Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4185 |
|---|---|
| ensemblid | ENSG00000073670.14 |
| hgncid | 189 |
| symbol | ADAM11 |
| name | ADAM metallopeptidase domain 11 |
| refseq_nuc | NM_002390.6 |
| refseq_prot | NP_002381.2 |
| ensembl_nuc | ENST00000200557.11 |
| ensembl_prot | ENSP00000200557.6 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 44758988 |
| end | 44781846 |
| strand | + |
| ver | v1.2 |
| region | chr17:44758988-44781846 |
| region5000 | chr17:44753988-44786846 |
| regionname0 | ADAM11_chr17_44758988_44781846 |
| regionname5000 | ADAM11_chr17_44753988_44786846 |
| 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 | 769 | 330 | 92 | 73 | 117 | 14 | 32 | 77 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0002 | 0/0 | 769 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0003 | 0/0 | 769 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0004 | 0/0 | 769 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0005 | 0/0 | 769 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0006 | 0/0 | 769 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0007 | 0/0 | 769 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2310 | 192 | 38 | 49 | 73 | 11 | 20 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0002 | 0/0 | 2310 | 85 | 45 | 18 | 15 | 2 | 5 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0003 | 1/0 | 2310 | 48 | 8 | 4 | 27 | 1 | 7 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0004 | 0/0 | 2310 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0005 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0006 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0007 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0008 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0009 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0010 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0011 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0012 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| c0013 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| 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 | 2306 | 166 | 28 | 48 | 59 | 11 | 19 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0002 | 1/0 | 2305 | 44 | 8 | 5 | 23 | 1 | 6 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0003 | 0/0 | 2305 | 39 | 19 | 7 | 8 | 2 | 3 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0004 | 0/0 | 2305 | 17 | 7 | 3 | 7 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0005 | 0/0 | 2306 | 13 | 11 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0006 | 0/0 | 2305 | 11 | 9 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0007 | 0/0 | 2305 | 8 | 8 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0008 | 0/0 | 2306 | 5 | 0 | 0 | 5 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0009 | 0/0 | 2305 | 5 | 0 | 2 | 2 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0010 | 0/0 | 2306 | 3 | 1 | 1 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0011 | 0/0 | 2306 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0012 | 0/0 | 2306 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0013 | 0/0 | 2305 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0014 | 0/0 | 2306 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0015 | 0/0 | 2306 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0016 | 0/0 | 2306 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0017 | 0/0 | 2305 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0018 | 0/0 | 2305 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0019 | 0/0 | 2305 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0020 | 0/0 | 2305 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0021 | 0/0 | 2305 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0022 | 0/0 | 2305 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0023 | 0/0 | 2306 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0024 | 0/0 | 2306 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0025 | 0/0 | 2305 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0026 | 0/0 | 2305 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0027 | 0/0 | 2305 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0028 | 0/0 | 2305 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0029 | 0/0 | 2305 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0030 | 0/0 | 2305 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0031 | 0/0 | 2306 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| t0032 | 0/0 | 2305 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| 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 | 33 | 6 | 7 | 15 | 3 | 2 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0002 | 0/0 | 12 | 1 | 9 | 0 | 0 | 2 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0003 | 0/0 | 9 | 0 | 4 | 4 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0004 | 0/0 | 8 | 1 | 2 | 3 | 0 | 2 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0005 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0009 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2310 | 192 | 38 | 49 | 73 | 11 | 20 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002 | 0/0 | 2310 | 85 | 45 | 18 | 15 | 2 | 5 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0003 | 1/0 | 2310 | 48 | 8 | 4 | 27 | 1 | 7 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0004 | 0/0 | 2310 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0005 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0007 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0009 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0002c0006 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0003c0008 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0004c0013 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0005c0010 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0006c0011 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0007c0012 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4615 | 161 | 27 | 46 | 57 | 11 | 19 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0005 | 0/0 | 4615 | 11 | 10 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0008 | 0/0 | 4615 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0009 | 0/0 | 4614 | 5 | 0 | 2 | 2 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0011 | 0/0 | 4615 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0012 | 0/0 | 4615 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0014 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0015 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0016 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0017 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0018 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0019 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0001t0031 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0002 | 0/0 | 4614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0003 | 0/0 | 4614 | 37 | 18 | 7 | 7 | 2 | 3 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0004 | 0/0 | 4614 | 17 | 7 | 3 | 7 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0006 | 0/0 | 4614 | 11 | 9 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0007 | 0/0 | 4614 | 8 | 8 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0010 | 0/0 | 4615 | 3 | 1 | 1 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0021 | 0/0 | 4614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0022 | 0/0 | 4614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0024 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0025 | 0/0 | 4614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0026 | 0/0 | 4614 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0028 | 0/0 | 4614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0030 | 0/0 | 4614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0002t0032 | 0/0 | 4614 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0003t0002 | 1/0 | 4614 | 43 | 8 | 4 | 23 | 1 | 6 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0003t0013 | 0/0 | 4614 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0003t0020 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0003t0023 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0003t0027 | 0/0 | 4614 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0004t0005 | 0/0 | 4615 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0005t0001 | 0/0 | 4615 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0007t0029 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0001c0009t0008 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0002c0006t0001 | 0/0 | 4615 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0003c0008t0003 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0004c0013t0001 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0005c0010t0001 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0006c0011t0001 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| a0007c0012t0003 | 0/0 | 4614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | copy fasta | chr17 | 44753988 | 44786846 |
| 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 | 29 | 6 | 7 | 11 | 3 | 2 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0002 | 0/0 | 10 | 1 | 7 | 0 | 0 | 2 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0008g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0009g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0009g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0009g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0011g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0011g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0012g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0012g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0014g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0015g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0016g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0019g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0031g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0005 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0010g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0021g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0022g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0024g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0025g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0026g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0028g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0030g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0032g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0004 | 0/0 | 7 | 1 | 2 | 3 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0013g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0013g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0020g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0023g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0027g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0004t0005g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0004t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0005t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0007t0029g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0009t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0002c0006t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0003c0008t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0004c0013t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0005c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0006c0011t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0007c0012t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0139 | EUR | GBR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00140 | hp1 | a0001 | c0003 | t0002 | g0017 | EUR | GBR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0138 | EUR | FIN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00544 | hp2 | a0001 | c0009 | t0008 | g0001 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00558 | hp1 | a0001 | c0007 | t0029 | g0191 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0016 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00621 | hp1 | a0001 | c0001 | t0031 | g0007 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00673 | hp1 | a0006 | c0011 | t0001 | g0010 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00733 | hp2 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01074 | hp1 | a0001 | c0002 | t0010 | g0161 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0160 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01109 | hp1 | a0001 | c0004 | t0005 | g0229 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0004 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01167 | hp2 | a0001 | c0002 | t0006 | g0029 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0171 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0172 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01169 | hp2 | a0001 | c0002 | t0006 | g0029 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0031 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0146 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0173 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01261 | hp1 | a0001 | c0005 | t0001 | g0003 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01261 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0175 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0170 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01433 | hp1 | a0001 | c0002 | t0028 | g0120 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0002 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0184 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0187 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01891 | hp2 | a0001 | c0002 | t0006 | g0129 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0004 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01952 | hp1 | a0002 | c0006 | t0001 | g0199 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01978 | hp1 | a0001 | c0002 | t0025 | g0005 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01993 | hp1 | a0001 | c0002 | t0022 | g0011 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02004 | hp1 | a0001 | c0003 | t0002 | g0019 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02004 | hp2 | a0001 | c0002 | t0004 | g0212 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02015 | hp1 | a0001 | c0002 | t0004 | g0213 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0043 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0167 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02056 | hp2 | a0001 | c0001 | t0008 | g0110 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02071 | hp1 | a0001 | c0001 | t0009 | g0087 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02080 | hp1 | a0001 | c0001 | t0009 | g0041 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02080 | hp2 | a0001 | c0001 | t0011 | g0116 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0035 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02129 | hp1 | a0001 | c0002 | t0004 | g0196 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02129 | hp2 | a0001 | c0003 | t0002 | g0188 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0036 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02132 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0044 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02145 | hp1 | a0001 | c0002 | t0007 | g0190 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02148 | hp2 | a0001 | c0002 | t0030 | g0164 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0018 | EAS | CDX | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02165 | hp2 | a0003 | c0008 | t0003 | g0180 | EAS | CDX | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02258 | hp2 | a0001 | c0002 | t0007 | g0189 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0017 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02451 | hp1 | a0001 | c0002 | t0021 | g0194 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0179 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02572 | hp2 | a0001 | c0002 | t0010 | g0166 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0018 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0222 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0143 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02622 | hp2 | a0001 | c0002 | t0006 | g0141 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02630 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02630 | hp2 | a0001 | c0002 | t0024 | g0193 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02647 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02723 | hp2 | a0001 | c0002 | t0007 | g0134 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0011 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02738 | hp2 | a0001 | c0001 | t0009 | g0009 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02809 | hp1 | a0004 | c0013 | t0001 | g0015 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02809 | hp2 | a0001 | c0002 | t0006 | g0140 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0031 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02818 | hp2 | a0001 | c0002 | t0006 | g0142 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0178 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0014 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0174 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02970 | hp1 | a0001 | c0002 | t0007 | g0032 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0195 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0028 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0137 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0014 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0225 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0207 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0051 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0059 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0165 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0158 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0014 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0218 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0058 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03453 | hp1 | a0001 | c0002 | t0006 | g0155 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0227 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03486 | hp1 | a0001 | c0002 | t0007 | g0177 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03492 | hp2 | a0001 | c0003 | t0002 | g0019 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0149 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03540 | hp2 | a0001 | c0002 | t0007 | g0032 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03579 | hp1 | a0001 | c0004 | t0005 | g0230 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03654 | hp2 | a0001 | c0002 | t0032 | g0215 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0181 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03710 | hp2 | a0001 | c0003 | t0002 | g0004 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03834 | hp1 | a0001 | c0002 | t0026 | g0083 | SAS | BEB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03927 | hp2 | a0001 | c0003 | t0002 | g0176 | SAS | BEB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0095 | SAS | STU | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0145 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18747 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | CHB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0183 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0056 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0046 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18948 | hp1 | a0001 | c0003 | t0002 | g0048 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18956 | hp1 | a0001 | c0001 | t0014 | g0104 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18962 | hp2 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0136 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18967 | hp1 | a0001 | c0003 | t0002 | g0040 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0049 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18973 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18973 | hp2 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18980 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18984 | hp2 | a0001 | c0002 | t0004 | g0216 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18987 | hp2 | a0001 | c0002 | t0010 | g0162 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18994 | hp1 | a0001 | c0001 | t0019 | g0070 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18994 | hp2 | a0001 | c0003 | t0020 | g0039 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19002 | hp1 | a0001 | c0001 | t0012 | g0023 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19002 | hp2 | a0001 | c0001 | t0016 | g0061 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19004 | hp1 | a0001 | c0001 | t0012 | g0007 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19005 | hp2 | a0001 | c0003 | t0002 | g0020 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19010 | hp1 | a0001 | c0003 | t0002 | g0054 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0159 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0228 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19043 | hp2 | a0001 | c0002 | t0006 | g0028 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19057 | hp2 | a0005 | c0010 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19062 | hp2 | a0001 | c0003 | t0002 | g0038 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19063 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19064 | hp2 | a0001 | c0003 | t0013 | g0016 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19067 | hp2 | a0001 | c0003 | t0002 | g0055 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19068 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19079 | hp1 | a0001 | c0001 | t0008 | g0122 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19079 | hp2 | a0001 | c0001 | t0008 | g0097 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19081 | hp2 | a0001 | c0003 | t0023 | g0034 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19085 | hp2 | a0001 | c0003 | t0013 | g0052 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0020 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0127 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19088 | hp2 | a0001 | c0001 | t0011 | g0063 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19089 | hp1 | a0001 | c0003 | t0002 | g0053 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19090 | hp1 | a0001 | c0002 | t0004 | g0217 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19090 | hp2 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0144 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | ASW | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0214 | AFR | ASW | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20905 | hp1 | a0001 | c0003 | t0027 | g0004 | SAS | GIH | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20905 | hp2 | a0001 | c0003 | t0002 | g0168 | SAS | GIH | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0042 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0163 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | USA | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0185 | AFR | USA | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20300 | hp2 | a0001 | c0002 | t0007 | g0192 | AFR | USA | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA21309 | hp1 | a0001 | c0002 | t0007 | g0208 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA21309 | hp2 | a0007 | c0012 | t0003 | g0126 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0198 | REF | REF | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0232 | REF | REF | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44772292
|
G | A | 1 | a0002 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.569G>A | p.Arg190Gln | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 7/27 | 781/4614 | 569/2310 | 190/769 | chr17 | 44772292 | ||
| chr17:44773288
|
A | G | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.853A>G | p.Ile285Val | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/27 | 1065/4614 | 853/2310 | 285/769 | chr17 | 44773288 | ||
| chr17:44774568
|
A | T | 1 | a0006 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.1154A>T | p.His385Leu | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 13/27 | 1366/4614 | 1154/2310 | 385/769 | chr17 | 44774568 | ||
| chr17:44774577
|
C | T | 1 | a0003 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.1163C>T | p.Ser388Leu | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 13/27 | 1375/4614 | 1163/2310 | 388/769 | chr17 | 44774577 | ||
| chr17:44777715
|
C | T | 1 | a0005 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.1922C>T | p.Ala641Val | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 23/27 | 2134/4614 | 1922/2310 | 641/769 | chr17 | 44777715 | ||
| chr17:44777720
|
G | A | 1 | a0004 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.1927G>A | p.Gly643Ser | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 23/27 | 2139/4614 | 1927/2310 | 643/769 | chr17 | 44777720 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44759765
|
C | T | 1 | a0001c0004 | 2 | HG01109.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.105C>T | p.Gly35Gly | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/27 | 317/4614 | 105/2310 | 35/769 | chr17 | 44759765 | ||
| chr17:44770027
|
G | A | 1 | a0001c0005 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.360G>A | p.Glu120Glu | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/27 | 572/4614 | 360/2310 | 120/769 | chr17 | 44770027 | ||
| chr17:44770048
|
C | T | 1 | a0004c0013 | 1 | HG02809.hp1 | splice_region_variant&synonymous_variant | LOW | c.381C>T | p.Thr127Thr | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/27 | 593/4614 | 381/2310 | 127/769 | chr17 | 44770048 | ||
| chr17:44774361
|
C | T | 8 | a0001c0001a0001c0004a0001c0005others(5): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
synonymous_variant | LOW | c.1059C>T | p.His353His | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 12/27 | 1271/4614 | 1059/2310 | 353/769 | chr17 | 44774361 | ||
| chr17:44775236
|
G | T | 8 | a0001c0001a0001c0004a0001c0005others(5): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
synonymous_variant | LOW | c.1245G>T | p.Ser415Ser | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 15/27 | 1457/4614 | 1245/2310 | 415/769 | chr17 | 44775236 | ||
| chr17:44775242
|
T | C | 12 | a0001c0001a0001c0002a0001c0004others(9): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
synonymous_variant | LOW | c.1251T>C | p.Cys417Cys | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 15/27 | 1463/4614 | 1251/2310 | 417/769 | chr17 | 44775242 | ||
| chr17:44777242
|
T | C | 8 | a0001c0001a0001c0004a0001c0005others(5): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
synonymous_variant | LOW | c.1758T>C | p.Ser586Ser | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 21/27 | 1970/4614 | 1758/2310 | 586/769 | chr17 | 44777242 | ||
| chr17:44777590
|
G | A | 1 | a0001c0009 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.1890G>A | p.Glu630Glu | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 22/27 | 2102/4614 | 1890/2310 | 630/769 | chr17 | 44777590 | ||
| chr17:44778053
|
G | A | 1 | a0001c0007 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.2172G>A | p.Thr724Thr | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 24/27 | 2384/4614 | 2172/2310 | 724/769 | chr17 | 44778053 | ||
| chr17:44778186
|
T | C | 8 | a0001c0001a0001c0004a0001c0005others(5): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
synonymous_variant | LOW | c.2220T>C | p.Ile740Ile | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/27 | 2432/4614 | 2220/2310 | 740/769 | chr17 | 44778186 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44759006
|
C | T | 1 | a0001c0002t0032 | 1 | HG03654.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-194C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 1/27 | chr17 | 44759006 | ||||||
| chr17:44779794
|
C | T | 1 | a0001c0001t0031 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 40 | chr17 | 44779794 | |||||
| chr17:44779807
|
C | T | 1 | a0001c0002t0030 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 53 | chr17 | 44779807 | |||||
| chr17:44780062
|
G | A | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(17): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*308G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 308 | chr17 | 44780062 | |||||
| chr17:44780149
|
C | T | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(17): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*395C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 395 | chr17 | 44780149 | |||||
| chr17:44780176
|
T | A | 1 | a0001c0001t0014 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*422T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 422 | chr17 | 44780176 | |||||
| chr17:44780209
|
C | T | 2 | a0001c0001t0012a0001c0001t0014 | 3 | NA18956.hp1 NA19002.hp1 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*455C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 455 | chr17 | 44780209 | |||||
| chr17:44780214
|
A | T | 1 | a0001c0001t0014 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*460A>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 460 | chr17 | 44780214 | |||||
| chr17:44780225
|
G | A | 2 | a0001c0001t0015a0001c0003t0020 | 2 | NA18994.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*471G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 471 | chr17 | 44780225 | |||||
| chr17:44780237
|
G | T | 1 | a0001c0007t0029 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*483G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 483 | chr17 | 44780237 | |||||
| chr17:44780255
|
A | T | 1 | a0001c0001t0019 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501A>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 501 | chr17 | 44780255 | |||||
| chr17:44780298
|
G | C | 1 | a0001c0001t0014 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*544G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 544 | chr17 | 44780298 | |||||
| chr17:44780323
|
A | C | 1 | a0001c0001t0014 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*569A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 569 | chr17 | 44780323 | |||||
| chr17:44780385
|
C | A | 1 | a0001c0001t0016 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*631C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 631 | chr17 | 44780385 | |||||
| chr17:44780425
|
T | G | 1 | a0001c0002t0021 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*671T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 671 | chr17 | 44780425 | |||||
| chr17:44780556
|
C | CG | 17 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(14): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*810dupG | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 811 | INFO_REALIGN_3_PRIME | chr17 | 44780556 | ||||
| chr17:44780556
|
C | G | 1 | a0001c0001t0018 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*802C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 802 | chr17 | 44780556 | |||||
| chr17:44780562
|
G | C | 1 | a0001c0002t0022 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*808G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 808 | chr17 | 44780562 | |||||
| chr17:44780562
|
G | GC | 2 | a0001c0001t0011a0001c0001t0014 | 3 | HG02080.hp2 NA18956.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*808_*809insC | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 809 | chr17 | 44780562 | |||||
| chr17:44780577
|
T | C | 4 | a0001c0002t0004a0001c0002t0021a0001c0002t0025others(1): Show | 20 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*823T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 823 | chr17 | 44780577 | |||||
| chr17:44780947
|
T | C | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(17): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*1193T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1193 | chr17 | 44780947 | |||||
| chr17:44780978
|
C | T | 3 | a0001c0001t0008a0001c0001t0017a0001c0009t0008 | 6 | HG00544.hp2 HG02056.hp2 HG02132.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1224C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1224 | chr17 | 44780978 | |||||
| chr17:44780991
|
G | A | 1 | a0001c0002t0006 | 11 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1237G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1237 | chr17 | 44780991 | |||||
| chr17:44781126
|
A | C | 4 | a0001c0002t0007a0001c0002t0024a0001c0002t0028others(1): Show | 11 | HG00558.hp1 HG01433.hp1 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1372A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1372 | chr17 | 44781126 | |||||
| chr17:44781210
|
C | A | 4 | a0001c0002t0004a0001c0002t0021a0001c0002t0025others(1): Show | 20 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1456C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1456 | chr17 | 44781210 | |||||
| chr17:44781287
|
G | A | 3 | a0001c0001t0005a0001c0001t0015a0001c0004t0005 | 14 | HG01109.hp1 HG01243.hp2 HG02486.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1533G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1533 | chr17 | 44781287 | |||||
| chr17:44781385
|
C | T | 1 | a0001c0003t0027 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1631C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1631 | chr17 | 44781385 | |||||
| chr17:44781433
|
G | A | 1 | a0001c0002t0021 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1679G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1679 | chr17 | 44781433 | |||||
| chr17:44781582
|
C | T | 13 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(10): Show | 84 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1828C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1828 | chr17 | 44781582 | |||||
| chr17:44781739
|
C | T | 1 | a0001c0003t0013 | 2 | NA19064.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1985C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1985 | chr17 | 44781739 | |||||
| chr17:44781796
|
G | A | 1 | a0001c0002t0026 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2042G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 2042 | chr17 | 44781796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44760090
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.237+193T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44760090 | ||||||
| chr17:44760112
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.237+215C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44760112 | ||||||
| chr17:44760332
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.237+435C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44760332 | ||||||
| chr17:44760436
|
A | G | 2 | a0001c0004t0005g0229a0001c0004t0005g0230 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.237+539A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44760436 | ||||||
| chr17:44760708
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.237+811G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44760708 | ||||||
| chr17:44760973
|
C | T | 1 | a0001c0001t0015g0228 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.237+1076C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44760973 | ||||||
| chr17:44761183
|
CTG | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(85): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.237+1289_237+1290d others(4): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44761183 | |||||
| chr17:44761383
|
C | G | 1 | a0001c0003t0002g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.237+1486C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761383 | ||||||
| chr17:44761486
|
T | G | 5 | a0001c0003t0002g0035a0001c0003t0002g0036a0001c0003t0002g0037others(2): Show | 5 | HG02083.hp2 HG02132.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.237+1589T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761486 | ||||||
| chr17:44761525
|
T | A | 1 | a0007c0012t0003g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.237+1628T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761525 | ||||||
| chr17:44761535
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.237+1638C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761535 | ||||||
| chr17:44761593
|
T | A | 1 | a0001c0001t0016g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+1696T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761593 | ||||||
| chr17:44761603
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.237+1706G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761603 | ||||||
| chr17:44761679
|
G | A | 1 | a0001c0001t0011g0063 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.237+1782G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761679 | ||||||
| chr17:44761692
|
G | C | 1 | a0001c0001t0016g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+1795G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761692 | ||||||
| chr17:44761698
|
T | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(167): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.237+1801T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761698 | ||||||
| chr17:44761749
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.237+1852G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761749 | ||||||
| chr17:44761824
|
GT | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0033others(40): Show | 58 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.237+1928delT | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761824 | ||||||
| chr17:44761899
|
C | A | 1 | a0001c0001t0016g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+2002C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761899 | ||||||
| chr17:44761948
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.237+2051G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761948 | ||||||
| chr17:44762051
|
C | T | 2 | a0001c0001t0015g0228a0007c0012t0003g0126 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.237+2154C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762051 | ||||||
| chr17:44762082
|
C | T | 2 | a0001c0002t0021g0194a0001c0003t0002g0195 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.237+2185C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762082 | ||||||
| chr17:44762137
|
G | A | 1 | a0001c0002t0004g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.237+2240G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762137 | ||||||
| chr17:44762183
|
C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.237+2286C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762183 | ||||||
| chr17:44762373
|
C | G | 1 | a0001c0003t0002g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.237+2476C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762373 | ||||||
| chr17:44762628
|
G | A | 2 | a0001c0001t0015g0228a0007c0012t0003g0126 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.237+2731G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762628 | ||||||
| chr17:44762778
|
A | G | 2 | a0001c0002t0021g0194a0001c0003t0002g0195 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.237+2881A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762778 | ||||||
| chr17:44762917
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.237+3020G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762917 | ||||||
| chr17:44762925
|
G | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0197others(12): Show | 23 | HG00323.hp2 HG00673.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.237+3028G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762925 | ||||||
| chr17:44762969
|
C | CA | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0068others(18): Show | 25 | HG00609.hp1 HG01074.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.237+3089dupA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44762969 | |||||
| chr17:44762969
|
C | CAA | 37 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0033others(34): Show | 52 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.237+3088_237+3089d others(4): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44762969 | |||||
| chr17:44763150
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02109.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.237+3253C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763150 | ||||||
| chr17:44763494
|
AG | A | 3 | a0001c0002t0003g0127a0001c0002t0003g0135a0001c0002t0003g0136 | 3 | NA18964.hp1 NA18973.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.237+3599delG | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44763494 | |||||
| chr17:44763565
|
C | T | 7 | a0001c0002t0007g0032a0001c0002t0007g0134a0001c0002t0007g0189others(4): Show | 8 | HG00558.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.237+3668C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763565 | ||||||
| chr17:44763721
|
CT | C | 9 | a0001c0001t0001g0072a0001c0001t0001g0128a0001c0001t0001g0197others(6): Show | 9 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(6): Show |
intron_variant | MODIFIER | c.237+3837delT | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44763721 | |||||
| chr17:44763747
|
C | T | 1 | a0001c0003t0002g0188 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.237+3850C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763747 | ||||||
| chr17:44763757
|
C | T | 3 | a0001c0001t0005g0221a0001c0001t0005g0222a0001c0003t0002g0227 | 3 | HG02615.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.237+3860C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763757 | ||||||
| chr17:44763799
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.237+3902C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763799 | ||||||
| chr17:44763878
|
A | G | 1 | a0001c0003t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.237+3981A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763878 | ||||||
| chr17:44763931
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.237+4034G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763931 | ||||||
| chr17:44763948
|
C | T | 1 | a0001c0003t0002g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.237+4051C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763948 | ||||||
| chr17:44764012
|
C | T | 1 | a0001c0002t0003g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.237+4115C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764012 | ||||||
| chr17:44764081
|
C | A | 2 | a0001c0002t0004g0014a0001c0002t0004g0207 | 4 | HG02922.hp1 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+4184C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764081 | ||||||
| chr17:44764156
|
T | A | 1 | a0001c0001t0016g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+4259T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764156 | ||||||
| chr17:44764262
|
C | A | 9 | a0001c0002t0006g0028a0001c0002t0006g0029a0001c0002t0006g0129others(6): Show | 11 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.237+4365C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764262 | ||||||
| chr17:44764390
|
G | C | 1 | a0001c0002t0004g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.237+4493G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764390 | ||||||
| chr17:44764476
|
C | A | 1 | a0001c0001t0016g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+4579C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764476 | ||||||
| chr17:44764610
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075 | 3 | HG00140.hp2 HG01361.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.237+4713G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764610 | ||||||
| chr17:44764711
|
A | T | 1 | a0001c0001t0016g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+4814A>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764711 | ||||||
| chr17:44764743
|
C | A | 1 | a0001c0001t0016g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+4846C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764743 | ||||||
| chr17:44764745
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.237+4848T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764745 | ||||||
| chr17:44764847
|
C | T | 41 | a0001c0002t0002g0173a0001c0002t0003g0011a0001c0002t0003g0012others(38): Show | 47 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.238-4871C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764847 | ||||||
| chr17:44765151
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.238-4567T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765151 | ||||||
| chr17:44765229
|
G | A | 7 | a0001c0001t0001g0148a0001c0001t0005g0030a0001c0001t0005g0130others(4): Show | 8 | HG01243.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-4489G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765229 | ||||||
| chr17:44765278
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(91): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.238-4440C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765278 | ||||||
| chr17:44765439
|
C | G | 1 | a0001c0001t0008g0122 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.238-4279C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765439 | ||||||
| chr17:44765533
|
A | T | 1 | a0001c0002t0006g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.238-4185A>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765533 | ||||||
| chr17:44765610
|
C | CT | 23 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0079others(20): Show | 27 | HG00558.hp1 HG02145.hp1 HG02165.hp1 others(24): Show |
intron_variant | MODIFIER | c.238-4085dupT | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | |||||
| chr17:44765610
|
C | CTT | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(67): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.238-4086_238-4085d others(4): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | |||||
| chr17:44765610
|
C | CTTT | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0071others(21): Show | 27 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.238-4087_238-4085d others(5): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | |||||
| chr17:44765610
|
C | CTTTT | 20 | a0001c0002t0002g0173a0001c0002t0003g0031a0001c0002t0003g0127others(17): Show | 21 | HG00099.hp1 HG00609.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.238-4088_238-4085d others(6): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | |||||
| chr17:44765610
|
C | CTTTTT | 20 | a0001c0001t0001g0148a0001c0001t0005g0030a0001c0001t0005g0130others(17): Show | 25 | HG01243.hp2 HG01358.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.238-4089_238-4085d others(7): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | |||||
| chr17:44765610
|
C | CTTTTTT | 6 | a0001c0001t0005g0149a0001c0002t0003g0183a0001c0002t0003g0184others(3): Show | 6 | HG01884.hp1 HG03195.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-4090_238-4085d others(8): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | |||||
| chr17:44765610
|
CTTTTT | C | 7 | a0001c0001t0001g0078a0001c0001t0001g0203a0001c0002t0004g0014others(4): Show | 9 | HG01433.hp2 HG02273.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.238-4089_238-4085d others(7): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | |||||
| chr17:44765610
|
CTTTTTT | C | 41 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0033others(38): Show | 56 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.238-4090_238-4085d others(8): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | |||||
| chr17:44765648
|
T | G | 1 | a0001c0001t0016g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.238-4070T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765648 | ||||||
| chr17:44765661
|
C | T | 1 | a0001c0002t0002g0173 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.238-4057C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765661 | ||||||
| chr17:44765673
|
T | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG00438.hp2 NA19000.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.238-4045T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765673 | ||||||
| chr17:44765779
|
C | T | 11 | a0001c0001t0001g0148a0001c0001t0005g0030a0001c0001t0005g0130others(8): Show | 12 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-3939C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765779 | ||||||
| chr17:44766143
|
C | T | 1 | a0001c0003t0002g0054 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.238-3575C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766143 | ||||||
| chr17:44766188
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.238-3530G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766188 | ||||||
| chr17:44766430
|
C | T | 1 | a0001c0002t0006g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238-3288C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766430 | ||||||
| chr17:44766479
|
T | G | 1 | a0001c0001t0016g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.238-3239T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766479 | ||||||
| chr17:44766528
|
G | A | 2 | a0001c0004t0005g0229a0001c0004t0005g0230 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.238-3190G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766528 | ||||||
| chr17:44766553
|
T | A | 1 | a0001c0001t0016g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.238-3165T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766553 | ||||||
| chr17:44766561
|
C | T | 2 | a0001c0001t0005g0221a0001c0001t0005g0222 | 2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.238-3157C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766561 | ||||||
| chr17:44766566
|
C | G | 7 | a0001c0002t0007g0032a0001c0002t0007g0134a0001c0002t0007g0189others(4): Show | 8 | HG00558.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-3152C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766566 | ||||||
| chr17:44766594
|
C | A | 3 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153 | 3 | HG03041.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.238-3124C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766594 | ||||||
| chr17:44766745
|
C | T | 1 | a0001c0001t0008g0110 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.238-2973C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766745 | ||||||
| chr17:44766746
|
G | A | 2 | a0001c0001t0005g0221a0001c0001t0005g0222 | 2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.238-2972G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766746 | ||||||
| chr17:44766795
|
T | A | 1 | a0001c0001t0016g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.238-2923T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766795 | ||||||
| chr17:44766869
|
A | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(141): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.238-2849A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766869 | ||||||
| chr17:44767097
|
A | C | 1 | a0001c0002t0003g0182 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.238-2621A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767097 | ||||||
| chr17:44767213
|
G | A | 1 | a0001c0002t0004g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.238-2505G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767213 | ||||||
| chr17:44767354
|
C | CA | 47 | a0001c0001t0001g0033a0001c0001t0001g0079a0001c0001t0001g0086others(44): Show | 54 | HG00408.hp1 HG00438.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.238-2341dupA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44767354 | |||||
| chr17:44767354
|
CA | C | 19 | a0001c0001t0001g0026a0001c0001t0001g0064a0001c0001t0001g0082others(16): Show | 20 | HG00099.hp1 HG01168.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.238-2341delA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44767354 | |||||
| chr17:44767685
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG00280.hp2 HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.238-2033G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767685 | ||||||
| chr17:44767896
|
C | T | 2 | a0001c0001t0015g0228a0007c0012t0003g0126 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.238-1822C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767896 | ||||||
| chr17:44767909
|
G | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0115a0001c0001t0016g0061 | 3 | NA18975.hp2 NA18984.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.238-1809G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767909 | ||||||
| chr17:44767979
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-1739A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767979 | ||||||
| chr17:44767997
|
T | C | 1 | a0002c0006t0001g0199 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.238-1721T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767997 | ||||||
| chr17:44768067
|
G | T | 1 | a0001c0003t0002g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.238-1651G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768067 | ||||||
| chr17:44768085
|
A | G | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0224 | 3 | HG01255.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.238-1633A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768085 | ||||||
| chr17:44768168
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG00408.hp2 HG00544.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-1550A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768168 | ||||||
| chr17:44768180
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.238-1538A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768180 | ||||||
| chr17:44768216
|
A | G | 1 | a0001c0003t0002g0051 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.238-1502A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768216 | ||||||
| chr17:44768266
|
A | G | 1 | a0001c0002t0006g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238-1452A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768266 | ||||||
| chr17:44768326
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(91): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.238-1392G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768326 | ||||||
| chr17:44768509
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.238-1209G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768509 | ||||||
| chr17:44768657
|
G | T | 1 | a0001c0001t0014g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.238-1061G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768657 | ||||||
| chr17:44768737
|
G | T | 3 | a0001c0003t0002g0037a0001c0003t0002g0038a0001c0003t0023g0034 | 3 | NA19062.hp2 NA19068.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.238-981G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768737 | ||||||
| chr17:44768761
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.238-957C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768761 | ||||||
| chr17:44768780
|
A | G | 3 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153 | 3 | HG03041.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.238-938A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768780 | ||||||
| chr17:44768824
|
C | A | 1 | a0001c0002t0004g0212 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.238-894C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768824 | ||||||
| chr17:44768937
|
C | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0033others(23): Show | 35 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.238-781C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768937 | ||||||
| chr17:44768963
|
G | T | 1 | a0001c0002t0030g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.238-755G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768963 | ||||||
| chr17:44768981
|
C | T | 1 | a0001c0002t0004g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.238-737C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768981 | ||||||
| chr17:44769040
|
T | C | 1 | a0001c0003t0002g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.238-678T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769040 | ||||||
| chr17:44769063
|
A | T | 1 | a0001c0003t0002g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.238-655A>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769063 | ||||||
| chr17:44769145
|
G | A | 1 | a0001c0002t0003g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.238-573G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769145 | ||||||
| chr17:44769261
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.238-457G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769261 | ||||||
| chr17:44769472
|
G | A | 1 | a0001c0002t0003g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.238-246G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769472 | ||||||
| chr17:44769521
|
C | T | 2 | a0001c0001t0015g0228a0007c0012t0003g0126 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.238-197C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769521 | ||||||
| chr17:44769626
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.238-92T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769626 | ||||||
| chr17:44769655
|
C | G | 1 | a0001c0003t0002g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.238-63C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769655 | ||||||
| chr17:44769660
|
C | G | 1 | a0001c0002t0006g0029 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.238-58C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769660 | ||||||
| chr17:44769665
|
C | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(90): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.238-53C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769665 | ||||||
| chr17:44769861
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.314+67G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 3/26 | chr17 | 44769861 | ||||||
| chr17:44769943
|
C | G | 1 | a0001c0003t0002g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.315-39C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 3/26 | chr17 | 44769943 | ||||||
| chr17:44770070
|
C | G | 41 | a0001c0002t0002g0173a0001c0002t0003g0011a0001c0002t0003g0012others(38): Show | 47 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.381+22C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770070 | ||||||
| chr17:44770288
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.381+240C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770288 | ||||||
| chr17:44770400
|
C | T | 15 | a0001c0001t0001g0148a0001c0001t0005g0030a0001c0001t0005g0130others(12): Show | 16 | HG01109.hp1 HG01243.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.381+352C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770400 | ||||||
| chr17:44770488
|
T | TC | 13 | a0001c0001t0001g0045a0001c0003t0002g0016a0001c0003t0002g0017others(10): Show | 14 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.381+451dupC | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44770488 | |||||
| chr17:44770488
|
TC | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0033others(23): Show | 36 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.381+451delC | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44770488 | |||||
| chr17:44770490
|
C | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(165): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.381+442C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770490 | ||||||
| chr17:44770495
|
CCCCCG | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(84): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.381+452_381+456del others(5): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44770495 | |||||
| chr17:44770496
|
C | G | 53 | a0001c0002t0002g0173a0001c0002t0003g0011a0001c0002t0003g0012others(50): Show | 63 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.381+448C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770496 | ||||||
| chr17:44770497
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+449C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770497 | ||||||
| chr17:44770497
|
CCCG | C | 67 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(64): Show | 81 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.381+452_381+454del others(3): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44770497 | |||||
| chr17:44770499
|
CG | C | 4 | a0001c0001t0015g0228a0001c0002t0007g0190a0001c0002t0032g0215others(1): Show | 4 | HG02145.hp1 HG03654.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+452delG | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770499 | ||||||
| chr17:44770500
|
G | C | 15 | a0001c0001t0001g0148a0001c0001t0005g0030a0001c0001t0005g0130others(12): Show | 16 | HG01109.hp1 HG01243.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.381+452G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770500 | ||||||
| chr17:44770501
|
C | G | 5 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+453C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770501 | ||||||
| chr17:44770502
|
C | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(84): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.381+454C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770502 | ||||||
| chr17:44770503
|
C | G | 3 | a0001c0004t0005g0229a0001c0004t0005g0230a0007c0012t0003g0126 | 3 | HG01109.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.381+455C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770503 | ||||||
| chr17:44770580
|
C | A | 1 | a0001c0002t0003g0181 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.381+532C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770580 | ||||||
| chr17:44770726
|
T | C | 86 | a0001c0001t0001g0148a0001c0001t0005g0030a0001c0001t0005g0130others(83): Show | 102 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.381+678T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770726 | ||||||
| chr17:44770820
|
A | C | 5 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-764A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770820 | ||||||
| chr17:44770872
|
TG | T | 3 | a0001c0001t0001g0121a0001c0001t0014g0104a0001c0003t0002g0037 | 3 | NA18956.hp1 NA18987.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.382-709delG | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44770872 | |||||
| chr17:44770952
|
T | C | 2 | a0001c0002t0028g0120a0001c0007t0029g0191 | 2 | HG00558.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.382-632T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770952 | ||||||
| chr17:44771152
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.382-432T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44771152 | ||||||
| chr17:44771279
|
G | A | 5 | a0001c0003t0002g0035a0001c0003t0002g0036a0001c0003t0002g0037others(2): Show | 5 | HG02083.hp2 HG02132.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-305G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44771279 | ||||||
| chr17:44771297
|
C | CA | 47 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0024others(44): Show | 63 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.382-269dupA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44771297 | |||||
| chr17:44771297
|
CA | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(98): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.382-269delA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44771297 | |||||
| chr17:44771336
|
C | T | 1 | a0001c0002t0004g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.382-248C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44771336 | ||||||
| chr17:44771557
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.382-27G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44771557 | ||||||
| chr17:44771726
|
C | T | 15 | a0001c0001t0001g0148a0001c0001t0005g0030a0001c0001t0005g0130others(12): Show | 16 | HG01109.hp1 HG01243.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.468-30C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 5/26 | chr17 | 44771726 | ||||||
| chr17:44771990
|
G | GCCCCAGC others(11): Show |
1 | a0001c0003t0020g0039 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.543+170_543+187dup others(18): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr17 | 44771990 | |||||
| chr17:44772135
|
C | T | 1 | a0001c0003t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544-132C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 6/26 | chr17 | 44772135 | ||||||
| chr17:44772353
|
G | T | 1 | a0001c0003t0002g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.610+20G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 7/26 | chr17 | 44772353 | ||||||
| chr17:44772545
|
G | A | 1 | a0001c0001t0005g0146 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.678+79G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 8/26 | chr17 | 44772545 | ||||||
| chr17:44772577
|
G | A | 2 | a0001c0001t0005g0156a0001c0001t0005g0157 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.678+111G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 8/26 | chr17 | 44772577 | ||||||
| chr17:44772843
|
C | T | 1 | a0001c0002t0028g0120 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.679-14C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 8/26 | chr17 | 44772843 | ||||||
| chr17:44772984
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(72): Show | 108 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.754-30T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 9/26 | chr17 | 44772984 | ||||||
| chr17:44773165
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.825+80C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 10/26 | chr17 | 44773165 | ||||||
| chr17:44773573
|
T | G | 11 | a0001c0001t0005g0030a0001c0001t0005g0130a0001c0001t0005g0145others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.992+146T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773573 | ||||||
| chr17:44773706
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.992+279G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773706 | ||||||
| chr17:44773749
|
T | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0128a0001c0001t0001g0132 | 4 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.992+322T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773749 | ||||||
| chr17:44773803
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 201 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.992+376A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773803 | ||||||
| chr17:44773816
|
C | T | 1 | a0001c0002t0032g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.992+389C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773816 | ||||||
| chr17:44773822
|
G | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0115a0001c0001t0016g0061 | 3 | NA18975.hp2 NA18984.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.992+395G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773822 | ||||||
| chr17:44773883
|
G | C | 9 | a0001c0002t0007g0032a0001c0002t0007g0134a0001c0002t0007g0189others(6): Show | 10 | HG00558.hp1 HG01433.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.993-412G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773883 | ||||||
| chr17:44773936
|
C | T | 1 | a0001c0002t0004g0214 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.993-359C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773936 | ||||||
| chr17:44774042
|
G | C | 6 | a0001c0002t0003g0127a0001c0002t0003g0135a0001c0002t0003g0136others(3): Show | 6 | HG01074.hp1 HG01358.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.993-253G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44774042 | ||||||
| chr17:44774097
|
A | AAAAAAG | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.993-188_993-183dup others(6): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr17 | 44774097 | |||||
| chr17:44774134
|
G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 201 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.993-161G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44774134 | ||||||
| chr17:44774135
|
G | T | 1 | a0001c0007t0029g0191 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.993-160G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44774135 | ||||||
| chr17:44774266
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 201 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.993-29G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44774266 | ||||||
| chr17:44774693
|
C | T | 59 | a0001c0002t0002g0173a0001c0002t0003g0011a0001c0002t0003g0012others(56): Show | 68 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(65): Show |
splice_region_variant&intron_variant | LOW | c.1169-5C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 13/26 | chr17 | 44774693 | ||||||
| chr17:44774777
|
A | G | 1 | a0001c0001t0014g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1220+28A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 14/26 | chr17 | 44774777 | ||||||
| chr17:44774846
|
C | A | 1 | a0001c0003t0002g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1220+97C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 14/26 | chr17 | 44774846 | ||||||
| chr17:44774894
|
C | A | 1 | a0001c0003t0002g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1220+145C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 14/26 | chr17 | 44774894 | ||||||
| chr17:44775043
|
A | ATGGGAGC others(28): Show |
1 | a0001c0001t0001g0201 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1221-168_1221-134d others(37): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr17 | 44775043 | |||||
| chr17:44775081
|
A | G | 2 | a0001c0002t0006g0028a0001c0002t0006g0129 | 3 | HG01891.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1221-131A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 14/26 | chr17 | 44775081 | ||||||
| chr17:44775780
|
C | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0033others(34): Show | 47 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.1485+104C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775780 | ||||||
| chr17:44775793
|
G | A | 1 | a0001c0003t0002g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1485+117G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775793 | ||||||
| chr17:44775878
|
A | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1485+202A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775878 | ||||||
| chr17:44775879
|
G | C | 1 | a0001c0001t0001g0201 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1485+203G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775879 | ||||||
| chr17:44775888
|
G | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0154 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1485+212G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775888 | ||||||
| chr17:44775965
|
G | A | 12 | a0001c0002t0004g0005a0001c0002t0004g0014a0001c0002t0004g0196others(9): Show | 18 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1486-162G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775965 | ||||||
| chr17:44776058
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1486-69G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44776058 | ||||||
| chr17:44776059
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1486-68A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44776059 | ||||||
| chr17:44776326
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(91): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1566+119C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776326 | ||||||
| chr17:44776473
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1566+266C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776473 | ||||||
| chr17:44776550
|
C | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0033others(34): Show | 47 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.1567-195C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776550 | ||||||
| chr17:44776582
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1567-163G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776582 | ||||||
| chr17:44776685
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0033others(34): Show | 47 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.1567-60G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776685 | ||||||
| chr17:44776687
|
G | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0128others(3): Show | 10 | HG02055.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1567-58G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776687 | ||||||
| chr17:44776840
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(91): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1617+45G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 19/26 | chr17 | 44776840 | ||||||
| chr17:44777134
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(91): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1682-32G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 20/26 | chr17 | 44777134 | ||||||
| chr17:44777421
|
G | C | 1 | a0001c0001t0008g0097 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1782-61G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 21/26 | chr17 | 44777421 | ||||||
| chr17:44777630
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1901+29G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 22/26 | chr17 | 44777630 | ||||||
| chr17:44777694
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA19063.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1902-1G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 22/26 | chr17 | 44777694 | ||||||
| chr17:44777880
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.2070+17T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 23/26 | chr17 | 44777880 | ||||||
| chr17:44778092
|
G | T | 1 | a0001c0003t0002g0049 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2185+26G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 24/26 | chr17 | 44778092 | ||||||
| chr17:44778104
|
T | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.2185+38T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 24/26 | chr17 | 44778104 | ||||||
| chr17:44778378
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0101a0001c0001t0001g0119 | 4 | HG00733.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2276+136A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778378 | ||||||
| chr17:44778563
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.2276+321G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778563 | ||||||
| chr17:44778586
|
C | T | 2 | a0001c0001t0001g0201a0007c0012t0003g0126 | 2 | NA19063.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2276+344C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778586 | ||||||
| chr17:44778615
|
G | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.2276+373G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778615 | ||||||
| chr17:44778646
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2276+404G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778646 | ||||||
| chr17:44778650
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 10 | HG00642.hp2 HG01069.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2276+408C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778650 | ||||||
| chr17:44778688
|
C | CA | 6 | a0001c0001t0001g0205a0001c0003t0002g0020a0001c0003t0002g0038others(3): Show | 7 | HG01175.hp1 HG02135.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.2276+471dupA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778688 | |||||
| chr17:44778688
|
C | CAAAAAAA others(12): Show |
1 | a0001c0002t0010g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2276+461_2276+462i others(21): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778688 | |||||
| chr17:44778688
|
CA | C | 10 | a0001c0001t0001g0197a0001c0002t0004g0014a0001c0002t0004g0213others(7): Show | 12 | HG00323.hp2 HG02015.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.2276+471delA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778688 | |||||
| chr17:44778688
|
CAA | C | 16 | a0001c0002t0004g0005a0001c0002t0004g0144a0001c0002t0004g0196others(13): Show | 22 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.2276+470_2276+471d others(4): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778688 | |||||
| chr17:44778688
|
CAAAAAAA others(4): Show |
C | 1 | a0007c0012t0003g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2276+461_2276+471d others(13): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778688 | |||||
| chr17:44778713
|
A | AAAAAAAA others(13): Show |
2 | a0001c0002t0003g0160a0001c0002t0024g0193 | 2 | HG01081.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2276+471_2276+472i others(22): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAAAAAA others(12): Show |
1 | a0001c0002t0028g0120 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2276+471_2276+472i others(21): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAAAAAA others(11): Show |
2 | a0001c0002t0003g0186a0001c0002t0007g0192 | 2 | NA19062.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2276+471_2276+472i others(20): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAAAAAA others(10): Show |
8 | a0001c0002t0002g0173a0001c0002t0003g0011a0001c0002t0003g0137others(5): Show | 10 | HG00323.hp1 HG00639.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(19): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAAAAAA others(9): Show |
1 | a0001c0002t0007g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2276+471_2276+472i others(18): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAAAAAA others(8): Show |
3 | a0001c0002t0003g0031a0001c0002t0003g0135a0001c0002t0003g0175 | 4 | HG01243.hp1 HG01358.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(17): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAAAAAA others(7): Show |
12 | a0001c0002t0003g0012a0001c0002t0003g0127a0001c0002t0003g0136others(9): Show | 14 | HG00099.hp1 HG00609.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(16): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAAAAAA others(6): Show |
8 | a0001c0002t0003g0013a0001c0002t0003g0159a0001c0002t0003g0167others(5): Show | 10 | HG00558.hp1 HG01074.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(15): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAAAAAA others(5): Show |
2 | a0001c0002t0003g0171a0001c0002t0003g0178 | 2 | HG01168.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2276+471_2276+472i others(14): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAAAAAA others(4): Show |
1 | a0001c0002t0003g0172 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2276+471_2276+472i others(13): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAAAAAA others(3): Show |
2 | a0001c0002t0003g0184a0001c0002t0007g0189 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2276+471_2276+472i others(12): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAAG | 16 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0209others(13): Show | 17 | HG00642.hp2 HG01069.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(6): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAAG | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(26): Show | 37 | HG00621.hp1 HG00642.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(5): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AAG | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(66): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(4): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778713
|
A | AG | 4 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0152others(1): Show | 4 | HG01070.hp1 HG01884.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.2276+472dupG | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778713 | |||||
| chr17:44778713
|
A | G | 30 | a0001c0001t0005g0157a0001c0002t0003g0179a0001c0002t0003g0185others(27): Show | 38 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.2276+471A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | ||||||
| chr17:44778714
|
G | A | 1 | a0001c0001t0014g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2276+472G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778714 | ||||||
| chr17:44778814
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG00408.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.2277-408A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778814 | ||||||
| chr17:44778989
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.2277-233T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778989 | ||||||
| chr17:44779082
|
T | C | 9 | a0001c0002t0006g0028a0001c0002t0006g0029a0001c0002t0006g0129others(6): Show | 11 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2277-140T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44779082 | ||||||
| chr17:44779253
|
C | T | 1 | a0001c0001t0014g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2294+14C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 26/26 | chr17 | 44779253 | ||||||
| chr17:44779348
|
G | A | 1 | a0001c0002t0003g0181 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2294+109G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 26/26 | chr17 | 44779348 |