Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57508 |
|---|---|
| ensemblid | ENSG00000108506.14 |
| hgncid | 29241 |
| symbol | INTS2 |
| name | integrator complex subunit 2 |
| refseq_nuc | NM_001351695.2 |
| refseq_prot | NP_001338624.2 |
| ensembl_nuc | ENST00000251334.7 |
| ensembl_prot | ENSP00000251334.6 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 61865367 |
| end | 61927982 |
| strand | - |
| ver | v1.2 |
| region | chr17:61865367-61927982 |
| region5000 | chr17:61860367-61932982 |
| regionname0 | INTS2_chr17_61865367_61927982 |
| regionname5000 | INTS2_chr17_61860367_61932982 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1196 | 360 | 84 | 59 | 169 | 12 | 35 | 131 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0002 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0003 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0004 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0005 | 0/0 | 1196 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0006 | 1/0 | 1196 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0007 | 0/0 | 1196 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3591 | 303 | 79 | 54 | 130 | 12 | 27 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| c0002 | 0/0 | 3591 | 51 | 1 | 5 | 37 | 0 | 8 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| c0003 | 0/0 | 3591 | 4 | 4 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| c0004 | 0/0 | 3591 | 2 | 0 | 0 | 2 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| c0005 | 0/0 | 3591 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| c0006 | 0/0 | 3591 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| c0007 | 0/0 | 3591 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| c0008 | 1/0 | 3591 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| c0009 | 0/0 | 3591 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| c0010 | 0/0 | 3591 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2538 | 100 | 15 | 27 | 41 | 6 | 10 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0002 | 0/0 | 2538 | 96 | 15 | 8 | 68 | 2 | 3 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0003 | 0/0 | 2538 | 75 | 36 | 17 | 12 | 2 | 8 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0004 | 0/0 | 2539 | 44 | 1 | 5 | 30 | 1 | 7 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0005 | 0/0 | 2538 | 7 | 7 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0006 | 0/0 | 2539 | 5 | 0 | 0 | 5 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0007 | 0/0 | 2539 | 5 | 2 | 0 | 3 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0008 | 0/0 | 2538 | 4 | 0 | 0 | 0 | 0 | 4 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0009 | 0/0 | 2540 | 4 | 0 | 0 | 4 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0010 | 0/0 | 2539 | 3 | 2 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0011 | 0/0 | 2524 | 3 | 0 | 0 | 3 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0012 | 0/0 | 2538 | 2 | 0 | 0 | 0 | 0 | 2 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0013 | 0/0 | 2539 | 2 | 2 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0014 | 0/0 | 2538 | 2 | 2 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0015 | 0/0 | 2538 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0016 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0017 | 0/0 | 2538 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0018 | 0/0 | 2538 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0019 | 1/0 | 2538 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0020 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0021 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0022 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0023 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0024 | 0/0 | 2538 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0025 | 0/0 | 2538 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0026 | 0/0 | 2538 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0027 | 0/0 | 2539 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| t0028 | 0/0 | 2524 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0132 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3591 | 303 | 79 | 54 | 130 | 12 | 27 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0002 | 0/0 | 3591 | 51 | 1 | 5 | 37 | 0 | 8 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0003 | 0/0 | 3591 | 4 | 4 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0004 | 0/0 | 3591 | 2 | 0 | 0 | 2 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0002c0006 | 0/0 | 3591 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0003c0007 | 0/0 | 3591 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0004c0010 | 0/0 | 3591 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0005c0009 | 0/0 | 3591 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0006c0008 | 1/0 | 3591 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0007c0005 | 0/0 | 3591 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6128 | 98 | 15 | 26 | 41 | 6 | 9 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0002 | 0/0 | 6128 | 89 | 11 | 8 | 65 | 2 | 3 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0003 | 0/0 | 6128 | 75 | 36 | 17 | 12 | 2 | 8 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0004 | 0/0 | 6129 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0005 | 0/0 | 6128 | 7 | 7 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0006 | 0/0 | 6129 | 5 | 0 | 0 | 5 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0007 | 0/0 | 6129 | 5 | 2 | 0 | 3 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0008 | 0/0 | 6128 | 4 | 0 | 0 | 0 | 0 | 4 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0010 | 0/0 | 6129 | 3 | 2 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0012 | 0/0 | 6128 | 2 | 0 | 0 | 0 | 0 | 2 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0013 | 0/0 | 6129 | 2 | 2 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0014 | 0/0 | 6128 | 2 | 2 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0015 | 0/0 | 6128 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0016 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0017 | 0/0 | 6128 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0018 | 0/0 | 6128 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0020 | 0/0 | 6129 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0021 | 0/0 | 6129 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0022 | 0/0 | 6129 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0023 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0025 | 0/0 | 6128 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0001t0026 | 0/0 | 6128 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0002t0004 | 0/0 | 6129 | 42 | 1 | 5 | 29 | 0 | 7 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0002t0009 | 0/0 | 6130 | 4 | 0 | 0 | 4 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0002t0011 | 0/0 | 6114 | 3 | 0 | 0 | 3 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0002t0027 | 0/0 | 6129 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0002t0028 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0003t0002 | 0/0 | 6128 | 4 | 4 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0001c0004t0002 | 0/0 | 6128 | 2 | 0 | 0 | 2 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0002c0006t0024 | 0/0 | 6128 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0003c0007t0004 | 0/0 | 6129 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0004c0010t0002 | 0/0 | 6128 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0005c0009t0001 | 0/0 | 6128 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0006c0008t0019 | 1/0 | 6128 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| a0007c0005t0001 | 0/0 | 6128 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | copy fasta | chr17 | 61860367 | 61932982 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0132 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0007g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0007g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0007g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0008g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0008g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0008g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0008g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0010g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0012g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0012g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0013g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0013g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0014g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0016g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0017g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0018g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0020g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0021g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0022g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0023g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0025g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0026g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0009g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0009g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0009g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0011g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0011g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0011g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0027g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0028g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0003t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0003t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0003t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0004t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0004t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0002c0006t0024g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0003c0007t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0004c0010t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0005c0009t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0006c0008t0019g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0007c0005t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0159 | EUR | GBR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00099 | hp2 | a0001 | c0001 | t0015 | g0001 | EUR | GBR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0162 | EUR | GBR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0087 | EUR | GBR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00423 | hp1 | a0001 | c0004 | t0002 | g0309 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00423 | hp2 | a0001 | c0002 | t0004 | g0075 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00438 | hp2 | a0001 | c0002 | t0004 | g0045 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0356 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0337 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00642 | hp1 | a0001 | c0002 | t0004 | g0042 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01081 | hp2 | a0001 | c0002 | t0004 | g0061 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01099 | hp2 | a0001 | c0001 | t0026 | g0349 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0352 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0054 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01175 | hp1 | a0001 | c0002 | t0004 | g0066 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0354 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01257 | hp2 | a0007 | c0005 | t0001 | g0086 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01346 | hp1 | a0001 | c0001 | t0018 | g0136 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0041 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | IBS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0330 | EUR | IBS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0343 | EUR | IBS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01928 | hp2 | a0001 | c0001 | t0025 | g0326 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0358 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0333 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02027 | hp1 | a0001 | c0001 | t0021 | g0245 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02055 | hp2 | a0001 | c0001 | t0013 | g0008 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02056 | hp1 | a0001 | c0002 | t0004 | g0078 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02071 | hp1 | a0001 | c0002 | t0028 | g0366 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02080 | hp1 | a0001 | c0002 | t0011 | g0363 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02132 | hp2 | a0001 | c0001 | t0022 | g0128 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | CDX | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | CDX | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0073 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0056 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0347 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0335 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0359 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02735 | hp1 | a0001 | c0002 | t0027 | g0362 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0250 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02738 | hp2 | a0001 | c0001 | t0012 | g0205 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0216 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0057 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0332 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0350 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0351 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0346 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03486 | hp2 | a0001 | c0001 | t0023 | g0178 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0338 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0339 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03540 | hp1 | a0001 | c0001 | t0016 | g0242 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0357 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03710 | hp1 | a0001 | c0002 | t0004 | g0080 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0340 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03831 | hp1 | a0001 | c0001 | t0008 | g0336 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0071 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03834 | hp2 | a0005 | c0009 | t0001 | g0140 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04184 | hp1 | a0001 | c0002 | t0004 | g0068 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04184 | hp2 | a0001 | c0001 | t0012 | g0207 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04199 | hp2 | a0001 | c0002 | t0004 | g0069 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04228 | hp2 | a0001 | c0002 | t0004 | g0053 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18612 | hp1 | a0001 | c0001 | t0020 | g0104 | EAS | CHB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | CHB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18747 | hp1 | a0001 | c0002 | t0004 | g0043 | EAS | CHB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | CHB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18940 | hp1 | a0001 | c0002 | t0011 | g0364 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18941 | hp2 | a0002 | c0006 | t0024 | g0282 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18943 | hp2 | a0001 | c0002 | t0004 | g0361 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0050 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18948 | hp1 | a0001 | c0002 | t0004 | g0063 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18949 | hp1 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18950 | hp2 | a0001 | c0002 | t0004 | g0082 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18952 | hp1 | a0001 | c0002 | t0004 | g0055 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18956 | hp2 | a0001 | c0001 | t0017 | g0268 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18962 | hp1 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0319 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18965 | hp1 | a0001 | c0002 | t0004 | g0047 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18966 | hp2 | a0001 | c0002 | t0004 | g0058 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18967 | hp1 | a0001 | c0004 | t0002 | g0308 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18967 | hp2 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18968 | hp2 | a0003 | c0007 | t0004 | g0067 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18970 | hp1 | a0001 | c0002 | t0004 | g0059 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18972 | hp1 | a0001 | c0002 | t0004 | g0076 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18981 | hp2 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18982 | hp2 | a0001 | c0002 | t0004 | g0072 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18985 | hp1 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18993 | hp2 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19007 | hp1 | a0001 | c0002 | t0004 | g0081 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0269 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19010 | hp1 | a0001 | c0002 | t0011 | g0365 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19010 | hp2 | a0001 | c0002 | t0009 | g0062 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19012 | hp1 | a0001 | c0002 | t0009 | g0046 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19030 | hp1 | a0001 | c0001 | t0013 | g0005 | AFR | LWK | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | LWK | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19054 | hp1 | a0001 | c0002 | t0009 | g0065 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19056 | hp2 | a0001 | c0002 | t0004 | g0280 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19058 | hp2 | a0001 | c0002 | t0009 | g0048 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19060 | hp2 | a0001 | c0002 | t0004 | g0084 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19074 | hp2 | a0001 | c0002 | t0004 | g0060 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19077 | hp2 | a0001 | c0002 | t0004 | g0085 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19079 | hp2 | a0001 | c0002 | t0004 | g0077 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19080 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19081 | hp2 | a0001 | c0002 | t0004 | g0049 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0107 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19082 | hp2 | a0001 | c0002 | t0004 | g0074 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19084 | hp1 | a0001 | c0002 | t0004 | g0070 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19085 | hp2 | a0001 | c0002 | t0004 | g0083 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19090 | hp2 | a0004 | c0010 | t0002 | g0038 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0064 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0014 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0345 | AFR | ASW | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ASW | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0238 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02486 | hp1 | a0001 | c0001 | t0014 | g0144 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | USA | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | USA | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | USA | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0360 | AFR | LWK | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA21309 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | LWK | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0132 | REF | REF | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| homoSapiens_grch38 | hp1 | a0006 | c0008 | t0019 | g0152 | REF | REF | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:61878065
|
T | G | 6 | a0001a0002a0003others(3): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
missense_variant | MODERATE | c.2278A>C | p.Asn760His | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/25 | 2625/6128 | 2278/3591 | 760/1196 | chr17 | 61878065 | ||
| chr17:61881042
|
T | A | 1 | a0005 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.2219A>T | p.Asn740Ile | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/25 | 2566/6128 | 2219/3591 | 740/1196 | chr17 | 61881042 | ||
| chr17:61907425
|
C | A | 1 | a0004 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.1164G>T | p.Met388Ile | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/25 | 1511/6128 | 1164/3591 | 388/1196 | chr17 | 61907425 | ||
| chr17:61907499
|
A | G | 1 | a0003 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.1090T>C | p.Ser364Pro | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/25 | 1437/6128 | 1090/3591 | 364/1196 | chr17 | 61907499 | ||
| chr17:61907627
|
C | T | 1 | a0002 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.962G>A | p.Arg321Lys | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/25 | 1309/6128 | 962/3591 | 321/1196 | chr17 | 61907627 | ||
| chr17:61925044
|
C | T | 1 | a0007 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.349G>A | p.Gly117Arg | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/25 | 696/6128 | 349/3591 | 117/1196 | chr17 | 61925044 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:61877919
|
T | C | 1 | a0001c0003 | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
synonymous_variant | LOW | c.2424A>G | p.Leu808Leu | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/25 | 2771/6128 | 2424/3591 | 808/1196 | chr17 | 61877919 | ||
| chr17:61877952
|
A | T | 1 | a0001c0004 | 2 | HG00423.hp1 NA18967.hp1 |
synonymous_variant | LOW | c.2391T>A | p.Val797Val | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/25 | 2738/6128 | 2391/3591 | 797/1196 | chr17 | 61877952 | ||
| chr17:61891639
|
T | C | 2 | a0001c0002a0003c0007 | 52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
synonymous_variant | LOW | c.1749A>G | p.Gln583Gln | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/25 | 2096/6128 | 1749/3591 | 583/1196 | chr17 | 61891639 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:61865470
|
C | T | 1 | a0001c0001t0025 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2087G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 2087 | chr17 | 61865470 | |||||
| chr17:61865553
|
G | C | 1 | a0001c0001t0022 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2004C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 2004 | chr17 | 61865553 | |||||
| chr17:61865707
|
T | TA | 10 | a0001c0001t0004a0001c0001t0020a0001c0001t0021others(7): Show | 56 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1849dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1849 | chr17 | 61865707 | |||||
| chr17:61865927
|
C | T | 2 | a0001c0001t0005a0001c0001t0013 | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1630G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1630 | chr17 | 61865927 | |||||
| chr17:61865973
|
G | A | 2 | a0001c0001t0021a0001c0001t0022 | 2 | HG02027.hp1 HG02132.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1584C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1584 | chr17 | 61865973 | |||||
| chr17:61866060
|
T | A | 1 | a0001c0001t0026 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1497A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1497 | chr17 | 61866060 | |||||
| chr17:61866092
|
C | T | 1 | a0001c0001t0023 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1465G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1465 | chr17 | 61866092 | |||||
| chr17:61866171
|
T | C | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*1386A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1386 | chr17 | 61866171 | |||||
| chr17:61866198
|
T | C | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*1359A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1359 | chr17 | 61866198 | |||||
| chr17:61866343
|
G | C | 10 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(7): Show | 109 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*1214C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1214 | chr17 | 61866343 | |||||
| chr17:61866346
|
G | A | 1 | a0001c0001t0012 | 2 | HG02738.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1211C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1211 | chr17 | 61866346 | |||||
| chr17:61866359
|
G | GA | 5 | a0001c0001t0006a0001c0001t0007a0001c0001t0010others(2): Show | 19 | HG00621.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1197dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1197 | chr17 | 61866359 | |||||
| chr17:61866375
|
A | C | 1 | a0001c0001t0018 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1182T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1182 | chr17 | 61866375 | |||||
| chr17:61866404
|
G | A | 1 | a0001c0002t0028 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1153C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1153 | chr17 | 61866404 | |||||
| chr17:61866451
|
A | T | 1 | a0001c0001t0008 | 4 | HG03491.hp1 HG03492.hp2 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1106T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1106 | chr17 | 61866451 | |||||
| chr17:61866920
|
A | C | 1 | a0001c0001t0017 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*637T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 637 | chr17 | 61866920 | |||||
| chr17:61867050
|
G | A | 1 | a0001c0001t0014 | 2 | HG02486.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*507C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 507 | chr17 | 61867050 | |||||
| chr17:61867108
|
C | T | 1 | a0001c0001t0016 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*449G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 449 | chr17 | 61867108 | |||||
| chr17:61927824
|
G | C | 1 | a0001c0002t0027 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-189C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/25 | 1180 | chr17 | 61927824 | |||||
| chr17:61927878
|
AGAACCGG others(8): Show |
A | 2 | a0001c0002t0011a0001c0002t0028 | 4 | HG02071.hp1 HG02080.hp1 NA18940.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-258_-244delCTACAG others(9): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/25 | 1235 | chr17 | 61927878 | |||||
| chr17:61927920
|
A | G | 1 | a0001c0001t0015 | 1 | HG00099.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-285T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/25 | chr17 | 61927920 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:61867817
|
A | G | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3421+16T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 24/24 | chr17 | 61867817 | ||||||
| chr17:61868111
|
A | C | 7 | a0001c0001t0003g0164a0001c0001t0003g0170a0001c0001t0003g0172others(4): Show | 7 | NA18951.hp1 NA18961.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.3245-102T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868111 | ||||||
| chr17:61868207
|
A | G | 34 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.3245-198T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868207 | ||||||
| chr17:61868465
|
T | C | 2 | a0001c0001t0003g0176a0001c0001t0003g0237 | 2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3245-456A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868465 | ||||||
| chr17:61868863
|
G | A | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3244+171C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868863 | ||||||
| chr17:61868889
|
G | A | 4 | a0001c0002t0009g0062a0001c0002t0011g0363a0001c0002t0011g0364others(1): Show | 4 | HG02071.hp1 HG02080.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.3244+145C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868889 | ||||||
| chr17:61868997
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3244+37A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868997 | ||||||
| chr17:61869643
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3030+94A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 21/24 | chr17 | 61869643 | ||||||
| chr17:61870055
|
A | C | 1 | a0001c0001t0002g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2779-67T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870055 | ||||||
| chr17:61870176
|
T | G | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2779-188A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870176 | ||||||
| chr17:61870264
|
A | C | 2 | a0001c0001t0003g0223a0001c0001t0015g0001 | 2 | HG00099.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2779-276T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870264 | ||||||
| chr17:61870503
|
C | T | 1 | a0001c0001t0002g0265 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2779-515G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870503 | ||||||
| chr17:61870669
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2779-681A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870669 | ||||||
| chr17:61870792
|
G | T | 1 | a0001c0001t0001g0103 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2779-804C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870792 | ||||||
| chr17:61871282
|
G | A | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2778+983C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871282 | ||||||
| chr17:61871392
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2778+873C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871392 | ||||||
| chr17:61871427
|
A | C | 1 | a0001c0003t0002g0013 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2778+838T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871427 | ||||||
| chr17:61871655
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2778+610G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871655 | ||||||
| chr17:61871814
|
G | A | 2 | a0001c0001t0005g0006a0001c0001t0005g0010 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2778+451C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871814 | ||||||
| chr17:61871940
|
C | CAA | 9 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2778+323_2778+324d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871940 | ||||||
| chr17:61872126
|
T | A | 45 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0088others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.2778+139A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61872126 | ||||||
| chr17:61872168
|
T | C | 1 | a0001c0001t0003g0232 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2778+97A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61872168 | ||||||
| chr17:61872689
|
A | T | 1 | a0001c0001t0002g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2583-229T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61872689 | ||||||
| chr17:61872730
|
C | T | 2 | a0001c0001t0002g0267a0001c0001t0002g0313 | 2 | NA18940.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2583-270G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61872730 | ||||||
| chr17:61872775
|
A | G | 5 | a0001c0001t0007g0002a0001c0003t0002g0012a0001c0003t0002g0013others(2): Show | 5 | HG02257.hp2 HG03540.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.2583-315T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61872775 | ||||||
| chr17:61872937
|
C | G | 1 | a0001c0001t0001g0132 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2583-477G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61872937 | ||||||
| chr17:61873014
|
T | C | 1 | a0001c0001t0014g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2583-554A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873014 | ||||||
| chr17:61873142
|
T | C | 103 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(100): Show | 103 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2583-682A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873142 | ||||||
| chr17:61873231
|
A | G | 1 | a0001c0001t0003g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2583-771T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873231 | ||||||
| chr17:61873293
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0191 | 2 | HG01261.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2583-833C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873293 | ||||||
| chr17:61873367
|
A | T | 2 | a0001c0001t0003g0179a0001c0001t0003g0180 | 2 | HG02300.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2583-907T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873367 | ||||||
| chr17:61873419
|
A | C | 1 | a0001c0001t0002g0337 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2583-959T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873419 | ||||||
| chr17:61873693
|
T | C | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG01109.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2582+1220A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873693 | ||||||
| chr17:61874079
|
C | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG01109.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2582+834G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874079 | ||||||
| chr17:61874104
|
T | C | 1 | a0001c0002t0011g0365 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2582+809A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874104 | ||||||
| chr17:61874121
|
C | G | 1 | a0001c0001t0003g0225 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2582+792G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874121 | ||||||
| chr17:61874202
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0134 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2582+711G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874202 | ||||||
| chr17:61874452
|
G | C | 30 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(27): Show | 30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.2582+461C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874452 | ||||||
| chr17:61874457
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2582+456G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874457 | ||||||
| chr17:61874640
|
T | C | 1 | a0001c0001t0003g0168 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2582+273A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874640 | ||||||
| chr17:61875326
|
T | C | 8 | a0001c0001t0003g0173a0001c0001t0003g0174a0001c0001t0003g0175others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2457-288A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875326 | ||||||
| chr17:61875379
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0001g0219 | 3 | HG03130.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2457-341C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875379 | ||||||
| chr17:61875605
|
A | C | 4 | a0001c0001t0003g0173a0001c0001t0003g0174a0001c0001t0003g0234others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2457-567T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875605 | ||||||
| chr17:61875673
|
C | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG01109.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2457-635G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875673 | ||||||
| chr17:61875755
|
G | A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2457-717C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875755 | ||||||
| chr17:61875891
|
A | G | 30 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(27): Show | 30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.2457-853T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875891 | ||||||
| chr17:61875953
|
G | C | 12 | a0001c0001t0003g0243a0001c0001t0003g0244a0001c0001t0005g0003others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2457-915C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875953 | ||||||
| chr17:61876029
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2457-991C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876029 | ||||||
| chr17:61876129
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2457-1091G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876129 | ||||||
| chr17:61876462
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2457-1424C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876462 | ||||||
| chr17:61876529
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2456+1358G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876529 | ||||||
| chr17:61876545
|
C | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0101others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2456+1342G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876545 | ||||||
| chr17:61876812
|
G | A | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2456+1075C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876812 | ||||||
| chr17:61877014
|
T | C | 1 | a0001c0001t0002g0264 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2456+873A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61877014 | ||||||
| chr17:61877169
|
T | C | 23 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0106others(20): Show | 23 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.2456+718A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61877169 | ||||||
| chr17:61877221
|
A | C | 1 | a0001c0001t0003g0229 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2456+666T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61877221 | ||||||
| chr17:61877349
|
G | A | 1 | a0001c0002t0004g0056 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2456+538C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61877349 | ||||||
| chr17:61878526
|
C | T | 45 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0088others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.2255-438G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878526 | ||||||
| chr17:61878637
|
A | AT | 42 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(39): Show | 42 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.2255-550dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878637 | ||||||
| chr17:61878833
|
G | C | 52 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0041others(49): Show | 52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.2255-745C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878833 | ||||||
| chr17:61878854
|
C | A | 1 | a0001c0001t0003g0169 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2255-766G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878854 | ||||||
| chr17:61878921
|
A | G | 42 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(39): Show | 42 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.2255-833T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878921 | ||||||
| chr17:61878931
|
C | CA | 80 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0099others(77): Show | 80 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.2255-844dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878931 | ||||||
| chr17:61878931
|
C | CAA | 101 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0098others(98): Show | 101 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.2255-845_2255-844d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878931 | ||||||
| chr17:61878931
|
C | CAAA | 73 | a0001c0001t0001g0100a0001c0001t0001g0188a0001c0001t0001g0189others(70): Show | 73 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2255-846_2255-844d others(5): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878931 | ||||||
| chr17:61878931
|
C | CAAAA | 26 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0145others(23): Show | 26 | HG00140.hp2 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2255-847_2255-844d others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878931 | ||||||
| chr17:61878944
|
A | AAAAAAAA others(3): Show |
10 | a0001c0001t0003g0021a0001c0001t0003g0023a0001c0001t0003g0025others(7): Show | 10 | HG01891.hp1 HG02257.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.2255-857_2255-856i others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878944 | ||||||
| chr17:61878944
|
A | AAAAAAAA others(2): Show |
23 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(20): Show | 23 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2255-857_2255-856i others(11): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878944 | ||||||
| chr17:61878944
|
A | AAAAAAAA others(1): Show |
8 | a0001c0001t0003g0243a0001c0001t0005g0003a0001c0001t0005g0004others(5): Show | 8 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2255-857_2255-856i others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878944 | ||||||
| chr17:61878944
|
A | C | 1 | a0001c0001t0003g0234 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2255-856T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878944 | ||||||
| chr17:61879071
|
C | CT | 49 | a0001c0001t0001g0092a0001c0001t0001g0098a0001c0001t0001g0099others(46): Show | 49 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.2255-984dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | ||||||
| chr17:61879071
|
C | CTT | 8 | a0001c0001t0001g0153a0001c0001t0002g0314a0001c0001t0002g0333others(5): Show | 8 | HG00140.hp2 HG01099.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.2255-985_2255-984d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | ||||||
| chr17:61879071
|
CT | C | 134 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0145others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2255-984delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | ||||||
| chr17:61879071
|
CTT | C | 16 | a0001c0001t0002g0328a0001c0001t0002g0334a0001c0001t0002g0346others(13): Show | 16 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2255-985_2255-984d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | ||||||
| chr17:61879071
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2255-995_2255-984d others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | ||||||
| chr17:61879071
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2255-998_2255-984d others(17): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | ||||||
| chr17:61879200
|
G | C | 13 | a0001c0001t0003g0151a0001c0001t0003g0155a0001c0001t0003g0156others(10): Show | 13 | HG01074.hp2 HG01106.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.2255-1112C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879200 | ||||||
| chr17:61879457
|
A | G | 1 | a0001c0001t0002g0335 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2255-1369T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879457 | ||||||
| chr17:61879875
|
T | G | 1 | a0001c0002t0004g0047 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2254+1132A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879875 | ||||||
| chr17:61879887
|
A | C | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2254+1120T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879887 | ||||||
| chr17:61880075
|
G | A | 1 | a0001c0001t0003g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2254+932C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880075 | ||||||
| chr17:61880169
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2254+838C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880169 | ||||||
| chr17:61880239
|
G | A | 2 | a0001c0001t0002g0262a0001c0001t0002g0264 | 2 | HG00673.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2254+768C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880239 | ||||||
| chr17:61880261
|
T | C | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2254+746A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880261 | ||||||
| chr17:61880709
|
G | A | 1 | a0001c0002t0004g0056 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2254+298C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880709 | ||||||
| chr17:61880787
|
G | C | 95 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(92): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2254+220C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880787 | ||||||
| chr17:61880819
|
A | G | 1 | a0001c0001t0023g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2254+188T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880819 | ||||||
| chr17:61880902
|
T | C | 111 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0145others(108): Show | 111 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2254+105A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880902 | ||||||
| chr17:61880929
|
T | C | 9 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2254+78A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880929 | ||||||
| chr17:61881274
|
G | T | 115 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0145others(112): Show | 115 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.2090-103C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61881274 | ||||||
| chr17:61881351
|
C | A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2090-180G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61881351 | ||||||
| chr17:61881426
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0222 | 2 | HG03490.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.2090-255C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61881426 | ||||||
| chr17:61882185
|
A | C | 45 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0088others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.2090-1014T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882185 | ||||||
| chr17:61882228
|
C | T | 109 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(106): Show | 109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2090-1057G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882228 | ||||||
| chr17:61882404
|
G | C | 81 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(78): Show | 81 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.2090-1233C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882404 | ||||||
| chr17:61882500
|
A | G | 2 | a0001c0001t0002g0344a0001c0001t0002g0353 | 2 | HG00438.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.2090-1329T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882500 | ||||||
| chr17:61882601
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2090-1430G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882601 | ||||||
| chr17:61882741
|
G | A | 1 | a0001c0001t0002g0265 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2090-1570C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882741 | ||||||
| chr17:61882809
|
A | C | 1 | a0001c0001t0016g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2090-1638T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882809 | ||||||
| chr17:61883056
|
C | T | 250 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2089+1845G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883056 | ||||||
| chr17:61883311
|
G | C | 16 | a0001c0001t0002g0095a0001c0001t0002g0184a0001c0001t0002g0265others(13): Show | 16 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.2089+1590C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883311 | ||||||
| chr17:61883343
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2089+1558A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883343 | ||||||
| chr17:61883378
|
C | T | 364 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2089+1523G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883378 | ||||||
| chr17:61883390
|
C | A | 364 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2089+1511G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883390 | ||||||
| chr17:61883406
|
G | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0135a0001c0001t0003g0091 | 3 | HG01358.hp2 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2089+1495C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883406 | ||||||
| chr17:61883523
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0214a0001c0001t0001g0221others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089+1378C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883523 | ||||||
| chr17:61883604
|
T | C | 2 | a0001c0001t0003g0157a0001c0001t0003g0160 | 2 | HG00408.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2089+1297A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883604 | ||||||
| chr17:61884001
|
G | GA | 51 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0041others(48): Show | 51 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.2089+899dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884001 | ||||||
| chr17:61884001
|
GA | G | 49 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(46): Show | 49 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.2089+899delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884001 | ||||||
| chr17:61884152
|
T | C | 30 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(27): Show | 30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.2089+749A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884152 | ||||||
| chr17:61884554
|
A | T | 1 | a0001c0001t0003g0358 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2089+347T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884554 | ||||||
| chr17:61884555
|
A | T | 95 | a0001c0001t0001g0097a0001c0001t0001g0256a0001c0001t0001g0259others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.2089+346T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884555 | ||||||
| chr17:61884556
|
T | A | 18 | a0001c0001t0001g0212a0001c0001t0002g0274a0001c0001t0003g0016others(15): Show | 18 | HG00639.hp1 HG00642.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2089+345A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884556 | ||||||
| chr17:61885113
|
A | G | 1 | a0001c0002t0004g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1985-108T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885113 | ||||||
| chr17:61885155
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1985-150G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885155 | ||||||
| chr17:61885223
|
T | C | 42 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(39): Show | 42 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1985-218A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885223 | ||||||
| chr17:61885359
|
T | C | 250 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1985-354A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885359 | ||||||
| chr17:61885360
|
G | T | 1 | a0001c0001t0002g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1985-355C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885360 | ||||||
| chr17:61885414
|
C | CT | 42 | a0001c0001t0001g0111a0001c0001t0001g0188a0001c0001t0001g0213others(39): Show | 42 | HG00639.hp1 HG00733.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.1985-410dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885414 | ||||||
| chr17:61885414
|
CT | C | 94 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0088others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.1985-410delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885414 | ||||||
| chr17:61885428
|
T | C | 110 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(107): Show | 110 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1985-423A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885428 | ||||||
| chr17:61885603
|
A | G | 42 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(39): Show | 42 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1985-598T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885603 | ||||||
| chr17:61885714
|
G | A | 1 | a0001c0001t0021g0245 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1985-709C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885714 | ||||||
| chr17:61885721
|
C | A | 3 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1985-716G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885721 | ||||||
| chr17:61885723
|
A | AT | 44 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0111others(41): Show | 44 | HG00642.hp1 HG01109.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.1985-719dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885723 | ||||||
| chr17:61885723
|
AT | A | 134 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(131): Show | 134 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.1985-719delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885723 | ||||||
| chr17:61885761
|
G | A | 1 | a0001c0001t0003g0155 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1985-756C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885761 | ||||||
| chr17:61885950
|
G | A | 1 | a0001c0001t0003g0025 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1985-945C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885950 | ||||||
| chr17:61886192
|
A | T | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1985-1187T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886192 | ||||||
| chr17:61886251
|
A | G | 51 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0041others(48): Show | 51 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1985-1246T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886251 | ||||||
| chr17:61886356
|
G | A | 109 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(106): Show | 109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1985-1351C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886356 | ||||||
| chr17:61886418
|
A | C | 152 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(149): Show | 152 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1985-1413T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886418 | ||||||
| chr17:61886550
|
C | T | 105 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(102): Show | 105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1985-1545G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886550 | ||||||
| chr17:61886553
|
C | A | 22 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(19): Show | 22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1985-1548G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886553 | ||||||
| chr17:61886658
|
A | C | 1 | a0001c0001t0026g0349 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1985-1653T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886658 | ||||||
| chr17:61886733
|
G | A | 22 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(19): Show | 22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1985-1728C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886733 | ||||||
| chr17:61887065
|
C | T | 1 | a0001c0002t0004g0045 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1985-2060G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887065 | ||||||
| chr17:61887183
|
A | T | 3 | a0001c0003t0002g0012a0001c0003t0002g0014a0001c0003t0002g0015 | 3 | HG02257.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1985-2178T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887183 | ||||||
| chr17:61887338
|
T | C | 145 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(142): Show | 145 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1985-2333A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887338 | ||||||
| chr17:61887405
|
C | G | 1 | a0001c0001t0003g0249 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1984+2381G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887405 | ||||||
| chr17:61887438
|
G | A | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1984+2348C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887438 | ||||||
| chr17:61887458
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1984+2328C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887458 | ||||||
| chr17:61887466
|
C | G | 1 | a0001c0001t0002g0297 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1984+2320G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887466 | ||||||
| chr17:61887482
|
C | CA | 27 | a0001c0001t0001g0100a0001c0001t0001g0133a0001c0001t0001g0241others(24): Show | 27 | HG00140.hp2 HG00597.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.1984+2303dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887482 | ||||||
| chr17:61887482
|
CA | C | 6 | a0001c0001t0001g0126a0001c0001t0001g0143a0001c0001t0001g0211others(3): Show | 6 | HG01243.hp1 HG01255.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1984+2303delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887482 | ||||||
| chr17:61887677
|
T | C | 365 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(362): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1984+2109A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887677 | ||||||
| chr17:61887722
|
A | G | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1984+2064T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887722 | ||||||
| chr17:61887746
|
G | C | 2 | a0001c0001t0005g0006a0001c0001t0005g0010 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1984+2040C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887746 | ||||||
| chr17:61887775
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1984+2011C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887775 | ||||||
| chr17:61887790
|
C | T | 1 | a0001c0001t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1984+1996G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887790 | ||||||
| chr17:61887815
|
G | A | 4 | a0001c0001t0002g0329a0001c0001t0002g0334a0001c0001t0002g0346others(1): Show | 4 | HG02717.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1984+1971C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887815 | ||||||
| chr17:61888235
|
T | C | 6 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(3): Show | 6 | HG00280.hp2 HG01071.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1984+1551A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888235 | ||||||
| chr17:61888389
|
A | G | 1 | a0001c0001t0002g0266 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1984+1397T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888389 | ||||||
| chr17:61888556
|
T | TGTGC | 8 | a0001c0001t0002g0288a0001c0001t0002g0329a0001c0001t0002g0334others(5): Show | 8 | HG01109.hp2 HG02717.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1984+1226_1984+122 others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888556 | ||||||
| chr17:61888556
|
T | TGTGCGTG others(5): Show |
1 | a0001c0001t0003g0179 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1984+1229_1984+123 others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888556 | ||||||
| chr17:61888564
|
C | CGT | 3 | a0001c0001t0001g0112a0001c0001t0001g0147a0001c0001t0006g0210 | 3 | HG01168.hp2 NA18959.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1984+1220_1984+122 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | ||||||
| chr17:61888564
|
C | CGTGCGTG others(5): Show |
25 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(22): Show | 25 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1984+1221_1984+122 others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | ||||||
| chr17:61888564
|
C | CGTGCGTG others(7): Show |
1 | a0001c0001t0003g0176 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1984+1221_1984+122 others(18): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | ||||||
| chr17:61888564
|
C | CGTGCGTG others(9): Show |
1 | a0001c0001t0003g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1984+1221_1984+122 others(20): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | ||||||
| chr17:61888564
|
C | CGTGCGTG others(3): Show |
2 | a0001c0001t0003g0025a0001c0001t0003g0091 | 2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1984+1221_1984+122 others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | ||||||
| chr17:61888564
|
CGT | C | 5 | a0001c0001t0001g0139a0001c0001t0003g0032a0001c0001t0003g0230others(2): Show | 5 | HG02698.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1984+1220_1984+122 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | ||||||
| chr17:61888566
|
T | TGC | 141 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.1984+1219_1984+122 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888566 | ||||||
| chr17:61888566
|
T | TGCGTGC | 12 | a0001c0001t0003g0243a0001c0001t0003g0244a0001c0001t0005g0003others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1984+1219_1984+122 others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888566 | ||||||
| chr17:61888568
|
T | C | 63 | a0001c0001t0001g0141a0001c0001t0002g0288a0001c0001t0002g0329others(60): Show | 63 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1984+1218A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888568 | ||||||
| chr17:61888570
|
T | C | 102 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(99): Show | 102 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1984+1216A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888570 | ||||||
| chr17:61888572
|
T | C | 2 | a0001c0001t0002g0345a0001c0001t0002g0354 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1984+1214A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888572 | ||||||
| chr17:61888574
|
T | C | 1 | a0001c0001t0023g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1984+1212A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888574 | ||||||
| chr17:61888681
|
T | C | 1 | a0001c0001t0002g0327 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1984+1105A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888681 | ||||||
| chr17:61888790
|
C | T | 1 | a0001c0002t0004g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1984+996G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888790 | ||||||
| chr17:61888810
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1984+976C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888810 | ||||||
| chr17:61888821
|
A | G | 365 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(362): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1984+965T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888821 | ||||||
| chr17:61889020
|
C | CAAAAACA | 22 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(19): Show | 22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1984+759_1984+765d others(9): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889020 | ||||||
| chr17:61889020
|
C | CAAAAACA others(7): Show |
9 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1984+752_1984+765d others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889020 | ||||||
| chr17:61889020
|
CAAAAACA | C | 51 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0041others(48): Show | 51 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1984+759_1984+765d others(9): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889020 | ||||||
| chr17:61889020
|
CAAAAACA others(7): Show |
C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1984+752_1984+765d others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889020 | ||||||
| chr17:61889067
|
A | C | 12 | a0001c0001t0002g0095a0001c0001t0002g0265a0001c0001t0002g0270others(9): Show | 12 | HG00423.hp1 HG00621.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.1984+719T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889067 | ||||||
| chr17:61889069
|
C | A | 108 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(105): Show | 108 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1984+717G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889069 | ||||||
| chr17:61889091
|
C | CT | 109 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(106): Show | 109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1984+694dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889091 | ||||||
| chr17:61889275
|
CG | C | 51 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0041others(48): Show | 51 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1984+510delC | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889275 | ||||||
| chr17:61889380
|
A | T | 241 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1984+406T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889380 | ||||||
| chr17:61889443
|
T | G | 42 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(39): Show | 42 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1984+343A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889443 | ||||||
| chr17:61889483
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1984+303G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889483 | ||||||
| chr17:61889625
|
G | T | 1 | a0001c0001t0018g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1984+161C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889625 | ||||||
| chr17:61889901
|
G | T | 1 | a0001c0001t0003g0088 | 1 | HG02717.hp2 | splice_region_variant&intron_variant | LOW | c.1876-7C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61889901 | ||||||
| chr17:61889929
|
T | C | 8 | a0001c0001t0002g0328a0001c0001t0002g0329a0001c0001t0002g0332others(5): Show | 8 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1876-35A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61889929 | ||||||
| chr17:61890026
|
T | C | 105 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(102): Show | 105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1876-132A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890026 | ||||||
| chr17:61890033
|
G | A | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1876-139C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890033 | ||||||
| chr17:61890312
|
C | T | 1 | a0001c0002t0011g0363 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1876-418G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890312 | ||||||
| chr17:61890343
|
G | A | 1 | a0001c0002t0011g0363 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1876-449C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890343 | ||||||
| chr17:61890418
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1876-524A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890418 | ||||||
| chr17:61890441
|
C | A | 1 | a0001c0001t0002g0337 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1876-547G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890441 | ||||||
| chr17:61890490
|
A | T | 1 | a0001c0002t0004g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1876-596T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890490 | ||||||
| chr17:61890491
|
T | C | 1 | a0001c0002t0004g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1876-597A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890491 | ||||||
| chr17:61890494
|
C | T | 1 | a0001c0002t0004g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1876-600G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890494 | ||||||
| chr17:61890513
|
G | A | 1 | a0001c0002t0004g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1876-619C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890513 | ||||||
| chr17:61890579
|
C | T | 97 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0088others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.1876-685G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890579 | ||||||
| chr17:61890609
|
C | CA | 90 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0105others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1876-716dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890609 | ||||||
| chr17:61890609
|
C | CAA | 16 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0158others(13): Show | 16 | HG01978.hp1 HG02055.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1876-717_1876-716d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890609 | ||||||
| chr17:61890609
|
CA | C | 128 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(125): Show | 128 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1876-716delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890609 | ||||||
| chr17:61890756
|
T | A | 22 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(19): Show | 22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1875+757A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890756 | ||||||
| chr17:61890789
|
C | T | 1 | a0001c0003t0002g0013 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1875+724G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890789 | ||||||
| chr17:61890864
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1875+649C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890864 | ||||||
| chr17:61890961
|
T | C | 1 | a0001c0001t0002g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1875+552A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890961 | ||||||
| chr17:61890983
|
C | CA | 165 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0097others(162): Show | 165 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.1875+529dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890983 | ||||||
| chr17:61890983
|
CA | C | 30 | a0001c0001t0002g0034a0001c0001t0002g0095a0001c0001t0002g0261others(27): Show | 30 | HG01099.hp2 HG01515.hp2 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.1875+529delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890983 | ||||||
| chr17:61890983
|
CAAAAAAA others(8): Show |
C | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1875+515_1875+529d others(17): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890983 | ||||||
| chr17:61891012
|
G | A | 2 | a0001c0001t0002g0296a0001c0001t0007g0002 | 2 | HG03579.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1875+501C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891012 | ||||||
| chr17:61891091
|
C | T | 52 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0041others(49): Show | 52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1875+422G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891091 | ||||||
| chr17:61891190
|
G | A | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1875+323C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891190 | ||||||
| chr17:61891210
|
A | C | 64 | a0001c0001t0003g0243a0001c0001t0003g0244a0001c0001t0005g0003others(61): Show | 64 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1875+303T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891210 | ||||||
| chr17:61891219
|
C | T | 2 | a0001c0001t0005g0006a0001c0001t0005g0010 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1875+294G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891219 | ||||||
| chr17:61891249
|
T | A | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1875+264A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891249 | ||||||
| chr17:61891260
|
T | C | 151 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(148): Show | 151 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1875+253A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891260 | ||||||
| chr17:61891464
|
G | A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1875+49C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891464 | ||||||
| chr17:61891871
|
A | T | 143 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(140): Show | 143 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1699-182T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61891871 | ||||||
| chr17:61891920
|
C | A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1699-231G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61891920 | ||||||
| chr17:61891924
|
T | TTAATCTA others(321): Show |
1 | a0003c0007t0004g0067 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1699-236_1699-235i others(330): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61891924 | ||||||
| chr17:61892019
|
G | A | 3 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1699-330C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892019 | ||||||
| chr17:61892172
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1699-483G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892172 | ||||||
| chr17:61892397
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1699-708G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892397 | ||||||
| chr17:61892444
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1699-755C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892444 | ||||||
| chr17:61892557
|
C | T | 2 | a0001c0001t0003g0179a0001c0001t0003g0180 | 2 | HG02300.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1699-868G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892557 | ||||||
| chr17:61892562
|
T | C | 6 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | NA18612.hp1 NA18946.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1699-873A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892562 | ||||||
| chr17:61892583
|
G | A | 14 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0243others(11): Show | 14 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1699-894C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892583 | ||||||
| chr17:61892586
|
G | T | 2 | a0001c0001t0003g0019a0001c0001t0003g0027 | 2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1699-897C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892586 | ||||||
| chr17:61892590
|
A | C | 1 | a0001c0001t0002g0348 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1699-901T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892590 | ||||||
| chr17:61892720
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1699-1031C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892720 | ||||||
| chr17:61892789
|
TA | T | 9 | a0001c0001t0001g0112a0001c0001t0002g0266a0001c0001t0002g0303others(6): Show | 9 | HG01074.hp2 HG01515.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1698+975delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892789 | ||||||
| chr17:61892854
|
G | A | 5 | a0001c0001t0003g0169a0001c0003t0002g0012a0001c0003t0002g0013others(2): Show | 5 | HG01978.hp1 HG02257.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1698+911C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892854 | ||||||
| chr17:61892953
|
C | CA | 17 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0110others(14): Show | 17 | HG01167.hp1 HG02622.hp1 HG02738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1698+811dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892953 | ||||||
| chr17:61892953
|
CA | C | 222 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1698+811delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892953 | ||||||
| chr17:61892953
|
CAA | C | 8 | a0001c0001t0002g0303a0001c0001t0002g0342a0001c0001t0002g0343others(5): Show | 8 | HG01074.hp2 HG01099.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1698+810_1698+811d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892953 | ||||||
| chr17:61892984
|
G | A | 1 | a0001c0001t0003g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1698+781C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892984 | ||||||
| chr17:61892991
|
C | CT | 45 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0088others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.1698+773dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892991 | ||||||
| chr17:61893004
|
T | C | 30 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(27): Show | 30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1698+761A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893004 | ||||||
| chr17:61893148
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1698+617A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893148 | ||||||
| chr17:61893154
|
A | G | 250 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1698+611T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893154 | ||||||
| chr17:61893236
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1698+529A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893236 | ||||||
| chr17:61893347
|
G | A | 4 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0166others(1): Show | 4 | HG02280.hp2 HG03490.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1698+418C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893347 | ||||||
| chr17:61893347
|
G | C | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1698+418C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893347 | ||||||
| chr17:61893435
|
C | T | 22 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(19): Show | 22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1698+330G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893435 | ||||||
| chr17:61893476
|
A | G | 30 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(27): Show | 30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1698+289T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893476 | ||||||
| chr17:61893546
|
T | C | 45 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0088others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.1698+219A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893546 | ||||||
| chr17:61893554
|
G | A | 1 | a0001c0002t0004g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1698+211C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893554 | ||||||
| chr17:61893691
|
T | C | 3 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1698+74A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893691 | ||||||
| chr17:61893706
|
A | T | 144 | a0001c0001t0002g0342a0001c0001t0002g0343a0001c0001t0002g0352others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1698+59T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893706 | ||||||
| chr17:61894402
|
T | C | 30 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(27): Show | 30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1564-503A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894402 | ||||||
| chr17:61894621
|
G | A | 104 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(101): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1563+694C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894621 | ||||||
| chr17:61894773
|
A | G | 2 | a0001c0001t0003g0032a0001c0001t0003g0252 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1563+542T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894773 | ||||||
| chr17:61894810
|
T | C | 108 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(105): Show | 108 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1563+505A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894810 | ||||||
| chr17:61894839
|
T | TTA | 30 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(27): Show | 30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1563+475_1563+476i others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894839 | ||||||
| chr17:61894839
|
TA | T | 161 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(158): Show | 161 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1563+475delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894839 | ||||||
| chr17:61894912
|
T | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1563+403A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894912 | ||||||
| chr17:61894930
|
T | C | 3 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1563+385A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894930 | ||||||
| chr17:61895116
|
C | G | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1563+199G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61895116 | ||||||
| chr17:61895516
|
T | G | 1 | a0001c0001t0003g0230 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1495-133A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61895516 | ||||||
| chr17:61895718
|
G | A | 242 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1495-335C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61895718 | ||||||
| chr17:61895891
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG01071.hp2 HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1495-508A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61895891 | ||||||
| chr17:61895894
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1495-511T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61895894 | ||||||
| chr17:61895998
|
T | A | 47 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(44): Show | 47 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1495-615A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61895998 | ||||||
| chr17:61896097
|
G | A | 1 | a0001c0001t0002g0314 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1495-714C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896097 | ||||||
| chr17:61896100
|
C | T | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495-717G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896100 | ||||||
| chr17:61896124
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1495-741G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896124 | ||||||
| chr17:61896171
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1495-788G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896171 | ||||||
| chr17:61896195
|
G | A | 53 | a0001c0001t0006g0107a0001c0002t0004g0039a0001c0002t0004g0040others(50): Show | 53 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1495-812C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896195 | ||||||
| chr17:61896239
|
C | CA | 18 | a0001c0001t0001g0092a0001c0001t0002g0275a0001c0001t0002g0278others(15): Show | 18 | HG00621.hp1 HG00621.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1495-857dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896239 | ||||||
| chr17:61896251
|
AC | A | 43 | a0001c0001t0002g0341a0001c0001t0003g0051a0001c0001t0003g0052others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(40): Show |
intron_variant | MODIFIER | c.1495-869delG | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896251 | ||||||
| chr17:61896252
|
C | A | 208 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(205): Show | 208 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.1495-869G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896252 | ||||||
| chr17:61896256
|
A | C | 1 | a0001c0002t0004g0082 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1495-873T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896256 | ||||||
| chr17:61896260
|
A | C | 1 | a0001c0001t0003g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1495-877T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896260 | ||||||
| chr17:61896471
|
C | T | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1494+998G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896471 | ||||||
| chr17:61896805
|
A | G | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+664T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896805 | ||||||
| chr17:61896856
|
C | A | 45 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0088others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.1494+613G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896856 | ||||||
| chr17:61896933
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1494+536G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896933 | ||||||
| chr17:61897027
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1494+442A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61897027 | ||||||
| chr17:61897290
|
A | G | 47 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(44): Show | 47 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1494+179T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61897290 | ||||||
| chr17:61897348
|
T | G | 30 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(27): Show | 30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1494+121A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61897348 | ||||||
| chr17:61897944
|
C | T | 1 | a0001c0002t0009g0062 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1308-205G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61897944 | ||||||
| chr17:61898011
|
T | C | 109 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(106): Show | 109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1308-272A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898011 | ||||||
| chr17:61898088
|
T | C | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308-349A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898088 | ||||||
| chr17:61898093
|
A | G | 2 | a0001c0001t0005g0007a0001c0001t0005g0011 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1308-354T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898093 | ||||||
| chr17:61898406
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1308-667G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898406 | ||||||
| chr17:61898407
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1308-668T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898407 | ||||||
| chr17:61898408
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1308-669G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898408 | ||||||
| chr17:61898578
|
G | A | 9 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1308-839C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898578 | ||||||
| chr17:61898602
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1308-863A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898602 | ||||||
| chr17:61898650
|
G | A | 8 | a0001c0001t0002g0328a0001c0001t0002g0329a0001c0001t0002g0332others(5): Show | 8 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1308-911C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898650 | ||||||
| chr17:61898675
|
G | C | 4 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0013g0005others(1): Show | 4 | HG02055.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1308-936C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898675 | ||||||
| chr17:61898716
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1308-977G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898716 | ||||||
| chr17:61898739
|
G | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0148a0001c0001t0001g0217others(1): Show | 4 | HG01099.hp1 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308-1000C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898739 | ||||||
| chr17:61899166
|
C | A | 3 | a0001c0001t0003g0175a0001c0001t0003g0235a0001c0001t0003g0236 | 3 | HG02809.hp1 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1308-1427G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899166 | ||||||
| chr17:61899179
|
T | C | 8 | a0001c0001t0002g0261a0001c0001t0002g0267a0001c0001t0002g0273others(5): Show | 8 | HG02129.hp1 HG02155.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1308-1440A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899179 | ||||||
| chr17:61899200
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1308-1461C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899200 | ||||||
| chr17:61899231
|
A | T | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1308-1492T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899231 | ||||||
| chr17:61899416
|
A | G | 9 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1308-1677T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899416 | ||||||
| chr17:61899482
|
C | A | 3 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1308-1743G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899482 | ||||||
| chr17:61899606
|
A | G | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1308-1867T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899606 | ||||||
| chr17:61899813
|
A | G | 105 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(102): Show | 105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1308-2074T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899813 | ||||||
| chr17:61899839
|
G | A | 1 | a0001c0002t0004g0058 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1308-2100C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899839 | ||||||
| chr17:61899908
|
T | C | 1 | a0001c0001t0018g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1308-2169A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899908 | ||||||
| chr17:61899910
|
TA | T | 254 | a0001c0001t0001g0111a0001c0001t0001g0123a0001c0001t0001g0129others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1308-2172delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899910 | ||||||
| chr17:61899927
|
T | A | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1308-2188A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899927 | ||||||
| chr17:61900205
|
A | G | 3 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1308-2466T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900205 | ||||||
| chr17:61900323
|
C | T | 1 | a0001c0002t0004g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1308-2584G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900323 | ||||||
| chr17:61900434
|
T | C | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308-2695A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900434 | ||||||
| chr17:61900673
|
A | C | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308-2934T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900673 | ||||||
| chr17:61900702
|
A | T | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308-2963T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900702 | ||||||
| chr17:61900756
|
G | A | 5 | a0001c0001t0002g0289a0001c0001t0002g0303a0001c0001t0002g0304others(2): Show | 5 | HG01993.hp1 NA18945.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1308-3017C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900756 | ||||||
| chr17:61900812
|
G | C | 105 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(102): Show | 105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1308-3073C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900812 | ||||||
| chr17:61900851
|
G | A | 3 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1308-3112C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900851 | ||||||
| chr17:61901015
|
C | T | 104 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(101): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1308-3276G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901015 | ||||||
| chr17:61901061
|
G | C | 1 | a0001c0002t0004g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1308-3322C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901061 | ||||||
| chr17:61901204
|
A | C | 1 | a0001c0001t0003g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1307+3256T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901204 | ||||||
| chr17:61901363
|
G | T | 108 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(105): Show | 108 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1307+3097C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901363 | ||||||
| chr17:61901435
|
T | G | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1307+3025A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901435 | ||||||
| chr17:61901491
|
G | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1307+2969C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901491 | ||||||
| chr17:61901577
|
C | CT | 63 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0001g0125others(60): Show | 63 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1307+2882dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
C | CTT | 34 | a0001c0001t0001g0103a0001c0001t0001g0240a0001c0001t0001g0241others(31): Show | 34 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1307+2881_1307+288 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
C | CTTT | 9 | a0001c0001t0002g0264a0001c0001t0002g0327a0001c0001t0002g0330others(6): Show | 9 | HG01081.hp1 HG01243.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1307+2880_1307+288 others(7): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CT | C | 29 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(26): Show | 29 | HG01070.hp1 HG01255.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1307+2882delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTT | C | 11 | a0001c0001t0001g0097a0001c0001t0003g0016a0001c0001t0003g0023others(8): Show | 11 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1307+2881_1307+288 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTT | C | 6 | a0001c0001t0003g0017a0001c0001t0003g0019a0001c0001t0003g0020others(3): Show | 6 | HG02451.hp1 HG02896.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1307+2880_1307+288 others(7): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTT | C | 7 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0037others(4): Show | 7 | HG02257.hp2 NA18993.hp1 NA19074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1307+2877_1307+288 others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090others(4): Show | 7 | HG02145.hp1 HG02717.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1307+2875_1307+288 others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTTT others(2): Show |
C | 35 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0151others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.1307+2874_1307+288 others(13): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0187 | 3 | HG00140.hp1 NA18942.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1307+2873_1307+288 others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0123a0001c0001t0001g0254 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1307+2872_1307+288 others(15): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTTT others(5): Show |
C | 54 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(51): Show | 54 | HG00280.hp2 HG00558.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.1307+2871_1307+288 others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0002g0262others(1): Show | 4 | HG00673.hp2 HG01346.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307+2870_1307+288 others(17): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | HG02040.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1307+2869_1307+288 others(18): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1307+2866_1307+288 others(21): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0002t0004g0044a0001c0002t0004g0053 | 2 | HG04228.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1307+2865_1307+288 others(22): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTTT others(12): Show |
C | 51 | a0001c0001t0001g0111a0001c0001t0006g0107a0001c0002t0004g0039others(48): Show | 51 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1307+2864_1307+288 others(23): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901577
|
CTTTTTTT others(13): Show |
C | 2 | a0001c0001t0002g0263a0001c0002t0004g0078 | 2 | HG02056.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1307+2863_1307+288 others(24): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | ||||||
| chr17:61901615
|
T | C | 3 | a0001c0001t0002g0348a0001c0001t0003g0243a0001c0001t0003g0244 | 3 | HG02280.hp1 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1307+2845A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901615 | ||||||
| chr17:61901631
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1307+2829C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901631 | ||||||
| chr17:61901775
|
T | C | 1 | a0001c0001t0003g0182 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1307+2685A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901775 | ||||||
| chr17:61901786
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0214a0001c0001t0001g0221 | 3 | HG02896.hp2 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1307+2674G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901786 | ||||||
| chr17:61901817
|
C | T | 1 | a0001c0001t0003g0165 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1307+2643G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901817 | ||||||
| chr17:61901873
|
C | T | 3 | a0001c0001t0003g0243a0001c0001t0003g0244a0001c0001t0016g0242 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1307+2587G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901873 | ||||||
| chr17:61901877
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1307+2583G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901877 | ||||||
| chr17:61901929
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1307+2531C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901929 | ||||||
| chr17:61902151
|
G | A | 19 | a0001c0001t0002g0330a0001c0001t0002g0331a0001c0001t0002g0333others(16): Show | 19 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.1307+2309C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902151 | ||||||
| chr17:61902491
|
C | A | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1307+1969G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902491 | ||||||
| chr17:61902518
|
A | G | 1 | a0001c0001t0002g0263 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1307+1942T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902518 | ||||||
| chr17:61902567
|
T | C | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1307+1893A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902567 | ||||||
| chr17:61902643
|
G | T | 8 | a0001c0001t0002g0328a0001c0001t0002g0329a0001c0001t0002g0332others(5): Show | 8 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1307+1817C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902643 | ||||||
| chr17:61902709
|
T | TA | 23 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0106others(20): Show | 23 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.1307+1750dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902709 | ||||||
| chr17:61902858
|
T | TA | 15 | a0001c0001t0001g0194a0001c0001t0002g0095a0001c0001t0002g0275others(12): Show | 15 | HG01978.hp2 HG02056.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1307+1601dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902858 | ||||||
| chr17:61902858
|
TA | T | 99 | a0001c0001t0001g0111a0001c0001t0001g0123a0001c0001t0001g0208others(96): Show | 99 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.1307+1601delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902858 | ||||||
| chr17:61902913
|
T | A | 2 | a0001c0001t0001g0097a0005c0009t0001g0140 | 2 | HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1307+1547A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902913 | ||||||
| chr17:61902937
|
C | A | 12 | a0001c0001t0003g0243a0001c0001t0003g0244a0001c0001t0005g0003others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1307+1523G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902937 | ||||||
| chr17:61902980
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1307+1480G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902980 | ||||||
| chr17:61902991
|
C | T | 1 | a0001c0001t0002g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1307+1469G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902991 | ||||||
| chr17:61903021
|
C | T | 1 | a0001c0001t0014g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1307+1439G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903021 | ||||||
| chr17:61903162
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1307+1298C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903162 | ||||||
| chr17:61903174
|
G | GA | 37 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0135others(34): Show | 37 | HG00621.hp1 HG00621.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1307+1285dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903174 | ||||||
| chr17:61903174
|
GA | G | 45 | a0001c0001t0006g0107a0001c0001t0007g0002a0001c0002t0004g0039others(42): Show | 45 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1307+1285delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903174 | ||||||
| chr17:61903220
|
A | AT | 106 | a0001c0001t0001g0117a0001c0001t0002g0033a0001c0001t0002g0034others(103): Show | 106 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1307+1239dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903220 | ||||||
| chr17:61903262
|
C | T | 4 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0193others(1): Show | 4 | NA18994.hp1 NA19011.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307+1198G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903262 | ||||||
| chr17:61903398
|
G | A | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307+1062C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903398 | ||||||
| chr17:61903612
|
T | C | 2 | a0001c0002t0004g0061a0001c0002t0004g0073 | 2 | HG01081.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1307+848A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903612 | ||||||
| chr17:61903665
|
C | CA | 6 | a0001c0001t0001g0189a0001c0001t0003g0021a0001c0001t0003g0091others(3): Show | 6 | HG02300.hp1 HG02630.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1307+794dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903665 | ||||||
| chr17:61903665
|
CA | C | 15 | a0001c0001t0001g0138a0001c0001t0001g0214a0001c0001t0002g0273others(12): Show | 15 | HG02300.hp2 HG02735.hp1 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1307+794delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903665 | ||||||
| chr17:61903809
|
G | C | 8 | a0001c0001t0002g0328a0001c0001t0002g0329a0001c0001t0002g0332others(5): Show | 8 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1307+651C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903809 | ||||||
| chr17:61904173
|
T | C | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307+287A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61904173 | ||||||
| chr17:61904379
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0239 | 2 | HG02083.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1307+81G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61904379 | ||||||
| chr17:61904405
|
T | C | 1 | a0001c0002t0004g0070 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1307+55A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61904405 | ||||||
| chr17:61904627
|
G | C | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-42C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61904627 | ||||||
| chr17:61904724
|
G | A | 45 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0088others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.1182-139C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61904724 | ||||||
| chr17:61904946
|
A | AT | 24 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0111others(21): Show | 24 | HG00558.hp2 HG01934.hp2 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.1182-362dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61904946 | ||||||
| chr17:61904946
|
AT | A | 123 | a0001c0001t0001g0106a0001c0001t0002g0305a0001c0001t0002g0334others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.1182-362delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61904946 | ||||||
| chr17:61905160
|
C | T | 52 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0041others(49): Show | 52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1182-575G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905160 | ||||||
| chr17:61905225
|
G | C | 1 | a0001c0002t0004g0070 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1182-640C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905225 | ||||||
| chr17:61905337
|
T | C | 1 | a0001c0002t0011g0364 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1182-752A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905337 | ||||||
| chr17:61905359
|
C | T | 52 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0041others(49): Show | 52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1182-774G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905359 | ||||||
| chr17:61905513
|
G | C | 1 | a0001c0001t0025g0326 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1182-928C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905513 | ||||||
| chr17:61905595
|
G | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1182-1010C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905595 | ||||||
| chr17:61905695
|
TTA | T | 5 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090others(2): Show | 5 | HG01109.hp2 HG01952.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-1112_1182-111 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905695 | ||||||
| chr17:61905700
|
T | C | 2 | a0001c0001t0003g0177a0001c0001t0010g0238 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1182-1115A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905700 | ||||||
| chr17:61905754
|
A | G | 1 | a0001c0001t0003g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1182-1169T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905754 | ||||||
| chr17:61905963
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1182-1378G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905963 | ||||||
| chr17:61905965
|
GGGATTAC others(6): Show |
G | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1182-1393_1182-138 others(17): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905965 | ||||||
| chr17:61906001
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1181+1407G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906001 | ||||||
| chr17:61906364
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1181+1044G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906364 | ||||||
| chr17:61906507
|
C | T | 1 | a0001c0001t0002g0299 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1181+901G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906507 | ||||||
| chr17:61906691
|
A | C | 47 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(44): Show | 47 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1181+717T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906691 | ||||||
| chr17:61906830
|
C | CA | 7 | a0001c0001t0001g0098a0001c0001t0001g0141a0001c0001t0006g0107others(4): Show | 7 | HG02486.hp2 HG03834.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181+577dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906830 | ||||||
| chr17:61906830
|
CA | C | 233 | a0001c0001t0001g0117a0001c0001t0002g0033a0001c0001t0002g0034others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1181+577delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906830 | ||||||
| chr17:61906910
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1181+498C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906910 | ||||||
| chr17:61906943
|
G | A | 5 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090others(2): Show | 5 | HG01109.hp2 HG01952.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+465C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906943 | ||||||
| chr17:61906963
|
C | CA | 139 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0099others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.1181+444dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906963 | ||||||
| chr17:61906963
|
C | CAA | 18 | a0001c0001t0001g0132a0001c0001t0001g0204a0001c0001t0003g0051others(15): Show | 18 | HG00438.hp2 HG01175.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.1181+443_1181+444d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906963 | ||||||
| chr17:61906963
|
C | CAAA | 26 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(23): Show | 26 | HG00639.hp1 HG02055.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1181+442_1181+444d others(5): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906963 | ||||||
| chr17:61906963
|
C | CAAAAAA | 85 | a0001c0001t0001g0117a0001c0001t0002g0033a0001c0001t0002g0034others(82): Show | 85 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1181+439_1181+444d others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906963 | ||||||
| chr17:61906963
|
C | CAAAAAAA | 22 | a0001c0001t0002g0037a0001c0001t0002g0095a0001c0001t0002g0264others(19): Show | 22 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1181+438_1181+444d others(9): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906963 | ||||||
| chr17:61906985
|
C | A | 2 | a0001c0001t0003g0358a0001c0001t0007g0002 | 2 | HG01975.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1181+423G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906985 | ||||||
| chr17:61907095
|
C | T | 1 | a0001c0001t0002g0321 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1181+313G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61907095 | ||||||
| chr17:61907167
|
T | A | 2 | a0001c0002t0004g0049a0001c0002t0009g0048 | 2 | NA19058.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1181+241A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61907167 | ||||||
| chr17:61907285
|
C | A | 1 | a0001c0001t0008g0340 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1181+123G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61907285 | ||||||
| chr17:61907670
|
T | A | 1 | a0001c0001t0012g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.955-36A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61907670 | ||||||
| chr17:61907865
|
A | T | 1 | a0004c0010t0002g0038 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.955-231T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61907865 | ||||||
| chr17:61907970
|
G | A | 1 | a0001c0001t0003g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.955-336C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61907970 | ||||||
| chr17:61908329
|
C | T | 45 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0088others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.955-695G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908329 | ||||||
| chr17:61908424
|
C | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0252 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.955-790G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908424 | ||||||
| chr17:61908473
|
A | C | 4 | a0001c0001t0008g0336a0001c0001t0008g0338a0001c0001t0008g0339others(1): Show | 4 | HG03491.hp1 HG03492.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.955-839T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908473 | ||||||
| chr17:61908502
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.955-868A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908502 | ||||||
| chr17:61908569
|
T | C | 1 | a0001c0001t0002g0301 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.955-935A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908569 | ||||||
| chr17:61908814
|
T | TAAAATCA others(305): Show |
1 | a0001c0002t0011g0363 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.955-1181_955-1180i others(314): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908814 | ||||||
| chr17:61908814
|
T | TAAAATCA others(305): Show |
42 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0041others(39): Show | 42 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.955-1181_955-1180i others(314): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908814 | ||||||
| chr17:61908814
|
T | TAAAATCA others(306): Show |
9 | a0001c0002t0004g0056a0001c0002t0004g0058a0001c0002t0004g0066others(6): Show | 9 | HG01175.hp1 HG02056.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-1181_955-1180i others(315): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908814 | ||||||
| chr17:61908860
|
A | T | 1 | a0001c0001t0006g0093 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.955-1226T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908860 | ||||||
| chr17:61908915
|
TGTTGTCT others(18): Show |
T | 1 | a0001c0001t0001g0209 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.955-1306_955-1282d others(27): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908915 | ||||||
| chr17:61908961
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.955-1327A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908961 | ||||||
| chr17:61909121
|
C | CT | 47 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(44): Show | 47 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.955-1488dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909121 | ||||||
| chr17:61909259
|
G | A | 1 | a0001c0001t0001g0132 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.955-1625C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909259 | ||||||
| chr17:61909435
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.955-1801C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909435 | ||||||
| chr17:61909554
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0134 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.955-1920G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909554 | ||||||
| chr17:61909611
|
T | A | 1 | a0001c0002t0011g0365 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.954+1909A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909611 | ||||||
| chr17:61909632
|
C | T | 52 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0041others(49): Show | 52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.954+1888G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909632 | ||||||
| chr17:61909769
|
G | A | 1 | a0001c0001t0002g0311 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.954+1751C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909769 | ||||||
| chr17:61909779
|
T | C | 1 | a0001c0001t0014g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.954+1741A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909779 | ||||||
| chr17:61909802
|
C | T | 2 | a0001c0001t0005g0007a0001c0001t0005g0011 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.954+1718G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909802 | ||||||
| chr17:61909811
|
G | A | 110 | a0001c0001t0001g0209a0001c0001t0002g0033a0001c0001t0002g0034others(107): Show | 110 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.954+1709C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909811 | ||||||
| chr17:61909815
|
A | ATATATAC others(3): Show |
20 | a0001c0001t0002g0261a0001c0001t0002g0267a0001c0001t0002g0271others(17): Show | 20 | HG00558.hp1 HG02071.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.954+1704_954+1705i others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909815 | ||||||
| chr17:61909815
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0209a0001c0001t0002g0296 | 2 | NA18991.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.954+1704_954+1705i others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909815 | ||||||
| chr17:61909815
|
ATGTGTGT others(5): Show |
A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.954+1693_954+1704d others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909815 | ||||||
| chr17:61909816
|
T | TATATAC | 81 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(78): Show | 81 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.954+1703_954+1704i others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909816 | ||||||
| chr17:61909817
|
G | A | 6 | a0001c0001t0002g0312a0001c0001t0002g0331a0001c0001t0002g0360others(3): Show | 6 | HG01081.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+1703C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909817 | ||||||
| chr17:61909818
|
T | TATAC | 6 | a0001c0001t0002g0312a0001c0001t0002g0331a0001c0001t0002g0360others(3): Show | 6 | HG01081.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+1701_954+1702i others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909818 | ||||||
| chr17:61909819
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.954+1701C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909819 | ||||||
| chr17:61909821
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.954+1699C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909821 | ||||||
| chr17:61909823
|
A | ACATGTG | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+1696_954+1697i others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | ||||||
| chr17:61909823
|
A | ATG | 3 | a0001c0001t0001g0147a0001c0001t0001g0204a0001c0001t0001g0215 | 3 | HG01168.hp2 HG01358.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.954+1695_954+1696d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | ||||||
| chr17:61909823
|
A | G | 90 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(87): Show | 90 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.954+1697T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | ||||||
| chr17:61909823
|
ATG | A | 33 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0103others(30): Show | 33 | HG00280.hp1 HG00544.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.954+1695_954+1696d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | ||||||
| chr17:61909823
|
ATGTG | A | 108 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0102others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.954+1693_954+1696d others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | ||||||
| chr17:61909823
|
ATGTGTG | A | 13 | a0001c0001t0003g0020a0001c0001t0003g0023a0001c0001t0003g0028others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.954+1691_954+1696d others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | ||||||
| chr17:61909823
|
ATGTGTGT others(1): Show |
A | 59 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0003g0016others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(56): Show |
intron_variant | MODIFIER | c.954+1689_954+1696d others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | ||||||
| chr17:61909823
|
ATGTGTGT others(3): Show |
A | 5 | a0001c0001t0001g0257a0001c0001t0005g0003a0001c0001t0005g0004others(2): Show | 5 | HG02004.hp2 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.954+1687_954+1696d others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | ||||||
| chr17:61909824
|
T | C | 18 | a0001c0001t0001g0209a0001c0001t0002g0261a0001c0001t0002g0262others(15): Show | 18 | HG00558.hp1 HG00673.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+1696A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909824 | ||||||
| chr17:61909826
|
T | TAC | 64 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(61): Show | 64 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.954+1693_954+1694i others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909826 | ||||||
| chr17:61909827
|
G | A | 21 | a0001c0001t0002g0095a0001c0001t0002g0330a0001c0001t0002g0335others(18): Show | 21 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.954+1693C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909827 | ||||||
| chr17:61909828
|
T | C | 17 | a0001c0001t0002g0095a0001c0001t0002g0330a0001c0001t0002g0335others(14): Show | 17 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.954+1692A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909828 | ||||||
| chr17:61909829
|
G | A | 6 | a0001c0001t0002g0312a0001c0001t0002g0331a0001c0001t0002g0360others(3): Show | 6 | HG01081.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+1691C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909829 | ||||||
| chr17:61909830
|
T | C | 6 | a0001c0001t0002g0312a0001c0001t0002g0331a0001c0001t0002g0360others(3): Show | 6 | HG01081.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+1690A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909830 | ||||||
| chr17:61909835
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.954+1685C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909835 | ||||||
| chr17:61909836
|
T | C | 1 | a0001c0001t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.954+1684A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909836 | ||||||
| chr17:61909915
|
T | A | 9 | a0001c0001t0002g0328a0001c0001t0002g0329a0001c0001t0002g0332others(6): Show | 9 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+1605A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909915 | ||||||
| chr17:61910006
|
T | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.954+1514A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910006 | ||||||
| chr17:61910200
|
C | T | 9 | a0001c0002t0004g0050a0001c0002t0004g0058a0001c0002t0004g0063others(6): Show | 9 | NA18945.hp2 NA18948.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.954+1320G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910200 | ||||||
| chr17:61910369
|
G | A | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.954+1151C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910369 | ||||||
| chr17:61910417
|
G | A | 110 | a0001c0001t0001g0209a0001c0001t0002g0033a0001c0001t0002g0034others(107): Show | 110 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.954+1103C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910417 | ||||||
| chr17:61910453
|
T | TGAG | 5 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090others(2): Show | 5 | HG01109.hp2 HG01952.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.954+1066_954+1067i others(5): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910453 | ||||||
| chr17:61910511
|
G | A | 1 | a0001c0002t0004g0049 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.954+1009C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910511 | ||||||
| chr17:61910553
|
T | C | 4 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0166others(1): Show | 4 | HG02280.hp2 HG03490.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+967A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910553 | ||||||
| chr17:61910583
|
C | A | 45 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0088others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.954+937G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910583 | ||||||
| chr17:61910591
|
C | CA | 105 | a0001c0001t0001g0117a0001c0001t0001g0189a0001c0001t0001g0209others(102): Show | 105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.954+928dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910591 | ||||||
| chr17:61910591
|
C | CAA | 11 | a0001c0001t0001g0213a0001c0001t0002g0272a0001c0001t0002g0279others(8): Show | 11 | HG01106.hp1 HG01175.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.954+927_954+928dup others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910591 | ||||||
| chr17:61910645
|
C | G | 1 | a0001c0001t0001g0185 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.954+875G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910645 | ||||||
| chr17:61910756
|
A | C | 1 | a0001c0001t0002g0312 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.954+764T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910756 | ||||||
| chr17:61910767
|
TATA | T | 8 | a0001c0001t0002g0328a0001c0001t0002g0329a0001c0001t0002g0332others(5): Show | 8 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+750_954+752del others(3): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910767 | ||||||
| chr17:61910885
|
G | A | 1 | a0001c0002t0004g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.954+635C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910885 | ||||||
| chr17:61911765
|
A | C | 109 | a0001c0001t0001g0209a0001c0001t0002g0033a0001c0001t0002g0034others(106): Show | 109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.781-72T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 6/24 | chr17 | 61911765 | ||||||
| chr17:61912212
|
T | A | 1 | a0001c0004t0002g0308 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.650-142A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912212 | ||||||
| chr17:61912217
|
A | G | 1 | a0001c0004t0002g0308 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.650-147T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912217 | ||||||
| chr17:61912220
|
A | G | 1 | a0001c0004t0002g0308 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.650-150T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912220 | ||||||
| chr17:61912221
|
A | T | 1 | a0001c0004t0002g0308 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.650-151T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912221 | ||||||
| chr17:61912339
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.650-269C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912339 | ||||||
| chr17:61912373
|
CG | C | 225 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0098others(222): Show | 225 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.650-304delC | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912373 | ||||||
| chr17:61912373
|
CGG | C | 99 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0103others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.650-305_650-304del others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912373 | ||||||
| chr17:61912375
|
G | C | 1 | a0001c0001t0001g0200 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.650-305C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912375 | ||||||
| chr17:61912384
|
G | C | 1 | a0001c0002t0028g0366 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.650-314C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912384 | ||||||
| chr17:61912385
|
G | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.650-315C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912385 | ||||||
| chr17:61912385
|
G | T | 22 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(19): Show | 22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.650-315C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912385 | ||||||
| chr17:61912391
|
G | A | 3 | a0001c0002t0004g0061a0001c0002t0004g0068a0001c0002t0004g0073 | 3 | HG01081.hp2 HG02258.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.650-321C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912391 | ||||||
| chr17:61912415
|
G | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.650-345C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912415 | ||||||
| chr17:61912520
|
C | G | 110 | a0001c0001t0001g0209a0001c0001t0002g0033a0001c0001t0002g0034others(107): Show | 110 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.650-450G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912520 | ||||||
| chr17:61912681
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.650-611A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912681 | ||||||
| chr17:61912706
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.650-636A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912706 | ||||||
| chr17:61912789
|
T | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.650-719A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912789 | ||||||
| chr17:61912865
|
T | C | 364 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.650-795A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912865 | ||||||
| chr17:61912907
|
C | A | 1 | a0001c0001t0003g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.650-837G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912907 | ||||||
| chr17:61912946
|
C | A | 1 | a0001c0001t0007g0351 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.650-876G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912946 | ||||||
| chr17:61912946
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.650-876G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912946 | ||||||
| chr17:61912953
|
A | G | 253 | a0001c0001t0001g0209a0001c0001t0002g0033a0001c0001t0002g0034others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.650-883T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912953 | ||||||
| chr17:61912968
|
C | G | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.650-898G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912968 | ||||||
| chr17:61913045
|
C | T | 3 | a0001c0001t0003g0243a0001c0001t0003g0244a0001c0001t0016g0242 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.650-975G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913045 | ||||||
| chr17:61913112
|
C | T | 1 | a0001c0002t0004g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.650-1042G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913112 | ||||||
| chr17:61913248
|
G | A | 52 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0041others(49): Show | 52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.650-1178C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913248 | ||||||
| chr17:61913283
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.650-1213C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913283 | ||||||
| chr17:61913342
|
C | CA | 9 | a0001c0001t0001g0241a0001c0001t0002g0315a0001c0001t0003g0031others(6): Show | 9 | HG00597.hp1 HG01175.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.650-1273dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913342 | ||||||
| chr17:61913362
|
A | AG | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.650-1293dupC | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913362 | ||||||
| chr17:61913373
|
G | A | 1 | a0001c0001t0002g0267 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.650-1303C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913373 | ||||||
| chr17:61913382
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.650-1312C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913382 | ||||||
| chr17:61913462
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.650-1392T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913462 | ||||||
| chr17:61914048
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.650-1978A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914048 | ||||||
| chr17:61914106
|
A | G | 1 | a0001c0001t0002g0297 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.650-2036T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914106 | ||||||
| chr17:61914338
|
C | T | 1 | a0001c0001t0002g0334 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.650-2268G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914338 | ||||||
| chr17:61914515
|
C | T | 1 | a0007c0005t0001g0086 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.650-2445G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914515 | ||||||
| chr17:61914571
|
C | T | 78 | a0001c0001t0001g0209a0001c0001t0002g0033a0001c0001t0002g0034others(75): Show | 78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.650-2501G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914571 | ||||||
| chr17:61914573
|
G | A | 6 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0145others(3): Show | 6 | HG02622.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.650-2503C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914573 | ||||||
| chr17:61914692
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.650-2622C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914692 | ||||||
| chr17:61914702
|
C | CA | 47 | a0001c0001t0001g0094a0001c0001t0001g0103a0001c0001t0001g0154others(44): Show | 47 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.650-2633dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | ||||||
| chr17:61914702
|
C | CAA | 6 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0001g0193others(3): Show | 6 | HG02602.hp2 HG03130.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.650-2634_650-2633d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | ||||||
| chr17:61914702
|
C | CAAAAAAA others(3): Show |
2 | a0001c0003t0002g0012a0001c0003t0002g0013 | 2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.650-2642_650-2633d others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | ||||||
| chr17:61914702
|
C | CAAAAAAA others(4): Show |
7 | a0001c0001t0002g0328a0001c0001t0002g0329a0001c0001t0002g0332others(4): Show | 7 | HG02257.hp2 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.650-2643_650-2633d others(13): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | ||||||
| chr17:61914702
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0002g0334a0001c0001t0002g0347a0001c0001t0002g0348others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.650-2644_650-2633d others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | ||||||
| chr17:61914702
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.650-2645_650-2633d others(15): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | ||||||
| chr17:61914702
|
CA | C | 13 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0002g0095others(10): Show | 13 | HG00558.hp2 HG01167.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.650-2633delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | ||||||
| chr17:61914873
|
C | CA | 9 | a0001c0001t0001g0105a0001c0001t0001g0189a0001c0001t0001g0254others(6): Show | 9 | HG01192.hp2 HG01346.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.650-2804dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914873 | ||||||
| chr17:61915067
|
G | A | 104 | a0001c0001t0001g0209a0001c0001t0002g0033a0001c0001t0002g0034others(101): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.650-2997C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915067 | ||||||
| chr17:61915165
|
C | T | 2 | a0001c0001t0003g0032a0001c0001t0003g0252 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.650-3095G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915165 | ||||||
| chr17:61915195
|
G | A | 45 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(42): Show | 45 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.650-3125C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915195 | ||||||
| chr17:61915333
|
G | A | 2 | a0001c0001t0005g0007a0001c0001t0005g0011 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.650-3263C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915333 | ||||||
| chr17:61915341
|
A | AAAAT | 70 | a0001c0001t0001g0109a0001c0001t0001g0117a0001c0001t0001g0186others(67): Show | 70 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.650-3275_650-3272d others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | ||||||
| chr17:61915341
|
A | AAAATAAA others(1): Show |
8 | a0001c0001t0003g0023a0001c0001t0003g0025a0001c0001t0003g0026others(5): Show | 8 | HG01109.hp2 HG01891.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.650-3279_650-3272d others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | ||||||
| chr17:61915341
|
A | AAAATAAA others(5): Show |
11 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(8): Show | 11 | HG00639.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.650-3283_650-3272d others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | ||||||
| chr17:61915341
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0003g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.650-3287_650-3272d others(18): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | ||||||
| chr17:61915341
|
A | T | 1 | a0001c0001t0001g0202 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.650-3271T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | ||||||
| chr17:61915341
|
AAAAT | A | 105 | a0001c0001t0001g0209a0001c0001t0002g0033a0001c0001t0002g0034others(102): Show | 105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.650-3275_650-3272d others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | ||||||
| chr17:61915414
|
A | T | 205 | a0001c0001t0001g0209a0001c0001t0002g0033a0001c0001t0002g0034others(202): Show | 205 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.650-3344T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915414 | ||||||
| chr17:61915489
|
G | A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.650-3419C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915489 | ||||||
| chr17:61915536
|
A | AC | 4 | a0001c0001t0002g0287a0001c0001t0002g0307a0001c0001t0002g0323others(1): Show | 4 | HG02083.hp1 HG02132.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.650-3467_650-3466i others(3): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915536 | ||||||
| chr17:61915536
|
A | C | 101 | a0001c0001t0001g0209a0001c0001t0002g0033a0001c0001t0002g0034others(98): Show | 101 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.650-3466T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915536 | ||||||
| chr17:61915547
|
G | A | 21 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(18): Show | 21 | HG00639.hp1 HG01109.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.650-3477C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915547 | ||||||
| chr17:61915655
|
TA | T | 249 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.650-3586delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915655 | ||||||
| chr17:61915661
|
A | T | 1 | a0001c0002t0004g0050 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.650-3591T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915661 | ||||||
| chr17:61915688
|
G | A | 15 | a0001c0001t0002g0328a0001c0001t0002g0329a0001c0001t0002g0332others(12): Show | 15 | HG02109.hp2 HG02258.hp1 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.650-3618C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915688 | ||||||
| chr17:61915724
|
G | A | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.650-3654C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915724 | ||||||
| chr17:61915781
|
G | C | 3 | a0001c0002t0004g0074a0001c0002t0004g0079a0001c0002t0004g0081 | 3 | NA18967.hp2 NA19007.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.649+3619C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915781 | ||||||
| chr17:61915796
|
C | T | 7 | a0001c0002t0004g0044a0001c0002t0004g0045a0001c0002t0004g0047others(4): Show | 7 | HG00438.hp2 NA18963.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.649+3604G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915796 | ||||||
| chr17:61915801
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.649+3599C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915801 | ||||||
| chr17:61915807
|
G | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.649+3593C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915807 | ||||||
| chr17:61915816
|
T | TA | 127 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0097others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.649+3583dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915816 | ||||||
| chr17:61915816
|
T | TAA | 12 | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0145others(9): Show | 12 | HG01978.hp1 HG02630.hp1 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.649+3582_649+3583d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915816 | ||||||
| chr17:61915816
|
TA | T | 12 | a0001c0001t0001g0129a0001c0001t0002g0305a0001c0001t0002g0332others(9): Show | 12 | HG01167.hp2 HG02145.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.649+3583delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915816 | ||||||
| chr17:61915816
|
TAAAAAAA others(4): Show |
T | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.649+3573_649+3583d others(13): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915816 | ||||||
| chr17:61915817
|
A | G | 2 | a0001c0001t0003g0176a0001c0001t0003g0237 | 2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.649+3583T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915817 | ||||||
| chr17:61916204
|
G | C | 1 | a0001c0001t0007g0351 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.649+3196C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916204 | ||||||
| chr17:61916385
|
G | A | 205 | a0001c0001t0001g0209a0001c0001t0002g0033a0001c0001t0002g0034others(202): Show | 205 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.649+3015C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916385 | ||||||
| chr17:61916411
|
T | C | 1 | a0007c0005t0001g0086 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.649+2989A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916411 | ||||||
| chr17:61916460
|
C | A | 3 | a0001c0001t0003g0243a0001c0001t0003g0244a0001c0001t0016g0242 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.649+2940G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916460 | ||||||
| chr17:61916772
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.649+2628A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916772 | ||||||
| chr17:61916983
|
G | A | 10 | a0001c0001t0002g0328a0001c0001t0002g0329a0001c0001t0002g0332others(7): Show | 10 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.649+2417C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916983 | ||||||
| chr17:61917262
|
C | T | 21 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(18): Show | 21 | HG00639.hp1 HG01109.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.649+2138G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61917262 | ||||||
| chr17:61917796
|
TA | T | 5 | a0001c0001t0002g0330a0001c0001t0002g0333a0001c0001t0002g0335others(2): Show | 5 | HG00140.hp2 HG01099.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.649+1603delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61917796 | ||||||
| chr17:61918099
|
T | C | 9 | a0001c0001t0003g0157a0001c0001t0003g0160a0001c0001t0003g0164others(6): Show | 9 | HG00408.hp1 NA18951.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.649+1301A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918099 | ||||||
| chr17:61918254
|
T | C | 1 | a0001c0001t0005g0009 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.649+1146A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918254 | ||||||
| chr17:61918311
|
G | A | 2 | a0001c0001t0005g0007a0001c0001t0005g0011 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.649+1089C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918311 | ||||||
| chr17:61918543
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.649+857C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918543 | ||||||
| chr17:61918631
|
A | G | 106 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(103): Show | 106 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.649+769T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918631 | ||||||
| chr17:61918818
|
G | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.649+582C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918818 | ||||||
| chr17:61918906
|
T | C | 2 | a0001c0002t0004g0064a0001c0002t0004g0077 | 2 | NA19079.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.649+494A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918906 | ||||||
| chr17:61918916
|
C | A | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.649+484G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918916 | ||||||
| chr17:61918923
|
G | GT | 37 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0116others(34): Show | 37 | HG00140.hp1 HG00438.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.649+476dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918923 | ||||||
| chr17:61918923
|
GT | G | 97 | a0001c0001t0001g0146a0001c0001t0001g0192a0001c0001t0001g0204others(94): Show | 97 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.649+476delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918923 | ||||||
| chr17:61918945
|
G | A | 1 | a0001c0001t0003g0358 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.649+455C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918945 | ||||||
| chr17:61918994
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.649+406C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918994 | ||||||
| chr17:61919155
|
C | A | 4 | a0001c0002t0004g0082a0001c0002t0004g0083a0001c0002t0004g0084others(1): Show | 4 | NA18950.hp2 NA19060.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.649+245G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61919155 | ||||||
| chr17:61919215
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.649+185C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61919215 | ||||||
| chr17:61919573
|
C | T | 2 | a0001c0001t0002g0328a0001c0001t0002g0332 | 2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.536-60G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61919573 | ||||||
| chr17:61919821
|
T | C | 4 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0036others(1): Show | 4 | HG02027.hp2 NA18993.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-308A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61919821 | ||||||
| chr17:61919990
|
G | A | 10 | a0001c0001t0003g0032a0001c0001t0003g0173a0001c0001t0003g0174others(7): Show | 10 | HG02257.hp1 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.536-477C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61919990 | ||||||
| chr17:61920052
|
A | G | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.536-539T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920052 | ||||||
| chr17:61920120
|
A | G | 20 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0111others(17): Show | 20 | HG00558.hp2 HG02083.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.536-607T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920120 | ||||||
| chr17:61920180
|
C | CT | 62 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0098others(59): Show | 62 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.536-668dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920180 | ||||||
| chr17:61920180
|
C | CTT | 85 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(82): Show | 85 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.536-669_536-668dup others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920180 | ||||||
| chr17:61920180
|
C | CTTT | 13 | a0001c0001t0002g0036a0001c0001t0002g0261a0001c0001t0002g0267others(10): Show | 13 | HG00558.hp1 HG00597.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.536-670_536-668dup others(3): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920180 | ||||||
| chr17:61920198
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.536-685A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920198 | ||||||
| chr17:61920200
|
C | T | 7 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0179others(4): Show | 7 | HG01346.hp2 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.536-687G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920200 | ||||||
| chr17:61920280
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.536-767G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920280 | ||||||
| chr17:61920486
|
C | CT | 39 | a0001c0001t0001g0096a0001c0001t0001g0102a0001c0001t0001g0108others(36): Show | 39 | HG00280.hp2 HG01071.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.536-974dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920486 | ||||||
| chr17:61920486
|
CT | C | 150 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0130others(147): Show | 150 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.536-974delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920486 | ||||||
| chr17:61920486
|
CTT | C | 21 | a0001c0001t0002g0035a0001c0001t0002g0261a0001c0001t0002g0266others(18): Show | 21 | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.536-975_536-974del others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920486 | ||||||
| chr17:61920499
|
T | G | 16 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(13): Show | 16 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.536-986A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920499 | ||||||
| chr17:61920504
|
T | G | 16 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(13): Show | 16 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.536-991A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920504 | ||||||
| chr17:61920521
|
TG | T | 365 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(362): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.536-1009delC | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920521 | ||||||
| chr17:61920526
|
C | T | 53 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0002t0004g0039others(50): Show | 53 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.536-1013G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920526 | ||||||
| chr17:61920580
|
C | A | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.536-1067G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920580 | ||||||
| chr17:61920622
|
G | A | 26 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(23): Show | 26 | HG00673.hp1 HG01928.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.535+1103C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920622 | ||||||
| chr17:61920789
|
T | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+936A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920789 | ||||||
| chr17:61920791
|
A | G | 1 | a0001c0001t0003g0358 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.535+934T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920791 | ||||||
| chr17:61920793
|
A | T | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+932T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920793 | ||||||
| chr17:61920796
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+929G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920796 | ||||||
| chr17:61920802
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+906_535+922del others(17): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920802 | ||||||
| chr17:61920821
|
C | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+904G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920821 | ||||||
| chr17:61920826
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+899A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920826 | ||||||
| chr17:61920828
|
T | A | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+897A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920828 | ||||||
| chr17:61920831
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+894T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920831 | ||||||
| chr17:61920832
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+893G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920832 | ||||||
| chr17:61920833
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+892T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920833 | ||||||
| chr17:61920841
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+884T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920841 | ||||||
| chr17:61920846
|
A | T | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+879T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920846 | ||||||
| chr17:61920847
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+878G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920847 | ||||||
| chr17:61920848
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+877T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920848 | ||||||
| chr17:61920865
|
G | T | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+860C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920865 | ||||||
| chr17:61920872
|
T | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+853A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920872 | ||||||
| chr17:61920876
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+849G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920876 | ||||||
| chr17:61920877
|
C | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+848G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920877 | ||||||
| chr17:61920878
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+847T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920878 | ||||||
| chr17:61920909
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+816G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920909 | ||||||
| chr17:61920910
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+815T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920910 | ||||||
| chr17:61920929
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+796A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920929 | ||||||
| chr17:61920933
|
C | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+792G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920933 | ||||||
| chr17:61921373
|
C | A | 102 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.535+352G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61921373 | ||||||
| chr17:61921492
|
T | C | 2 | a0001c0001t0002g0344a0001c0001t0002g0353 | 2 | HG00438.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.535+233A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61921492 | ||||||
| chr17:61921591
|
C | G | 7 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0113others(4): Show | 7 | NA18949.hp1 NA18952.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.535+134G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61921591 | ||||||
| chr17:61921670
|
G | A | 9 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.535+55C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61921670 | ||||||
| chr17:61922029
|
T | C | 106 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(103): Show | 106 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.433-202A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922029 | ||||||
| chr17:61922352
|
TAGCTACT others(1): Show |
T | 93 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(90): Show | 93 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.433-533_433-526del others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922352 | ||||||
| chr17:61922383
|
G | T | 1 | a0001c0001t0003g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.433-556C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922383 | ||||||
| chr17:61922444
|
G | T | 21 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(18): Show | 21 | HG00639.hp1 HG01109.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.433-617C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922444 | ||||||
| chr17:61922467
|
CA | C | 95 | a0001c0001t0001g0097a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.433-641delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922467 | ||||||
| chr17:61922511
|
C | CAT | 20 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0105others(17): Show | 20 | HG00408.hp2 HG00597.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.433-686_433-685dup others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
C | CATAT | 14 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(11): Show | 14 | HG00280.hp1 HG01168.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.433-688_433-685dup others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
C | CATATAT | 17 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0212others(14): Show | 17 | HG00642.hp2 HG00733.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-690_433-685dup others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
C | CATATATA others(1): Show |
31 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0098others(28): Show | 31 | HG01074.hp1 HG01167.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.433-692_433-685dup others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
C | CATATATA others(3): Show |
49 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(46): Show | 49 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.433-694_433-685dup others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
C | CATATATA others(5): Show |
34 | a0001c0001t0001g0097a0001c0001t0001g0115a0001c0001t0001g0116others(31): Show | 34 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.433-696_433-685dup others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
C | CATATATA others(7): Show |
23 | a0001c0001t0001g0102a0001c0001t0001g0112a0001c0001t0001g0113others(20): Show | 23 | HG00140.hp2 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.433-698_433-685dup others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
C | CATATATA others(9): Show |
15 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0197others(12): Show | 15 | HG00621.hp2 HG01516.hp2 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.433-700_433-685dup others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
C | CATATATA others(11): Show |
13 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0195others(10): Show | 13 | HG00621.hp1 HG00673.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.433-702_433-685dup others(18): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
C | CATATATA others(13): Show |
4 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(1): Show | 4 | HG01993.hp1 HG02083.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-704_433-685dup others(20): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
C | CATATATA others(15): Show |
2 | a0001c0001t0002g0184a0001c0001t0002g0310 | 2 | NA18985.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.433-706_433-685dup others(22): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
CAT | C | 8 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-686_433-685del others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
CATAT | C | 3 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0005g0007 | 3 | HG02132.hp1 HG03453.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.433-688_433-685del others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
CATATAT | C | 3 | a0001c0001t0002g0342a0001c0001t0002g0343a0001c0001t0002g0352 | 3 | HG01106.hp1 HG01433.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.433-690_433-685del others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
CATATATA others(3): Show |
C | 4 | a0001c0001t0001g0222a0001c0002t0004g0066a0001c0002t0011g0363others(1): Show | 4 | HG01175.hp1 HG02080.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-694_433-685del others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
CATATATA others(5): Show |
C | 58 | a0001c0001t0001g0154a0001c0001t0003g0051a0001c0001t0003g0052others(55): Show | 58 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.433-696_433-685del others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
CATATATA others(7): Show |
C | 29 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0163others(26): Show | 29 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.433-698_433-685del others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
CATATATA others(9): Show |
C | 2 | a0001c0001t0002g0286a0001c0001t0025g0326 | 2 | HG01928.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.433-700_433-685del others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
CATATATA others(11): Show |
C | 6 | a0001c0001t0002g0344a0001c0001t0002g0353a0001c0003t0002g0012others(3): Show | 6 | HG00438.hp1 HG00597.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-702_433-685del others(18): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922511
|
CATATATA others(13): Show |
C | 21 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(18): Show | 21 | HG00639.hp1 HG01109.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.433-704_433-685del others(20): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | ||||||
| chr17:61922543
|
T | TATATATA others(7): Show |
1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.433-717_433-716ins others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922543 | ||||||
| chr17:61922547
|
C | T | 6 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | NA18612.hp1 NA18946.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.433-720G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922547 | ||||||
| chr17:61922548
|
G | A | 214 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(211): Show | 214 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.433-721C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922548 | ||||||
| chr17:61922611
|
T | C | 28 | a0001c0001t0002g0095a0001c0001t0002g0287a0001c0001t0002g0288others(25): Show | 28 | HG00673.hp1 HG01928.hp2 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.433-784A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922611 | ||||||
| chr17:61922676
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.433-849T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922676 | ||||||
| chr17:61922747
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.433-920C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922747 | ||||||
| chr17:61923079
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.433-1252T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923079 | ||||||
| chr17:61923098
|
T | A | 2 | a0001c0001t0005g0007a0001c0001t0005g0011 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.433-1271A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923098 | ||||||
| chr17:61923145
|
T | C | 2 | a0001c0001t0002g0035a0004c0010t0002g0038 | 2 | NA19074.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.433-1318A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923145 | ||||||
| chr17:61923214
|
G | A | 3 | a0001c0001t0003g0243a0001c0001t0003g0244a0001c0001t0016g0242 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.433-1387C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923214 | ||||||
| chr17:61923215
|
T | C | 3 | a0001c0001t0003g0243a0001c0001t0003g0244a0001c0001t0016g0242 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.433-1388A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923215 | ||||||
| chr17:61923263
|
A | G | 3 | a0001c0001t0003g0243a0001c0001t0003g0244a0001c0001t0016g0242 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.433-1436T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923263 | ||||||
| chr17:61923273
|
C | T | 1 | a0001c0001t0002g0261 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.433-1446G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923273 | ||||||
| chr17:61923278
|
C | T | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.433-1451G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923278 | ||||||
| chr17:61923280
|
A | G | 1 | a0001c0001t0003g0025 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433-1453T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923280 | ||||||
| chr17:61923288
|
T | C | 106 | a0001c0001t0001g0097a0001c0001t0001g0239a0001c0001t0002g0033others(103): Show | 106 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.433-1461A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923288 | ||||||
| chr17:61923305
|
G | A | 4 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0240others(1): Show | 4 | HG00408.hp2 HG00597.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-1478C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923305 | ||||||
| chr17:61923401
|
C | CGGGAGGC others(10): Show |
1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.432+1543_432+1559d others(19): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923401 | ||||||
| chr17:61923409
|
G | A | 1 | a0001c0001t0003g0187 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.432+1552C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923409 | ||||||
| chr17:61923425
|
C | T | 9 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(6): Show | 9 | HG01070.hp1 HG01255.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.432+1536G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923425 | ||||||
| chr17:61923450
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.432+1511G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923450 | ||||||
| chr17:61923477
|
C | CA | 121 | a0001c0001t0001g0094a0001c0001t0001g0188a0001c0001t0001g0189others(118): Show | 121 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.432+1483dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923477 | ||||||
| chr17:61923477
|
C | CAA | 14 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0002g0327others(11): Show | 14 | HG00733.hp1 HG00733.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.432+1482_432+1483d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923477 | ||||||
| chr17:61923477
|
CA | C | 7 | a0001c0001t0001g0096a0001c0001t0003g0091a0001c0002t0004g0039others(4): Show | 7 | HG00642.hp1 HG01433.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+1483delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923477 | ||||||
| chr17:61923665
|
G | A | 4 | a0001c0003t0002g0012a0001c0003t0002g0013a0001c0003t0002g0014others(1): Show | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+1296C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923665 | ||||||
| chr17:61923674
|
T | TGTG | 53 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0002t0004g0039others(50): Show | 53 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.432+1284_432+1286d others(5): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923674 | ||||||
| chr17:61923686
|
G | T | 106 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(103): Show | 106 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.432+1275C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923686 | ||||||
| chr17:61923689
|
T | G | 1 | a0001c0002t0004g0081 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.432+1272A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923689 | ||||||
| chr17:61923750
|
G | A | 4 | a0001c0002t0004g0082a0001c0002t0004g0083a0001c0002t0004g0084others(1): Show | 4 | NA18950.hp2 NA19060.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+1211C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923750 | ||||||
| chr17:61923945
|
G | A | 1 | a0001c0001t0010g0250 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.432+1016C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923945 | ||||||
| chr17:61924030
|
A | C | 3 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0006g0093 | 3 | NA18985.hp1 NA19005.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.432+931T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924030 | ||||||
| chr17:61924244
|
T | C | 1 | a0001c0001t0003g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.432+717A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924244 | ||||||
| chr17:61924293
|
T | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0252 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.432+668A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924293 | ||||||
| chr17:61924483
|
A | G | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.432+478T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924483 | ||||||
| chr17:61924546
|
C | T | 75 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(72): Show | 75 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.432+415G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924546 | ||||||
| chr17:61924556
|
T | G | 8 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.432+405A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924556 | ||||||
| chr17:61924600
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.432+361G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924600 | ||||||
| chr17:61924617
|
G | A | 108 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(105): Show | 108 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.432+344C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924617 | ||||||
| chr17:61924679
|
A | G | 3 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.432+282T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924679 | ||||||
| chr17:61924698
|
G | A | 1 | a0001c0001t0002g0355 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.432+263C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924698 | ||||||
| chr17:61924722
|
A | C | 1 | a0001c0001t0004g0087 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.432+239T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924722 | ||||||
| chr17:61924937
|
G | A | 4 | a0001c0002t0004g0082a0001c0002t0004g0083a0001c0002t0004g0084others(1): Show | 4 | NA18950.hp2 NA19060.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+24C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924937 | ||||||
| chr17:61925433
|
C | T | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.294-334G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925433 | ||||||
| chr17:61925526
|
G | C | 1 | a0001c0001t0007g0356 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.294-427C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925526 | ||||||
| chr17:61925737
|
C | T | 53 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0002t0004g0039others(50): Show | 53 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.293+615G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925737 | ||||||
| chr17:61925820
|
T | C | 1 | a0001c0001t0003g0357 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.293+532A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925820 | ||||||
| chr17:61925882
|
C | G | 6 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(3): Show | 6 | HG02027.hp2 NA18993.hp1 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+470G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925882 | ||||||
| chr17:61925957
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.293+395G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925957 | ||||||
| chr17:61925966
|
C | A | 1 | a0001c0001t0003g0358 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.293+386G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925966 | ||||||
| chr17:61926033
|
GA | G | 16 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(13): Show | 16 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.293+318delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61926033 | ||||||
| chr17:61926095
|
C | A | 1 | a0001c0001t0003g0359 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.293+257G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61926095 | ||||||
| chr17:61927217
|
T | C | 1 | a0001c0001t0002g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19+437A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/24 | chr17 | 61927217 | ||||||
| chr17:61927567
|
A | G | 13 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0006others(10): Show | 13 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+87T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/24 | chr17 | 61927567 | ||||||
| chr17:61927586
|
C | G | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+68G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/24 | chr17 | 61927586 | ||||||
| chr17:61927610
|
G | A | 1 | a0001c0002t0004g0361 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-19+44C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/24 | chr17 | 61927610 |