Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 26512 |
|---|---|
| ensemblid | ENSG00000102786.15 |
| hgncid | 14879 |
| symbol | INTS6 |
| name | integrator complex subunit 6 |
| refseq_nuc | NM_012141.3 |
| refseq_prot | NP_036273.1 |
| ensembl_nuc | ENST00000311234.9 |
| ensembl_prot | ENSP00000310260.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 51361577 |
| end | 51453036 |
| strand | - |
| ver | v1.2 |
| region | chr13:51361577-51453036 |
| region5000 | chr13:51356577-51458036 |
| regionname0 | INTS6_chr13_51361577_51453036 |
| regionname5000 | INTS6_chr13_51356577_51458036 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 887 | 357 | 81 | 68 | 152 | 12 | 42 | 120 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0002 | 0/0 | 887 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2664 | 338 | 81 | 67 | 138 | 12 | 38 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| c0002 | 0/0 | 2664 | 17 | 0 | 1 | 12 | 0 | 4 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| c0003 | 0/0 | 2664 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| c0004 | 0/0 | 2664 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| c0005 | 0/0 | 2664 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4687 | 149 | 31 | 28 | 69 | 2 | 17 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0002 | 0/0 | 4687 | 31 | 22 | 6 | 2 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0003 | 0/0 | 4686 | 25 | 5 | 0 | 16 | 0 | 4 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0004 | 0/0 | 4686 | 23 | 4 | 2 | 14 | 2 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0005 | 0/0 | 4688 | 15 | 1 | 4 | 5 | 3 | 2 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0006 | 0/0 | 4688 | 13 | 0 | 1 | 9 | 1 | 2 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0007 | 0/0 | 4686 | 13 | 0 | 10 | 0 | 0 | 3 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0008 | 0/0 | 4687 | 9 | 0 | 1 | 7 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0009 | 0/0 | 4687 | 7 | 0 | 3 | 3 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0010 | 0/0 | 4687 | 6 | 6 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0011 | 0/0 | 4687 | 6 | 0 | 0 | 6 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0012 | 0/0 | 4688 | 5 | 0 | 0 | 2 | 0 | 3 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0013 | 0/0 | 4688 | 5 | 1 | 3 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0014 | 0/0 | 4687 | 5 | 0 | 1 | 1 | 0 | 3 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0015 | 0/0 | 4685 | 5 | 0 | 0 | 5 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0016 | 0/0 | 4687 | 4 | 0 | 0 | 4 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0017 | 0/0 | 4687 | 3 | 3 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0018 | 0/0 | 4688 | 2 | 0 | 1 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0019 | 0/0 | 4687 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0020 | 0/0 | 4687 | 2 | 0 | 0 | 0 | 0 | 2 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0021 | 0/0 | 4688 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0022 | 0/0 | 4687 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0023 | 0/0 | 4688 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0024 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0025 | 0/0 | 4688 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0026 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0027 | 0/0 | 4688 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0028 | 0/0 | 4688 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0029 | 0/0 | 4687 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0030 | 0/0 | 4687 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0031 | 0/0 | 4687 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0032 | 0/0 | 4687 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0033 | 0/0 | 4687 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0034 | 0/0 | 4687 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0035 | 0/0 | 4687 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0036 | 0/0 | 4687 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0037 | 0/0 | 4687 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0038 | 0/0 | 4686 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0039 | 0/0 | 4686 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0040 | 0/0 | 4686 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0041 | 0/0 | 4686 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0042 | 0/0 | 4687 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0043 | 0/0 | 4687 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0044 | 0/0 | 4686 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0045 | 0/0 | 4687 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0046 | 0/0 | 4687 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| t0047 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2664 | 338 | 81 | 67 | 138 | 12 | 38 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0002 | 0/0 | 2664 | 17 | 0 | 1 | 12 | 0 | 4 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0004 | 0/0 | 2664 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0005 | 0/0 | 2664 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0002c0003 | 0/0 | 2664 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7350 | 147 | 30 | 28 | 68 | 2 | 17 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0002 | 0/0 | 7350 | 31 | 22 | 6 | 2 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0003 | 0/0 | 7349 | 25 | 5 | 0 | 16 | 0 | 4 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0004 | 0/0 | 7349 | 23 | 4 | 2 | 14 | 2 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0005 | 0/0 | 7351 | 15 | 1 | 4 | 5 | 3 | 2 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0006 | 0/0 | 7351 | 13 | 0 | 1 | 9 | 1 | 2 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0007 | 0/0 | 7349 | 13 | 0 | 10 | 0 | 0 | 3 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0009 | 0/0 | 7350 | 7 | 0 | 3 | 3 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0010 | 0/0 | 7350 | 6 | 6 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0012 | 0/0 | 7351 | 5 | 0 | 0 | 2 | 0 | 3 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0013 | 0/0 | 7351 | 5 | 1 | 3 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0014 | 0/0 | 7350 | 5 | 0 | 1 | 1 | 0 | 3 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0015 | 0/0 | 7348 | 5 | 0 | 0 | 5 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0016 | 0/0 | 7350 | 4 | 0 | 0 | 4 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0017 | 0/0 | 7350 | 3 | 3 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0018 | 0/0 | 7351 | 2 | 0 | 1 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0019 | 0/0 | 7350 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0021 | 0/0 | 7351 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0022 | 0/0 | 7350 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0023 | 0/0 | 7351 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0024 | 0/0 | 7351 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0025 | 0/0 | 7351 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0026 | 0/0 | 7351 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0027 | 0/0 | 7351 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0028 | 0/0 | 7351 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0029 | 0/0 | 7350 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0030 | 0/0 | 7350 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0032 | 0/0 | 7350 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0033 | 0/0 | 7350 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0034 | 0/0 | 7350 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0035 | 0/0 | 7350 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0036 | 0/0 | 7350 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0037 | 0/0 | 7350 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0038 | 0/0 | 7349 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0039 | 0/0 | 7349 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0040 | 0/0 | 7349 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0041 | 0/0 | 7349 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0042 | 0/0 | 7350 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0043 | 0/0 | 7350 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0044 | 0/0 | 7349 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0045 | 0/0 | 7350 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0046 | 0/0 | 7350 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0001t0047 | 0/0 | 7351 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0002t0008 | 0/0 | 7350 | 9 | 0 | 1 | 7 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0002t0011 | 0/0 | 7350 | 5 | 0 | 0 | 5 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0002t0020 | 0/0 | 7350 | 2 | 0 | 0 | 0 | 0 | 2 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0002t0031 | 0/0 | 7350 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0004t0011 | 0/0 | 7350 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0001c0005t0001 | 0/0 | 7350 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| a0002c0003t0001 | 0/0 | 7350 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | copy fasta | chr13 | 51356577 | 51458036 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0006g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0007g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0009g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0009g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0009g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0009g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0009g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0009g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0009g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0010g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0010g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0010g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0010g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0010g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0010g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0012g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0012g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0012g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0012g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0012g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0013g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0013g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0013g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0013g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0014g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0014g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0014g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0014g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0014g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0015g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0015g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0015g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0015g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0016g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0016g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0016g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0016g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0017g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0017g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0017g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0018g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0018g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0019g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0019g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0021g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0021g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0022g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0023g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0024g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0025g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0026g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0027g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0028g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0029g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0030g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0032g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0033g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0034g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0035g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0036g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0037g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0038g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0039g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0040g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0041g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0042g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0043g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0044g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0045g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0046g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0001t0047g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0008g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0008g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0008g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0008g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0008g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0008g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0008g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0008g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0008g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0011g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0011g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0011g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0011g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0011g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0020g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0002t0031g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0004t0011g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0001c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| a0002c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0265 | EUR | GBR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0292 | EUR | GBR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0139 | EUR | GBR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00280 | hp1 | a0001 | c0001 | t0044 | g0215 | EUR | FIN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00280 | hp2 | a0001 | c0001 | t0013 | g0156 | EUR | FIN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00438 | hp2 | a0001 | c0002 | t0011 | g0334 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00558 | hp1 | a0001 | c0001 | t0012 | g0248 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00639 | hp1 | a0001 | c0001 | t0013 | g0106 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0140 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00642 | hp2 | a0001 | c0001 | t0027 | g0268 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0262 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00733 | hp2 | a0001 | c0001 | t0035 | g0081 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00735 | hp2 | a0001 | c0001 | t0041 | g0208 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0282 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01069 | hp2 | a0001 | c0002 | t0008 | g0336 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0212 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0217 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0209 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01175 | hp2 | a0001 | c0001 | t0013 | g0179 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0277 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01243 | hp2 | a0001 | c0001 | t0029 | g0306 | AMR | PUR | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01255 | hp1 | a0001 | c0001 | t0043 | g0029 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0266 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01346 | hp1 | a0001 | c0001 | t0018 | g0264 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01346 | hp2 | a0001 | c0001 | t0009 | g0132 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01358 | hp1 | a0001 | c0001 | t0028 | g0288 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01358 | hp2 | a0001 | c0001 | t0013 | g0184 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01361 | hp2 | a0001 | c0001 | t0009 | g0131 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0285 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0261 | EUR | IBS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0202 | EUR | IBS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0283 | EUR | IBS | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01891 | hp1 | a0001 | c0001 | t0019 | g0308 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01928 | hp1 | a0001 | c0001 | t0038 | g0195 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01928 | hp2 | a0001 | c0001 | t0009 | g0134 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0200 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0158 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01943 | hp2 | a0001 | c0001 | t0023 | g0121 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01952 | hp1 | a0001 | c0001 | t0014 | g0129 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0216 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01981 | hp2 | a0001 | c0001 | t0007 | g0196 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0141 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG01993 | hp2 | a0001 | c0001 | t0007 | g0199 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0201 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02056 | hp1 | a0001 | c0001 | t0024 | g0275 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02074 | hp1 | a0001 | c0001 | t0021 | g0347 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0326 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02083 | hp2 | a0001 | c0001 | t0021 | g0346 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02135 | hp2 | a0001 | c0001 | t0039 | g0099 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02293 | hp2 | a0001 | c0001 | t0007 | g0161 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0313 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0290 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | KHV | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0314 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02602 | hp2 | a0001 | c0001 | t0012 | g0270 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0318 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0267 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02698 | hp2 | a0001 | c0002 | t0008 | g0247 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02717 | hp2 | a0001 | c0001 | t0022 | g0239 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0316 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02735 | hp2 | a0001 | c0001 | t0014 | g0128 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02896 | hp2 | a0001 | c0001 | t0017 | g0301 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02897 | hp1 | a0001 | c0001 | t0017 | g0302 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02976 | hp1 | a0001 | c0001 | t0030 | g0138 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0298 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0311 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0211 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03239 | hp2 | a0001 | c0001 | t0014 | g0127 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0310 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03491 | hp1 | a0001 | c0002 | t0020 | g0008 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03492 | hp1 | a0001 | c0002 | t0020 | g0008 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03540 | hp2 | a0001 | c0001 | t0019 | g0307 | AFR | GWD | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0287 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0187 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | STU | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03704 | hp1 | a0001 | c0002 | t0031 | g0344 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0294 | SAS | BEB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0233 | SAS | BEB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0197 | SAS | BEB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | BEB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | BEB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0210 | SAS | STU | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG04199 | hp1 | a0001 | c0001 | t0012 | g0291 | SAS | STU | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG04199 | hp2 | a0001 | c0001 | t0014 | g0088 | SAS | STU | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG04204 | hp1 | a0001 | c0001 | t0025 | g0117 | SAS | STU | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0289 | SAS | STU | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG04228 | hp2 | a0001 | c0001 | t0046 | g0349 | SAS | STU | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18522 | hp1 | a0001 | c0001 | t0036 | g0300 | AFR | YRI | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0315 | AFR | YRI | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | CHB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | CHB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | CHB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | YRI | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18939 | hp1 | a0001 | c0002 | t0008 | g0341 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0280 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18944 | hp2 | a0001 | c0001 | t0040 | g0327 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18945 | hp2 | a0001 | c0001 | t0016 | g0100 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18947 | hp1 | a0001 | c0002 | t0008 | g0332 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18949 | hp1 | a0001 | c0001 | t0026 | g0271 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18950 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0274 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18956 | hp2 | a0001 | c0001 | t0006 | g0286 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18957 | hp2 | a0001 | c0002 | t0008 | g0333 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18973 | hp1 | a0001 | c0001 | t0012 | g0293 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18974 | hp1 | a0001 | c0001 | t0006 | g0281 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18974 | hp2 | a0001 | c0002 | t0011 | g0338 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18980 | hp2 | a0001 | c0001 | t0047 | g0350 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18981 | hp1 | a0001 | c0002 | t0008 | g0335 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18982 | hp2 | a0001 | c0001 | t0015 | g0045 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18984 | hp1 | a0001 | c0002 | t0008 | g0343 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0260 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18992 | hp1 | a0001 | c0001 | t0016 | g0101 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18997 | hp2 | a0001 | c0001 | t0005 | g0259 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18998 | hp1 | a0001 | c0002 | t0008 | g0345 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19000 | hp2 | a0001 | c0001 | t0014 | g0136 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19003 | hp1 | a0001 | c0001 | t0016 | g0125 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19004 | hp1 | a0001 | c0001 | t0006 | g0272 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0273 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19012 | hp2 | a0001 | c0001 | t0033 | g0263 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19030 | hp1 | a0001 | c0001 | t0034 | g0295 | AFR | LWK | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19030 | hp2 | a0001 | c0001 | t0013 | g0153 | AFR | LWK | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | LWK | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | LWK | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19055 | hp1 | a0001 | c0002 | t0011 | g0342 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19057 | hp2 | a0001 | c0002 | t0011 | g0339 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19060 | hp2 | a0001 | c0005 | t0001 | g0065 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19062 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19062 | hp2 | a0001 | c0002 | t0011 | g0340 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19063 | hp1 | a0001 | c0001 | t0042 | g0023 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19070 | hp1 | a0001 | c0001 | t0015 | g0035 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19074 | hp2 | a0001 | c0004 | t0011 | g0337 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19079 | hp1 | a0001 | c0001 | t0009 | g0133 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19081 | hp1 | a0001 | c0001 | t0009 | g0135 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19082 | hp1 | a0001 | c0001 | t0009 | g0130 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19083 | hp2 | a0001 | c0001 | t0015 | g0032 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA19090 | hp2 | a0001 | c0002 | t0008 | g0331 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ASW | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | ASW | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0137 | EUR | TSI | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA20752 | hp2 | a0001 | c0001 | t0018 | g0279 | EUR | TSI | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA20905 | hp1 | a0001 | c0001 | t0012 | g0284 | SAS | GIH | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | GIH | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02559 | hp1 | a0001 | c0001 | t0045 | g0348 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | MSL | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | USA | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| HG06807 | hp2 | a0001 | c0001 | t0037 | g0312 | AFR | USA | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA18955 | hp2 | a0001 | c0001 | t0016 | g0048 | EAS | JPT | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | USA | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA20300 | hp2 | a0001 | c0001 | t0032 | g0299 | AFR | USA | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0269 | AFR | LWK | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0166 | REF | REF | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0108 | REF | REF | INTS6_chr13_51356577_51458036 | INTS6 | chr13 | 51356577 | 51458036 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51369170
|
T | C | 1 | a0002 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.2245A>G | p.Thr749Ala | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 16/18 | 2756/7350 | 2245/2664 | 749/887 | chr13 | 51369170 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51367807
|
T | C | 2 | a0001c0002a0001c0004 | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
splice_region_variant&synonymous_variant | LOW | c.2568A>G | p.Ser856Ser | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/18 | 3079/7350 | 2568/2664 | 856/887 | chr13 | 51367807 | ||
| chr13:51378287
|
G | A | 1 | a0001c0004 | 1 | NA19074.hp2 | synonymous_variant | LOW | c.1554C>T | p.Asp518Asp | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/18 | 2065/7350 | 1554/2664 | 518/887 | chr13 | 51378287 | ||
| chr13:51382089
|
T | G | 2 | a0001c0002a0001c0004 | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
synonymous_variant | LOW | c.1215A>C | p.Thr405Thr | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/18 | 1726/7350 | 1215/2664 | 405/887 | chr13 | 51382089 | ||
| chr13:51383456
|
G | A | 1 | a0001c0005 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.1053C>T | p.Tyr351Tyr | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 9/18 | 1564/7350 | 1053/2664 | 351/887 | chr13 | 51383456 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51361614
|
G | C | 1 | a0001c0001t0036 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4138C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 4138 | chr13 | 51361614 | |||||
| chr13:51361651
|
C | A | 1 | a0001c0001t0040 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4101G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 4101 | chr13 | 51361651 | |||||
| chr13:51361943
|
T | C | 1 | a0001c0001t0032 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3809A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 3809 | chr13 | 51361943 | |||||
| chr13:51362055
|
G | T | 1 | a0001c0001t0030 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3697C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 3697 | chr13 | 51362055 | |||||
| chr13:51362064
|
G | A | 5 | a0001c0002t0008a0001c0002t0011a0001c0002t0020others(2): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3688C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 3688 | chr13 | 51362064 | |||||
| chr13:51362136
|
G | A | 9 | a0001c0001t0005a0001c0001t0006a0001c0001t0012others(6): Show | 40 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*3616C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 3616 | chr13 | 51362136 | |||||
| chr13:51362268
|
A | G | 5 | a0001c0002t0008a0001c0002t0011a0001c0002t0020others(2): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3484T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 3484 | chr13 | 51362268 | |||||
| chr13:51362287
|
G | A | 4 | a0001c0001t0017a0001c0001t0032a0001c0001t0034others(1): Show | 6 | HG02896.hp2 HG02897.hp1 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3465C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 3465 | chr13 | 51362287 | |||||
| chr13:51362375
|
G | T | 5 | a0001c0002t0008a0001c0002t0011a0001c0002t0020others(2): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3377C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 3377 | chr13 | 51362375 | |||||
| chr13:51362499
|
A | T | 5 | a0001c0002t0008a0001c0002t0011a0001c0002t0020others(2): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3253T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 3253 | chr13 | 51362499 | |||||
| chr13:51362841
|
G | A | 1 | a0001c0001t0026 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2911C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 2911 | chr13 | 51362841 | |||||
| chr13:51362954
|
A | G | 4 | a0001c0001t0007a0001c0001t0018a0001c0001t0038others(1): Show | 17 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2798T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 2798 | chr13 | 51362954 | |||||
| chr13:51363370
|
AAC | A | 1 | a0001c0001t0015 | 5 | NA18950.hp2 NA18982.hp2 NA19062.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2380_*2381delGT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 2380 | chr13 | 51363370 | |||||
| chr13:51363544
|
A | C | 1 | a0001c0001t0029 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2208T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 2208 | chr13 | 51363544 | |||||
| chr13:51363965
|
T | C | 1 | a0001c0001t0016 | 4 | NA18945.hp2 NA18955.hp2 NA18992.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1787A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 1787 | chr13 | 51363965 | |||||
| chr13:51364117
|
A | T | 1 | a0001c0001t0030 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1635T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 1635 | chr13 | 51364117 | |||||
| chr13:51364333
|
C | T | 1 | a0001c0001t0035 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1419G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 1419 | chr13 | 51364333 | |||||
| chr13:51364430
|
G | A | 10 | a0001c0001t0006a0001c0001t0018a0001c0001t0026others(7): Show | 24 | HG00099.hp1 HG00733.hp1 HG00735.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1322C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 1322 | chr13 | 51364430 | |||||
| chr13:51364440
|
G | T | 21 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(18): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1312C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 1312 | chr13 | 51364440 | |||||
| chr13:51364658
|
T | C | 1 | a0001c0001t0037 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1094A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 1094 | chr13 | 51364658 | |||||
| chr13:51364740
|
A | G | 9 | a0001c0001t0009a0001c0001t0014a0001c0001t0023others(6): Show | 32 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1012T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 1012 | chr13 | 51364740 | |||||
| chr13:51364823
|
A | G | 1 | a0001c0001t0038 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*929T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 929 | chr13 | 51364823 | |||||
| chr13:51364855
|
C | T | 1 | a0001c0001t0019 | 2 | HG01891.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*897G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 897 | chr13 | 51364855 | |||||
| chr13:51364867
|
C | T | 1 | a0001c0001t0045 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*885G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 885 | chr13 | 51364867 | |||||
| chr13:51364881
|
T | C | 1 | a0001c0001t0013 | 5 | HG00280.hp2 HG00639.hp1 HG01175.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*871A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 871 | chr13 | 51364881 | |||||
| chr13:51364993
|
C | T | 2 | a0001c0001t0010a0001c0001t0029 | 7 | HG01243.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*759G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 759 | chr13 | 51364993 | |||||
| chr13:51365391
|
C | CT | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0012others(10): Show | 49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*360dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 360 | chr13 | 51365391 | |||||
| chr13:51365391
|
CT | C | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(5): Show | 66 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*360delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 360 | chr13 | 51365391 | |||||
| chr13:51365504
|
T | A | 1 | a0001c0001t0042 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 248 | chr13 | 51365504 | |||||
| chr13:51365623
|
T | C | 1 | a0001c0001t0043 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*129A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 129 | chr13 | 51365623 | |||||
| chr13:51365654
|
C | G | 1 | a0001c0001t0022 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*98G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 98 | chr13 | 51365654 | |||||
| chr13:51365676
|
G | A | 1 | a0001c0001t0044 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*76C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 18/18 | 76 | chr13 | 51365676 | |||||
| chr13:51452621
|
G | A | 1 | a0001c0001t0021 | 2 | HG02074.hp1 HG02083.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-96C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 1/18 | chr13 | 51452621 | ||||||
| chr13:51452673
|
G | A | 1 | a0001c0001t0045 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 1/18 | 148 | chr13 | 51452673 | |||||
| chr13:51452752
|
T | G | 1 | a0001c0001t0046 | 1 | HG04228.hp2 | 5_prime_UTR_variant | MODIFIER | c.-227A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 1/18 | 227 | chr13 | 51452752 | |||||
| chr13:51452929
|
G | A | 1 | a0001c0001t0047 | 1 | NA18980.hp2 | 5_prime_UTR_variant | MODIFIER | c.-404C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 1/18 | 404 | chr13 | 51452929 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51365894
|
A | G | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2571-49T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51365894 | ||||||
| chr13:51365909
|
T | C | 1 | a0001c0001t0023g0121 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2571-64A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51365909 | ||||||
| chr13:51365920
|
AGGAGAGA others(6): Show |
A | 1 | a0001c0001t0001g0231 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2571-88_2571-76del others(13): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51365920 | ||||||
| chr13:51365980
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2571-135G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51365980 | ||||||
| chr13:51365999
|
G | T | 1 | a0001c0001t0007g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2571-154C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51365999 | ||||||
| chr13:51366307
|
G | T | 1 | a0001c0001t0001g0231 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2571-462C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51366307 | ||||||
| chr13:51366471
|
G | T | 1 | a0001c0001t0009g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2571-626C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51366471 | ||||||
| chr13:51366778
|
C | CAA | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.2571-935_2571-934d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51366778 | ||||||
| chr13:51366943
|
C | T | 1 | a0001c0001t0012g0248 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2570+862G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51366943 | ||||||
| chr13:51366961
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2570+844T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51366961 | ||||||
| chr13:51366993
|
C | A | 13 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2570+812G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51366993 | ||||||
| chr13:51367196
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2570+609T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51367196 | ||||||
| chr13:51367331
|
C | G | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0032g0299others(2): Show | 5 | HG02965.hp2 HG03139.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2570+474G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51367331 | ||||||
| chr13:51367458
|
C | T | 1 | a0001c0001t0004g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2570+347G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51367458 | ||||||
| chr13:51367787
|
A | G | 1 | a0001c0002t0008g0331 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2570+18T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 17/17 | chr13 | 51367787 | ||||||
| chr13:51368296
|
G | A | 1 | a0001c0001t0003g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2477-398C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 16/17 | chr13 | 51368296 | ||||||
| chr13:51368303
|
A | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0069others(17): Show | 22 | HG00423.hp2 HG00609.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.2477-405T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 16/17 | chr13 | 51368303 | ||||||
| chr13:51368394
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.2477-496C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 16/17 | chr13 | 51368394 | ||||||
| chr13:51368783
|
G | T | 1 | a0001c0001t0013g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2476+156C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 16/17 | chr13 | 51368783 | ||||||
| chr13:51368867
|
CT | C | 8 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0017g0298others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2476+71delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 16/17 | chr13 | 51368867 | ||||||
| chr13:51368921
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0014g0088 | 2 | HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2476+18C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 16/17 | chr13 | 51368921 | ||||||
| chr13:51369326
|
C | T | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.2105-16G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51369326 | ||||||
| chr13:51369774
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2105-464A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51369774 | ||||||
| chr13:51369846
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2105-536A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51369846 | ||||||
| chr13:51369896
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.2105-586A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51369896 | ||||||
| chr13:51370019
|
C | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0003g0150others(1): Show | 4 | HG01255.hp2 HG02258.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2105-709G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370019 | ||||||
| chr13:51370073
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.2105-763G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370073 | ||||||
| chr13:51370094
|
T | TTTC | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.2105-785_2105-784i others(5): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370094 | ||||||
| chr13:51370285
|
G | A | 1 | a0001c0001t0024g0275 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2105-975C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370285 | ||||||
| chr13:51370436
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1126G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370436 | ||||||
| chr13:51370438
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1128G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370438 | ||||||
| chr13:51370442
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1132G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370442 | ||||||
| chr13:51370444
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1134G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370444 | ||||||
| chr13:51370445
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1135G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370445 | ||||||
| chr13:51370446
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1136G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370446 | ||||||
| chr13:51370449
|
T | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1139A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370449 | ||||||
| chr13:51370451
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1141G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370451 | ||||||
| chr13:51370453
|
T | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1143A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370453 | ||||||
| chr13:51370456
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1146G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370456 | ||||||
| chr13:51370479
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1169G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370479 | ||||||
| chr13:51370480
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1170G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370480 | ||||||
| chr13:51370481
|
T | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1171A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370481 | ||||||
| chr13:51370482
|
A | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1172T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370482 | ||||||
| chr13:51370483
|
T | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1173A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370483 | ||||||
| chr13:51370484
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1174G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370484 | ||||||
| chr13:51370485
|
A | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1175T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370485 | ||||||
| chr13:51370487
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1177G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370487 | ||||||
| chr13:51370489
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1179G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370489 | ||||||
| chr13:51370490
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1180G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370490 | ||||||
| chr13:51370495
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1185C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370495 | ||||||
| chr13:51370497
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1187C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370497 | ||||||
| chr13:51370502
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1192G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370502 | ||||||
| chr13:51370541
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1231G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370541 | ||||||
| chr13:51370543
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1233T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370543 | ||||||
| chr13:51370559
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1249A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370559 | ||||||
| chr13:51370560
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1250A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370560 | ||||||
| chr13:51370562
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1252A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370562 | ||||||
| chr13:51370563
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1253A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370563 | ||||||
| chr13:51370564
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1254C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370564 | ||||||
| chr13:51370571
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1261T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370571 | ||||||
| chr13:51370572
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1262G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370572 | ||||||
| chr13:51370576
|
A | C | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1266T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370576 | ||||||
| chr13:51370578
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1268C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370578 | ||||||
| chr13:51370579
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1269C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370579 | ||||||
| chr13:51370582
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1272T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370582 | ||||||
| chr13:51370583
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1273C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370583 | ||||||
| chr13:51370584
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1274G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370584 | ||||||
| chr13:51370596
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1286A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370596 | ||||||
| chr13:51370612
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1302T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370612 | ||||||
| chr13:51370614
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1304T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370614 | ||||||
| chr13:51370617
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1307G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370617 | ||||||
| chr13:51370620
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1310G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370620 | ||||||
| chr13:51370623
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1313T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370623 | ||||||
| chr13:51370624
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1314G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370624 | ||||||
| chr13:51370625
|
A | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1315T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370625 | ||||||
| chr13:51370630
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2105-1320C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370630 | ||||||
| chr13:51370655
|
A | G | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.2105-1345T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370655 | ||||||
| chr13:51370818
|
G | T | 13 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2105-1508C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370818 | ||||||
| chr13:51370925
|
T | C | 2 | a0001c0001t0013g0156a0001c0001t0013g0184 | 2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2105-1615A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51370925 | ||||||
| chr13:51371159
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.2105-1849G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51371159 | ||||||
| chr13:51371416
|
T | C | 4 | a0001c0001t0016g0048a0001c0001t0017g0298a0001c0001t0017g0301others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2105-2106A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51371416 | ||||||
| chr13:51371419
|
C | T | 1 | a0001c0001t0007g0212 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2105-2109G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51371419 | ||||||
| chr13:51371490
|
T | C | 1 | a0001c0001t0003g0221 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2105-2180A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51371490 | ||||||
| chr13:51371597
|
C | T | 1 | a0001c0001t0036g0300 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2105-2287G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51371597 | ||||||
| chr13:51371605
|
G | A | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.2105-2295C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51371605 | ||||||
| chr13:51371807
|
C | T | 1 | a0001c0002t0031g0344 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2104+2401G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51371807 | ||||||
| chr13:51371808
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0113a0001c0001t0001g0118 | 4 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2104+2400C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51371808 | ||||||
| chr13:51371876
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0228 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2104+2332C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51371876 | ||||||
| chr13:51372239
|
C | T | 16 | a0001c0001t0001g0227a0001c0001t0001g0303a0001c0001t0001g0304others(13): Show | 16 | HG01243.hp2 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2104+1969G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372239 | ||||||
| chr13:51372247
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.2104+1961G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372247 | ||||||
| chr13:51372303
|
CAGT | C | 16 | a0001c0002t0008g0331a0001c0002t0008g0332a0001c0002t0008g0333others(13): Show | 17 | HG00438.hp2 HG01069.hp2 HG03491.hp1 others(14): Show |
intron_variant | MODIFIER | c.2104+1902_2104+190 others(7): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372303 | ||||||
| chr13:51372305
|
G | GT | 33 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0028others(30): Show | 34 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2104+1902dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372305 | ||||||
| chr13:51372305
|
GT | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0030others(54): Show | 59 | HG01074.hp1 HG01243.hp2 HG01257.hp1 others(56): Show |
intron_variant | MODIFIER | c.2104+1902delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372305 | ||||||
| chr13:51372308
|
T | G | 16 | a0001c0002t0008g0331a0001c0002t0008g0332a0001c0002t0008g0333others(13): Show | 17 | HG00438.hp2 HG01069.hp2 HG03491.hp1 others(14): Show |
intron_variant | MODIFIER | c.2104+1900A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372308 | ||||||
| chr13:51372309
|
T | G | 1 | a0001c0002t0008g0247 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2104+1899A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372309 | ||||||
| chr13:51372336
|
A | G | 8 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0017g0298others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+1872T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372336 | ||||||
| chr13:51372574
|
C | T | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2104+1634G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372574 | ||||||
| chr13:51372691
|
G | C | 1 | a0001c0001t0005g0259 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2104+1517C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372691 | ||||||
| chr13:51372819
|
C | T | 1 | a0001c0001t0006g0274 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2104+1389G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372819 | ||||||
| chr13:51372984
|
A | G | 2 | a0001c0001t0002g0188a0001c0001t0002g0194 | 2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2104+1224T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51372984 | ||||||
| chr13:51373097
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2104+1111C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373097 | ||||||
| chr13:51373137
|
T | C | 1 | a0001c0001t0005g0269 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2104+1071A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373137 | ||||||
| chr13:51373202
|
G | GT | 8 | a0001c0001t0001g0089a0001c0001t0001g0305a0001c0001t0003g0230others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+1005dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373202 | ||||||
| chr13:51373202
|
G | GTT | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2104+1004_2104+100 others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373202 | ||||||
| chr13:51373202
|
GT | G | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.2104+1005delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373202 | ||||||
| chr13:51373351
|
C | G | 2 | a0001c0001t0001g0182a0001c0001t0002g0181 | 2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2104+857G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373351 | ||||||
| chr13:51373446
|
T | G | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2104+762A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373446 | ||||||
| chr13:51373493
|
T | C | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.2104+715A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373493 | ||||||
| chr13:51373560
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2104+648G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373560 | ||||||
| chr13:51373578
|
T | C | 91 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.2104+630A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373578 | ||||||
| chr13:51373644
|
C | T | 1 | a0001c0001t0004g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2104+564G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373644 | ||||||
| chr13:51373941
|
T | C | 1 | a0001c0001t0032g0299 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2104+267A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 15/17 | chr13 | 51373941 | ||||||
| chr13:51375113
|
G | A | 7 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1730-317C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375113 | ||||||
| chr13:51375130
|
G | A | 1 | a0001c0001t0032g0299 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1730-334C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375130 | ||||||
| chr13:51375189
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1730-393A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375189 | ||||||
| chr13:51375267
|
G | A | 3 | a0001c0001t0001g0231a0001c0001t0002g0188a0001c0001t0002g0194 | 3 | HG02647.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1730-471C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375267 | ||||||
| chr13:51375279
|
G | T | 1 | a0001c0001t0013g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1730-483C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375279 | ||||||
| chr13:51375300
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1730-504G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375300 | ||||||
| chr13:51375351
|
C | CA | 159 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0014others(156): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1730-556dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375351 | ||||||
| chr13:51375351
|
CA | C | 31 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(28): Show | 31 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.1730-556delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375351 | ||||||
| chr13:51375351
|
CAAAAAAA others(2): Show |
C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1730-564_1730-556d others(11): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375351 | ||||||
| chr13:51375476
|
T | A | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1729+572A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375476 | ||||||
| chr13:51375476
|
T | TA | 150 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0025others(147): Show | 150 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1729+571dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375476 | ||||||
| chr13:51375476
|
T | TAA | 120 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(117): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.1729+570_1729+571d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375476 | ||||||
| chr13:51375494
|
G | A | 90 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1729+554C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375494 | ||||||
| chr13:51375556
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1729+492A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375556 | ||||||
| chr13:51375567
|
T | C | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1729+481A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375567 | ||||||
| chr13:51375655
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1729+393G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375655 | ||||||
| chr13:51375730
|
AGTGGGTG others(3): Show |
A | 15 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(12): Show | 16 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.1729+308_1729+317d others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375730 | ||||||
| chr13:51375734
|
G | GAT | 4 | a0001c0001t0001g0182a0001c0001t0002g0181a0001c0001t0013g0106others(1): Show | 4 | HG00639.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1729+313_1729+314i others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
G | GATGT | 5 | a0001c0001t0002g0234a0001c0001t0013g0153a0001c0001t0013g0156others(2): Show | 5 | HG00280.hp2 HG01175.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1729+313_1729+314i others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
G | GGT | 68 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(65): Show | 71 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1729+312_1729+313d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
G | GGTGT | 14 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0036others(11): Show | 14 | HG00735.hp2 HG01106.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1729+310_1729+313d others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
G | GGTGTGT | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0103others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1729+308_1729+313d others(8): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
G | GGTGTGTG others(1): Show |
4 | a0001c0001t0001g0014a0001c0001t0010g0318a0001c0001t0036g0300others(1): Show | 4 | HG02615.hp1 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1729+306_1729+313d others(10): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0034g0295 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1729+302_1729+313d others(14): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
G | GT | 9 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0094others(6): Show | 9 | HG00735.hp1 HG01993.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1729+313_1729+314i others(3): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
G | T | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.1729+314C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
GGT | G | 44 | a0001c0001t0001g0110a0001c0001t0001g0166a0001c0001t0001g0227others(41): Show | 44 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1729+312_1729+313d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
GGTGT | G | 19 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0167others(16): Show | 19 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1729+310_1729+313d others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
GGTGTGTG others(7): Show |
G | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1729+300_1729+313d others(16): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375734
|
GGTGTGTG others(9): Show |
G | 1 | a0001c0001t0037g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1729+298_1729+313d others(18): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375734 | ||||||
| chr13:51375735
|
G | A | 3 | a0001c0001t0001g0191a0001c0001t0002g0188a0001c0001t0002g0194 | 3 | HG02647.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1729+313C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375735 | ||||||
| chr13:51375737
|
G | A | 3 | a0001c0001t0002g0154a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG02897.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1729+311C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375737 | ||||||
| chr13:51375739
|
G | A | 3 | a0001c0001t0001g0231a0001c0001t0002g0192a0001c0001t0002g0193 | 3 | HG02615.hp2 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1729+309C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375739 | ||||||
| chr13:51375740
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1729+308A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375740 | ||||||
| chr13:51375764
|
T | C | 1 | a0001c0001t0023g0121 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1729+284A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375764 | ||||||
| chr13:51375764
|
T | TGC | 3 | a0001c0001t0009g0133a0001c0001t0014g0129a0001c0001t0014g0136 | 3 | HG01952.hp1 NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1729+283_1729+284i others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375764 | ||||||
| chr13:51375764
|
T | TGTGC | 5 | a0001c0001t0009g0130a0001c0001t0009g0132a0001c0001t0009g0134others(2): Show | 5 | HG01346.hp2 HG01928.hp2 NA19081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1729+280_1729+283d others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375764 | ||||||
| chr13:51375766
|
T | C | 8 | a0001c0001t0001g0176a0001c0001t0001g0191a0001c0001t0002g0234others(5): Show | 9 | HG01074.hp1 HG02698.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1729+282A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375766 | ||||||
| chr13:51375766
|
T | TGC | 4 | a0001c0001t0001g0149a0001c0001t0001g0168a0001c0001t0001g0171others(1): Show | 4 | HG03130.hp1 NA19083.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1729+280_1729+281d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375766 | ||||||
| chr13:51375768
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1729+280G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375768 | ||||||
| chr13:51375769
|
G | A | 2 | a0001c0001t0018g0264a0001c0001t0018g0279 | 2 | HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1729+279C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375769 | ||||||
| chr13:51375775
|
G | A | 1 | a0001c0001t0036g0300 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1729+273C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375775 | ||||||
| chr13:51375999
|
CTA | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1729+47_1729+48del others(2): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 13/17 | chr13 | 51375999 | ||||||
| chr13:51376213
|
C | T | 1 | a0001c0001t0010g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1603-39G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51376213 | ||||||
| chr13:51376225
|
A | G | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1603-51T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51376225 | ||||||
| chr13:51376255
|
G | A | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1603-81C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51376255 | ||||||
| chr13:51376329
|
C | T | 5 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(2): Show | 5 | HG02074.hp1 HG02083.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603-155G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51376329 | ||||||
| chr13:51376615
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1603-441A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51376615 | ||||||
| chr13:51376712
|
C | T | 22 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0173others(19): Show | 22 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-538G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51376712 | ||||||
| chr13:51376717
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1603-543T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51376717 | ||||||
| chr13:51376836
|
C | T | 1 | a0001c0001t0003g0095 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1603-662G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51376836 | ||||||
| chr13:51377030
|
C | G | 1 | a0001c0001t0004g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1603-856G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51377030 | ||||||
| chr13:51377048
|
T | C | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1603-874A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51377048 | ||||||
| chr13:51377100
|
C | T | 1 | a0001c0001t0014g0129 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1603-926G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51377100 | ||||||
| chr13:51377580
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1602+659A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51377580 | ||||||
| chr13:51377805
|
A | C | 1 | a0001c0001t0002g0250 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1602+434T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51377805 | ||||||
| chr13:51377826
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1602+413A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51377826 | ||||||
| chr13:51377916
|
T | C | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.1602+323A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51377916 | ||||||
| chr13:51377971
|
C | T | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.1602+268G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51377971 | ||||||
| chr13:51378187
|
C | T | 2 | a0001c0001t0006g0265a0001c0001t0006g0289 | 2 | HG00099.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1602+52G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 12/17 | chr13 | 51378187 | ||||||
| chr13:51378741
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1387-287A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 11/17 | chr13 | 51378741 | ||||||
| chr13:51378745
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1387-291A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 11/17 | chr13 | 51378745 | ||||||
| chr13:51378960
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1386+502A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 11/17 | chr13 | 51378960 | ||||||
| chr13:51379135
|
GT | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1386+326delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 11/17 | chr13 | 51379135 | ||||||
| chr13:51379215
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1386+247A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 11/17 | chr13 | 51379215 | ||||||
| chr13:51379348
|
A | G | 2 | a0001c0001t0006g0290a0001c0001t0047g0350 | 2 | HG02523.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1386+114T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 11/17 | chr13 | 51379348 | ||||||
| chr13:51379405
|
C | T | 91 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1386+57G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 11/17 | chr13 | 51379405 | ||||||
| chr13:51379438
|
G | C | 1 | a0001c0001t0005g0269 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1386+24C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 11/17 | chr13 | 51379438 | ||||||
| chr13:51379620
|
T | C | 2 | a0001c0001t0004g0197a0001c0001t0039g0099 | 2 | HG02135.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1276-48A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51379620 | ||||||
| chr13:51379623
|
T | C | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1276-51A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51379623 | ||||||
| chr13:51379657
|
C | CA | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1276-86dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51379657 | ||||||
| chr13:51379704
|
C | T | 161 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(158): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1276-132G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51379704 | ||||||
| chr13:51379753
|
G | T | 2 | a0001c0001t0001g0067a0001c0001t0002g0068 | 2 | HG02683.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1276-181C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51379753 | ||||||
| chr13:51379762
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0030 | 3 | NA18960.hp2 NA19002.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1276-190T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51379762 | ||||||
| chr13:51379935
|
T | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0034g0295 | 3 | HG02965.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1276-363A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51379935 | ||||||
| chr13:51380083
|
T | C | 1 | a0001c0002t0008g0335 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1276-511A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51380083 | ||||||
| chr13:51380175
|
A | G | 1 | a0001c0001t0036g0300 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1276-603T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51380175 | ||||||
| chr13:51380300
|
T | A | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.1276-728A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51380300 | ||||||
| chr13:51380382
|
A | G | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1276-810T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51380382 | ||||||
| chr13:51380442
|
A | G | 1 | a0001c0001t0040g0327 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1276-870T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51380442 | ||||||
| chr13:51380478
|
C | T | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258 | 3 | HG02486.hp2 HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1276-906G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51380478 | ||||||
| chr13:51380663
|
A | G | 9 | a0001c0001t0001g0317a0001c0001t0010g0310a0001c0001t0010g0313others(6): Show | 9 | HG01243.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1276-1091T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51380663 | ||||||
| chr13:51380725
|
C | A | 2 | a0001c0001t0002g0188a0001c0001t0002g0194 | 2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1276-1153G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51380725 | ||||||
| chr13:51380882
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1275+1147A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51380882 | ||||||
| chr13:51380917
|
T | C | 1 | a0001c0001t0007g0212 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1275+1112A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51380917 | ||||||
| chr13:51381024
|
G | A | 4 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(1): Show | 4 | HG02257.hp1 HG03098.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275+1005C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381024 | ||||||
| chr13:51381076
|
C | T | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1275+953G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381076 | ||||||
| chr13:51381498
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0053 | 2 | NA18979.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1275+531C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381498 | ||||||
| chr13:51381527
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1275+502T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381527 | ||||||
| chr13:51381599
|
C | T | 48 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(45): Show | 49 | HG00438.hp2 HG01069.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.1275+430G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381599 | ||||||
| chr13:51381605
|
G | A | 267 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(264): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1275+424C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381605 | ||||||
| chr13:51381701
|
G | GT | 202 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1275+327dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381701 | ||||||
| chr13:51381701
|
G | GTT | 11 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0180others(8): Show | 11 | HG01934.hp2 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1275+326_1275+327d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381701 | ||||||
| chr13:51381701
|
GT | G | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.1275+327delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381701 | ||||||
| chr13:51381923
|
G | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1275+106C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381923 | ||||||
| chr13:51381933
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1275+96G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381933 | ||||||
| chr13:51381986
|
T | C | 271 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(268): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1275+43A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 10/17 | chr13 | 51381986 | ||||||
| chr13:51382489
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1181-366A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 9/17 | chr13 | 51382489 | ||||||
| chr13:51382665
|
AACTAT | A | 8 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0017g0298others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181-547_1181-543d others(7): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 9/17 | chr13 | 51382665 | ||||||
| chr13:51382787
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.1180+542T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 9/17 | chr13 | 51382787 | ||||||
| chr13:51383059
|
T | C | 1 | a0001c0001t0009g0131 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1180+270A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 9/17 | chr13 | 51383059 | ||||||
| chr13:51383092
|
A | AC | 45 | a0001c0001t0001g0178a0001c0001t0005g0244a0001c0001t0005g0245others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1180+236dupG | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 9/17 | chr13 | 51383092 | ||||||
| chr13:51383092
|
A | C | 1 | a0001c0002t0008g0335 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1180+237T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 9/17 | chr13 | 51383092 | ||||||
| chr13:51383101
|
C | CA | 11 | a0001c0001t0001g0017a0001c0001t0002g0249a0001c0001t0002g0250others(8): Show | 11 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1180+227dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 9/17 | chr13 | 51383101 | ||||||
| chr13:51383833
|
G | A | 5 | a0001c0001t0002g0154a0001c0001t0002g0189a0001c0001t0002g0190others(2): Show | 5 | HG02615.hp2 HG02818.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-92C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51383833 | ||||||
| chr13:51383873
|
T | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.895-132A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51383873 | ||||||
| chr13:51383982
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.895-241G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51383982 | ||||||
| chr13:51384064
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.895-323A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384064 | ||||||
| chr13:51384116
|
T | C | 1 | a0001c0001t0045g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.895-375A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384116 | ||||||
| chr13:51384132
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.895-391T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384132 | ||||||
| chr13:51384191
|
C | T | 1 | a0001c0001t0040g0327 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.895-450G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384191 | ||||||
| chr13:51384310
|
CCT | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.895-571_895-570del others(2): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384310 | ||||||
| chr13:51384491
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.895-750G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384491 | ||||||
| chr13:51384504
|
A | G | 1 | a0001c0001t0042g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.895-763T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384504 | ||||||
| chr13:51384575
|
C | A | 5 | a0001c0002t0008g0333a0001c0002t0008g0341a0001c0002t0008g0345others(2): Show | 5 | NA18939.hp1 NA18957.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-834G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384575 | ||||||
| chr13:51384620
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.895-879G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384620 | ||||||
| chr13:51384704
|
G | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.895-963C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384704 | ||||||
| chr13:51384890
|
CT | C | 13 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.895-1150delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384890 | ||||||
| chr13:51384938
|
G | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.895-1197C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51384938 | ||||||
| chr13:51385004
|
A | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.895-1263T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51385004 | ||||||
| chr13:51385070
|
A | G | 1 | a0001c0001t0004g0140 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.895-1329T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51385070 | ||||||
| chr13:51385096
|
C | G | 1 | a0001c0001t0002g0256 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.895-1355G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51385096 | ||||||
| chr13:51385129
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.895-1388A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51385129 | ||||||
| chr13:51385278
|
C | T | 1 | a0001c0001t0012g0284 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.895-1537G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51385278 | ||||||
| chr13:51385420
|
A | G | 3 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0089 | 3 | NA18964.hp2 NA18977.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.895-1679T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51385420 | ||||||
| chr13:51385552
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.895-1811G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51385552 | ||||||
| chr13:51385597
|
A | T | 1 | a0001c0001t0001g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.894+1789T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51385597 | ||||||
| chr13:51385693
|
TTTC | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.894+1690_894+1692d others(5): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51385693 | ||||||
| chr13:51385703
|
A | G | 1 | a0001c0002t0008g0332 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.894+1683T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51385703 | ||||||
| chr13:51385836
|
T | C | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.894+1550A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51385836 | ||||||
| chr13:51386159
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0002g0181 | 2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.894+1227T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51386159 | ||||||
| chr13:51386231
|
G | A | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.894+1155C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51386231 | ||||||
| chr13:51386259
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.894+1127A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51386259 | ||||||
| chr13:51386280
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.894+1106A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51386280 | ||||||
| chr13:51386304
|
A | AAATAG | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.894+1077_894+1081d others(7): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51386304 | ||||||
| chr13:51386386
|
A | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.894+1000T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51386386 | ||||||
| chr13:51386407
|
T | C | 1 | a0001c0001t0003g0090 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.894+979A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51386407 | ||||||
| chr13:51386438
|
A | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.894+948T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51386438 | ||||||
| chr13:51386770
|
AT | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.894+615delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51386770 | ||||||
| chr13:51386782
|
A | G | 1 | a0001c0001t0001g0322 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.894+604T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51386782 | ||||||
| chr13:51386884
|
C | T | 1 | a0001c0001t0034g0295 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.894+502G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51386884 | ||||||
| chr13:51387264
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.894+122A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51387264 | ||||||
| chr13:51387282
|
T | C | 4 | a0001c0001t0009g0131a0001c0001t0009g0132a0001c0001t0009g0134others(1): Show | 4 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+104A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 7/17 | chr13 | 51387282 | ||||||
| chr13:51387543
|
A | G | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02965.hp2 HG03139.hp1 |
splice_region_variant&intron_variant | LOW | c.740-3T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51387543 | ||||||
| chr13:51387747
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.740-207G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51387747 | ||||||
| chr13:51387775
|
G | A | 1 | a0001c0001t0012g0270 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.740-235C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51387775 | ||||||
| chr13:51387831
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.740-291T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51387831 | ||||||
| chr13:51387840
|
T | C | 1 | a0001c0001t0004g0224 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.740-300A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51387840 | ||||||
| chr13:51387892
|
C | T | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.740-352G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51387892 | ||||||
| chr13:51387999
|
C | T | 1 | a0001c0001t0002g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.740-459G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51387999 | ||||||
| chr13:51388354
|
T | TTG | 17 | a0001c0001t0004g0232a0001c0002t0008g0247a0001c0002t0008g0331others(14): Show | 18 | HG01069.hp2 HG02647.hp1 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.740-816_740-815dup others(2): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51388354 | ||||||
| chr13:51388370
|
T | G | 1 | a0001c0002t0008g0345 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-830A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51388370 | ||||||
| chr13:51388373
|
G | GT | 14 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.740-834dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51388373 | ||||||
| chr13:51388373
|
G | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.740-833C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51388373 | ||||||
| chr13:51388383
|
G | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.740-843C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51388383 | ||||||
| chr13:51388389
|
G | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.740-849C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51388389 | ||||||
| chr13:51388391
|
T | G | 1 | a0001c0002t0020g0008 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.740-851A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51388391 | ||||||
| chr13:51388471
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.739+848C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51388471 | ||||||
| chr13:51388582
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.739+737C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51388582 | ||||||
| chr13:51388647
|
C | T | 7 | a0001c0001t0001g0329a0001c0001t0004g0039a0001c0001t0004g0321others(4): Show | 7 | HG02074.hp2 NA18943.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.739+672G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51388647 | ||||||
| chr13:51388899
|
CA | C | 265 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(262): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.739+419delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51388899 | ||||||
| chr13:51389141
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.739+178A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51389141 | ||||||
| chr13:51389146
|
T | C | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.739+173A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51389146 | ||||||
| chr13:51389212
|
T | C | 91 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.739+107A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 6/17 | chr13 | 51389212 | ||||||
| chr13:51389458
|
AAAG | A | 13 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.614-17_614-15delCT others(1): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51389458 | ||||||
| chr13:51389725
|
A | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0040 | 2 | NA18947.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.614-281T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51389725 | ||||||
| chr13:51390357
|
G | T | 16 | a0001c0001t0002g0009a0001c0001t0003g0013a0001c0001t0007g0158others(13): Show | 16 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.614-913C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51390357 | ||||||
| chr13:51390363
|
T | C | 1 | a0001c0001t0012g0248 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.614-919A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51390363 | ||||||
| chr13:51390388
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.614-944T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51390388 | ||||||
| chr13:51390435
|
T | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.614-991A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51390435 | ||||||
| chr13:51390524
|
C | T | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.614-1080G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51390524 | ||||||
| chr13:51390605
|
C | T | 3 | a0001c0001t0003g0150a0001c0001t0003g0151a0001c0001t0003g0152 | 3 | HG02258.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.614-1161G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51390605 | ||||||
| chr13:51390629
|
T | C | 13 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.614-1185A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51390629 | ||||||
| chr13:51390829
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.614-1385G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51390829 | ||||||
| chr13:51390873
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0242a0001c0001t0001g0243 | 4 | HG03490.hp2 HG03492.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-1429A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51390873 | ||||||
| chr13:51390999
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.614-1555C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51390999 | ||||||
| chr13:51391012
|
T | C | 2 | a0001c0001t0014g0127a0001c0001t0014g0128 | 2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.614-1568A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51391012 | ||||||
| chr13:51391242
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0070others(7): Show | 11 | HG02015.hp2 NA18948.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.614-1798G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51391242 | ||||||
| chr13:51391316
|
G | A | 13 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.614-1872C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51391316 | ||||||
| chr13:51391353
|
C | G | 6 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(3): Show | 6 | HG02074.hp1 HG02083.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.614-1909G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51391353 | ||||||
| chr13:51391382
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.614-1938T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51391382 | ||||||
| chr13:51391744
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.614-2300T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51391744 | ||||||
| chr13:51391834
|
T | C | 1 | a0001c0001t0014g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.614-2390A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51391834 | ||||||
| chr13:51392140
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.614-2696G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392140 | ||||||
| chr13:51392169
|
G | A | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.614-2725C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392169 | ||||||
| chr13:51392193
|
G | A | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.614-2749C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392193 | ||||||
| chr13:51392197
|
C | A | 1 | a0001c0001t0001g0191 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.614-2753G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392197 | ||||||
| chr13:51392200
|
C | T | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.614-2756G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392200 | ||||||
| chr13:51392202
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.614-2758G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392202 | ||||||
| chr13:51392251
|
T | C | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.614-2807A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392251 | ||||||
| chr13:51392258
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.614-2814A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392258 | ||||||
| chr13:51392325
|
C | T | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.614-2881G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392325 | ||||||
| chr13:51392438
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.613+2862T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392438 | ||||||
| chr13:51392600
|
C | T | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.613+2700G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392600 | ||||||
| chr13:51392633
|
T | C | 1 | a0001c0001t0032g0299 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.613+2667A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392633 | ||||||
| chr13:51392709
|
T | C | 15 | a0001c0001t0002g0009a0001c0001t0007g0158a0001c0001t0007g0187others(12): Show | 15 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.613+2591A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392709 | ||||||
| chr13:51392782
|
C | A | 91 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.613+2518G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51392782 | ||||||
| chr13:51393040
|
A | G | 1 | a0001c0001t0007g0187 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.613+2260T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393040 | ||||||
| chr13:51393071
|
T | G | 1 | a0001c0001t0004g0139 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.613+2229A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393071 | ||||||
| chr13:51393074
|
A | AT | 13 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0001g0089others(10): Show | 13 | HG00597.hp2 HG01175.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.613+2225dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393074 | ||||||
| chr13:51393074
|
AT | A | 22 | a0001c0001t0001g0113a0001c0001t0001g0191a0001c0001t0001g0231others(19): Show | 22 | HG01069.hp1 HG01346.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.613+2225delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393074 | ||||||
| chr13:51393166
|
C | T | 1 | a0001c0001t0007g0201 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.613+2134G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393166 | ||||||
| chr13:51393222
|
C | T | 23 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0160others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.613+2078G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393222 | ||||||
| chr13:51393234
|
C | T | 13 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.613+2066G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393234 | ||||||
| chr13:51393358
|
A | G | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.613+1942T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393358 | ||||||
| chr13:51393369
|
C | T | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258 | 3 | HG02486.hp2 HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.613+1931G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393369 | ||||||
| chr13:51393373
|
C | T | 2 | a0001c0001t0002g0169a0001c0001t0007g0161 | 2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.613+1927G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393373 | ||||||
| chr13:51393766
|
A | T | 16 | a0001c0001t0002g0009a0001c0001t0003g0013a0001c0001t0007g0158others(13): Show | 16 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.613+1534T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393766 | ||||||
| chr13:51393848
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.613+1452T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393848 | ||||||
| chr13:51393985
|
C | T | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+1315G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51393985 | ||||||
| chr13:51394108
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.613+1192G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51394108 | ||||||
| chr13:51394188
|
T | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG02280.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.613+1112A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51394188 | ||||||
| chr13:51394201
|
A | G | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.613+1099T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51394201 | ||||||
| chr13:51394220
|
T | C | 8 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0017g0298others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.613+1080A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51394220 | ||||||
| chr13:51394266
|
G | A | 266 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.613+1034C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51394266 | ||||||
| chr13:51394277
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.613+1023T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51394277 | ||||||
| chr13:51394469
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.613+831G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51394469 | ||||||
| chr13:51394646
|
G | A | 1 | a0001c0001t0032g0299 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.613+654C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51394646 | ||||||
| chr13:51395071
|
A | G | 1 | a0001c0001t0025g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.613+229T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51395071 | ||||||
| chr13:51395163
|
A | G | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.613+137T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51395163 | ||||||
| chr13:51395202
|
G | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.613+98C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51395202 | ||||||
| chr13:51395247
|
A | G | 36 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(33): Show | 36 | HG00099.hp1 HG00558.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.613+53T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 5/17 | chr13 | 51395247 | ||||||
| chr13:51395560
|
C | T | 91 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.430-77G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51395560 | ||||||
| chr13:51395681
|
G | A | 1 | a0001c0001t0038g0195 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.430-198C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51395681 | ||||||
| chr13:51395771
|
A | G | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.430-288T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51395771 | ||||||
| chr13:51396044
|
C | T | 1 | a0001c0001t0032g0299 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.430-561G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396044 | ||||||
| chr13:51396112
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.430-629A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396112 | ||||||
| chr13:51396124
|
T | C | 1 | a0001c0001t0032g0299 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.430-641A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396124 | ||||||
| chr13:51396242
|
T | A | 1 | a0001c0001t0002g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.430-759A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396242 | ||||||
| chr13:51396255
|
C | T | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-772G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396255 | ||||||
| chr13:51396305
|
A | G | 1 | a0001c0001t0002g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430-822T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396305 | ||||||
| chr13:51396369
|
C | A | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.430-886G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396369 | ||||||
| chr13:51396482
|
C | T | 1 | a0001c0001t0034g0295 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.430-999G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396482 | ||||||
| chr13:51396637
|
T | G | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-1154A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396637 | ||||||
| chr13:51396638
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0002g0188a0001c0001t0002g0194 | 3 | HG02647.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.430-1155G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396638 | ||||||
| chr13:51396829
|
A | G | 267 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(264): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.430-1346T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396829 | ||||||
| chr13:51396860
|
C | T | 5 | a0001c0001t0002g0009a0001c0001t0007g0196a0001c0001t0007g0216others(2): Show | 5 | HG01081.hp2 HG01928.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-1377G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396860 | ||||||
| chr13:51396993
|
T | A | 6 | a0001c0001t0002g0043a0001c0001t0002g0154a0001c0001t0002g0189others(3): Show | 6 | HG02615.hp2 HG02818.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-1510A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51396993 | ||||||
| chr13:51397106
|
C | A | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-1623G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397106 | ||||||
| chr13:51397215
|
T | C | 2 | a0001c0001t0002g0169a0001c0001t0007g0161 | 2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.430-1732A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397215 | ||||||
| chr13:51397346
|
T | A | 15 | a0001c0001t0002g0009a0001c0001t0007g0158a0001c0001t0007g0187others(12): Show | 15 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.430-1863A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397346 | ||||||
| chr13:51397425
|
G | A | 1 | a0001c0001t0003g0150 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.430-1942C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397425 | ||||||
| chr13:51397474
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.430-1991C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397474 | ||||||
| chr13:51397488
|
G | A | 1 | a0001c0001t0019g0307 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.430-2005C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397488 | ||||||
| chr13:51397728
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.430-2245G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397728 | ||||||
| chr13:51397815
|
C | CCA | 27 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0317others(24): Show | 27 | HG01243.hp2 HG01346.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.430-2334_430-2333d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397815 | ||||||
| chr13:51397834
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.430-2351A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397834 | ||||||
| chr13:51397835
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.430-2352C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397835 | ||||||
| chr13:51397836
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.430-2353G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397836 | ||||||
| chr13:51397837
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.430-2354T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51397837 | ||||||
| chr13:51398207
|
T | C | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-2724A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51398207 | ||||||
| chr13:51398290
|
T | G | 1 | a0001c0001t0002g0256 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.430-2807A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51398290 | ||||||
| chr13:51398344
|
G | C | 2 | a0001c0001t0002g0077a0001c0001t0002g0078 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.430-2861C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51398344 | ||||||
| chr13:51398408
|
A | G | 14 | a0001c0001t0001g0229a0001c0001t0005g0267a0001c0001t0009g0130others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-2925T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51398408 | ||||||
| chr13:51398554
|
G | A | 1 | a0001c0001t0019g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430-3071C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51398554 | ||||||
| chr13:51398591
|
T | C | 60 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(57): Show | 61 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.430-3108A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51398591 | ||||||
| chr13:51398647
|
G | C | 1 | a0001c0001t0005g0282 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.430-3164C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51398647 | ||||||
| chr13:51398729
|
TA | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0005g0269others(21): Show | 25 | HG00438.hp2 HG01069.hp2 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.430-3247delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51398729 | ||||||
| chr13:51398889
|
T | C | 1 | a0001c0001t0001g0329 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.430-3406A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51398889 | ||||||
| chr13:51399212
|
GTTTTATT | G | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.430-3736_430-3730d others(9): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51399212 | ||||||
| chr13:51399228
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-3745T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51399228 | ||||||
| chr13:51399630
|
G | A | 13 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.430-4147C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51399630 | ||||||
| chr13:51399702
|
T | TTGTGTGT others(3): Show |
1 | a0001c0002t0008g0335 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.430-4220_430-4219i others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51399702 | ||||||
| chr13:51399705
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.430-4222A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51399705 | ||||||
| chr13:51399707
|
G | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-4224C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51399707 | ||||||
| chr13:51399713
|
TGTGTGTG others(3): Show |
T | 44 | a0001c0001t0002g0252a0001c0001t0005g0244a0001c0001t0005g0245others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.430-4240_430-4231d others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51399713 | ||||||
| chr13:51399973
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-4490T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51399973 | ||||||
| chr13:51400132
|
A | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-4649T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51400132 | ||||||
| chr13:51400232
|
G | T | 9 | a0001c0001t0001g0317a0001c0001t0010g0310a0001c0001t0010g0313others(6): Show | 9 | HG01243.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.430-4749C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51400232 | ||||||
| chr13:51400264
|
A | C | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.430-4781T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51400264 | ||||||
| chr13:51400554
|
C | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-5071G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51400554 | ||||||
| chr13:51400802
|
C | T | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-5319G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51400802 | ||||||
| chr13:51400914
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.430-5431T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51400914 | ||||||
| chr13:51401385
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-5902C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51401385 | ||||||
| chr13:51401621
|
G | T | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-6138C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51401621 | ||||||
| chr13:51401888
|
T | C | 9 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0213others(6): Show | 9 | HG01192.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.430-6405A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51401888 | ||||||
| chr13:51402015
|
A | G | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.430-6532T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402015 | ||||||
| chr13:51402186
|
AC | A | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258 | 3 | HG02486.hp2 HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430-6704delG | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402186 | ||||||
| chr13:51402193
|
G | A | 266 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.430-6710C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402193 | ||||||
| chr13:51402198
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-6715G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402198 | ||||||
| chr13:51402223
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.430-6740T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402223 | ||||||
| chr13:51402228
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-6745C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402228 | ||||||
| chr13:51402359
|
G | A | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.430-6876C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402359 | ||||||
| chr13:51402446
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0053 | 2 | NA18979.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.430-6963G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402446 | ||||||
| chr13:51402508
|
T | C | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.430-7025A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402508 | ||||||
| chr13:51402812
|
C | A | 1 | a0001c0001t0012g0248 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.430-7329G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402812 | ||||||
| chr13:51402888
|
C | CTTTA | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-7406_430-7405i others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402888 | ||||||
| chr13:51402966
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.430-7483T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51402966 | ||||||
| chr13:51403004
|
C | T | 1 | a0001c0001t0036g0300 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.430-7521G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403004 | ||||||
| chr13:51403005
|
G | A | 4 | a0001c0001t0001g0166a0001c0001t0002g0169a0001c0001t0007g0161others(1): Show | 4 | HG01978.hp2 HG02293.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-7522C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403005 | ||||||
| chr13:51403057
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.430-7574C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403057 | ||||||
| chr13:51403069
|
T | C | 270 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.430-7586A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403069 | ||||||
| chr13:51403269
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.430-7786C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403269 | ||||||
| chr13:51403357
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.430-7874G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403357 | ||||||
| chr13:51403439
|
G | A | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.430-7956C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403439 | ||||||
| chr13:51403489
|
G | A | 1 | a0001c0001t0045g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.430-8006C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403489 | ||||||
| chr13:51403543
|
C | G | 1 | a0001c0001t0012g0291 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.430-8060G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403543 | ||||||
| chr13:51403573
|
C | T | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.430-8090G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403573 | ||||||
| chr13:51403583
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0005g0276 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.430-8101_430-8100i others(14): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403583 | ||||||
| chr13:51403583
|
A | AAAAAAAA others(4): Show |
155 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.430-8111_430-8101d others(13): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403583 | ||||||
| chr13:51403583
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0164 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.430-8101_430-8100i others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403583 | ||||||
| chr13:51403583
|
AAAAAAAA others(4): Show |
A | 8 | a0001c0001t0001g0004a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 9 | HG01256.hp1 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.430-8111_430-8101d others(13): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403583 | ||||||
| chr13:51403592
|
A | G | 1 | a0001c0002t0008g0335 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.430-8109T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403592 | ||||||
| chr13:51403593
|
A | AAGAAAAA others(6): Show |
1 | a0001c0001t0005g0259 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.430-8111_430-8110i others(15): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403593 | ||||||
| chr13:51403594
|
G | A | 2 | a0001c0001t0005g0259a0001c0002t0008g0335 | 2 | NA18981.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.430-8111C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403594 | ||||||
| chr13:51403594
|
G | GAAAAAAA others(5): Show |
4 | a0001c0001t0001g0329a0001c0001t0002g0193a0001c0001t0002g0254others(1): Show | 4 | HG02615.hp2 HG03688.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-8123_430-8112d others(14): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403594 | ||||||
| chr13:51403594
|
GA | G | 16 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(13): Show | 17 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(14): Show |
intron_variant | MODIFIER | c.430-8112delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403594 | ||||||
| chr13:51403595
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0042 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.430-8122_430-8113d others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403595 | ||||||
| chr13:51403595
|
A | G | 1 | a0001c0002t0008g0335 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.430-8112T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403595 | ||||||
| chr13:51403603
|
A | AAGAAAAA others(4): Show |
1 | a0001c0001t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.430-8121_430-8120i others(13): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403603 | ||||||
| chr13:51403605
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.430-8122C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403605 | ||||||
| chr13:51403605
|
G | GA | 25 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0033others(22): Show | 26 | HG00741.hp2 HG01106.hp1 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.430-8123dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403605 | ||||||
| chr13:51403605
|
G | GAAAAAAA others(6): Show |
2 | a0001c0001t0001g0170a0001c0001t0001g0172 | 2 | HG01175.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.430-8123_430-8122i others(15): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403605 | ||||||
| chr13:51403605
|
G | GAAAAAAA others(5): Show |
45 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0030others(42): Show | 45 | HG00423.hp1 HG00642.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.430-8123_430-8122i others(14): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51403605 | ||||||
| chr13:51404063
|
T | TAC | 12 | a0001c0001t0001g0002a0001c0001t0001g0056a0001c0001t0001g0060others(9): Show | 13 | HG01106.hp1 HG02135.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.430-8582_430-8581d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404063
|
T | TACAC | 8 | a0001c0001t0004g0098a0001c0001t0009g0133a0001c0001t0009g0137others(5): Show | 8 | HG01243.hp2 HG02523.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-8584_430-8581d others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404063
|
T | TACACAC | 15 | a0001c0001t0001g0170a0001c0001t0002g0009a0001c0001t0003g0013others(12): Show | 15 | HG01081.hp2 HG01175.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.430-8586_430-8581d others(8): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404063
|
T | TACACACA others(1): Show |
14 | a0001c0001t0004g0096a0001c0001t0004g0097a0001c0001t0007g0187others(11): Show | 14 | HG00735.hp2 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-8588_430-8581d others(10): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404063
|
T | TACACACA others(3): Show |
6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0172others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-8590_430-8581d others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404063
|
T | TACACACA others(5): Show |
1 | a0001c0001t0001g0164 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.430-8592_430-8581d others(14): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404063
|
T | TACACACA others(17): Show |
1 | a0001c0001t0004g0174 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.430-8604_430-8581d others(26): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404063
|
TAC | T | 54 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0047others(51): Show | 55 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.430-8582_430-8581d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404063
|
TACAC | T | 7 | a0001c0001t0001g0064a0001c0001t0001g0102a0001c0001t0002g0255others(4): Show | 7 | HG00597.hp2 HG00741.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-8584_430-8581d others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404063
|
TACACAC | T | 40 | a0001c0001t0001g0309a0001c0001t0003g0185a0001c0001t0003g0203others(37): Show | 40 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.430-8586_430-8581d others(8): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404063
|
TACACACA others(1): Show |
T | 8 | a0001c0001t0001g0087a0001c0001t0005g0261a0001c0001t0005g0282others(5): Show | 8 | HG00642.hp2 HG00741.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-8588_430-8581d others(10): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404063
|
TACACACA others(9): Show |
T | 1 | a0001c0001t0006g0280 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.430-8596_430-8581d others(18): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404063 | ||||||
| chr13:51404097
|
C | G | 1 | a0001c0001t0006g0265 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.430-8614G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404097 | ||||||
| chr13:51404099
|
C | G | 4 | a0001c0001t0005g0244a0001c0001t0005g0246a0001c0001t0005g0267others(1): Show | 4 | HG00099.hp1 HG02683.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-8616G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404099 | ||||||
| chr13:51404101
|
C | G | 43 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0002g0234others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.430-8618G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404101 | ||||||
| chr13:51404103
|
C | CACACACA others(15): Show |
1 | a0001c0001t0001g0162 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.430-8621_430-8620i others(24): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACACACA others(9): Show |
2 | a0001c0001t0001g0168a0001c0001t0015g0032 | 2 | NA19083.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.430-8621_430-8620i others(18): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACACACA others(7): Show |
4 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0176others(1): Show | 4 | HG02559.hp1 NA18992.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-8621_430-8620i others(16): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACACACA others(5): Show |
8 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0173others(5): Show | 8 | HG00423.hp1 HG01978.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-8621_430-8620i others(14): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACACACA others(9): Show |
1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.430-8621_430-8620i others(18): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACACACA others(3): Show |
13 | a0001c0001t0001g0017a0001c0001t0001g0159a0001c0001t0001g0163others(10): Show | 13 | HG00544.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.430-8621_430-8620i others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACACACA others(1): Show |
14 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0040others(11): Show | 14 | HG01255.hp1 HG01255.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.430-8621_430-8620i others(10): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACACACA others(3): Show |
3 | a0001c0001t0001g0020a0001c0001t0001g0305a0001c0001t0002g0046 | 3 | HG02109.hp2 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.430-8621_430-8620i others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACACAG | 55 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(52): Show | 57 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.430-8621_430-8620i others(8): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACACAGA others(1): Show |
7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(4): Show | 7 | HG01891.hp1 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-8621_430-8620i others(10): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACACAGA others(3): Show |
1 | a0001c0001t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.430-8621_430-8620i others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACACAGA others(5): Show |
1 | a0001c0001t0001g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.430-8621_430-8620i others(14): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACAG | 6 | a0001c0001t0001g0227a0001c0001t0002g0043a0001c0001t0002g0190others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-8621_430-8620i others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CACAGAG | 5 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(2): Show | 5 | HG00099.hp2 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-8621_430-8620i others(8): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | CAG | 3 | a0001c0001t0001g0191a0001c0001t0003g0198a0001c0001t0004g0232 | 3 | HG02647.hp1 HG03942.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.430-8622_430-8621d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
C | G | 72 | a0001c0001t0001g0102a0001c0001t0001g0182a0001c0001t0001g0296others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.430-8620G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
CAG | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0103a0001c0001t0001g0104others(15): Show | 20 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.430-8622_430-8621d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404103
|
CAGAG | C | 4 | a0001c0002t0008g0247a0001c0002t0008g0336a0001c0002t0031g0344others(1): Show | 4 | HG01069.hp2 HG02698.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-8624_430-8621d others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404103 | ||||||
| chr13:51404105
|
G | C | 5 | a0001c0001t0002g0078a0001c0001t0030g0138a0001c0001t0038g0195others(2): Show | 5 | HG01928.hp1 HG02257.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-8622C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404105 | ||||||
| chr13:51404107
|
G | C | 12 | a0001c0002t0008g0331a0001c0002t0008g0332a0001c0002t0008g0333others(9): Show | 13 | HG00438.hp2 HG03491.hp1 HG03492.hp1 others(10): Show |
intron_variant | MODIFIER | c.430-8624C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404107 | ||||||
| chr13:51404121
|
G | C | 1 | a0001c0001t0006g0265 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.430-8638C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404121 | ||||||
| chr13:51404164
|
G | C | 71 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0160others(68): Show | 72 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.430-8681C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404164 | ||||||
| chr13:51404213
|
G | C | 6 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(3): Show | 6 | HG02074.hp1 HG02083.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-8730C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404213 | ||||||
| chr13:51404293
|
T | TA | 19 | a0001c0001t0001g0062a0001c0001t0001g0167a0001c0001t0004g0325others(16): Show | 20 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(17): Show |
intron_variant | MODIFIER | c.430-8811dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404293 | ||||||
| chr13:51404293
|
TA | T | 75 | a0001c0001t0001g0074a0001c0001t0001g0231a0001c0001t0001g0296others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.430-8811delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404293 | ||||||
| chr13:51404507
|
C | T | 5 | a0001c0001t0003g0218a0001c0001t0004g0157a0001c0001t0004g0219others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-9024G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404507 | ||||||
| chr13:51404851
|
A | C | 91 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.430-9368T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404851 | ||||||
| chr13:51404895
|
C | T | 3 | a0001c0001t0001g0235a0001c0001t0002g0237a0001c0001t0002g0238 | 3 | HG02559.hp2 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.430-9412G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404895 | ||||||
| chr13:51404930
|
C | A | 1 | a0001c0001t0003g0152 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.430-9447G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404930 | ||||||
| chr13:51404937
|
ATCT | A | 161 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(158): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.430-9457_430-9455d others(5): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51404937 | ||||||
| chr13:51405114
|
C | G | 1 | a0001c0001t0004g0224 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.430-9631G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51405114 | ||||||
| chr13:51405187
|
T | C | 1 | a0001c0001t0032g0299 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.430-9704A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51405187 | ||||||
| chr13:51405251
|
G | C | 1 | a0001c0001t0003g0152 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.430-9768C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51405251 | ||||||
| chr13:51405305
|
A | T | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.430-9822T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51405305 | ||||||
| chr13:51405424
|
T | A | 1 | a0001c0001t0001g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.430-9941A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51405424 | ||||||
| chr13:51405606
|
C | T | 1 | a0001c0001t0004g0140 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.430-10123G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51405606 | ||||||
| chr13:51405870
|
T | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0053 | 2 | NA18979.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.430-10387A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51405870 | ||||||
| chr13:51405949
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.430-10466A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51405949 | ||||||
| chr13:51406091
|
C | A | 1 | a0001c0001t0006g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.430-10608G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406091 | ||||||
| chr13:51406405
|
T | A | 1 | a0001c0001t0006g0274 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.430-10922A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406405 | ||||||
| chr13:51406421
|
A | AT | 180 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(177): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.430-10939dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406421 | ||||||
| chr13:51406432
|
CCACCTCC others(16): Show |
C | 1 | a0001c0001t0001g0064 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.430-10972_430-1095 others(27): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406432 | ||||||
| chr13:51406442
|
CCT | C | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.430-10961_430-1096 others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406442 | ||||||
| chr13:51406519
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0002g0188a0001c0001t0002g0194 | 3 | HG02647.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.430-11036G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406519 | ||||||
| chr13:51406560
|
C | A | 5 | a0001c0001t0001g0142a0001c0001t0003g0143a0001c0001t0004g0139others(2): Show | 5 | HG00140.hp2 HG00642.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-11077G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406560 | ||||||
| chr13:51406763
|
G | A | 3 | a0001c0001t0005g0269a0001c0001t0012g0270a0001c0001t0012g0284 | 3 | HG02602.hp2 NA20905.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.430-11280C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406763 | ||||||
| chr13:51406831
|
G | T | 2 | a0001c0001t0007g0209a0001c0001t0041g0208 | 2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.430-11348C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406831 | ||||||
| chr13:51406899
|
A | AT | 19 | a0001c0001t0001g0036a0001c0001t0001g0159a0001c0001t0001g0182others(16): Show | 19 | HG00597.hp1 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.430-11417dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406899 | ||||||
| chr13:51406899
|
AT | A | 10 | a0001c0001t0001g0087a0001c0001t0001g0297a0001c0001t0003g0205others(7): Show | 10 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-11417delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406899 | ||||||
| chr13:51406899
|
ATT | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-11418_430-1141 others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406899 | ||||||
| chr13:51406900
|
T | A | 1 | a0001c0001t0001g0296 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.430-11417A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51406900 | ||||||
| chr13:51407033
|
G | A | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.430-11550C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51407033 | ||||||
| chr13:51407080
|
GA | G | 11 | a0001c0001t0001g0166a0001c0001t0002g0249a0001c0001t0002g0250others(8): Show | 11 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-11598delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51407080 | ||||||
| chr13:51407392
|
C | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-11909G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51407392 | ||||||
| chr13:51408016
|
C | CA | 26 | a0001c0001t0001g0025a0001c0001t0003g0222a0001c0001t0004g0140others(23): Show | 26 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.430-12534dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51408016 | ||||||
| chr13:51408060
|
A | G | 161 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(158): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.430-12577T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51408060 | ||||||
| chr13:51408146
|
G | GT | 43 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0053others(40): Show | 44 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.430-12664dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51408146 | ||||||
| chr13:51408146
|
GT | G | 13 | a0001c0001t0001g0116a0001c0001t0001g0235a0001c0001t0002g0249others(10): Show | 13 | HG01074.hp1 HG01081.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.430-12664delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51408146 | ||||||
| chr13:51408290
|
C | G | 1 | a0001c0001t0001g0018 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.430-12807G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51408290 | ||||||
| chr13:51408333
|
C | T | 1 | a0001c0001t0005g0259 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.430-12850G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51408333 | ||||||
| chr13:51408612
|
GTATGT | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0059a0001c0001t0001g0061 | 3 | NA18944.hp1 NA18965.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.430-13134_430-1313 others(9): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51408612 | ||||||
| chr13:51408729
|
T | C | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-13246A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51408729 | ||||||
| chr13:51408986
|
T | G | 1 | a0001c0001t0006g0287 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.430-13503A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51408986 | ||||||
| chr13:51409040
|
C | A | 1 | a0001c0001t0045g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.430-13557G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409040 | ||||||
| chr13:51409082
|
T | C | 4 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0213others(1): Show | 4 | HG01192.hp2 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-13599A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409082 | ||||||
| chr13:51409168
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-13685C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409168 | ||||||
| chr13:51409194
|
C | T | 1 | a0001c0001t0002g0043 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.430-13711G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409194 | ||||||
| chr13:51409263
|
A | AAAT | 19 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0028others(16): Show | 21 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.430-13783_430-1378 others(7): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409263 | ||||||
| chr13:51409263
|
A | AAATAAT | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0002g0188 | 3 | HG03130.hp2 HG03688.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.430-13786_430-1378 others(10): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409263 | ||||||
| chr13:51409263
|
AAAT | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(101): Show | 106 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.430-13783_430-1378 others(7): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409263 | ||||||
| chr13:51409263
|
AAATAAT | A | 52 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0037others(49): Show | 53 | HG00423.hp2 HG00642.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.430-13786_430-1378 others(10): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409263 | ||||||
| chr13:51409263
|
AAATAATA others(2): Show |
A | 95 | a0001c0001t0001g0020a0001c0001t0001g0111a0001c0001t0001g0115others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.430-13789_430-1378 others(13): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409263 | ||||||
| chr13:51409263
|
AAATAATA others(5): Show |
A | 14 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0030others(11): Show | 14 | HG01192.hp1 HG01358.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.430-13792_430-1378 others(16): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409263 | ||||||
| chr13:51409263
|
AAATAATA others(8): Show |
A | 6 | a0001c0001t0001g0155a0001c0001t0001g0305a0001c0001t0003g0222others(3): Show | 6 | HG00597.hp1 HG00609.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-13795_430-1378 others(19): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409263 | ||||||
| chr13:51409263
|
AAATAATA others(11): Show |
A | 1 | a0001c0001t0004g0197 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.430-13798_430-1378 others(22): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409263 | ||||||
| chr13:51409263
|
AAATAATA others(14): Show |
A | 2 | a0001c0001t0002g0249a0001c0001t0002g0251 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.430-13801_430-1378 others(25): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409263 | ||||||
| chr13:51409299
|
T | G | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.430-13816A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409299 | ||||||
| chr13:51409580
|
T | C | 2 | a0001c0001t0003g0218a0001c0001t0004g0157 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.430-14097A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409580 | ||||||
| chr13:51409641
|
A | AT | 23 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(20): Show | 24 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.430-14159dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409641 | ||||||
| chr13:51409664
|
ATTGGTG | A | 8 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0017g0298others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-14187_430-1418 others(10): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409664 | ||||||
| chr13:51409855
|
G | A | 2 | a0001c0001t0019g0307a0001c0001t0019g0308 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.430-14372C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51409855 | ||||||
| chr13:51410015
|
A | G | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-14532T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51410015 | ||||||
| chr13:51410072
|
G | A | 1 | a0001c0001t0003g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.430-14589C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51410072 | ||||||
| chr13:51410124
|
T | C | 1 | a0001c0001t0036g0300 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.430-14641A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51410124 | ||||||
| chr13:51410169
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.430-14686A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51410169 | ||||||
| chr13:51410493
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.430-15010A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51410493 | ||||||
| chr13:51410834
|
C | T | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.430-15351G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51410834 | ||||||
| chr13:51410844
|
A | C | 1 | a0001c0001t0004g0140 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.430-15361T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51410844 | ||||||
| chr13:51411125
|
A | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-15642T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411125 | ||||||
| chr13:51411127
|
T | C | 16 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(13): Show | 16 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.430-15644A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411127 | ||||||
| chr13:51411187
|
C | T | 91 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.430-15704G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411187 | ||||||
| chr13:51411190
|
G | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0034g0295 | 3 | HG02965.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.430-15707C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411190 | ||||||
| chr13:51411214
|
A | AAAAT | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 71 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.430-15735_430-1573 others(8): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411214 | ||||||
| chr13:51411214
|
A | AAAATAAA others(1): Show |
10 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(7): Show | 10 | HG01106.hp1 HG01358.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.430-15739_430-1573 others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411214 | ||||||
| chr13:51411214
|
AAAAT | A | 9 | a0001c0001t0001g0086a0001c0001t0001g0191a0001c0001t0002g0249others(6): Show | 9 | HG01257.hp1 HG01258.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.430-15735_430-1573 others(8): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411214 | ||||||
| chr13:51411214
|
AAAATAAA others(5): Show |
A | 3 | a0001c0001t0019g0307a0001c0001t0019g0308a0001c0001t0032g0299 | 3 | HG01891.hp1 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.430-15743_430-1573 others(16): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411214 | ||||||
| chr13:51411214
|
AAAATAAA others(9): Show |
A | 159 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.430-15747_430-1573 others(20): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411214 | ||||||
| chr13:51411351
|
CGAGACCA others(1): Show |
C | 5 | a0001c0001t0002g0154a0001c0001t0002g0189a0001c0001t0002g0190others(2): Show | 5 | HG02615.hp2 HG02818.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-15876_430-1586 others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411351 | ||||||
| chr13:51411382
|
G | A | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.430-15899C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411382 | ||||||
| chr13:51411513
|
G | A | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-16030C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411513 | ||||||
| chr13:51411517
|
C | T | 1 | a0001c0001t0004g0197 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.430-16034G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411517 | ||||||
| chr13:51411552
|
CA | C | 31 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(28): Show | 31 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.430-16070delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411552 | ||||||
| chr13:51411553
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-16070T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411553 | ||||||
| chr13:51411803
|
CA | C | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-16321delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411803 | ||||||
| chr13:51411973
|
C | A | 1 | a0001c0001t0040g0327 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.430-16490G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411973 | ||||||
| chr13:51411999
|
T | C | 1 | a0001c0001t0006g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.430-16516A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51411999 | ||||||
| chr13:51412008
|
A | C | 1 | a0001c0001t0006g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.430-16525T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51412008 | ||||||
| chr13:51412109
|
C | A | 1 | a0001c0001t0004g0220 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.430-16626G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51412109 | ||||||
| chr13:51412190
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-16707C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51412190 | ||||||
| chr13:51412242
|
T | A | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.430-16759A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51412242 | ||||||
| chr13:51412286
|
TTA | T | 3 | a0001c0001t0001g0231a0001c0001t0002g0188a0001c0001t0002g0194 | 3 | HG02647.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.430-16805_430-1680 others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51412286 | ||||||
| chr13:51412370
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.430-16887A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51412370 | ||||||
| chr13:51412428
|
T | G | 1 | a0001c0001t0001g0226 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.430-16945A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51412428 | ||||||
| chr13:51412558
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.430-17075G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51412558 | ||||||
| chr13:51412586
|
C | T | 1 | a0001c0001t0004g0325 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.430-17103G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51412586 | ||||||
| chr13:51412886
|
T | C | 2 | a0001c0001t0002g0077a0001c0001t0002g0078 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.430-17403A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51412886 | ||||||
| chr13:51412974
|
A | G | 162 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.429+17320T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51412974 | ||||||
| chr13:51413007
|
A | G | 2 | a0001c0001t0002g0169a0001c0001t0007g0161 | 2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.429+17287T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51413007 | ||||||
| chr13:51413008
|
A | G | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.429+17286T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51413008 | ||||||
| chr13:51413106
|
T | C | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+17188A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51413106 | ||||||
| chr13:51413202
|
T | G | 78 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 80 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.429+17092A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51413202 | ||||||
| chr13:51413253
|
G | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0034g0295 | 3 | HG02965.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.429+17041C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51413253 | ||||||
| chr13:51413287
|
G | A | 1 | a0001c0001t0004g0140 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.429+17007C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51413287 | ||||||
| chr13:51413582
|
T | C | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.429+16712A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51413582 | ||||||
| chr13:51413628
|
A | G | 8 | a0001c0001t0003g0185a0001c0001t0003g0203a0001c0001t0003g0204others(5): Show | 8 | HG00544.hp2 NA18612.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+16666T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51413628 | ||||||
| chr13:51413887
|
T | G | 1 | a0001c0001t0001g0038 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.429+16407A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51413887 | ||||||
| chr13:51414168
|
C | T | 3 | a0001c0001t0004g0139a0001c0001t0004g0140a0001c0001t0004g0141 | 3 | HG00140.hp2 HG00642.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.429+16126G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51414168 | ||||||
| chr13:51414678
|
G | A | 9 | a0001c0001t0001g0317a0001c0001t0010g0310a0001c0001t0010g0313others(6): Show | 9 | HG01243.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.429+15616C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51414678 | ||||||
| chr13:51414833
|
T | TAC | 152 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0020others(149): Show | 154 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.429+15459_429+1546 others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51414833 | ||||||
| chr13:51414833
|
T | TACAC | 57 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(54): Show | 58 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.429+15457_429+1546 others(8): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51414833 | ||||||
| chr13:51414833
|
T | TACACAC | 20 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(17): Show | 20 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.429+15455_429+1546 others(10): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51414833 | ||||||
| chr13:51414833
|
T | TACACACA others(1): Show |
6 | a0001c0001t0003g0223a0001c0001t0004g0202a0001c0001t0010g0314others(3): Show | 6 | HG00280.hp1 HG01517.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+15453_429+1546 others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51414833 | ||||||
| chr13:51414833
|
T | TACACACA others(3): Show |
2 | a0001c0001t0006g0287a0001c0001t0032g0299 | 2 | HG03654.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.429+15451_429+1546 others(14): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51414833 | ||||||
| chr13:51414833
|
TAC | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0053others(8): Show | 12 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+15459_429+1546 others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51414833 | ||||||
| chr13:51414833
|
TACACACA others(5): Show |
T | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+15449_429+1546 others(16): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51414833 | ||||||
| chr13:51415019
|
A | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0034g0295 | 3 | HG02965.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.429+15275T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415019 | ||||||
| chr13:51415099
|
C | G | 9 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(6): Show | 9 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+15195G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415099 | ||||||
| chr13:51415123
|
GT | G | 19 | a0001c0001t0007g0196a0001c0001t0010g0310a0001c0002t0008g0247others(16): Show | 20 | HG00438.hp2 HG01069.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.429+15170delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415123 | ||||||
| chr13:51415185
|
T | A | 2 | a0001c0001t0007g0209a0001c0001t0041g0208 | 2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.429+15109A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415185 | ||||||
| chr13:51415214
|
T | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+15080A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415214 | ||||||
| chr13:51415228
|
A | C | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+15066T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415228 | ||||||
| chr13:51415244
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.429+15050A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415244 | ||||||
| chr13:51415270
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0002g0181 | 2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.429+15024A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415270 | ||||||
| chr13:51415455
|
G | A | 13 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.429+14839C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415455 | ||||||
| chr13:51415486
|
A | T | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+14808T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415486 | ||||||
| chr13:51415653
|
CCT | C | 145 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.429+14639_429+1464 others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415653 | ||||||
| chr13:51415766
|
T | G | 2 | a0001c0001t0003g0150a0001c0001t0003g0151 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.429+14528A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415766 | ||||||
| chr13:51415768
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.429+14526C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415768 | ||||||
| chr13:51415865
|
C | T | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+14429G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415865 | ||||||
| chr13:51415866
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+14428C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51415866 | ||||||
| chr13:51416019
|
T | C | 5 | a0001c0001t0002g0154a0001c0001t0002g0189a0001c0001t0002g0190others(2): Show | 5 | HG02615.hp2 HG02818.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+14275A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51416019 | ||||||
| chr13:51416099
|
T | C | 1 | a0001c0001t0007g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.429+14195A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51416099 | ||||||
| chr13:51416111
|
G | A | 2 | a0001c0001t0006g0265a0001c0001t0006g0289 | 2 | HG00099.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.429+14183C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51416111 | ||||||
| chr13:51416181
|
T | A | 1 | a0001c0001t0033g0263 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.429+14113A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51416181 | ||||||
| chr13:51416204
|
G | T | 8 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0017g0298others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+14090C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51416204 | ||||||
| chr13:51416320
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0069 | 3 | NA19063.hp2 NA19065.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.429+13974G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51416320 | ||||||
| chr13:51416352
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+13942A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51416352 | ||||||
| chr13:51416465
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+13829A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51416465 | ||||||
| chr13:51416497
|
G | A | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.429+13797C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51416497 | ||||||
| chr13:51417098
|
T | G | 1 | a0001c0001t0001g0164 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.429+13196A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417098 | ||||||
| chr13:51417452
|
C | CT | 7 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0085others(4): Show | 8 | HG00639.hp1 HG00639.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+12841dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417452 | ||||||
| chr13:51417452
|
C | CTTTT | 8 | a0001c0001t0009g0133a0001c0001t0009g0137a0001c0001t0014g0127others(5): Show | 8 | HG02735.hp2 HG03239.hp2 NA18974.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+12838_429+1284 others(8): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417452 | ||||||
| chr13:51417452
|
C | CTTTTT | 20 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(17): Show | 21 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.429+12837_429+1284 others(9): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417452 | ||||||
| chr13:51417452
|
CT | C | 6 | a0001c0001t0001g0242a0001c0001t0003g0233a0001c0001t0010g0314others(3): Show | 6 | HG01891.hp1 HG02572.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+12841delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417452 | ||||||
| chr13:51417452
|
CTT | C | 168 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0014others(165): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.429+12840_429+1284 others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417452 | ||||||
| chr13:51417452
|
CTTT | C | 61 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0296others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.429+12839_429+1284 others(7): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417452 | ||||||
| chr13:51417595
|
C | G | 1 | a0001c0001t0044g0215 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.429+12699G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417595 | ||||||
| chr13:51417605
|
C | G | 16 | a0001c0001t0001g0227a0001c0001t0001g0303a0001c0001t0001g0304others(13): Show | 16 | HG01243.hp2 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.429+12689G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417605 | ||||||
| chr13:51417616
|
G | A | 3 | a0001c0001t0003g0150a0001c0001t0003g0151a0001c0001t0003g0152 | 3 | HG02258.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.429+12678C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417616 | ||||||
| chr13:51417685
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.429+12609C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417685 | ||||||
| chr13:51417768
|
CTTT | C | 3 | a0001c0001t0001g0231a0001c0001t0002g0188a0001c0001t0002g0194 | 3 | HG02647.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.429+12523_429+1252 others(7): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417768 | ||||||
| chr13:51417806
|
G | A | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+12488C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417806 | ||||||
| chr13:51417850
|
T | C | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.429+12444A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417850 | ||||||
| chr13:51417874
|
C | A | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+12420G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417874 | ||||||
| chr13:51417989
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.429+12305C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51417989 | ||||||
| chr13:51418025
|
G | A | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.429+12269C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418025 | ||||||
| chr13:51418058
|
T | A | 1 | a0001c0001t0045g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.429+12236A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418058 | ||||||
| chr13:51418086
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+12208G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418086 | ||||||
| chr13:51418175
|
T | C | 18 | a0001c0001t0001g0322a0001c0001t0001g0329a0001c0001t0003g0090others(15): Show | 18 | HG02071.hp2 HG02074.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.429+12119A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418175 | ||||||
| chr13:51418214
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0228 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.429+12080A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418214 | ||||||
| chr13:51418371
|
GA | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+11922delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418371 | ||||||
| chr13:51418441
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.429+11853A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418441 | ||||||
| chr13:51418534
|
T | TA | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+11759dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418534 | ||||||
| chr13:51418581
|
A | G | 162 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.429+11713T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418581 | ||||||
| chr13:51418593
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+11701A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418593 | ||||||
| chr13:51418752
|
T | C | 1 | a0001c0001t0012g0248 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.429+11542A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418752 | ||||||
| chr13:51418969
|
A | T | 1 | a0001c0001t0001g0213 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.429+11325T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51418969 | ||||||
| chr13:51419089
|
A | AC | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+11204dupG | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51419089 | ||||||
| chr13:51419135
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+11159A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51419135 | ||||||
| chr13:51419323
|
T | C | 2 | a0001c0001t0018g0264a0001c0001t0018g0279 | 2 | HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.429+10971A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51419323 | ||||||
| chr13:51419970
|
C | T | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.429+10324G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51419970 | ||||||
| chr13:51419999
|
C | T | 2 | a0001c0001t0019g0307a0001c0001t0019g0308 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.429+10295G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51419999 | ||||||
| chr13:51420050
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+10244G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51420050 | ||||||
| chr13:51420080
|
T | C | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.429+10214A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51420080 | ||||||
| chr13:51420204
|
AAT | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+10088_429+1008 others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51420204 | ||||||
| chr13:51420244
|
CAT | C | 175 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(172): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.429+10048_429+1004 others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51420244 | ||||||
| chr13:51420314
|
T | TA | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+9979dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51420314 | ||||||
| chr13:51420332
|
A | AT | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+9961dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51420332 | ||||||
| chr13:51420533
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.429+9761A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51420533 | ||||||
| chr13:51420756
|
T | TA | 19 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0003g0207others(16): Show | 20 | HG00438.hp2 HG01069.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.429+9537dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51420756 | ||||||
| chr13:51420756
|
TA | T | 31 | a0001c0001t0001g0072a0001c0001t0001g0112a0001c0001t0001g0119others(28): Show | 31 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.429+9537delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51420756 | ||||||
| chr13:51420910
|
C | G | 2 | a0001c0001t0001g0162a0001c0001t0004g0174 | 2 | NA18968.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.429+9384G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51420910 | ||||||
| chr13:51421151
|
T | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0228 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.429+9143A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51421151 | ||||||
| chr13:51421465
|
T | C | 1 | a0001c0001t0007g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.429+8829A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51421465 | ||||||
| chr13:51421624
|
A | G | 8 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0017g0298others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+8670T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51421624 | ||||||
| chr13:51421635
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG02280.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.429+8659G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51421635 | ||||||
| chr13:51421765
|
T | C | 1 | a0001c0001t0004g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.429+8529A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51421765 | ||||||
| chr13:51421806
|
A | T | 1 | a0001c0001t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.429+8488T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51421806 | ||||||
| chr13:51421855
|
A | AAC | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+8437_429+8438d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51421855 | ||||||
| chr13:51421861
|
C | A | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+8433G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51421861 | ||||||
| chr13:51421905
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+8389A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51421905 | ||||||
| chr13:51422048
|
A | G | 1 | a0001c0001t0045g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.429+8246T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51422048 | ||||||
| chr13:51422171
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.429+8123A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51422171 | ||||||
| chr13:51422198
|
C | T | 1 | a0001c0001t0012g0248 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.429+8096G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51422198 | ||||||
| chr13:51422199
|
C | T | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.429+8095G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51422199 | ||||||
| chr13:51422446
|
G | C | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+7848C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51422446 | ||||||
| chr13:51422766
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.429+7528T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51422766 | ||||||
| chr13:51422767
|
T | A | 1 | a0001c0001t0001g0089 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.429+7527A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51422767 | ||||||
| chr13:51422771
|
C | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0003g0150others(1): Show | 4 | HG01255.hp2 HG02258.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+7523G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51422771 | ||||||
| chr13:51422940
|
T | C | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+7354A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51422940 | ||||||
| chr13:51422956
|
C | T | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.429+7338G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51422956 | ||||||
| chr13:51423063
|
C | T | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+7231G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51423063 | ||||||
| chr13:51423095
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.429+7199T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51423095 | ||||||
| chr13:51423204
|
T | C | 1 | a0001c0001t0007g0212 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.429+7090A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51423204 | ||||||
| chr13:51423297
|
T | C | 1 | a0001c0001t0002g0257 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.429+6997A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51423297 | ||||||
| chr13:51423512
|
C | T | 3 | a0001c0001t0017g0298a0001c0001t0017g0301a0001c0001t0017g0302 | 3 | HG02896.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.429+6782G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51423512 | ||||||
| chr13:51423633
|
T | C | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.429+6661A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51423633 | ||||||
| chr13:51423867
|
T | A | 9 | a0001c0001t0001g0191a0001c0001t0001g0231a0001c0001t0002g0154others(6): Show | 9 | HG02615.hp2 HG02647.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.429+6427A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51423867 | ||||||
| chr13:51424101
|
T | C | 12 | a0001c0001t0001g0322a0001c0001t0001g0329a0001c0001t0003g0324others(9): Show | 12 | HG02074.hp2 NA18943.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+6193A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51424101 | ||||||
| chr13:51424225
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.429+6069A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51424225 | ||||||
| chr13:51424375
|
G | GA | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0032g0299others(2): Show | 5 | HG02965.hp2 HG03139.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+5918dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51424375 | ||||||
| chr13:51424879
|
C | T | 90 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.429+5415G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51424879 | ||||||
| chr13:51424880
|
A | T | 1 | a0001c0002t0011g0342 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.429+5414T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51424880 | ||||||
| chr13:51424916
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+5378T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51424916 | ||||||
| chr13:51424933
|
T | A | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.429+5361A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51424933 | ||||||
| chr13:51425034
|
G | A | 2 | a0001c0001t0002g0253a0001c0001t0002g0255 | 2 | HG01074.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.429+5260C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51425034 | ||||||
| chr13:51425049
|
T | A | 1 | a0001c0001t0004g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.429+5245A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51425049 | ||||||
| chr13:51425521
|
GA | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+4772delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51425521 | ||||||
| chr13:51425720
|
C | G | 15 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(12): Show | 15 | HG01243.hp2 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.429+4574G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51425720 | ||||||
| chr13:51425730
|
C | G | 2 | a0001c0001t0001g0303a0001c0001t0001g0304 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.429+4564G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51425730 | ||||||
| chr13:51425755
|
C | CTAATTA | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+4538_429+4539i others(8): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51425755 | ||||||
| chr13:51425852
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0228 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.429+4442G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51425852 | ||||||
| chr13:51425945
|
A | C | 13 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.429+4349T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51425945 | ||||||
| chr13:51425960
|
T | A | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+4334A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51425960 | ||||||
| chr13:51426188
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+4106G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51426188 | ||||||
| chr13:51426302
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.429+3992T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51426302 | ||||||
| chr13:51426331
|
C | T | 2 | a0001c0001t0019g0307a0001c0001t0019g0308 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.429+3963G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51426331 | ||||||
| chr13:51426349
|
G | A | 5 | a0001c0001t0001g0235a0001c0001t0002g0236a0001c0001t0002g0237others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+3945C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51426349 | ||||||
| chr13:51426500
|
G | T | 38 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0009g0130others(35): Show | 39 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.429+3794C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51426500 | ||||||
| chr13:51426536
|
T | G | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.429+3758A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51426536 | ||||||
| chr13:51426564
|
AC | A | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+3729delG | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51426564 | ||||||
| chr13:51427160
|
T | C | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0003g0150others(2): Show | 5 | HG01255.hp2 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+3134A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51427160 | ||||||
| chr13:51427250
|
GACACATT others(3): Show |
G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+3034_429+3043d others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51427250 | ||||||
| chr13:51427334
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.429+2960A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51427334 | ||||||
| chr13:51427574
|
C | T | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.429+2720G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51427574 | ||||||
| chr13:51427820
|
A | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 41 | HG00099.hp2 HG01255.hp1 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.429+2474T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51427820 | ||||||
| chr13:51427849
|
A | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+2445T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51427849 | ||||||
| chr13:51428015
|
C | G | 1 | a0001c0002t0008g0336 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.429+2279G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428015 | ||||||
| chr13:51428087
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.429+2207G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428087 | ||||||
| chr13:51428131
|
G | A | 162 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.429+2163C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428131 | ||||||
| chr13:51428326
|
CT | C | 19 | a0001c0001t0001g0142a0001c0001t0001g0159a0001c0001t0007g0217others(16): Show | 20 | HG00438.hp2 HG01069.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.429+1967delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428326 | ||||||
| chr13:51428344
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.429+1950T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428344 | ||||||
| chr13:51428411
|
A | G | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.429+1883T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428411 | ||||||
| chr13:51428426
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0067a0001c0001t0001g0080others(11): Show | 15 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.429+1868C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428426 | ||||||
| chr13:51428472
|
G | T | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+1822C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428472 | ||||||
| chr13:51428486
|
A | G | 1 | a0001c0001t0004g0039 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.429+1808T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428486 | ||||||
| chr13:51428608
|
A | G | 267 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(264): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.429+1686T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428608 | ||||||
| chr13:51428615
|
C | T | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+1679G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428615 | ||||||
| chr13:51428949
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.429+1345G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51428949 | ||||||
| chr13:51429125
|
G | C | 9 | a0001c0001t0002g0009a0001c0001t0007g0158a0001c0001t0007g0196others(6): Show | 9 | HG01081.hp2 HG01928.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+1169C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429125 | ||||||
| chr13:51429140
|
C | G | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.429+1154G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429140 | ||||||
| chr13:51429237
|
T | C | 1 | a0001c0001t0010g0313 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.429+1057A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429237 | ||||||
| chr13:51429260
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+1034A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429260 | ||||||
| chr13:51429387
|
A | T | 1 | a0001c0001t0001g0240 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.429+907T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429387 | ||||||
| chr13:51429714
|
A | G | 1 | a0001c0001t0018g0264 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.429+580T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429714 | ||||||
| chr13:51429758
|
T | C | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.429+536A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429758 | ||||||
| chr13:51429763
|
C | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+531G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429763 | ||||||
| chr13:51429763
|
C | CA | 48 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0020others(45): Show | 48 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.429+530dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429763 | ||||||
| chr13:51429763
|
C | CAA | 10 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0170others(7): Show | 10 | HG00423.hp1 HG00642.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.429+529_429+530dup others(2): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429763 | ||||||
| chr13:51429772
|
AAAAAAAA others(14): Show |
A | 1 | a0001c0001t0002g0190 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.429+501_429+521del others(21): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429772 | ||||||
| chr13:51429785
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0014g0129 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.429+508_429+509ins others(30): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0009g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.429+508_429+509ins others(32): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAAAA others(27): Show |
2 | a0001c0001t0009g0131a0001c0001t0009g0135 | 2 | HG01361.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.429+508_429+509ins others(34): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0032g0299 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.429+508_429+509ins others(19): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0009g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.429+508_429+509ins others(21): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0009g0134 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.429+508_429+509ins others(33): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0014g0136 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.429+508_429+509ins others(36): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0023g0121 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.429+508_429+509ins others(17): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0009g0133 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.429+508_429+509ins others(37): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.429+508_429+509ins others(12): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0009g0130 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.429+508_429+509ins others(36): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAAAT others(36): Show |
1 | a0001c0002t0008g0333 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.429+508_429+509ins others(43): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAAATA others(3): Show |
1 | a0001c0001t0036g0300 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.429+508_429+509ins others(10): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAATAT others(36): Show |
1 | a0001c0002t0008g0341 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.429+508_429+509ins others(43): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAAATAT others(38): Show |
2 | a0001c0002t0011g0334a0001c0002t0020g0008 | 3 | HG00438.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.429+508_429+509ins others(45): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAAATATA others(37): Show |
2 | a0001c0002t0008g0345a0001c0002t0011g0340 | 2 | NA18998.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.429+508_429+509ins others(44): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAATATAT others(4): Show |
1 | a0001c0001t0034g0295 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429+508_429+509ins others(11): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAATATAT others(26): Show |
1 | a0001c0002t0011g0338 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.429+508_429+509ins others(33): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAATATAT others(32): Show |
1 | a0001c0002t0031g0344 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.429+508_429+509ins others(39): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAATATAT others(36): Show |
1 | a0001c0002t0011g0339 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.429+508_429+509ins others(43): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAATATAT others(38): Show |
4 | a0001c0002t0008g0247a0001c0002t0008g0335a0001c0002t0008g0343others(1): Show | 4 | HG02698.hp2 NA18981.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+508_429+509ins others(45): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAATATAT others(40): Show |
1 | a0001c0002t0008g0332 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.429+508_429+509ins others(47): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | AAATATAT others(36): Show |
1 | a0001c0002t0008g0336 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.429+508_429+509ins others(43): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | ATAT | 5 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0070others(2): Show | 6 | HG02015.hp2 NA18952.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+508_429+509ins others(3): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | ATATATAT others(36): Show |
1 | a0001c0002t0008g0331 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.429+508_429+509ins others(43): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
A | T | 12 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0054others(9): Show | 12 | HG00741.hp2 HG02602.hp1 HG03669.hp1 others(9): Show |
intron_variant | MODIFIER | c.429+509T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429785
|
AAT | A | 14 | a0001c0001t0001g0182a0001c0001t0001g0191a0001c0001t0001g0231others(11): Show | 14 | HG00735.hp2 HG01106.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.429+507_429+508del others(2): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429785 | ||||||
| chr13:51429786
|
AT | A | 58 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0116others(55): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.429+507delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429786 | ||||||
| chr13:51429787
|
T | A | 139 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(136): Show | 140 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.429+507A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429787 | ||||||
| chr13:51429789
|
T | A | 173 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(170): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.429+505A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429789 | ||||||
| chr13:51429791
|
T | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 124 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.429+503A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429791 | ||||||
| chr13:51429793
|
T | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(44): Show | 49 | HG00099.hp2 HG01081.hp2 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.429+501A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429793 | ||||||
| chr13:51429795
|
T | A | 5 | a0001c0001t0001g0191a0001c0001t0002g0154a0001c0001t0002g0189others(2): Show | 5 | HG02615.hp2 HG02818.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+499A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429795 | ||||||
| chr13:51429800
|
A | ATATATAT others(37): Show |
1 | a0001c0002t0011g0342 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.429+493_429+494ins others(44): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429800 | ||||||
| chr13:51429800
|
A | G | 16 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(13): Show | 17 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(14): Show |
intron_variant | MODIFIER | c.429+494T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429800 | ||||||
| chr13:51429807
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.429+487A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429807 | ||||||
| chr13:51429829
|
G | C | 128 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.429+465C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429829 | ||||||
| chr13:51429829
|
G | T | 33 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 35 | HG00099.hp2 HG01255.hp1 HG02015.hp1 others(32): Show |
intron_variant | MODIFIER | c.429+465C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429829 | ||||||
| chr13:51429846
|
G | A | 1 | a0001c0001t0025g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.429+448C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429846 | ||||||
| chr13:51429921
|
G | T | 1 | a0001c0001t0004g0202 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.429+373C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429921 | ||||||
| chr13:51429971
|
C | T | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+323G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51429971 | ||||||
| chr13:51430225
|
A | C | 3 | a0001c0001t0001g0231a0001c0001t0002g0188a0001c0001t0002g0194 | 3 | HG02647.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.429+69T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 4/17 | chr13 | 51430225 | ||||||
| chr13:51430427
|
G | A | 1 | a0002c0003t0001g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.340-44C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51430427 | ||||||
| chr13:51430469
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.340-86G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51430469 | ||||||
| chr13:51430540
|
C | T | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.340-157G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51430540 | ||||||
| chr13:51430863
|
T | C | 1 | a0001c0001t0037g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.340-480A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51430863 | ||||||
| chr13:51430865
|
G | C | 2 | a0001c0001t0019g0307a0001c0001t0019g0308 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.340-482C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51430865 | ||||||
| chr13:51431036
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.340-653G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51431036 | ||||||
| chr13:51431113
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0014g0088 | 2 | HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.340-730G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51431113 | ||||||
| chr13:51431295
|
G | A | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.340-912C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51431295 | ||||||
| chr13:51431302
|
G | T | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.340-919C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51431302 | ||||||
| chr13:51431691
|
G | A | 1 | a0001c0001t0004g0328 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.340-1308C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51431691 | ||||||
| chr13:51431835
|
A | T | 3 | a0001c0001t0005g0269a0001c0001t0012g0270a0001c0001t0012g0284 | 3 | HG02602.hp2 NA20905.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.340-1452T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51431835 | ||||||
| chr13:51431862
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.340-1479A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51431862 | ||||||
| chr13:51431884
|
C | A | 74 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0249others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.340-1501G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51431884 | ||||||
| chr13:51431893
|
T | G | 1 | a0001c0001t0001g0231 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.340-1510A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51431893 | ||||||
| chr13:51431923
|
TATTAC | T | 11 | a0001c0001t0001g0182a0001c0001t0001g0191a0001c0001t0001g0231others(8): Show | 11 | HG02615.hp2 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-1545_340-1541d others(7): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51431923 | ||||||
| chr13:51432105
|
C | T | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.340-1722G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432105 | ||||||
| chr13:51432448
|
AATTT | A | 5 | a0001c0001t0001g0183a0001c0001t0013g0153a0001c0001t0013g0156others(2): Show | 5 | HG00280.hp2 HG00639.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-2069_340-2066d others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432448 | ||||||
| chr13:51432455
|
T | TA | 20 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0034g0295others(17): Show | 21 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(18): Show |
intron_variant | MODIFIER | c.340-2073dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432455 | ||||||
| chr13:51432455
|
TA | T | 12 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0235others(9): Show | 12 | HG00597.hp1 HG00609.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.340-2073delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432455 | ||||||
| chr13:51432500
|
G | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-2117C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432500 | ||||||
| chr13:51432509
|
C | T | 196 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(193): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.340-2126G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432509 | ||||||
| chr13:51432540
|
T | C | 1 | a0001c0001t0047g0350 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.340-2157A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432540 | ||||||
| chr13:51432590
|
T | C | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.340-2207A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432590 | ||||||
| chr13:51432597
|
A | G | 13 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.340-2214T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432597 | ||||||
| chr13:51432625
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.340-2242A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432625 | ||||||
| chr13:51432886
|
A | G | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.340-2503T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432886 | ||||||
| chr13:51432997
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-2614G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51432997 | ||||||
| chr13:51433065
|
A | C | 346 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(343): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.340-2682T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51433065 | ||||||
| chr13:51433085
|
A | C | 1 | a0001c0001t0001g0033 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.340-2702T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51433085 | ||||||
| chr13:51433169
|
A | C | 30 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(27): Show | 31 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.340-2786T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51433169 | ||||||
| chr13:51433218
|
C | T | 4 | a0001c0001t0017g0298a0001c0001t0017g0301a0001c0001t0017g0302others(1): Show | 4 | HG01069.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-2835G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51433218 | ||||||
| chr13:51433401
|
T | C | 10 | a0001c0002t0008g0331a0001c0002t0008g0333a0001c0002t0008g0335others(7): Show | 10 | HG00438.hp2 NA18939.hp1 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.340-3018A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51433401 | ||||||
| chr13:51433423
|
G | A | 1 | a0001c0001t0003g0207 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.340-3040C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51433423 | ||||||
| chr13:51433597
|
AGAT | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-3217_340-3215d others(5): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51433597 | ||||||
| chr13:51434102
|
T | C | 266 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.340-3719A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51434102 | ||||||
| chr13:51434364
|
A | T | 16 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(13): Show | 17 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(14): Show |
intron_variant | MODIFIER | c.340-3981T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51434364 | ||||||
| chr13:51434388
|
G | A | 11 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(8): Show | 11 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.340-4005C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51434388 | ||||||
| chr13:51434560
|
C | T | 1 | a0001c0001t0003g0152 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.340-4177G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51434560 | ||||||
| chr13:51434592
|
T | G | 2 | a0001c0001t0014g0127a0001c0001t0014g0128 | 2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.340-4209A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51434592 | ||||||
| chr13:51434654
|
T | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-4271A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51434654 | ||||||
| chr13:51434749
|
G | A | 1 | a0001c0001t0006g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.340-4366C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51434749 | ||||||
| chr13:51434759
|
GT | G | 275 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(272): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.340-4377delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51434759 | ||||||
| chr13:51434764
|
G | C | 275 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(272): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.340-4381C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51434764 | ||||||
| chr13:51434844
|
T | A | 1 | a0001c0002t0031g0344 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.340-4461A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51434844 | ||||||
| chr13:51434971
|
C | T | 1 | a0001c0001t0003g0143 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.340-4588G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51434971 | ||||||
| chr13:51435243
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.340-4860A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51435243 | ||||||
| chr13:51435302
|
G | A | 1 | a0001c0001t0045g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.340-4919C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51435302 | ||||||
| chr13:51435337
|
A | ATCTT | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-4955_340-4954i others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51435337 | ||||||
| chr13:51435356
|
T | G | 1 | a0001c0001t0001g0297 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.340-4973A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51435356 | ||||||
| chr13:51435396
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0013g0106 | 4 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-5013G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51435396 | ||||||
| chr13:51435459
|
A | G | 1 | a0001c0001t0022g0239 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.340-5076T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51435459 | ||||||
| chr13:51435527
|
G | T | 4 | a0001c0001t0009g0131a0001c0001t0009g0132a0001c0001t0009g0134others(1): Show | 4 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-5144C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51435527 | ||||||
| chr13:51435933
|
C | T | 1 | a0001c0001t0001g0329 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.340-5550G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51435933 | ||||||
| chr13:51436031
|
G | C | 11 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(8): Show | 11 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.340-5648C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51436031 | ||||||
| chr13:51436140
|
G | A | 9 | a0001c0001t0002g0009a0001c0001t0007g0158a0001c0001t0007g0196others(6): Show | 9 | HG01081.hp2 HG01928.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.340-5757C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51436140 | ||||||
| chr13:51436148
|
C | G | 1 | a0001c0001t0002g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.340-5765G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51436148 | ||||||
| chr13:51436237
|
T | A | 1 | a0001c0001t0002g0194 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.340-5854A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51436237 | ||||||
| chr13:51436419
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-6036G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51436419 | ||||||
| chr13:51436452
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-6069C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51436452 | ||||||
| chr13:51436483
|
T | G | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.340-6100A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51436483 | ||||||
| chr13:51436669
|
A | T | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.340-6286T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51436669 | ||||||
| chr13:51436672
|
T | C | 1 | a0001c0001t0009g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.340-6289A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51436672 | ||||||
| chr13:51436884
|
T | C | 8 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0017g0298others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-6501A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51436884 | ||||||
| chr13:51437046
|
A | C | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.340-6663T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51437046 | ||||||
| chr13:51437133
|
T | A | 15 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(12): Show | 15 | HG01243.hp2 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.340-6750A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51437133 | ||||||
| chr13:51437391
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-7008G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51437391 | ||||||
| chr13:51437454
|
C | CA | 23 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(20): Show | 24 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.340-7072dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51437454 | ||||||
| chr13:51437678
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.340-7295A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51437678 | ||||||
| chr13:51437955
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-7572C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51437955 | ||||||
| chr13:51437967
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-7584G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51437967 | ||||||
| chr13:51438004
|
G | A | 1 | a0001c0001t0013g0179 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.340-7621C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51438004 | ||||||
| chr13:51438025
|
A | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-7642T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51438025 | ||||||
| chr13:51438070
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-7687C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51438070 | ||||||
| chr13:51438120
|
A | C | 2 | a0001c0001t0001g0303a0001c0001t0001g0304 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.340-7737T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51438120 | ||||||
| chr13:51438350
|
TA | T | 29 | a0001c0001t0001g0041a0001c0001t0001g0083a0001c0001t0001g0142others(26): Show | 29 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.340-7968delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51438350 | ||||||
| chr13:51438360
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-7977T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51438360 | ||||||
| chr13:51438697
|
A | C | 8 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0017g0298others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-8314T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51438697 | ||||||
| chr13:51438732
|
A | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-8349T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51438732 | ||||||
| chr13:51438770
|
A | T | 2 | a0001c0001t0001g0182a0001c0001t0002g0181 | 2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.340-8387T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51438770 | ||||||
| chr13:51438795
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-8412T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51438795 | ||||||
| chr13:51438898
|
G | A | 5 | a0001c0001t0001g0235a0001c0001t0002g0236a0001c0001t0002g0237others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-8515C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51438898 | ||||||
| chr13:51439096
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.340-8713C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439096 | ||||||
| chr13:51439112
|
T | C | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0003g0150others(2): Show | 5 | HG01255.hp2 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-8729A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439112 | ||||||
| chr13:51439256
|
CA | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-8874delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439256 | ||||||
| chr13:51439331
|
G | C | 2 | a0001c0001t0006g0262a0001c0001t0006g0287 | 2 | HG00733.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.340-8948C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439331 | ||||||
| chr13:51439480
|
A | G | 9 | a0001c0001t0002g0009a0001c0001t0007g0158a0001c0001t0007g0196others(6): Show | 9 | HG01081.hp2 HG01928.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.340-9097T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439480 | ||||||
| chr13:51439582
|
T | A | 1 | a0001c0001t0002g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.340-9199A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439582 | ||||||
| chr13:51439677
|
C | T | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-9294G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439677 | ||||||
| chr13:51439733
|
A | G | 1 | a0001c0001t0002g0043 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.340-9350T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439733 | ||||||
| chr13:51439768
|
T | C | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.340-9385A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439768 | ||||||
| chr13:51439789
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.340-9406G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439789 | ||||||
| chr13:51439859
|
A | T | 1 | a0001c0001t0012g0248 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.340-9476T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439859 | ||||||
| chr13:51439915
|
T | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0228 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.340-9532A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439915 | ||||||
| chr13:51439919
|
C | T | 3 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078 | 3 | HG01106.hp1 HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.340-9536G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439919 | ||||||
| chr13:51439982
|
T | C | 1 | a0001c0001t0004g0330 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.340-9599A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439982 | ||||||
| chr13:51439993
|
C | A | 1 | a0001c0001t0009g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.340-9610G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51439993 | ||||||
| chr13:51440005
|
G | A | 1 | a0001c0001t0003g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.340-9622C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440005 | ||||||
| chr13:51440045
|
G | A | 1 | a0001c0001t0028g0288 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.340-9662C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440045 | ||||||
| chr13:51440092
|
C | CA | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.340-9710dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440092 | ||||||
| chr13:51440153
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-9770T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440153 | ||||||
| chr13:51440177
|
G | C | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.340-9794C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440177 | ||||||
| chr13:51440205
|
C | T | 1 | a0001c0001t0038g0195 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.340-9822G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440205 | ||||||
| chr13:51440206
|
G | A | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.340-9823C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440206 | ||||||
| chr13:51440210
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.340-9827G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440210 | ||||||
| chr13:51440250
|
C | CA | 12 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.340-9868dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440250 | ||||||
| chr13:51440329
|
A | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-9946T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440329 | ||||||
| chr13:51440384
|
CT | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-10002delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440384 | ||||||
| chr13:51440589
|
T | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-10206A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440589 | ||||||
| chr13:51440744
|
A | G | 11 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(8): Show | 11 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.339+10281T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440744 | ||||||
| chr13:51440775
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.339+10250A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440775 | ||||||
| chr13:51440842
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.339+10183A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440842 | ||||||
| chr13:51440910
|
C | T | 1 | a0001c0001t0016g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.339+10115G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51440910 | ||||||
| chr13:51441150
|
T | C | 6 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0124others(3): Show | 6 | NA18945.hp2 NA18953.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+9875A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51441150 | ||||||
| chr13:51441199
|
C | T | 29 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(26): Show | 30 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.339+9826G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51441199 | ||||||
| chr13:51441204
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.339+9821C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51441204 | ||||||
| chr13:51441247
|
A | G | 1 | a0001c0001t0010g0313 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.339+9778T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51441247 | ||||||
| chr13:51441322
|
T | C | 3 | a0001c0001t0017g0298a0001c0001t0017g0301a0001c0001t0017g0302 | 3 | HG02896.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+9703A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51441322 | ||||||
| chr13:51441355
|
A | C | 1 | a0001c0001t0012g0293 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.339+9670T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51441355 | ||||||
| chr13:51441384
|
G | A | 1 | a0001c0001t0018g0264 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.339+9641C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51441384 | ||||||
| chr13:51441633
|
A | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG02280.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.339+9392T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51441633 | ||||||
| chr13:51441637
|
T | C | 264 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(261): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.339+9388A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51441637 | ||||||
| chr13:51441824
|
C | CT | 160 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(157): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.339+9200dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51441824 | ||||||
| chr13:51441996
|
T | G | 1 | a0001c0001t0034g0295 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.339+9029A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51441996 | ||||||
| chr13:51442141
|
A | AT | 150 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.339+8883dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51442141 | ||||||
| chr13:51442296
|
C | T | 1 | a0001c0001t0042g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.339+8729G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51442296 | ||||||
| chr13:51442415
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.339+8610C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51442415 | ||||||
| chr13:51442420
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.339+8605C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51442420 | ||||||
| chr13:51442509
|
C | T | 3 | a0001c0001t0003g0198a0001c0001t0003g0233a0001c0001t0004g0197 | 3 | HG03831.hp2 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.339+8516G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51442509 | ||||||
| chr13:51442649
|
C | A | 5 | a0001c0001t0002g0009a0001c0001t0007g0196a0001c0001t0007g0216others(2): Show | 5 | HG01081.hp2 HG01928.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+8376G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51442649 | ||||||
| chr13:51442798
|
A | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.339+8227T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51442798 | ||||||
| chr13:51442953
|
T | C | 1 | a0001c0001t0002g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.339+8072A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51442953 | ||||||
| chr13:51443119
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0004g0174 | 2 | NA18968.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.339+7906A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51443119 | ||||||
| chr13:51443266
|
A | T | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.339+7759T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51443266 | ||||||
| chr13:51443295
|
A | C | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.339+7730T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51443295 | ||||||
| chr13:51443386
|
G | A | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.339+7639C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51443386 | ||||||
| chr13:51443400
|
ATTTG | A | 5 | a0001c0001t0003g0218a0001c0001t0004g0157a0001c0001t0004g0219others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+7621_339+7624d others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51443400 | ||||||
| chr13:51443485
|
T | A | 1 | a0001c0001t0045g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.339+7540A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51443485 | ||||||
| chr13:51443554
|
T | C | 3 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251 | 3 | HG01257.hp1 HG01258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.339+7471A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51443554 | ||||||
| chr13:51443618
|
G | A | 1 | a0001c0001t0006g0289 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.339+7407C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51443618 | ||||||
| chr13:51443672
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.339+7353T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51443672 | ||||||
| chr13:51443835
|
C | T | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.339+7190G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51443835 | ||||||
| chr13:51444091
|
GT | G | 11 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(8): Show | 11 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.339+6933delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444091 | ||||||
| chr13:51444251
|
AATTT | A | 14 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(11): Show | 15 | HG01069.hp2 HG02698.hp2 HG03491.hp1 others(12): Show |
intron_variant | MODIFIER | c.339+6770_339+6773d others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444251 | ||||||
| chr13:51444252
|
A | AT | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(54): Show | 59 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.339+6772dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444252 | ||||||
| chr13:51444252
|
A | ATT | 9 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0123others(6): Show | 9 | HG01175.hp2 HG02129.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.339+6771_339+6772d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444252 | ||||||
| chr13:51444252
|
AT | A | 115 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0014others(112): Show | 117 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.339+6772delA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444252 | ||||||
| chr13:51444252
|
ATT | A | 15 | a0001c0001t0001g0011a0001c0001t0001g0040a0001c0001t0001g0175others(12): Show | 15 | HG00544.hp1 HG01074.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.339+6771_339+6772d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444252 | ||||||
| chr13:51444252
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0064 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.339+6762_339+6772d others(13): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444252 | ||||||
| chr13:51444252
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | NA18952.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.339+6761_339+6772d others(14): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444252 | ||||||
| chr13:51444252
|
ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0004g0220 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.339+6758_339+6772d others(17): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444252 | ||||||
| chr13:51444401
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.339+6624C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444401 | ||||||
| chr13:51444460
|
A | T | 1 | a0001c0001t0001g0142 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.339+6565T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444460 | ||||||
| chr13:51444473
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.339+6552C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444473 | ||||||
| chr13:51444485
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.339+6540G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444485 | ||||||
| chr13:51444717
|
C | A | 2 | a0001c0001t0006g0290a0001c0001t0047g0350 | 2 | HG02523.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.339+6308G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444717 | ||||||
| chr13:51444750
|
A | C | 1 | a0001c0001t0042g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.339+6275T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444750 | ||||||
| chr13:51444795
|
T | TTTTTC | 38 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(35): Show | 39 | HG00438.hp2 HG01069.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.339+6225_339+6229d others(7): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444795 | ||||||
| chr13:51444800
|
C | CT | 12 | a0001c0001t0001g0178a0001c0001t0001g0322a0001c0001t0003g0324others(9): Show | 12 | HG01192.hp2 HG02074.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.339+6224dupA | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444800 | ||||||
| chr13:51444801
|
T | C | 1 | a0001c0001t0042g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.339+6224A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444801 | ||||||
| chr13:51444801
|
T | TTTTC | 43 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.339+6223_339+6224i others(6): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444801 | ||||||
| chr13:51444969
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.339+6056A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444969 | ||||||
| chr13:51444982
|
T | C | 6 | a0001c0001t0001g0226a0001c0001t0003g0221a0001c0001t0003g0222others(3): Show | 6 | HG00597.hp1 HG00609.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+6043A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51444982 | ||||||
| chr13:51445085
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.339+5940A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51445085 | ||||||
| chr13:51445443
|
A | G | 22 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0160others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.339+5582T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51445443 | ||||||
| chr13:51445498
|
G | GC | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.339+5526_339+5527i others(3): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51445498 | ||||||
| chr13:51445501
|
A | G | 11 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(8): Show | 11 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.339+5524T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51445501 | ||||||
| chr13:51445517
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0228 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.339+5508A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51445517 | ||||||
| chr13:51445529
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0014g0088 | 2 | HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.339+5496G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51445529 | ||||||
| chr13:51445606
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.339+5419C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51445606 | ||||||
| chr13:51445657
|
T | C | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.339+5368A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51445657 | ||||||
| chr13:51445661
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA18953.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.339+5364C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51445661 | ||||||
| chr13:51445726
|
T | C | 1 | a0001c0001t0003g0143 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.339+5299A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51445726 | ||||||
| chr13:51445827
|
T | G | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.339+5198A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51445827 | ||||||
| chr13:51446060
|
TA | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0082a0001c0001t0001g0083others(3): Show | 7 | HG01256.hp1 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+4964delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51446060 | ||||||
| chr13:51446122
|
A | G | 29 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(26): Show | 30 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.339+4903T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51446122 | ||||||
| chr13:51446135
|
A | T | 1 | a0001c0001t0033g0263 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.339+4890T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51446135 | ||||||
| chr13:51446157
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.339+4868G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51446157 | ||||||
| chr13:51446268
|
G | A | 5 | a0001c0001t0010g0313a0001c0001t0010g0314a0001c0001t0010g0315others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+4757C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51446268 | ||||||
| chr13:51446268
|
G | C | 29 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(26): Show | 30 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.339+4757C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51446268 | ||||||
| chr13:51446377
|
G | C | 1 | a0001c0001t0045g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.339+4648C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51446377 | ||||||
| chr13:51446441
|
C | T | 3 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251 | 3 | HG01257.hp1 HG01258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.339+4584G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51446441 | ||||||
| chr13:51446554
|
G | T | 1 | a0001c0001t0012g0291 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.339+4471C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51446554 | ||||||
| chr13:51446668
|
T | C | 1 | a0001c0001t0012g0291 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.339+4357A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51446668 | ||||||
| chr13:51446920
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01255.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.339+4105T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51446920 | ||||||
| chr13:51447047
|
A | T | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.339+3978T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447047 | ||||||
| chr13:51447096
|
A | G | 11 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(8): Show | 11 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.339+3929T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447096 | ||||||
| chr13:51447392
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.339+3633A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447392 | ||||||
| chr13:51447521
|
A | G | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.339+3504T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447521 | ||||||
| chr13:51447625
|
T | C | 25 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(22): Show | 26 | HG01255.hp1 HG02300.hp1 NA18947.hp2 others(23): Show |
intron_variant | MODIFIER | c.339+3400A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447625 | ||||||
| chr13:51447733
|
G | GA | 56 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0123others(53): Show | 56 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.339+3291dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447733 | ||||||
| chr13:51447733
|
G | GAA | 6 | a0001c0001t0002g0234a0001c0001t0005g0292a0001c0001t0005g0294others(3): Show | 6 | HG00140.hp1 HG02074.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+3290_339+3291d others(4): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447733 | ||||||
| chr13:51447733
|
GA | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0070others(27): Show | 31 | HG00280.hp2 HG00733.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.339+3291delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447733 | ||||||
| chr13:51447780
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0069 | 3 | NA19063.hp2 NA19065.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.339+3245G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447780 | ||||||
| chr13:51447902
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.339+3123A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447902 | ||||||
| chr13:51447909
|
T | C | 5 | a0001c0001t0001g0235a0001c0001t0002g0236a0001c0001t0002g0237others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+3116A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447909 | ||||||
| chr13:51447994
|
G | T | 2 | a0001c0001t0001g0303a0001c0001t0001g0304 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.339+3031C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447994 | ||||||
| chr13:51447999
|
G | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.339+3026C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51447999 | ||||||
| chr13:51448040
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0002g0068 | 2 | HG02683.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.339+2985T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51448040 | ||||||
| chr13:51448341
|
C | T | 10 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.339+2684G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51448341 | ||||||
| chr13:51448422
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.339+2603A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51448422 | ||||||
| chr13:51448453
|
A | G | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.339+2572T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51448453 | ||||||
| chr13:51448567
|
A | T | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0003g0150others(2): Show | 5 | HG01255.hp2 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+2458T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51448567 | ||||||
| chr13:51448570
|
A | C | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+2455T>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51448570 | ||||||
| chr13:51448679
|
A | G | 1 | a0001c0001t0012g0248 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.339+2346T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51448679 | ||||||
| chr13:51448724
|
T | C | 1 | a0001c0001t0045g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.339+2301A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51448724 | ||||||
| chr13:51448882
|
G | A | 1 | a0001c0001t0004g0330 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.339+2143C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51448882 | ||||||
| chr13:51449105
|
C | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016 | 3 | HG02280.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.339+1920G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51449105 | ||||||
| chr13:51449170
|
A | G | 2 | a0001c0001t0014g0127a0001c0001t0014g0128 | 2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.339+1855T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51449170 | ||||||
| chr13:51449192
|
T | A | 11 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(8): Show | 11 | HG01346.hp2 HG01361.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.339+1833A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51449192 | ||||||
| chr13:51449251
|
T | C | 1 | a0001c0001t0010g0318 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.339+1774A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51449251 | ||||||
| chr13:51449397
|
A | G | 174 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(171): Show | 176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.339+1628T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51449397 | ||||||
| chr13:51449663
|
G | A | 2 | a0001c0001t0017g0301a0001c0001t0017g0302 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.339+1362C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51449663 | ||||||
| chr13:51449705
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.339+1320T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51449705 | ||||||
| chr13:51449868
|
A | T | 2 | a0001c0001t0001g0303a0001c0001t0001g0304 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.339+1157T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51449868 | ||||||
| chr13:51449900
|
A | G | 1 | a0001c0001t0004g0319 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.339+1125T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51449900 | ||||||
| chr13:51450072
|
T | G | 1 | a0001c0001t0002g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.339+953A>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51450072 | ||||||
| chr13:51450261
|
TATC | T | 5 | a0001c0001t0001g0142a0001c0001t0003g0143a0001c0001t0004g0139others(2): Show | 5 | HG00140.hp2 HG00642.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+761_339+763del others(3): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51450261 | ||||||
| chr13:51450281
|
G | A | 8 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0017g0298others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.339+744C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51450281 | ||||||
| chr13:51450287
|
C | G | 21 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0049others(18): Show | 22 | HG00438.hp1 HG00597.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.339+738G>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51450287 | ||||||
| chr13:51450374
|
G | A | 1 | a0001c0001t0030g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.339+651C>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51450374 | ||||||
| chr13:51450413
|
AGT | A | 17 | a0001c0002t0008g0247a0001c0002t0008g0331a0001c0002t0008g0332others(14): Show | 18 | HG00438.hp2 HG01069.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.339+610_339+611del others(2): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51450413 | ||||||
| chr13:51450522
|
TA | T | 29 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(26): Show | 30 | HG00438.hp2 HG01069.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.339+502delT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51450522 | ||||||
| chr13:51450684
|
C | T | 3 | a0001c0001t0005g0244a0001c0001t0005g0245a0001c0001t0005g0246 | 3 | NA18943.hp1 NA19065.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.339+341G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51450684 | ||||||
| chr13:51450800
|
T | A | 264 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(261): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.339+225A>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51450800 | ||||||
| chr13:51450846
|
A | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 41 | HG00099.hp2 HG01255.hp1 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.339+179T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51450846 | ||||||
| chr13:51450985
|
T | C | 1 | a0001c0002t0020g0008 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.339+40A>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 3/17 | chr13 | 51450985 | ||||||
| chr13:51451287
|
G | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | NA18952.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.190-113C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 2/17 | chr13 | 51451287 | ||||||
| chr13:51451432
|
A | G | 1 | a0001c0001t0003g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.190-258T>C | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 2/17 | chr13 | 51451432 | ||||||
| chr13:51451460
|
A | T | 1 | a0001c0001t0001g0012 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.190-286T>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 2/17 | chr13 | 51451460 | ||||||
| chr13:51451461
|
G | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.190-287C>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 2/17 | chr13 | 51451461 | ||||||
| chr13:51451517
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.190-343G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 2/17 | chr13 | 51451517 | ||||||
| chr13:51451720
|
G | GCGC | 81 | a0001c0001t0001g0007a0001c0001t0001g0242a0001c0001t0001g0243others(78): Show | 83 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.189+255_189+257dup others(3): Show |
INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 2/17 | chr13 | 51451720 | ||||||
| chr13:51451812
|
C | T | 1 | a0001c0001t0047g0350 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.189+166G>A | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 2/17 | chr13 | 51451812 | ||||||
| chr13:51452152
|
C | CA | 16 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(13): Show | 16 | HG01243.hp2 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.112-98dupT | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 1/17 | chr13 | 51452152 | ||||||
| chr13:51452165
|
G | C | 12 | a0001c0001t0001g0322a0001c0001t0001g0329a0001c0001t0003g0324others(9): Show | 12 | HG02074.hp2 NA18943.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.112-110C>G | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 1/17 | chr13 | 51452165 | ||||||
| chr13:51452193
|
C | A | 16 | a0001c0002t0008g0331a0001c0002t0008g0332a0001c0002t0008g0333others(13): Show | 17 | HG00438.hp2 HG01069.hp2 HG03491.hp1 others(14): Show |
intron_variant | MODIFIER | c.112-138G>T | INTS6 | ENSG00000102786.15 | transcript | ENST00000311234.9 | protein_coding | 1/17 | chr13 | 51452193 |