Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 22937 |
|---|---|
| ensemblid | ENSG00000114650.21 |
| hgncid | 30634 |
| symbol | SCAP |
| name | SREBF chaperone |
| refseq_nuc | NM_012235.4 |
| refseq_prot | NP_036367.2 |
| ensembl_nuc | ENST00000265565.10 |
| ensembl_prot | ENSP00000265565.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 47413681 |
| end | 47475941 |
| strand | - |
| ver | v1.2 |
| region | chr3:47413681-47475941 |
| region5000 | chr3:47408681-47480941 |
| regionname0 | SCAP_chr3_47413681_47475941 |
| regionname5000 | SCAP_chr3_47408681_47480941 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1279 | 176 | 67 | 27 | 57 | 7 | 17 | 39 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0002 | 0/1 | 1279 | 113 | 15 | 30 | 46 | 3 | 18 | 37 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0003 | 0/0 | 1279 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0004 | 0/0 | 1279 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0005 | 0/0 | 1279 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0006 | 0/0 | 1279 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0007 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0008 | 0/0 | 1279 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0009 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0010 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0011 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0012 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0013 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3840 | 151 | 45 | 26 | 57 | 7 | 16 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0002 | 0/1 | 3840 | 112 | 15 | 30 | 46 | 3 | 17 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0003 | 1/0 | 3840 | 15 | 14 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0004 | 0/0 | 3840 | 3 | 0 | 0 | 3 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0005 | 0/0 | 3840 | 3 | 3 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0006 | 0/0 | 3840 | 2 | 0 | 0 | 2 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0007 | 0/0 | 3840 | 2 | 0 | 0 | 2 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0008 | 0/0 | 3840 | 2 | 1 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0009 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0010 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0011 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0012 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0013 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0014 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0015 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0016 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0017 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0018 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0019 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0020 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0021 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| c0022 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 415 | 264 | 75 | 46 | 104 | 6 | 31 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| t0002 | 0/0 | 415 | 17 | 2 | 6 | 0 | 4 | 5 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| t0003 | 0/0 | 420 | 15 | 0 | 3 | 12 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| t0004 | 0/0 | 418 | 3 | 2 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| t0005 | 0/0 | 415 | 2 | 1 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| t0006 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| t0007 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| t0008 | 0/0 | 415 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0005 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3840 | 151 | 45 | 26 | 57 | 7 | 16 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0003 | 1/0 | 3840 | 15 | 14 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0005 | 0/0 | 3840 | 3 | 3 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0008 | 0/0 | 3840 | 2 | 1 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0009 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0010 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0018 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0019 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0022 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0002c0002 | 0/1 | 3840 | 112 | 15 | 30 | 46 | 3 | 17 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0002c0011 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0003c0004 | 0/0 | 3840 | 3 | 0 | 0 | 3 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0004c0006 | 0/0 | 3840 | 2 | 0 | 0 | 2 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0005c0007 | 0/0 | 3840 | 2 | 0 | 0 | 2 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0006c0021 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0007c0012 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0008c0013 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0009c0014 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0010c0015 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0011c0017 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0012c0016 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0013c0020 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4254 | 116 | 41 | 16 | 45 | 3 | 11 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0001t0002 | 0/0 | 4254 | 16 | 1 | 6 | 0 | 4 | 5 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0001t0003 | 0/0 | 4259 | 15 | 0 | 3 | 12 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0001t0005 | 0/0 | 4254 | 2 | 1 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0001t0006 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0001t0007 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0003t0001 | 1/0 | 4254 | 15 | 14 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0005t0001 | 0/0 | 4254 | 3 | 3 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0008t0001 | 0/0 | 4254 | 2 | 1 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0009t0001 | 0/0 | 4254 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0010t0001 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0018t0002 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0019t0001 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0001c0022t0001 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0002c0002t0001 | 0/1 | 4254 | 108 | 13 | 28 | 46 | 3 | 17 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0002c0002t0004 | 0/0 | 4257 | 3 | 2 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0002c0002t0008 | 0/0 | 4254 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0002c0011t0001 | 0/0 | 4254 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0003c0004t0001 | 0/0 | 4254 | 3 | 0 | 0 | 3 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0004c0006t0001 | 0/0 | 4254 | 2 | 0 | 0 | 2 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0005c0007t0001 | 0/0 | 4254 | 2 | 0 | 0 | 2 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0006c0021t0001 | 0/0 | 4254 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0007c0012t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0008c0013t0001 | 0/0 | 4254 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0009c0014t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0010c0015t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0011c0017t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0012c0016t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| a0013c0020t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | copy fasta | chr3 | 47408681 | 47480941 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0006g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0001t0007g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0005 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0005t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0005t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0005t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0008t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0008t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0009t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0010t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0018t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0019t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0001c0022t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0002t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0002c0011t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0003c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0003c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0003c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0004c0006t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0004c0006t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0005c0007t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0005c0007t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0006c0021t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0007c0012t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0008c0013t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0009c0014t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0010c0015t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0011c0017t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0012c0016t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| a0013c0020t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0291 | EUR | GBR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0085 | EUR | GBR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0293 | EUR | GBR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00408 | hp1 | a0003 | c0004 | t0001 | g0073 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00544 | hp2 | a0004 | c0006 | t0001 | g0072 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0115 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01069 | hp2 | a0008 | c0013 | t0001 | g0266 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0168 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01074 | hp1 | a0002 | c0002 | t0004 | g0287 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0156 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01106 | hp2 | a0002 | c0002 | t0008 | g0113 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0079 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0152 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0122 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0104 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0238 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0290 | EUR | IBS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0153 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01934 | hp1 | a0001 | c0008 | t0001 | g0024 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0125 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0102 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02027 | hp1 | a0009 | c0014 | t0001 | g0128 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02055 | hp2 | a0001 | c0018 | t0002 | g0301 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0159 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CDX | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0236 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0188 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0099 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0110 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0164 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0108 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0078 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0068 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02965 | hp1 | a0002 | c0002 | t0004 | g0285 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0196 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0195 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0089 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03453 | hp1 | a0001 | c0022 | t0001 | g0197 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03453 | hp2 | a0001 | c0019 | t0001 | g0046 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03516 | hp2 | a0001 | c0010 | t0001 | g0180 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0114 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03704 | hp2 | a0006 | c0021 | t0001 | g0211 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03710 | hp2 | a0002 | c0011 | t0001 | g0096 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0100 | SAS | BEB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | BEB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03942 | hp1 | a0001 | c0009 | t0001 | g0267 | SAS | BEB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0143 | SAS | BEB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0088 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0087 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0103 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18906 | hp2 | a0002 | c0002 | t0004 | g0286 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18944 | hp2 | a0003 | c0004 | t0001 | g0160 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18947 | hp2 | a0010 | c0015 | t0001 | g0074 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18967 | hp1 | a0007 | c0012 | t0001 | g0083 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18969 | hp1 | a0005 | c0007 | t0001 | g0116 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18979 | hp2 | a0003 | c0004 | t0001 | g0140 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18984 | hp1 | a0005 | c0007 | t0001 | g0055 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19001 | hp2 | a0011 | c0017 | t0001 | g0261 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19002 | hp2 | a0013 | c0020 | t0001 | g0224 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19060 | hp2 | a0004 | c0006 | t0001 | g0076 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19084 | hp2 | a0012 | c0016 | t0001 | g0247 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0106 | AFR | ASW | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | TSI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0167 | EUR | TSI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0295 | EUR | TSI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0166 | EUR | TSI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0109 | SAS | GIH | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | GIH | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02486 | hp1 | a0001 | c0008 | t0001 | g0023 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0145 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | USA | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | USA | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0149 | REF | REF | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0005 | REF | REF | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:47413976
|
T | C | 1 | a0012 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.3718A>G | p.Lys1240Glu | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 23/23 | 3959/4254 | 3718/3840 | 1240/1279 | chr3 | 47413976 | ||
| chr3:47417135
|
A | G | 1 | a0010 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.3043T>C | p.Phe1015Leu | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/23 | 3284/4254 | 3043/3840 | 1015/1279 | chr3 | 47417135 | ||
| chr3:47417443
|
T | G | 1 | a0011 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.2831A>C | p.Gln944Pro | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 17/23 | 3072/4254 | 2831/3840 | 944/1279 | chr3 | 47417443 | ||
| chr3:47417456
|
G | A | 1 | a0004 | 2 | HG00544.hp2 NA19060.hp2 |
missense_variant | MODERATE | c.2818C>T | p.Pro940Ser | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 17/23 | 3059/4254 | 2818/3840 | 940/1279 | chr3 | 47417456 | ||
| chr3:47417497
|
G | A | 1 | a0005 | 2 | NA18969.hp1 NA18984.hp1 |
missense_variant | MODERATE | c.2777C>T | p.Ala926Val | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 17/23 | 3018/4254 | 2777/3840 | 926/1279 | chr3 | 47417497 | ||
| chr3:47417560
|
C | T | 2 | a0003a0004 | 5 | HG00408.hp1 HG00544.hp2 NA18944.hp2 others(2): Show |
missense_variant | MODERATE | c.2714G>A | p.Arg905Gln | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 17/23 | 2955/4254 | 2714/3840 | 905/1279 | chr3 | 47417560 | ||
| chr3:47418189
|
C | T | 7 | a0002a0003a0004others(4): Show | 123 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(120): Show |
missense_variant | MODERATE | c.2392G>A | p.Val798Ile | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/23 | 2633/4254 | 2392/3840 | 798/1279 | chr3 | 47418189 | ||
| chr3:47419469
|
C | T | 1 | a0009 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1799G>A | p.Arg600His | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/23 | 2040/4254 | 1799/3840 | 600/1279 | chr3 | 47419469 | ||
| chr3:47420690
|
C | T | 1 | a0008 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.1427G>A | p.Arg476Gln | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1668/4254 | 1427/3840 | 476/1279 | chr3 | 47420690 | ||
| chr3:47420693
|
T | A | 1 | a0007 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.1424A>T | p.Glu475Val | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1665/4254 | 1424/3840 | 475/1279 | chr3 | 47420693 | ||
| chr3:47420694
|
C | G | 1 | a0007 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.1423G>C | p.Glu475Gln | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1664/4254 | 1423/3840 | 475/1279 | chr3 | 47420694 | ||
| chr3:47420697
|
A | C | 1 | a0007 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.1420T>G | p.Tyr474Asp | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1661/4254 | 1420/3840 | 474/1279 | chr3 | 47420697 | ||
| chr3:47428637
|
T | C | 1 | a0013 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.286A>G | p.Ile96Val | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/23 | 527/4254 | 286/3840 | 96/1279 | chr3 | 47428637 | ||
| chr3:47435087
|
G | A | 1 | a0006 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.173C>T | p.Thr58Ile | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/23 | 414/4254 | 173/3840 | 58/1279 | chr3 | 47435087 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:47414240
|
C | T | 1 | a0001c0005 | 3 | HG02258.hp1 HG03098.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.3534G>A | p.Leu1178Leu | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 22/23 | 3775/4254 | 3534/3840 | 1178/1279 | chr3 | 47414240 | ||
| chr3:47418357
|
C | T | 1 | a0001c0008 | 2 | HG01934.hp1 HG02486.hp1 |
synonymous_variant | LOW | c.2295G>A | p.Thr765Thr | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 15/23 | 2536/4254 | 2295/3840 | 765/1279 | chr3 | 47418357 | ||
| chr3:47418402
|
G | A | 1 | a0001c0018 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2250C>T | p.Arg750Arg | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 15/23 | 2491/4254 | 2250/3840 | 750/1279 | chr3 | 47418402 | ||
| chr3:47419387
|
T | C | 1 | a0001c0019 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1881A>G | p.Lys627Lys | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/23 | 2122/4254 | 1881/3840 | 627/1279 | chr3 | 47419387 | ||
| chr3:47419582
|
G | A | 1 | a0001c0008 | 2 | HG01934.hp1 HG02486.hp1 |
synonymous_variant | LOW | c.1686C>T | p.Pro562Pro | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/23 | 1927/4254 | 1686/3840 | 562/1279 | chr3 | 47419582 | ||
| chr3:47420692
|
C | T | 1 | a0007c0012 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.1425G>A | p.Glu475Glu | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1666/4254 | 1425/3840 | 475/1279 | chr3 | 47420692 | ||
| chr3:47420695
|
G | A | 1 | a0007c0012 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.1422C>T | p.Tyr474Tyr | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1663/4254 | 1422/3840 | 474/1279 | chr3 | 47420695 | ||
| chr3:47420701
|
C | T | 1 | a0007c0012 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.1416G>A | p.Thr472Thr | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1657/4254 | 1416/3840 | 472/1279 | chr3 | 47420701 | ||
| chr3:47420710
|
T | C | 21 | a0001c0001a0001c0005a0001c0008others(18): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
synonymous_variant | LOW | c.1407A>G | p.Gly469Gly | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1648/4254 | 1407/3840 | 469/1279 | chr3 | 47420710 | ||
| chr3:47423979
|
C | T | 1 | a0002c0011 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1104G>A | p.Val368Val | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/23 | 1345/4254 | 1104/3840 | 368/1279 | chr3 | 47423979 | ||
| chr3:47427562
|
C | G | 1 | a0001c0010 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.516G>C | p.Leu172Leu | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 5/23 | 757/4254 | 516/3840 | 172/1279 | chr3 | 47427562 | ||
| chr3:47428545
|
C | T | 1 | a0001c0009 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.378G>A | p.Val126Val | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/23 | 619/4254 | 378/3840 | 126/1279 | chr3 | 47428545 | ||
| chr3:47442883
|
G | A | 1 | a0001c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.111C>T | p.Ile37Ile | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/23 | 352/4254 | 111/3840 | 37/1279 | chr3 | 47442883 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:47413771
|
G | A | 1 | a0001c0001t0005 | 2 | HG01261.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*83C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 23/23 | 83 | chr3 | 47413771 | |||||
| chr3:47413783
|
C | A | 1 | a0002c0002t0008 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 23/23 | 71 | chr3 | 47413783 | |||||
| chr3:47413804
|
G | GGCCCC | 1 | a0001c0001t0003 | 15 | HG00408.hp2 HG01928.hp2 HG01952.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*45_*49dupGGGGC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 23/23 | 49 | chr3 | 47413804 | |||||
| chr3:47475809
|
A | T | 1 | a0001c0001t0007 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-109T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/23 | 32816 | chr3 | 47475809 | |||||
| chr3:47475812
|
A | T | 1 | a0001c0001t0006 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-112T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/23 | 32819 | chr3 | 47475812 | |||||
| chr3:47475823
|
T | TGCG | 1 | a0002c0002t0004 | 3 | HG01074.hp1 HG02965.hp1 NA18906.hp2 |
5_prime_UTR_variant | MODIFIER | c.-126_-124dupCGC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/23 | 32831 | chr3 | 47475823 | |||||
| chr3:47475926
|
T | C | 2 | a0001c0001t0002a0001c0018t0002 | 17 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-226A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/23 | 32933 | chr3 | 47475926 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:47414448
|
T | G | 1 | a0001c0005t0001g0188 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3388-62A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 21/22 | chr3 | 47414448 | ||||||
| chr3:47414566
|
G | A | 2 | a0002c0002t0001g0156a0002c0002t0001g0168 | 2 | HG01070.hp1 HG01074.hp2 |
splice_region_variant&intron_variant | LOW | c.3387+6C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 21/22 | chr3 | 47414566 | ||||||
| chr3:47414735
|
T | C | 296 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.3307-83A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 20/22 | chr3 | 47414735 | ||||||
| chr3:47414761
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3306+66G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 20/22 | chr3 | 47414761 | ||||||
| chr3:47414800
|
G | GCACCCAA others(4): Show |
1 | a0002c0002t0001g0137 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3306+16_3306+26dup others(11): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 20/22 | chr3 | 47414800 | ||||||
| chr3:47415068
|
T | C | 2 | a0001c0001t0001g0044a0001c0019t0001g0046 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3139+30A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 19/22 | chr3 | 47415068 | ||||||
| chr3:47415199
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG04199.hp2 NA19010.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3057-19A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415199 | ||||||
| chr3:47415384
|
G | A | 2 | a0001c0001t0001g0235a0001c0001t0001g0257 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.3057-204C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415384 | ||||||
| chr3:47415386
|
A | G | 2 | a0002c0002t0001g0126a0002c0002t0001g0129 | 2 | HG00558.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.3057-206T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415386 | ||||||
| chr3:47415399
|
G | A | 1 | a0002c0002t0001g0090 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3057-219C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415399 | ||||||
| chr3:47415465
|
A | G | 1 | a0001c0001t0002g0298 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3057-285T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415465 | ||||||
| chr3:47415544
|
A | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | NA19010.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3057-364T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415544 | ||||||
| chr3:47415614
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3057-434G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415614 | ||||||
| chr3:47415917
|
C | T | 1 | a0002c0002t0001g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3057-737G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415917 | ||||||
| chr3:47416098
|
C | T | 3 | a0001c0001t0001g0228a0001c0005t0001g0195a0001c0005t0001g0196 | 3 | HG02132.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3057-918G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416098 | ||||||
| chr3:47416099
|
G | A | 2 | a0001c0001t0005g0236a0001c0001t0005g0238 | 2 | HG01261.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3057-919C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416099 | ||||||
| chr3:47416228
|
C | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0271 | 2 | HG00738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3056+894G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416228 | ||||||
| chr3:47416311
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0208a0011c0017t0001g0261 | 3 | HG02155.hp2 NA18966.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.3056+811G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416311 | ||||||
| chr3:47416613
|
C | T | 1 | a0002c0002t0001g0112 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3056+509G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416613 | ||||||
| chr3:47416615
|
C | CT | 13 | a0001c0001t0001g0255a0001c0001t0001g0271a0001c0001t0001g0283others(10): Show | 13 | HG01981.hp2 HG02486.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.3056+506dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | ||||||
| chr3:47416615
|
C | CTTTTTTT others(167): Show |
1 | a0002c0002t0001g0063 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3056+506_3056+507i others(176): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | ||||||
| chr3:47416615
|
C | CTTTTTTT others(178): Show |
1 | a0002c0002t0001g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3056+506_3056+507i others(187): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | ||||||
| chr3:47416615
|
CT | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0022others(69): Show | 72 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.3056+506delA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | ||||||
| chr3:47416615
|
CTT | C | 74 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0026others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.3056+505_3056+506d others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | ||||||
| chr3:47416615
|
CTTTTTTT others(1): Show |
C | 41 | a0002c0002t0001g0050a0002c0002t0001g0059a0002c0002t0001g0060others(38): Show | 41 | HG00544.hp2 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.3056+499_3056+506d others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | ||||||
| chr3:47416615
|
CTTTTTTT others(2): Show |
C | 78 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0051others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.3056+498_3056+506d others(11): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | ||||||
| chr3:47416615
|
CTTTTTTT others(3): Show |
C | 2 | a0002c0002t0001g0082a0002c0002t0001g0167 | 2 | HG00597.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3056+497_3056+506d others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | ||||||
| chr3:47416696
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3056+426C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416696 | ||||||
| chr3:47416712
|
C | T | 1 | a0002c0002t0001g0054 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3056+410G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416712 | ||||||
| chr3:47416749
|
C | A | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3056+373G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416749 | ||||||
| chr3:47416784
|
G | GCCCGGCT others(134): Show |
2 | a0002c0002t0001g0063a0002c0002t0001g0098 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3056+337_3056+338i others(143): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416784 | ||||||
| chr3:47416787
|
C | T | 1 | a0002c0002t0008g0113 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3056+335G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416787 | ||||||
| chr3:47416788
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3056+334C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416788 | ||||||
| chr3:47416820
|
G | T | 1 | a0011c0017t0001g0261 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3056+302C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416820 | ||||||
| chr3:47416869
|
G | A | 1 | a0001c0022t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3056+253C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416869 | ||||||
| chr3:47417260
|
C | T | 12 | a0002c0002t0001g0050a0002c0002t0001g0053a0002c0002t0001g0064others(9): Show | 12 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.2970+44G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 17/22 | chr3 | 47417260 | ||||||
| chr3:47417850
|
A | AGAGGGGG others(4): Show |
1 | a0011c0017t0001g0261 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2448-35_2448-25dup others(11): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417850 | ||||||
| chr3:47417860
|
C | T | 1 | a0001c0019t0001g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2448-34G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417860 | ||||||
| chr3:47417866
|
A | AG | 9 | a0001c0001t0001g0207a0001c0001t0001g0233a0001c0001t0001g0256others(6): Show | 9 | HG00597.hp2 HG01433.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.2448-41dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417866 | ||||||
| chr3:47417882
|
G | GCA | 123 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0050others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.2448-57_2448-56ins others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417882 | ||||||
| chr3:47417890
|
C | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.2448-64G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417890 | ||||||
| chr3:47417893
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0007g0002 | 2 | HG02559.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2448-67C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417893 | ||||||
| chr3:47417894
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0007g0002 | 2 | HG02559.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2448-68C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGGTGAGA others(15): Show |
2 | a0001c0001t0001g0255a0001c0001t0002g0303 | 2 | HG01981.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGGTGAGA others(39): Show |
1 | a0002c0002t0001g0172 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(46): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGGTGAGA others(38): Show |
2 | a0002c0002t0001g0097a0002c0002t0001g0143 | 2 | HG03942.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAG others(14): Show |
153 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(21): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAG others(35): Show |
1 | a0001c0001t0001g0230 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(42): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAG others(38): Show |
2 | a0002c0002t0001g0120a0002c0002t0001g0150 | 2 | NA18961.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAG others(37): Show |
102 | a0001c0001t0001g0067a0001c0001t0001g0107a0001c0001t0001g0217others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(44): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAG others(60): Show |
1 | a0002c0002t0001g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(67): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAG others(38): Show |
2 | a0002c0002t0001g0059a0002c0002t0001g0123 | 2 | HG02083.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAG others(38): Show |
6 | a0002c0002t0001g0071a0002c0002t0001g0121a0002c0002t0001g0125others(3): Show | 6 | HG01256.hp1 HG01934.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAG others(15): Show |
1 | a0001c0001t0002g0304 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAG others(15): Show |
1 | a0001c0001t0001g0240 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAG others(39): Show |
2 | a0002c0002t0001g0068a0009c0014t0001g0128 | 2 | HG02027.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(46): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAG others(38): Show |
3 | a0002c0002t0001g0064a0002c0002t0001g0092a0002c0002t0001g0105 | 3 | HG01433.hp1 HG02148.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGAT others(38): Show |
1 | a0002c0002t0001g0131 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417894
|
G | GGTGAGGG others(35): Show |
2 | a0002c0002t0001g0087a0002c0002t0001g0088 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(42): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | ||||||
| chr3:47417900
|
A | AGGGGGCG others(15): Show |
1 | a0001c0001t0001g0268 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2448-75_2448-74ins others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417900 | ||||||
| chr3:47417901
|
G | GGGGGCGG others(13): Show |
2 | a0001c0001t0001g0136a0011c0017t0001g0261 | 2 | NA18972.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2448-76_2448-75ins others(20): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417901 | ||||||
| chr3:47417903
|
G | GGGCGGGG others(15): Show |
1 | a0002c0002t0001g0227 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2448-78_2448-77ins others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417903 | ||||||
| chr3:47417908
|
T | G | 1 | a0002c0002t0001g0129 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2448-82A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417908 | ||||||
| chr3:47417909
|
G | GGGAGGGG others(36): Show |
1 | a0002c0002t0001g0129 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2448-84_2448-83ins others(43): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417909 | ||||||
| chr3:47417933
|
A | AG | 17 | a0001c0001t0001g0040a0001c0001t0001g0136a0001c0001t0001g0174others(14): Show | 17 | HG00558.hp2 HG00621.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.2448-108dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417933 | ||||||
| chr3:47417939
|
T | G | 3 | a0002c0002t0001g0065a0002c0002t0001g0068a0002c0002t0001g0123 | 3 | HG02083.hp2 HG02738.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.2448-113A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417939 | ||||||
| chr3:47417939
|
T | TG | 18 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0178others(15): Show | 18 | HG00673.hp1 HG00741.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.2448-114dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417939 | ||||||
| chr3:47417939
|
T | TGGGGGGA others(15): Show |
2 | a0001c0005t0001g0195a0001c0005t0001g0196 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2448-135_2448-114d others(24): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417939 | ||||||
| chr3:47417957
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2448-131G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417957 | ||||||
| chr3:47417958
|
G | A | 2 | a0002c0002t0001g0095a0002c0002t0001g0099 | 2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2448-132C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417958 | ||||||
| chr3:47417962
|
T | G | 1 | a0002c0002t0001g0162 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2448-136A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417962 | ||||||
| chr3:47417969
|
A | AG | 13 | a0001c0001t0001g0222a0001c0001t0001g0240a0001c0001t0001g0241others(10): Show | 13 | HG00642.hp1 HG01192.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2448-144dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417969 | ||||||
| chr3:47417970
|
G | A | 1 | a0002c0002t0001g0079 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2448-144C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417970 | ||||||
| chr3:47417978
|
C | CG | 8 | a0001c0001t0001g0136a0001c0001t0001g0222a0001c0001t0001g0239others(5): Show | 8 | HG00621.hp2 HG01175.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.2448-153dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417978 | ||||||
| chr3:47417990
|
A | AG | 6 | a0001c0001t0001g0027a0001c0001t0001g0192a0001c0001t0001g0208others(3): Show | 6 | HG01496.hp1 HG02027.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.2447+143dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417990 | ||||||
| chr3:47417995
|
G | C | 1 | a0001c0001t0001g0232 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2447+139C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417995 | ||||||
| chr3:47417998
|
C | CG | 15 | a0001c0001t0001g0034a0001c0001t0001g0136a0001c0001t0001g0205others(12): Show | 15 | HG00741.hp1 HG00741.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.2447+135dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417998 | ||||||
| chr3:47418004
|
T | G | 4 | a0001c0001t0001g0181a0001c0001t0001g0185a0001c0001t0001g0207others(1): Show | 4 | HG00597.hp2 HG01261.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.2447+130A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418004 | ||||||
| chr3:47418004
|
T | TG | 19 | a0001c0001t0001g0067a0001c0001t0001g0237a0001c0001t0001g0242others(16): Show | 19 | HG00642.hp2 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2447+129dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418004 | ||||||
| chr3:47418039
|
C | T | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2447+95G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418039 | ||||||
| chr3:47418074
|
C | CG | 9 | a0001c0001t0001g0027a0002c0002t0001g0082a0002c0002t0001g0092others(6): Show | 9 | HG00597.hp1 HG00621.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2447+59dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418074 | ||||||
| chr3:47418074
|
CG | C | 124 | a0001c0001t0001g0030a0001c0001t0001g0136a0001c0001t0001g0173others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.2447+59delC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418074 | ||||||
| chr3:47418080
|
G | T | 2 | a0001c0001t0001g0281a0011c0017t0001g0261 | 2 | HG00558.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2447+54C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418080 | ||||||
| chr3:47418081
|
T | G | 2 | a0001c0001t0001g0281a0011c0017t0001g0261 | 2 | HG00558.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2447+53A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418081 | ||||||
| chr3:47418084
|
G | T | 1 | a0011c0017t0001g0261 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2447+50C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418084 | ||||||
| chr3:47418852
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1941-9C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/22 | chr3 | 47418852 | ||||||
| chr3:47419064
|
G | A | 1 | a0001c0022t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1941-221C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/22 | chr3 | 47419064 | ||||||
| chr3:47419136
|
AGT | A | 12 | a0002c0002t0001g0050a0002c0002t0001g0053a0002c0002t0001g0064others(9): Show | 12 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1940+190_1940+191d others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/22 | chr3 | 47419136 | ||||||
| chr3:47419140
|
A | C | 12 | a0002c0002t0001g0050a0002c0002t0001g0053a0002c0002t0001g0064others(9): Show | 12 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1940+188T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/22 | chr3 | 47419140 | ||||||
| chr3:47419231
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1940+97A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/22 | chr3 | 47419231 | ||||||
| chr3:47419974
|
C | A | 1 | a0002c0002t0001g0127 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1564-270G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/22 | chr3 | 47419974 | ||||||
| chr3:47420240
|
G | A | 1 | a0002c0002t0001g0064 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1563+314C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/22 | chr3 | 47420240 | ||||||
| chr3:47420329
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1563+225A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/22 | chr3 | 47420329 | ||||||
| chr3:47420409
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1563+145C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/22 | chr3 | 47420409 | ||||||
| chr3:47420823
|
C | T | 1 | a0005c0007t0001g0116 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1345-51G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 11/22 | chr3 | 47420823 | ||||||
| chr3:47421084
|
C | T | 1 | a0002c0002t0001g0117 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1246-55G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421084 | ||||||
| chr3:47421097
|
A | G | 294 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1246-68T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421097 | ||||||
| chr3:47421236
|
C | G | 1 | a0001c0001t0001g0210 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1246-207G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421236 | ||||||
| chr3:47421277
|
T | C | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1246-248A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421277 | ||||||
| chr3:47421324
|
A | C | 1 | a0001c0001t0001g0241 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1246-295T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421324 | ||||||
| chr3:47421326
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1246-297G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421326 | ||||||
| chr3:47421371
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1246-342G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421371 | ||||||
| chr3:47421386
|
G | A | 10 | a0002c0002t0001g0059a0002c0002t0001g0060a0002c0002t0001g0061others(7): Show | 10 | HG00408.hp1 HG00544.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.1246-357C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421386 | ||||||
| chr3:47421531
|
T | C | 1 | a0002c0002t0001g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1246-502A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421531 | ||||||
| chr3:47421790
|
A | T | 2 | a0002c0002t0001g0063a0002c0002t0001g0098 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1245+652T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421790 | ||||||
| chr3:47421794
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(27): Show | 30 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1245+648C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421794 | ||||||
| chr3:47421795
|
C | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1245+647G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421795 | ||||||
| chr3:47421870
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1245+572A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421870 | ||||||
| chr3:47422004
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0257 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1245+438G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47422004 | ||||||
| chr3:47422018
|
G | A | 1 | a0001c0022t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1245+424C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47422018 | ||||||
| chr3:47422077
|
T | C | 130 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1245+365A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47422077 | ||||||
| chr3:47422369
|
C | T | 2 | a0001c0001t0005g0236a0001c0001t0005g0238 | 2 | HG01261.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1245+73G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47422369 | ||||||
| chr3:47422612
|
C | T | 3 | a0001c0005t0001g0188a0001c0005t0001g0195a0001c0005t0001g0196 | 3 | HG02258.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1151-76G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47422612 | ||||||
| chr3:47422628
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1151-92A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47422628 | ||||||
| chr3:47422632
|
A | G | 123 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0050others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1151-96T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47422632 | ||||||
| chr3:47422654
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1151-118C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47422654 | ||||||
| chr3:47422739
|
G | T | 1 | a0001c0022t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1151-203C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47422739 | ||||||
| chr3:47423029
|
TCTAAGGC others(38): Show |
T | 1 | a0002c0002t0001g0252 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1151-538_1151-494d others(47): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423029 | ||||||
| chr3:47423126
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1151-590T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423126 | ||||||
| chr3:47423267
|
T | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1150+666A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423267 | ||||||
| chr3:47423375
|
G | A | 1 | a0001c0001t0003g0244 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1150+558C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423375 | ||||||
| chr3:47423603
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1150+330T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423603 | ||||||
| chr3:47423690
|
A | C | 1 | a0002c0002t0001g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1150+243T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423690 | ||||||
| chr3:47423691
|
G | A | 1 | a0002c0002t0001g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1150+242C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423691 | ||||||
| chr3:47423692
|
C | G | 1 | a0002c0002t0001g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1150+241G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423692 | ||||||
| chr3:47423727
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1150+206G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423727 | ||||||
| chr3:47424179
|
C | A | 1 | a0002c0002t0008g0113 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1038-134G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47424179 | ||||||
| chr3:47424549
|
C | G | 1 | a0002c0002t0001g0092 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1038-504G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47424549 | ||||||
| chr3:47424671
|
A | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1038-626T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47424671 | ||||||
| chr3:47424678
|
T | C | 1 | a0001c0001t0003g0270 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1038-633A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47424678 | ||||||
| chr3:47424695
|
G | A | 5 | a0002c0002t0001g0103a0002c0002t0001g0109a0002c0002t0001g0114others(2): Show | 5 | HG03654.hp2 HG03710.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038-650C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47424695 | ||||||
| chr3:47425036
|
G | A | 1 | a0001c0003t0001g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1037+449C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47425036 | ||||||
| chr3:47425639
|
C | A | 1 | a0001c0001t0002g0289 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.911-28G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 7/22 | chr3 | 47425639 | ||||||
| chr3:47425659
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.911-48C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 7/22 | chr3 | 47425659 | ||||||
| chr3:47425779
|
T | C | 2 | a0001c0001t0001g0044a0001c0019t0001g0046 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.911-168A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 7/22 | chr3 | 47425779 | ||||||
| chr3:47425795
|
C | CAGGAAGG others(10): Show |
1 | a0001c0001t0001g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.910+185_911-185dup others(17): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 7/22 | chr3 | 47425795 | ||||||
| chr3:47426290
|
T | A | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.738-121A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 6/22 | chr3 | 47426290 | ||||||
| chr3:47426771
|
C | T | 124 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0050others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.737+386G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 6/22 | chr3 | 47426771 | ||||||
| chr3:47426854
|
G | A | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.737+303C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 6/22 | chr3 | 47426854 | ||||||
| chr3:47427877
|
G | C | 1 | a0002c0002t0001g0120 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.411-210C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/22 | chr3 | 47427877 | ||||||
| chr3:47428029
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.411-362G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/22 | chr3 | 47428029 | ||||||
| chr3:47428182
|
G | A | 1 | a0001c0003t0001g0006 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.410+331C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/22 | chr3 | 47428182 | ||||||
| chr3:47428239
|
G | A | 2 | a0002c0002t0001g0075a0010c0015t0001g0074 | 2 | NA18947.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.410+274C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/22 | chr3 | 47428239 | ||||||
| chr3:47428345
|
G | A | 1 | a0002c0002t0001g0167 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.410+168C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/22 | chr3 | 47428345 | ||||||
| chr3:47428994
|
G | A | 129 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.253-324C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47428994 | ||||||
| chr3:47429079
|
T | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.253-409A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47429079 | ||||||
| chr3:47429297
|
T | A | 159 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(156): Show | 159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.253-627A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47429297 | ||||||
| chr3:47429354
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.253-684C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47429354 | ||||||
| chr3:47429381
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.253-711G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47429381 | ||||||
| chr3:47430232
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.253-1562G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430232 | ||||||
| chr3:47430288
|
T | C | 2 | a0001c0008t0001g0023a0001c0008t0001g0024 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.253-1618A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430288 | ||||||
| chr3:47430368
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.253-1698G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430368 | ||||||
| chr3:47430513
|
C | A | 1 | a0001c0022t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.253-1843G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430513 | ||||||
| chr3:47430710
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.253-2040G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430710 | ||||||
| chr3:47430743
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0002c0002t0001g0057 | 3 | HG02109.hp2 NA18522.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.253-2073A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430743 | ||||||
| chr3:47431004
|
C | T | 1 | a0002c0002t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.253-2334G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431004 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
2 | a0001c0008t0001g0023a0001c0008t0001g0024 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0170 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
1 | a0001c0009t0001g0267 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
1 | a0001c0001t0001g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
150 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
9 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG01070.hp2 HG01175.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0227 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0153 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0060 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
2 | a0002c0002t0001g0075a0010c0015t0001g0074 | 2 | NA18947.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
31 | a0002c0002t0001g0059a0002c0002t0001g0061a0002c0002t0001g0062others(28): Show | 31 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0155 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
3 | a0002c0002t0001g0131a0002c0002t0001g0132a0002c0002t0001g0133 | 3 | NA18977.hp1 NA18999.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431267
|
T | TACTTAAT others(2661): Show |
83 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0050others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | ||||||
| chr3:47431450
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.253-2780G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431450 | ||||||
| chr3:47431491
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(27): Show | 30 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.253-2821C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431491 | ||||||
| chr3:47431678
|
C | T | 130 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.253-3008G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431678 | ||||||
| chr3:47431756
|
A | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0033others(2): Show | 5 | HG02055.hp1 HG02976.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-3086T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431756 | ||||||
| chr3:47432272
|
G | A | 1 | a0002c0002t0001g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.252+2736C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432272 | ||||||
| chr3:47432314
|
GA | G | 278 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.252+2693delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432314 | ||||||
| chr3:47432420
|
T | C | 1 | a0002c0002t0001g0227 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.252+2588A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432420 | ||||||
| chr3:47432614
|
A | G | 3 | a0002c0002t0004g0285a0002c0002t0004g0286a0002c0002t0004g0287 | 3 | HG01074.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.252+2394T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432614 | ||||||
| chr3:47432634
|
T | C | 16 | a0001c0001t0001g0217a0001c0001t0001g0221a0001c0001t0003g0215others(13): Show | 16 | HG00408.hp2 HG01928.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.252+2374A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432634 | ||||||
| chr3:47432669
|
A | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0239 | 2 | HG01070.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.252+2339T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432669 | ||||||
| chr3:47432842
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.252+2166G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432842 | ||||||
| chr3:47432890
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.252+2118T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432890 | ||||||
| chr3:47433101
|
A | G | 1 | a0002c0002t0001g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.252+1907T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47433101 | ||||||
| chr3:47433259
|
C | T | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.252+1749G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47433259 | ||||||
| chr3:47433499
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252+1509G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47433499 | ||||||
| chr3:47433782
|
C | T | 1 | a0002c0002t0001g0066 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.252+1226G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47433782 | ||||||
| chr3:47433953
|
C | G | 1 | a0001c0001t0001g0276 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.252+1055G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47433953 | ||||||
| chr3:47434234
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.252+774G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47434234 | ||||||
| chr3:47434705
|
C | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(27): Show | 30 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.252+303G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47434705 | ||||||
| chr3:47434740
|
G | C | 1 | a0001c0009t0001g0267 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.252+268C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47434740 | ||||||
| chr3:47435195
|
G | A | 1 | a0002c0002t0001g0142 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.123-58C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435195 | ||||||
| chr3:47435308
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.123-171A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435308 | ||||||
| chr3:47435428
|
TTATAACA others(5): Show |
T | 1 | a0001c0001t0003g0218 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.123-303_123-292del others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435428 | ||||||
| chr3:47435464
|
AAAC | A | 3 | a0002c0002t0001g0097a0002c0002t0001g0143a0002c0002t0001g0146 | 3 | HG00738.hp2 HG03942.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.123-330_123-328del others(3): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435464 | ||||||
| chr3:47435465
|
AACAT | A | 38 | a0001c0001t0001g0107a0002c0002t0001g0051a0002c0002t0001g0052others(35): Show | 38 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.123-332_123-329del others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | ||||||
| chr3:47435465
|
AACATAC | A | 21 | a0002c0002t0001g0050a0002c0002t0001g0059a0002c0002t0001g0060others(18): Show | 21 | HG00408.hp1 HG01106.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.123-334_123-329del others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | ||||||
| chr3:47435465
|
AACATACA others(1): Show |
A | 27 | a0002c0002t0001g0062a0002c0002t0001g0065a0002c0002t0001g0075others(24): Show | 27 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.123-336_123-329del others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | ||||||
| chr3:47435465
|
AACATACA others(3): Show |
A | 13 | a0002c0002t0001g0053a0002c0002t0001g0064a0002c0002t0001g0066others(10): Show | 13 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.123-338_123-329del others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | ||||||
| chr3:47435465
|
AACATACA others(5): Show |
A | 2 | a0002c0002t0001g0158a0003c0004t0001g0140 | 2 | HG00741.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.123-340_123-329del others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | ||||||
| chr3:47435465
|
AACATACA others(9): Show |
A | 1 | a0007c0012t0001g0083 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.123-344_123-329del others(16): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | ||||||
| chr3:47435467
|
CAT | C | 12 | a0001c0001t0001g0067a0002c0002t0001g0054a0002c0002t0001g0058others(9): Show | 12 | HG01346.hp1 HG01884.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-332_123-331del others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435467 | ||||||
| chr3:47435469
|
T | C | 9 | a0002c0002t0001g0088a0002c0002t0001g0089a0002c0002t0001g0097others(6): Show | 9 | HG00738.hp2 HG01106.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-332A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
T | TAC | 10 | a0001c0001t0001g0181a0001c0001t0001g0203a0001c0001t0001g0220others(7): Show | 10 | HG01515.hp2 HG02080.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-334_123-333dup others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
T | TACAC | 5 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0202others(2): Show | 5 | HG01109.hp1 HG01934.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-336_123-333dup others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
T | TACACAC | 19 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0031others(16): Show | 19 | HG01928.hp2 HG01952.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.123-338_123-333dup others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
T | TACACACA others(1): Show |
7 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG02004.hp1 HG02056.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-340_123-333dup others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
T | TACACACA others(3): Show |
9 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0047others(6): Show | 9 | HG00408.hp2 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-342_123-333dup others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
T | TACACACA others(5): Show |
5 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0045others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-344_123-333dup others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
T | TACACACA others(7): Show |
4 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0036others(1): Show | 4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-346_123-333dup others(14): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
T | TACACACA others(9): Show |
1 | a0001c0001t0001g0021 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.123-348_123-333dup others(16): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
TAC | T | 50 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.123-334_123-333del others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
TACAC | T | 8 | a0001c0001t0001g0199a0001c0001t0001g0233a0001c0001t0001g0239others(5): Show | 8 | HG01123.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-336_123-333del others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
TACACAC | T | 31 | a0001c0001t0001g0020a0001c0001t0001g0136a0001c0001t0001g0175others(28): Show | 31 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.123-338_123-333del others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435469
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG02083.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.123-342_123-333del others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | ||||||
| chr3:47435493
|
C | T | 1 | a0002c0002t0001g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.123-356G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435493 | ||||||
| chr3:47435494
|
A | T | 1 | a0002c0002t0001g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.123-357T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435494 | ||||||
| chr3:47435529
|
C | T | 124 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0050others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.123-392G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435529 | ||||||
| chr3:47435774
|
C | T | 1 | a0001c0001t0003g0260 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.123-637G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435774 | ||||||
| chr3:47436038
|
C | T | 4 | a0002c0002t0001g0103a0002c0002t0001g0109a0002c0002t0001g0114others(1): Show | 4 | HG03654.hp2 HG03710.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-901G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436038 | ||||||
| chr3:47436325
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.123-1188G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436325 | ||||||
| chr3:47436408
|
G | A | 1 | a0002c0002t0001g0097 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.123-1271C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436408 | ||||||
| chr3:47436413
|
A | G | 1 | a0002c0002t0001g0086 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.123-1276T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436413 | ||||||
| chr3:47436504
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.123-1367A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436504 | ||||||
| chr3:47436969
|
T | C | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.123-1832A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436969 | ||||||
| chr3:47437213
|
G | A | 3 | a0002c0002t0001g0103a0002c0002t0001g0109a0002c0002t0001g0145 | 3 | HG02559.hp2 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.123-2076C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437213 | ||||||
| chr3:47437340
|
G | A | 65 | a0001c0001t0001g0067a0001c0001t0001g0107a0001c0001t0003g0260others(62): Show | 65 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.123-2203C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437340 | ||||||
| chr3:47437419
|
T | C | 1 | a0002c0002t0001g0162 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.123-2282A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437419 | ||||||
| chr3:47437422
|
C | CA | 234 | a0001c0001t0001g0035a0001c0001t0001g0067a0001c0001t0001g0107others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.123-2286dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437422 | ||||||
| chr3:47437422
|
C | CAA | 16 | a0001c0001t0001g0241a0001c0001t0001g0256a0002c0002t0001g0051others(13): Show | 16 | HG00597.hp1 HG01952.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.123-2287_123-2286d others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437422 | ||||||
| chr3:47437585
|
A | C | 2 | a0002c0002t0001g0095a0002c0002t0001g0099 | 2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.123-2448T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437585 | ||||||
| chr3:47437688
|
G | A | 2 | a0001c0001t0001g0044a0001c0019t0001g0046 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.123-2551C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437688 | ||||||
| chr3:47437777
|
T | C | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123-2640A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437777 | ||||||
| chr3:47437860
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.123-2723C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437860 | ||||||
| chr3:47437862
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.123-2725C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437862 | ||||||
| chr3:47437945
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.123-2808C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437945 | ||||||
| chr3:47438024
|
C | T | 1 | a0001c0022t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.123-2887G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438024 | ||||||
| chr3:47438041
|
G | A | 1 | a0002c0002t0001g0167 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.123-2904C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438041 | ||||||
| chr3:47438245
|
A | C | 130 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.123-3108T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438245 | ||||||
| chr3:47438429
|
A | AGAGAAT | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.123-3293_123-3292i others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438429 | ||||||
| chr3:47438485
|
T | C | 1 | a0001c0010t0001g0180 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.123-3348A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438485 | ||||||
| chr3:47438500
|
AACTTGCT others(3): Show |
A | 3 | a0002c0002t0001g0103a0002c0002t0001g0109a0002c0002t0001g0114 | 3 | HG03654.hp2 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.123-3373_123-3364d others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438500 | ||||||
| chr3:47438580
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.123-3443C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438580 | ||||||
| chr3:47438867
|
A | G | 24 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0208others(21): Show | 24 | HG00408.hp2 HG01515.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.123-3730T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438867 | ||||||
| chr3:47439034
|
G | C | 130 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.122+3838C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439034 | ||||||
| chr3:47439036
|
T | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.122+3836A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439036 | ||||||
| chr3:47439148
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122+3724G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439148 | ||||||
| chr3:47439170
|
A | G | 1 | a0001c0001t0003g0259 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.122+3702T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439170 | ||||||
| chr3:47439171
|
G | A | 1 | a0001c0001t0003g0259 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.122+3701C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439171 | ||||||
| chr3:47439621
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0257 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.122+3251G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439621 | ||||||
| chr3:47440039
|
T | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0269 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.122+2833A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440039 | ||||||
| chr3:47440436
|
A | G | 1 | a0001c0001t0003g0259 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.122+2436T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440436 | ||||||
| chr3:47440437
|
G | A | 1 | a0001c0001t0003g0259 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.122+2435C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440437 | ||||||
| chr3:47440448
|
T | C | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.122+2424A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440448 | ||||||
| chr3:47440609
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.122+2263T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440609 | ||||||
| chr3:47440658
|
C | T | 1 | a0001c0001t0003g0259 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.122+2214G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440658 | ||||||
| chr3:47440732
|
C | T | 85 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0050others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.122+2140G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440732 | ||||||
| chr3:47440774
|
C | T | 1 | a0002c0002t0001g0064 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.122+2098G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440774 | ||||||
| chr3:47440879
|
T | G | 1 | a0001c0001t0001g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.122+1993A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440879 | ||||||
| chr3:47440964
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122+1908G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440964 | ||||||
| chr3:47441125
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122+1747G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441125 | ||||||
| chr3:47441337
|
G | A | 1 | a0001c0001t0002g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122+1535C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441337 | ||||||
| chr3:47441516
|
G | A | 1 | a0002c0002t0001g0065 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.122+1356C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441516 | ||||||
| chr3:47441526
|
C | T | 1 | a0002c0002t0001g0061 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.122+1346G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441526 | ||||||
| chr3:47441874
|
C | CT | 150 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(147): Show | 150 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.122+997dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441874 | ||||||
| chr3:47441874
|
C | CTT | 16 | a0001c0001t0001g0041a0001c0001t0001g0136a0001c0001t0001g0175others(13): Show | 16 | HG01175.hp2 HG01934.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.122+996_122+997dup others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441874 | ||||||
| chr3:47442236
|
A | C | 1 | a0001c0022t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122+636T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442236 | ||||||
| chr3:47442501
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.122+371G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442501 | ||||||
| chr3:47442525
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.122+347G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442525 | ||||||
| chr3:47442535
|
G | C | 1 | a0002c0002t0001g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122+337C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442535 | ||||||
| chr3:47442636
|
G | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.122+236C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442636 | ||||||
| chr3:47442765
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.122+107A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442765 | ||||||
| chr3:47442840
|
C | T | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.122+32G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442840 | ||||||
| chr3:47443149
|
C | A | 1 | a0001c0008t0001g0024 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-98-58G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443149 | ||||||
| chr3:47443233
|
TAC | T | 14 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0036others(11): Show | 14 | HG01975.hp1 HG02109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-98-144_-98-143del others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | ||||||
| chr3:47443233
|
TACAC | T | 42 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.-98-146_-98-143del others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | ||||||
| chr3:47443233
|
TACACAC | T | 111 | a0001c0001t0001g0067a0001c0001t0001g0136a0001c0001t0001g0173others(108): Show | 111 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.-98-148_-98-143del others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | ||||||
| chr3:47443233
|
TACACACA others(1): Show |
T | 69 | a0001c0001t0001g0107a0001c0001t0001g0198a0001c0003t0001g0006others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-98-150_-98-143del others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | ||||||
| chr3:47443233
|
TACACACA others(3): Show |
T | 8 | a0001c0001t0001g0003a0001c0001t0001g0217a0001c0001t0006g0001others(5): Show | 8 | HG02027.hp1 HG02572.hp2 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.-98-152_-98-143del others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | ||||||
| chr3:47443233
|
TACACACA others(5): Show |
T | 14 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(11): Show | 14 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-98-154_-98-143del others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | ||||||
| chr3:47443233
|
TACACACA others(7): Show |
T | 2 | a0002c0002t0001g0094a0002c0002t0001g0154 | 2 | HG02132.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.-98-156_-98-143del others(14): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | ||||||
| chr3:47443264
|
ACACACAC others(9): Show |
A | 1 | a0001c0001t0001g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-98-189_-98-174del others(16): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443264 | ||||||
| chr3:47443266
|
ACACACAC others(7): Show |
A | 1 | a0002c0002t0001g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-98-189_-98-176del others(14): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443266 | ||||||
| chr3:47443268
|
A | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0265 | 2 | HG01975.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-98-177T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443268 | ||||||
| chr3:47443268
|
ACACACAC others(3): Show |
A | 1 | a0002c0002t0001g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-98-187_-98-178del others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443268 | ||||||
| chr3:47443270
|
A | T | 9 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0221others(6): Show | 9 | HG00642.hp1 HG01975.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-98-179T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443270 | ||||||
| chr3:47443272
|
A | T | 19 | a0001c0001t0001g0179a0001c0001t0001g0200a0001c0001t0001g0201others(16): Show | 19 | HG00642.hp1 HG01168.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.-98-181T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443272 | ||||||
| chr3:47443272
|
ACACACT | A | 6 | a0001c0003t0001g0004a0002c0002t0001g0102a0002c0002t0001g0115others(3): Show | 6 | HG00735.hp1 HG01192.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-98-187_-98-182del others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443272 | ||||||
| chr3:47443274
|
A | T | 140 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0001g0136others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-98-183T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443274 | ||||||
| chr3:47443276
|
A | T | 199 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0067others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-98-185T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443276 | ||||||
| chr3:47443278
|
T | A | 2 | a0001c0001t0001g0028a0001c0008t0001g0023 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-98-187A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443278 | ||||||
| chr3:47443306
|
T | C | 272 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-98-215A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443306 | ||||||
| chr3:47443306
|
T | TCC | 3 | a0001c0001t0001g0179a0001c0001t0001g0256a0001c0001t0001g0265 | 3 | HG01168.hp1 NA18977.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-98-216_-98-215ins others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443306 | ||||||
| chr3:47443306
|
T | TCTCTCCC others(5): Show |
5 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0230others(2): Show | 5 | HG01515.hp2 HG02056.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.-98-216_-98-215ins others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443306 | ||||||
| chr3:47443306
|
T | TCTCTCTC others(7): Show |
3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0208 | 3 | HG02155.hp2 NA18966.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-98-216_-98-215ins others(14): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443306 | ||||||
| chr3:47443306
|
T | TCTCTCTC others(6): Show |
1 | a0001c0001t0001g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-98-216_-98-215ins others(13): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443306 | ||||||
| chr3:47443307
|
C | T | 156 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(153): Show | 156 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.-98-216G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443307 | ||||||
| chr3:47443462
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-98-371G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443462 | ||||||
| chr3:47443463
|
C | A | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-98-372G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443463 | ||||||
| chr3:47443463
|
C | G | 124 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0050others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-98-372G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443463 | ||||||
| chr3:47443539
|
C | T | 77 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(74): Show | 77 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-98-448G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443539 | ||||||
| chr3:47444156
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-98-1065C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47444156 | ||||||
| chr3:47444157
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-98-1066T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47444157 | ||||||
| chr3:47444857
|
T | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-98-1766A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47444857 | ||||||
| chr3:47445069
|
G | A | 2 | a0001c0008t0001g0023a0001c0008t0001g0024 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-98-1978C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445069 | ||||||
| chr3:47445077
|
A | G | 1 | a0001c0005t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-98-1986T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445077 | ||||||
| chr3:47445142
|
T | C | 130 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-98-2051A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445142 | ||||||
| chr3:47445243
|
C | CT | 6 | a0001c0018t0002g0301a0002c0002t0001g0068a0002c0002t0001g0095others(3): Show | 6 | HG00741.hp1 HG02055.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-98-2153dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445243 | ||||||
| chr3:47445243
|
CT | C | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(16): Show | 19 | HG01943.hp2 HG01952.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-98-2153delA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445243 | ||||||
| chr3:47445292
|
G | A | 2 | a0001c0001t0001g0044a0001c0019t0001g0046 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-98-2201C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445292 | ||||||
| chr3:47445328
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-98-2237G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445328 | ||||||
| chr3:47445405
|
C | G | 2 | a0001c0001t0001g0044a0001c0019t0001g0046 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-98-2314G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445405 | ||||||
| chr3:47445492
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-98-2401C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445492 | ||||||
| chr3:47445657
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-98-2566G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445657 | ||||||
| chr3:47445874
|
A | AT | 18 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(15): Show | 18 | HG00099.hp2 HG00741.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-98-2784dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445874 | ||||||
| chr3:47445876
|
T | A | 1 | a0002c0002t0001g0100 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-98-2785A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445876 | ||||||
| chr3:47445895
|
G | A | 1 | a0002c0002t0001g0100 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-98-2804C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445895 | ||||||
| chr3:47445897
|
G | A | 1 | a0002c0002t0001g0100 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-98-2806C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445897 | ||||||
| chr3:47445931
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-98-2840C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445931 | ||||||
| chr3:47446120
|
C | T | 1 | a0001c0001t0006g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-98-3029G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47446120 | ||||||
| chr3:47446583
|
G | A | 1 | a0001c0008t0001g0024 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-98-3492C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47446583 | ||||||
| chr3:47446765
|
G | A | 1 | a0002c0002t0001g0077 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-98-3674C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47446765 | ||||||
| chr3:47446806
|
G | T | 1 | a0002c0002t0001g0120 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-98-3715C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47446806 | ||||||
| chr3:47447224
|
G | A | 303 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-98-4133C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47447224 | ||||||
| chr3:47447298
|
C | T | 4 | a0003c0004t0001g0073a0003c0004t0001g0140a0004c0006t0001g0072others(1): Show | 4 | HG00408.hp1 HG00544.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-98-4207G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47447298 | ||||||
| chr3:47447387
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-98-4296G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47447387 | ||||||
| chr3:47447418
|
G | A | 1 | a0002c0002t0001g0080 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-98-4327C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47447418 | ||||||
| chr3:47447801
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0234 | 2 | NA18967.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-98-4710C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47447801 | ||||||
| chr3:47448002
|
C | CA | 19 | a0001c0001t0001g0041a0001c0001t0001g0173a0001c0001t0001g0174others(16): Show | 19 | HG00597.hp2 HG01261.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.-98-4912dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448002 | ||||||
| chr3:47448002
|
CA | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-98-4912delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448002 | ||||||
| chr3:47448002
|
CAA | C | 52 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(49): Show | 52 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-98-4913_-98-4912d others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448002 | ||||||
| chr3:47448002
|
CAAA | C | 88 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0107others(85): Show | 88 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.-98-4914_-98-4912d others(5): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448002 | ||||||
| chr3:47448312
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-98-5221C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448312 | ||||||
| chr3:47448330
|
C | T | 124 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0050others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-98-5239G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448330 | ||||||
| chr3:47448395
|
G | C | 129 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.-98-5304C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448395 | ||||||
| chr3:47448724
|
GTTCAT | G | 130 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-98-5638_-98-5634d others(7): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448724 | ||||||
| chr3:47448833
|
G | A | 1 | a0002c0002t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-98-5742C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448833 | ||||||
| chr3:47448931
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-98-5840T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448931 | ||||||
| chr3:47449003
|
G | A | 124 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0050others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-98-5912C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449003 | ||||||
| chr3:47449177
|
TGCTGTTT others(2766): Show |
T | 130 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-98-8859_-98-6087d others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449177 | ||||||
| chr3:47449199
|
G | A | 1 | a0001c0008t0001g0024 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-98-6108C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449199 | ||||||
| chr3:47449222
|
C | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-98-6131G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449222 | ||||||
| chr3:47449535
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-98-6444C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449535 | ||||||
| chr3:47449697
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-98-6606G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449697 | ||||||
| chr3:47449811
|
T | A | 2 | a0002c0002t0001g0095a0002c0002t0001g0099 | 2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-98-6720A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449811 | ||||||
| chr3:47450083
|
C | T | 1 | a0001c0003t0001g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-98-6992G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450083 | ||||||
| chr3:47450143
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-98-7052C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450143 | ||||||
| chr3:47450457
|
G | C | 1 | a0002c0002t0001g0100 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-98-7366C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450457 | ||||||
| chr3:47450511
|
G | GT | 45 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(42): Show | 45 | HG01175.hp1 HG01934.hp1 HG01981.hp1 others(42): Show |
intron_variant | MODIFIER | c.-98-7421dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450511 | ||||||
| chr3:47450647
|
G | A | 1 | a0001c0003t0001g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-98-7556C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450647 | ||||||
| chr3:47450772
|
G | C | 1 | a0002c0002t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-98-7681C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450772 | ||||||
| chr3:47450863
|
T | G | 1 | a0001c0001t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-98-7772A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450863 | ||||||
| chr3:47451143
|
G | A | 2 | a0002c0002t0001g0075a0010c0015t0001g0074 | 2 | NA18947.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-98-8052C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47451143 | ||||||
| chr3:47451201
|
C | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(156): Show | 159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.-98-8110G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47451201 | ||||||
| chr3:47451394
|
CT | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-98-8304delA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47451394 | ||||||
| chr3:47452052
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG00544.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-98-8961G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452052 | ||||||
| chr3:47452667
|
T | C | 77 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(74): Show | 77 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-98-9576A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452667 | ||||||
| chr3:47452813
|
G | A | 130 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-98-9722C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452813 | ||||||
| chr3:47452861
|
G | A | 1 | a0002c0002t0001g0110 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-98-9770C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452861 | ||||||
| chr3:47452890
|
G | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(155): Show | 158 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.-98-9799C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452890 | ||||||
| chr3:47452926
|
CA | C | 287 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-98-9836delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452926 | ||||||
| chr3:47453252
|
C | T | 2 | a0001c0001t0002g0292a0001c0001t0002g0293 | 2 | HG00140.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-98-10161G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47453252 | ||||||
| chr3:47453379
|
T | TA | 13 | a0002c0002t0001g0051a0002c0002t0001g0053a0002c0002t0001g0064others(10): Show | 13 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-10289dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47453379 | ||||||
| chr3:47453397
|
G | GA | 288 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-98-10307dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47453397 | ||||||
| chr3:47454065
|
C | G | 2 | a0001c0001t0001g0044a0001c0019t0001g0046 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-98-10974G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454065 | ||||||
| chr3:47454163
|
T | C | 1 | a0003c0004t0001g0140 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-98-11072A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454163 | ||||||
| chr3:47454194
|
T | C | 4 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG00597.hp2 HG04199.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-98-11103A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454194 | ||||||
| chr3:47454205
|
A | C | 1 | a0002c0002t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-98-11114T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454205 | ||||||
| chr3:47454361
|
C | G | 1 | a0001c0003t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-98-11270G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454361 | ||||||
| chr3:47454688
|
C | T | 3 | a0002c0002t0001g0062a0002c0002t0001g0094a0002c0002t0001g0154 | 3 | HG02132.hp2 NA18951.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-98-11597G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454688 | ||||||
| chr3:47454748
|
A | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0035others(3): Show | 6 | HG02280.hp1 HG03130.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-98-11657T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454748 | ||||||
| chr3:47454792
|
C | T | 2 | a0001c0001t0001g0044a0001c0019t0001g0046 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-98-11701G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454792 | ||||||
| chr3:47454880
|
T | A | 1 | a0002c0002t0001g0111 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-98-11789A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454880 | ||||||
| chr3:47454974
|
G | A | 62 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(59): Show | 62 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-98-11883C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454974 | ||||||
| chr3:47455062
|
C | CAT | 14 | a0001c0003t0001g0004a0002c0002t0001g0061a0002c0002t0001g0064others(11): Show | 14 | HG00099.hp2 HG00621.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.-98-11973_-98-1197 others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | ||||||
| chr3:47455062
|
C | CATAT | 5 | a0002c0002t0001g0082a0002c0002t0001g0143a0002c0002t0001g0145others(2): Show | 5 | HG00597.hp1 HG02559.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-98-11975_-98-1197 others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | ||||||
| chr3:47455062
|
CAT | C | 31 | a0001c0001t0007g0002a0001c0003t0001g0010a0001c0003t0001g0014others(28): Show | 31 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-98-11973_-98-1197 others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | ||||||
| chr3:47455062
|
CATAT | C | 28 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0008t0001g0023others(25): Show | 28 | HG00609.hp1 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.-98-11975_-98-1197 others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | ||||||
| chr3:47455062
|
CATATAT | C | 50 | a0001c0001t0001g0107a0001c0001t0001g0181a0001c0001t0001g0182others(47): Show | 50 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-98-11977_-98-1197 others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | ||||||
| chr3:47455062
|
CATATATA others(1): Show |
C | 33 | a0001c0001t0001g0019a0001c0001t0001g0179a0001c0001t0001g0184others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.-98-11979_-98-1197 others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | ||||||
| chr3:47455062
|
CATATATA others(3): Show |
C | 33 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(30): Show | 33 | HG00408.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-98-11981_-98-1197 others(14): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | ||||||
| chr3:47455062
|
CATATATA others(5): Show |
C | 85 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(82): Show | 85 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.-98-11983_-98-1197 others(16): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | ||||||
| chr3:47455062
|
CATATATA others(7): Show |
C | 2 | a0001c0001t0001g0169a0001c0001t0001g0283 | 2 | HG02922.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-98-11985_-98-1197 others(18): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | ||||||
| chr3:47455062
|
CATATATA others(15): Show |
C | 1 | a0002c0002t0001g0053 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-98-11993_-98-1197 others(26): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | ||||||
| chr3:47455084
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0203 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-98-12004_-98-1199 others(15): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455084 | ||||||
| chr3:47455094
|
T | A | 29 | a0001c0001t0001g0194a0001c0001t0001g0198a0001c0001t0001g0199others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-98-12003A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455094 | ||||||
| chr3:47455146
|
A | G | 1 | a0002c0002t0001g0064 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-98-12055T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455146 | ||||||
| chr3:47455332
|
C | T | 1 | a0002c0002t0001g0065 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-98-12241G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455332 | ||||||
| chr3:47455364
|
A | G | 297 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-98-12273T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455364 | ||||||
| chr3:47455517
|
C | T | 21 | a0002c0002t0001g0050a0002c0002t0001g0051a0002c0002t0001g0053others(18): Show | 21 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.-98-12426G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455517 | ||||||
| chr3:47455594
|
C | CA | 25 | a0001c0001t0001g0044a0001c0001t0001g0134a0001c0001t0001g0175others(22): Show | 25 | HG01106.hp2 HG01175.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.-98-12504dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455594 | ||||||
| chr3:47455594
|
CA | C | 13 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0035others(10): Show | 13 | HG01069.hp1 HG02280.hp1 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-12504delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455594 | ||||||
| chr3:47455759
|
C | T | 1 | a0002c0002t0001g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-98-12668G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455759 | ||||||
| chr3:47456041
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0240 | 2 | HG02135.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-98-12950C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47456041 | ||||||
| chr3:47456362
|
T | G | 1 | a0001c0001t0003g0273 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-98-13271A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47456362 | ||||||
| chr3:47456851
|
A | G | 2 | a0002c0002t0001g0121a0002c0002t0001g0122 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-98-13760T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47456851 | ||||||
| chr3:47456857
|
G | A | 2 | a0001c0001t0002g0304a0001c0019t0001g0046 | 2 | HG01192.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-98-13766C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47456857 | ||||||
| chr3:47457130
|
T | C | 1 | a0002c0002t0001g0115 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-98-14039A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47457130 | ||||||
| chr3:47457508
|
T | C | 1 | a0004c0006t0001g0076 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-98-14417A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47457508 | ||||||
| chr3:47457635
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-98-14544G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47457635 | ||||||
| chr3:47457636
|
G | A | 1 | a0001c0003t0001g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-98-14545C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47457636 | ||||||
| chr3:47457918
|
A | G | 1 | a0002c0002t0001g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-98-14827T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47457918 | ||||||
| chr3:47458082
|
G | A | 1 | a0002c0002t0001g0146 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-98-14991C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458082 | ||||||
| chr3:47458116
|
C | T | 1 | a0001c0022t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-98-15025G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458116 | ||||||
| chr3:47458140
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-98-15049A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458140 | ||||||
| chr3:47458498
|
T | G | 1 | a0001c0022t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-98-15407A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458498 | ||||||
| chr3:47458647
|
C | T | 1 | a0002c0002t0001g0146 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-98-15556G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458647 | ||||||
| chr3:47458811
|
A | G | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-98-15720T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458811 | ||||||
| chr3:47458962
|
T | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(27): Show | 30 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.-98-15871A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458962 | ||||||
| chr3:47459080
|
C | T | 1 | a0005c0007t0001g0116 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-98-15989G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459080 | ||||||
| chr3:47459172
|
G | A | 122 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0050others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-98-16081C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459172 | ||||||
| chr3:47459442
|
T | G | 1 | a0005c0007t0001g0116 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-98-16351A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459442 | ||||||
| chr3:47459759
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-99+16040G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459759 | ||||||
| chr3:47459760
|
G | A | 1 | a0002c0002t0001g0117 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-99+16039C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459760 | ||||||
| chr3:47459763
|
T | C | 28 | a0001c0001t0001g0194a0001c0001t0001g0198a0001c0001t0001g0199others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.-99+16036A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459763 | ||||||
| chr3:47459947
|
T | C | 2 | a0002c0002t0001g0121a0002c0002t0001g0122 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-99+15852A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459947 | ||||||
| chr3:47460268
|
A | G | 4 | a0001c0001t0001g0193a0001c0001t0001g0251a0001c0001t0001g0254others(1): Show | 4 | HG02027.hp2 NA18947.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+15531T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460268 | ||||||
| chr3:47460363
|
G | A | 1 | a0001c0001t0003g0246 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-99+15436C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460363 | ||||||
| chr3:47460363
|
G | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0035others(3): Show | 6 | HG02280.hp1 HG03130.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+15436C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460363 | ||||||
| chr3:47460443
|
A | G | 1 | a0002c0002t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-99+15356T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460443 | ||||||
| chr3:47460524
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-99+15275T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460524 | ||||||
| chr3:47460547
|
G | T | 1 | a0002c0002t0001g0081 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-99+15252C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460547 | ||||||
| chr3:47460576
|
A | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-99+15223T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460576 | ||||||
| chr3:47460660
|
C | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0035others(3): Show | 6 | HG02280.hp1 HG03130.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+15139G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460660 | ||||||
| chr3:47460910
|
G | A | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-99+14889C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460910 | ||||||
| chr3:47461693
|
T | C | 2 | a0002c0002t0001g0118a0002c0002t0001g0149 | 2 | HG01952.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-99+14106A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47461693 | ||||||
| chr3:47461859
|
C | T | 132 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0001g0174others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.-99+13940G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47461859 | ||||||
| chr3:47461872
|
A | T | 2 | a0002c0002t0001g0150a0002c0002t0001g0151 | 2 | NA19004.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-99+13927T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47461872 | ||||||
| chr3:47461912
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-99+13887A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47461912 | ||||||
| chr3:47462343
|
A | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-99+13456T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462343 | ||||||
| chr3:47462610
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(12): Show | 15 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.-99+13189C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462610 | ||||||
| chr3:47462704
|
G | C | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-99+13095C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462704 | ||||||
| chr3:47462705
|
A | G | 1 | a0001c0001t0002g0291 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-99+13094T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462705 | ||||||
| chr3:47462709
|
C | T | 1 | a0002c0002t0001g0080 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-99+13090G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462709 | ||||||
| chr3:47462753
|
C | CA | 8 | a0001c0001t0001g0028a0001c0001t0001g0045a0002c0002t0001g0119others(5): Show | 8 | HG00621.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-99+13045dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462753 | ||||||
| chr3:47462753
|
CA | C | 127 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0173others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-99+13045delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462753 | ||||||
| chr3:47462767
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-99+13032T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462767 | ||||||
| chr3:47462771
|
A | G | 54 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0198others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-99+13028T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462771 | ||||||
| chr3:47463021
|
A | C | 1 | a0002c0002t0001g0149 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-99+12778T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47463021 | ||||||
| chr3:47463359
|
G | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-99+12440C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47463359 | ||||||
| chr3:47463430
|
G | A | 2 | a0001c0022t0001g0197a0002c0002t0001g0123 | 2 | HG02083.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-99+12369C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47463430 | ||||||
| chr3:47463514
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-99+12285G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47463514 | ||||||
| chr3:47464031
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-99+11768A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464031 | ||||||
| chr3:47464134
|
G | C | 1 | a0001c0001t0001g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-99+11665C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464134 | ||||||
| chr3:47464204
|
C | T | 8 | a0002c0002t0001g0052a0002c0002t0001g0146a0002c0002t0001g0147others(5): Show | 8 | HG00738.hp2 HG01074.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+11595G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464204 | ||||||
| chr3:47464235
|
T | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-99+11564A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464235 | ||||||
| chr3:47464332
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-99+11467C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464332 | ||||||
| chr3:47464481
|
C | T | 3 | a0001c0005t0001g0188a0001c0005t0001g0195a0001c0005t0001g0196 | 3 | HG02258.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-99+11318G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464481 | ||||||
| chr3:47464489
|
T | C | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-99+11310A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464489 | ||||||
| chr3:47464740
|
G | A | 3 | a0002c0002t0001g0124a0002c0002t0001g0125a0002c0002t0001g0163 | 3 | HG01175.hp1 HG01934.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-99+11059C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464740 | ||||||
| chr3:47464837
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-99+10962G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464837 | ||||||
| chr3:47464921
|
T | C | 5 | a0001c0001t0002g0289a0001c0001t0002g0302a0001c0001t0002g0303others(2): Show | 5 | HG01192.hp2 HG02055.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.-99+10878A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464921 | ||||||
| chr3:47464951
|
T | C | 1 | a0001c0003t0001g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-99+10848A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464951 | ||||||
| chr3:47465168
|
C | CT | 23 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(20): Show | 23 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-99+10630dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465168 | ||||||
| chr3:47465785
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-99+10014A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465785 | ||||||
| chr3:47465841
|
C | CA | 117 | a0001c0001t0001g0067a0001c0001t0001g0107a0001c0001t0001g0175others(114): Show | 117 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-99+9957dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465841 | ||||||
| chr3:47465841
|
CA | C | 100 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0176others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-99+9957delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465841 | ||||||
| chr3:47465844
|
A | AC | 3 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070 | 3 | HG01106.hp1 HG02738.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-99+9954_-99+9955i others(3): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465844 | ||||||
| chr3:47465845
|
A | C | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-99+9954T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465845 | ||||||
| chr3:47466129
|
T | TA | 8 | a0001c0001t0001g0169a0001c0001t0007g0002a0002c0002t0001g0061others(5): Show | 8 | HG00558.hp1 HG01069.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.-99+9669dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466129 | ||||||
| chr3:47466135
|
C | A | 294 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-99+9664G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466135 | ||||||
| chr3:47466136
|
C | A | 11 | a0001c0001t0001g0169a0001c0001t0007g0002a0002c0002t0001g0061others(8): Show | 11 | HG00558.hp1 HG01069.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.-99+9663G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466136 | ||||||
| chr3:47466136
|
CA | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 7 | HG01168.hp1 HG01258.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-99+9662delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466136 | ||||||
| chr3:47466138
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-99+9661T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466138 | ||||||
| chr3:47466150
|
A | G | 2 | a0001c0001t0001g0208a0001c0001t0002g0297 | 2 | HG00735.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-99+9649T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466150 | ||||||
| chr3:47466154
|
A | AG | 35 | a0001c0001t0001g0190a0001c0001t0001g0193a0001c0001t0001g0205others(32): Show | 35 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-99+9644_-99+9645i others(3): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466154 | ||||||
| chr3:47466154
|
A | G | 98 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0176others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-99+9645T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466154 | ||||||
| chr3:47466345
|
C | T | 1 | a0001c0001t0002g0290 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-99+9454G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466345 | ||||||
| chr3:47466589
|
T | C | 1 | a0002c0002t0001g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-99+9210A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466589 | ||||||
| chr3:47466858
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-99+8941G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466858 | ||||||
| chr3:47466886
|
C | A | 8 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0182others(5): Show | 8 | HG00544.hp1 HG00673.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+8913G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466886 | ||||||
| chr3:47466963
|
T | A | 1 | a0002c0002t0001g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-99+8836A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466963 | ||||||
| chr3:47466979
|
G | C | 1 | a0002c0002t0001g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-99+8820C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466979 | ||||||
| chr3:47467099
|
GA | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0035others(5): Show | 8 | HG02280.hp1 HG02922.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+8699delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467099 | ||||||
| chr3:47467327
|
C | T | 1 | a0001c0003t0001g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-99+8472G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467327 | ||||||
| chr3:47467434
|
A | G | 1 | a0002c0002t0001g0063 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-99+8365T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467434 | ||||||
| chr3:47467605
|
G | A | 289 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-99+8194C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467605 | ||||||
| chr3:47467879
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-99+7920G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467879 | ||||||
| chr3:47467890
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-99+7909C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467890 | ||||||
| chr3:47468163
|
A | C | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-99+7636T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47468163 | ||||||
| chr3:47468285
|
G | C | 1 | a0001c0001t0007g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-99+7514C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47468285 | ||||||
| chr3:47468663
|
G | T | 1 | a0001c0022t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-99+7136C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47468663 | ||||||
| chr3:47468921
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-99+6878A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47468921 | ||||||
| chr3:47468962
|
G | A | 3 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139 | 3 | HG02135.hp2 NA19002.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-99+6837C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47468962 | ||||||
| chr3:47469003
|
G | A | 1 | a0001c0001t0003g0231 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-99+6796C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469003 | ||||||
| chr3:47469075
|
C | T | 1 | a0002c0002t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-99+6724G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469075 | ||||||
| chr3:47469090
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0255a0001c0001t0001g0271 | 3 | HG00738.hp1 HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-99+6709C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469090 | ||||||
| chr3:47469156
|
T | C | 1 | a0001c0022t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-99+6643A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469156 | ||||||
| chr3:47469288
|
G | A | 10 | a0001c0001t0002g0290a0001c0001t0002g0291a0001c0001t0002g0292others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.-99+6511C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469288 | ||||||
| chr3:47469339
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-99+6460G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469339 | ||||||
| chr3:47469401
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-99+6398T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469401 | ||||||
| chr3:47469957
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0034 | 3 | HG02055.hp1 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-99+5842G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469957 | ||||||
| chr3:47470208
|
T | C | 17 | a0001c0001t0002g0288a0001c0001t0002g0289a0001c0001t0002g0290others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.-99+5591A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470208 | ||||||
| chr3:47470600
|
C | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(24): Show | 27 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-99+5199G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470600 | ||||||
| chr3:47470614
|
A | G | 1 | a0002c0002t0001g0053 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-99+5185T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470614 | ||||||
| chr3:47470675
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-99+5124G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470675 | ||||||
| chr3:47470841
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(27): Show | 30 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.-99+4958C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470841 | ||||||
| chr3:47470865
|
G | GA | 4 | a0002c0002t0001g0165a0002c0002t0001g0166a0002c0002t0001g0167others(1): Show | 4 | HG00639.hp2 HG01070.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+4933dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470865 | ||||||
| chr3:47470965
|
A | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0200 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-99+4834T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470965 | ||||||
| chr3:47471070
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-99+4729A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471070 | ||||||
| chr3:47471189
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-99+4610C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471189 | ||||||
| chr3:47471418
|
C | A | 1 | a0003c0004t0001g0140 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-99+4381G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471418 | ||||||
| chr3:47471436
|
C | G | 1 | a0001c0001t0001g0268 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-99+4363G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471436 | ||||||
| chr3:47471844
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-99+3955A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471844 | ||||||
| chr3:47471928
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-99+3871C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471928 | ||||||
| chr3:47472055
|
A | C | 1 | a0002c0002t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-99+3744T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472055 | ||||||
| chr3:47472268
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-99+3531G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472268 | ||||||
| chr3:47472291
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-99+3508C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472291 | ||||||
| chr3:47472398
|
C | T | 4 | a0002c0002t0001g0059a0002c0002t0001g0060a0002c0002t0001g0061others(1): Show | 4 | NA18969.hp2 NA18988.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+3401G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472398 | ||||||
| chr3:47472431
|
A | G | 1 | a0002c0002t0001g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-99+3368T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472431 | ||||||
| chr3:47472453
|
T | A | 2 | a0001c0001t0001g0199a0002c0002t0001g0141 | 2 | HG02300.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-99+3346A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472453 | ||||||
| chr3:47472460
|
A | AAAT | 260 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.-99+3336_-99+3338d others(5): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472460 | ||||||
| chr3:47472460
|
A | AAATAAT | 5 | a0001c0001t0001g0169a0001c0005t0001g0188a0001c0022t0001g0197others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-99+3333_-99+3338d others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472460 | ||||||
| chr3:47472460
|
AAAT | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 22 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.-99+3336_-99+3338d others(5): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472460 | ||||||
| chr3:47472846
|
C | A | 1 | a0002c0002t0001g0142 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-99+2953G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472846 | ||||||
| chr3:47472914
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0234 | 2 | NA18967.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-99+2885G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472914 | ||||||
| chr3:47473079
|
T | TCAAAAAA others(15): Show |
2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-99+2719_-99+2720i others(24): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473079 | ||||||
| chr3:47473080
|
C | CAAA | 7 | a0001c0001t0001g0193a0001c0001t0001g0194a0002c0002t0001g0053others(4): Show | 7 | HG01884.hp2 HG01975.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-99+2716_-99+2718d others(5): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAA | 88 | a0001c0001t0001g0067a0001c0001t0001g0107a0001c0001t0001g0134others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-99+2715_-99+2718d others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAA | 33 | a0001c0001t0007g0002a0001c0005t0001g0195a0001c0005t0001g0196others(30): Show | 33 | HG00609.hp1 HG00639.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-99+2714_-99+2718d others(7): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02109.hp2 HG02922.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-99+2712_-99+2718d others(9): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-99+2709_-99+2718d others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-99+2706_-99+2718d others(15): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(10): Show |
4 | a0001c0001t0001g0049a0001c0001t0001g0199a0001c0008t0001g0023others(1): Show | 4 | HG01934.hp1 HG02300.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2702_-99+2718d others(19): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(11): Show |
10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(7): Show | 10 | HG01109.hp1 HG02922.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-99+2701_-99+2718d others(20): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(12): Show |
7 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(4): Show | 7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-99+2700_-99+2718d others(21): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(13): Show |
6 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0201others(3): Show | 6 | HG01975.hp1 HG02155.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(14): Show |
34 | a0001c0001t0001g0173a0001c0001t0001g0205a0001c0001t0001g0206others(31): Show | 34 | HG00597.hp2 HG00673.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(23): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(15): Show |
26 | a0001c0001t0001g0043a0001c0001t0001g0174a0001c0001t0001g0175others(23): Show | 26 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(24): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(16): Show |
11 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0045others(8): Show | 11 | HG01123.hp2 HG02148.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(25): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(17): Show |
3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0019t0001g0046 | 3 | HG03225.hp2 HG03453.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(26): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(18): Show |
9 | a0001c0001t0002g0289a0001c0001t0002g0290a0001c0001t0002g0291others(6): Show | 9 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(27): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(19): Show |
14 | a0001c0001t0001g0047a0001c0001t0001g0268a0001c0001t0001g0269others(11): Show | 14 | HG00558.hp2 HG00642.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(28): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(20): Show |
7 | a0001c0001t0001g0048a0001c0001t0001g0176a0001c0001t0001g0177others(4): Show | 7 | HG02080.hp1 HG02080.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(29): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(21): Show |
1 | a0001c0018t0002g0301 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-99+2718_-99+2719i others(30): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473080
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | HG00741.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(34): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | ||||||
| chr3:47473085
|
A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG00544.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-99+2713_-99+2714i others(23): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473085 | ||||||
| chr3:47473086
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0185 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-99+2712_-99+2713i others(23): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473086 | ||||||
| chr3:47473086
|
A | AAAAAAAA others(13): Show |
4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | NA18951.hp1 NA18954.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2712_-99+2713i others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473086 | ||||||
| chr3:47473086
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0178 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-99+2712_-99+2713i others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473086 | ||||||
| chr3:47473086
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0179a0001c0010t0001g0180 | 2 | HG01168.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-99+2712_-99+2713i others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473086 | ||||||
| chr3:47473145
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-99+2654A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473145 | ||||||
| chr3:47473273
|
G | T | 1 | a0002c0002t0001g0050 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-99+2526C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473273 | ||||||
| chr3:47473933
|
T | C | 1 | a0002c0002t0001g0170 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-99+1866A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473933 | ||||||
| chr3:47474060
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-99+1739A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474060 | ||||||
| chr3:47474067
|
G | A | 126 | a0001c0001t0001g0067a0001c0001t0001g0107a0001c0001t0001g0134others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-99+1732C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474067 | ||||||
| chr3:47474146
|
T | C | 3 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0304 | 3 | HG01192.hp2 HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-99+1653A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474146 | ||||||
| chr3:47474264
|
C | CA | 126 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-99+1534dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474264 | ||||||
| chr3:47474371
|
T | C | 1 | a0002c0002t0001g0172 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-99+1428A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474371 | ||||||
| chr3:47474658
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-99+1141C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474658 | ||||||
| chr3:47474782
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG00558.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-99+1017C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474782 | ||||||
| chr3:47475238
|
G | A | 130 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-99+561C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47475238 | ||||||
| chr3:47475268
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-99+531G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47475268 | ||||||
| chr3:47475548
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG00639.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-99+251C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47475548 | ||||||
| chr3:47475601
|
C | A | 1 | a0001c0001t0003g0284 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-99+198G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47475601 |