001c0001t0005g0081a0001c0001t0010g0080 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.613+1633T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890757 | ||||||
| chr13:46890804
|
C | A | 4 | a0001c0001t0042g0289a0001c0001t0043g0290a0001c0001t0044g0291others(1): Show | 4 | HG00639.hp2 HG02723.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+1586G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890804 | ||||||
| chr13:46890902
|
G | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 38 | HG00558.hp2 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.613+1488C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890902 | ||||||
| chr13:46890939
|
G | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0132a0001c0001t0006g0163others(132): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.613+1451C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890939 | ||||||
| chr13:46891009
|
C | T | 1 | a0001c0002t0002g0171 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.613+1381G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891009 | ||||||
| chr13:46891124
|
G | A | 1 | a0001c0002t0002g0274 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.613+1266C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891124 | ||||||
| chr13:46891139
|
T | C | 1 | a0001c0001t0017g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.613+1251A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891139 | ||||||
| chr13:46891303
|
A | C | 2 | a0001c0001t0011g0003a0001c0005t0027g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+1087T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891303 | ||||||
| chr13:46891379
|
A | G | 7 | a0001c0002t0001g0165a0001c0002t0001g0166a0001c0002t0001g0167others(4): Show | 7 | NA18962.hp1 NA18971.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.613+1011T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891379 | ||||||
| chr13:46891554
|
G | A | 1 | a0001c0002t0001g0275 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.613+836C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891554 | ||||||
| chr13:46891604
|
C | A | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+786G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891604 | ||||||
| chr13:46891648
|
A | G | 5 | a0001c0001t0017g0292a0001c0001t0017g0294a0001c0001t0045g0293others(2): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+742T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891648 | ||||||
| chr13:46891796
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA18986.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.613+594C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891796 | ||||||
| chr13:46891893
|
G | A | 2 | a0002c0003t0003g0048a0002c0003t0003g0049 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.613+497C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891893 | ||||||
| chr13:46891948
|
C | A | 1 | a0001c0001t0010g0129 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.613+442G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891948 | ||||||
| chr13:46892095
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.613+295G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46892095 | ||||||
| chr13:46892249
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.613+141A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46892249 | ||||||
| chr13:46892646
|
T | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(199): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.413-56A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892646 | ||||||
| chr13:46892815
|
T | G | 55 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0083others(52): Show | 56 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.413-225A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892815 | ||||||
| chr13:46892902
|
G | T | 2 | a0001c0001t0001g0050a0001c0001t0002g0051 | 2 | HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.413-312C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892902 | ||||||
| chr13:46892935
|
T | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 97 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.413-345A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892935 | ||||||
| chr13:46892969
|
A | C | 11 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(8): Show | 11 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.413-379T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892969 | ||||||
| chr13:46892981
|
C | A | 2 | a0003c0007t0007g0149a0003c0007t0007g0150 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.413-391G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892981 | ||||||
| chr13:46893060
|
A | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(24): Show | 28 | HG00280.hp1 HG01081.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.413-470T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893060 | ||||||
| chr13:46893228
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(317): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.413-638T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893228 | ||||||
| chr13:46893232
|
G | C | 1 | a0001c0002t0002g0278 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.413-642C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893232 | ||||||
| chr13:46893305
|
C | G | 1 | a0001c0001t0046g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413-715G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893305 | ||||||
| chr13:46893326
|
C | A | 6 | a0001c0002t0001g0279a0001c0002t0001g0280a0001c0002t0001g0283others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-736G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893326 | ||||||
| chr13:46893351
|
T | G | 1 | a0001c0001t0046g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413-761A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893351 | ||||||
| chr13:46893469
|
C | G | 1 | a0001c0002t0001g0012 | 2 | NA18971.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.413-879G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893469 | ||||||
| chr13:46893491
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 124 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.413-901C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893491 | ||||||
| chr13:46893638
|
T | C | 7 | a0001c0001t0011g0003a0001c0001t0017g0292a0001c0001t0017g0294others(4): Show | 9 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.413-1048A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893638 | ||||||
| chr13:46893743
|
C | T | 24 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.413-1153G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893743 | ||||||
| chr13:46893836
|
C | G | 5 | a0001c0001t0017g0292a0001c0001t0017g0294a0001c0001t0045g0293others(2): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-1246G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893836 | ||||||
| chr13:46894117
|
G | C | 11 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(8): Show | 11 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+1378C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894117 | ||||||
| chr13:46894174
|
T | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0130others(169): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.412+1321A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894174 | ||||||
| chr13:46894277
|
G | A | 11 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0156others(8): Show | 11 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+1218C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894277 | ||||||
| chr13:46894414
|
T | G | 2 | a0001c0002t0001g0285a0001c0002t0006g0286 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.412+1081A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894414 | ||||||
| chr13:46894420
|
A | G | 1 | a0001c0002t0001g0164 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.412+1075T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894420 | ||||||
| chr13:46894445
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0132others(167): Show | 176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.412+1050A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894445 | ||||||
| chr13:46894702
|
G | A | 1 | a0001c0001t0020g0319 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.412+793C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894702 | ||||||
| chr13:46894726
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.412+769A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894726 | ||||||
| chr13:46895177
|
G | A | 1 | a0001c0001t0006g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.412+318C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46895177 | ||||||
| chr13:46895200
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(283): Show | 297 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.412+295A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46895200 | ||||||
| chr13:46895301
|
G | A | 1 | a0001c0001t0021g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.412+194C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46895301 | ||||||
| chr13:46896306
|
C | T | 2 | a0001c0002t0002g0022a0001c0002t0005g0021 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-328-72G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/3 | chr13 | 46896306 | ||||||
| chr13:46896346
|
G | T | 1 | a0001c0001t0001g0020 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-328-112C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/3 | chr13 | 46896346 | ||||||
| chr13:46896465
|
A | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(313): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.-329+209T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/3 | chr13 | 46896465 | ||||||
| chr13:46896655
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-329+19A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/3 | chr13 | 46896655 |