| geneid | 135112 |
|---|---|
| ensemblid | ENSG00000111912.20 |
| hgncid | 21081 |
| symbol | NCOA7 |
| name | nuclear receptor coactivator 7 |
| refseq_nuc | NM_181782.5 |
| refseq_prot | NP_861447.3 |
| ensembl_nuc | ENST00000392477.7 |
| ensembl_prot | ENSP00000376269.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 125790960 |
| end | 125932034 |
| strand | + |
| ver | v1.2 |
| region | chr6:125790960-125932034 |
| region5000 | chr6:125785960-125937034 |
| regionname0 | NCOA7_chr6_125790960_125932034 |
| regionname5000 | NCOA7_chr6_125785960_125937034 |
| 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 | 0/0 | 942 | 127 | 25 | 28 | 54 | 7 | 13 | 48 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002 | 1/1 | 942 | 88 | 22 | 15 | 30 | 7 | 12 | 26 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0003 | 0/0 | 942 | 47 | 19 | 3 | 19 | 2 | 4 | 16 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0004 | 0/0 | 942 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0005 | 0/0 | 942 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0006 | 0/0 | 16 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0007 | 0/0 | 942 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0008 | 0/0 | 942 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| 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 | 0/0 | 2829 | 124 | 23 | 28 | 54 | 7 | 12 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0002 | 1/1 | 2829 | 83 | 17 | 15 | 30 | 7 | 12 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0003 | 0/0 | 2829 | 47 | 19 | 3 | 19 | 2 | 4 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0004 | 0/0 | 2829 | 4 | 4 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0005 | 0/0 | 2829 | 2 | 0 | 0 | 2 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0006 | 0/0 | 2829 | 2 | 0 | 2 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0007 | 0/0 | 2829 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0008 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0009 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0010 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0011 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0012 | 0/0 | 2829 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0013 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| c0014 | 0/0 | 2829 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| 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 | 3436 | 91 | 9 | 26 | 33 | 8 | 14 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0002 | 1/0 | 3436 | 68 | 12 | 17 | 23 | 5 | 10 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0003 | 0/0 | 3425 | 48 | 18 | 3 | 20 | 2 | 5 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0004 | 0/0 | 3437 | 21 | 5 | 1 | 15 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0005 | 0/0 | 3437 | 7 | 5 | 1 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0006 | 0/0 | 3436 | 5 | 5 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0007 | 0/0 | 3436 | 4 | 2 | 0 | 1 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0008 | 0/0 | 3436 | 4 | 0 | 0 | 4 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0009 | 0/0 | 3437 | 3 | 0 | 0 | 3 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0010 | 0/0 | 3436 | 2 | 2 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0011 | 0/0 | 3437 | 2 | 2 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0012 | 0/0 | 3436 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0013 | 0/0 | 3425 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0014 | 0/0 | 3436 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0015 | 0/0 | 3436 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0016 | 0/0 | 3436 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0017 | 0/0 | 3436 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0018 | 0/0 | 3425 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0019 | 0/0 | 3425 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0020 | 0/0 | 3425 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0021 | 0/0 | 3425 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0022 | 0/0 | 3436 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0023 | 0/0 | 3436 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0024 | 0/0 | 3436 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0025 | 0/0 | 3437 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| t0026 | 0/0 | 3436 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| 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 | 0/0 | 2829 | 124 | 23 | 28 | 54 | 7 | 12 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0007 | 0/0 | 2829 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0009 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0010 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002 | 1/1 | 2829 | 83 | 17 | 15 | 30 | 7 | 12 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0004 | 0/0 | 2829 | 4 | 4 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0008 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0003c0003 | 0/0 | 2829 | 47 | 19 | 3 | 19 | 2 | 4 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0004c0005 | 0/0 | 2829 | 2 | 0 | 0 | 2 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0004c0013 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0005c0006 | 0/0 | 2829 | 2 | 0 | 2 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0006c0014 | 0/0 | 2829 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0007c0011 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0008c0012 | 0/0 | 2829 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6264 | 77 | 4 | 23 | 32 | 6 | 12 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0002 | 0/0 | 6264 | 7 | 3 | 3 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0004 | 0/0 | 6265 | 19 | 4 | 1 | 14 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0005 | 0/0 | 6265 | 5 | 3 | 1 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0006 | 0/0 | 6264 | 5 | 5 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0007 | 0/0 | 6264 | 2 | 1 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0009 | 0/0 | 6265 | 3 | 0 | 0 | 3 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0011 | 0/0 | 6265 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0016 | 0/0 | 6264 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0017 | 0/0 | 6264 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0024 | 0/0 | 6264 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0025 | 0/0 | 6265 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0001t0026 | 0/0 | 6264 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0007t0001 | 0/0 | 6264 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0009t0022 | 0/0 | 6264 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0001c0010t0005 | 0/0 | 6265 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002t0001 | 0/1 | 6264 | 13 | 5 | 3 | 1 | 2 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002t0002 | 1/0 | 6264 | 55 | 5 | 12 | 23 | 4 | 10 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002t0004 | 0/0 | 6265 | 2 | 1 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002t0005 | 0/0 | 6265 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002t0007 | 0/0 | 6264 | 2 | 1 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002t0008 | 0/0 | 6264 | 4 | 0 | 0 | 4 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002t0010 | 0/0 | 6264 | 2 | 2 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002t0011 | 0/0 | 6265 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002t0012 | 0/0 | 6264 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002t0014 | 0/0 | 6264 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0002t0023 | 0/0 | 6264 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0004t0002 | 0/0 | 6264 | 4 | 4 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0002c0008t0015 | 0/0 | 6264 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0003c0003t0003 | 0/0 | 6253 | 43 | 17 | 3 | 17 | 2 | 4 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0003c0003t0018 | 0/0 | 6253 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0003c0003t0019 | 0/0 | 6253 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0003c0003t0020 | 0/0 | 6253 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0003c0003t0021 | 0/0 | 6253 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0004c0005t0003 | 0/0 | 6253 | 2 | 0 | 0 | 2 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0004c0013t0013 | 0/0 | 6253 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0005c0006t0002 | 0/0 | 6264 | 2 | 0 | 2 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0006c0014t0003 | 0/0 | 6253 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0007c0011t0003 | 0/0 | 6253 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| a0008c0012t0003 | 0/0 | 6253 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | copy fasta | chr6 | 125785960 | 125937034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0009g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0016g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0017g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0024g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0025g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0026g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0007t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0009t0022g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0010t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0007g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0010g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0012g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0014g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0023g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0004t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0004t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0004t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0004t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0008t0015g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0018g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0019g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0020g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0021g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0004c0005t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0004c0005t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0004c0013t0013g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0005c0006t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0006c0014t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0007c0011t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0008c0012t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0179 | EUR | GBR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0055 | EUR | GBR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | FIN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00280 | hp2 | a0003 | c0003 | t0003 | g0050 | EUR | FIN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0229 | EUR | FIN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0233 | EAS | CHS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | CHS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0063 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0215 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00738 | hp1 | a0005 | c0006 | t0002 | g0001 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01071 | hp2 | a0005 | c0006 | t0002 | g0001 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01106 | hp2 | a0003 | c0003 | t0003 | g0248 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0107 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01175 | hp1 | a0003 | c0003 | t0003 | g0138 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01192 | hp2 | a0003 | c0003 | t0003 | g0134 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0077 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0071 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0076 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0145 | EUR | IBS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01515 | hp2 | a0002 | c0002 | t0007 | g0153 | EUR | IBS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0144 | EUR | IBS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0152 | EUR | IBS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01884 | hp1 | a0003 | c0003 | t0003 | g0147 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01891 | hp2 | a0001 | c0001 | t0026 | g0261 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0088 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02027 | hp2 | a0003 | c0003 | t0003 | g0119 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02080 | hp1 | a0003 | c0003 | t0003 | g0116 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02135 | hp2 | a0003 | c0003 | t0019 | g0211 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02257 | hp1 | a0007 | c0011 | t0003 | g0129 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0268 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0234 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02523 | hp1 | a0008 | c0012 | t0003 | g0113 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02523 | hp2 | a0002 | c0002 | t0023 | g0074 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02572 | hp1 | a0002 | c0002 | t0010 | g0133 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0090 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02615 | hp1 | a0003 | c0003 | t0003 | g0034 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02615 | hp2 | a0002 | c0004 | t0002 | g0151 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02630 | hp1 | a0002 | c0004 | t0002 | g0027 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02630 | hp2 | a0003 | c0003 | t0003 | g0124 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02647 | hp1 | a0003 | c0003 | t0003 | g0130 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0053 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02717 | hp1 | a0003 | c0003 | t0003 | g0139 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02717 | hp2 | a0002 | c0002 | t0005 | g0253 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0048 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02723 | hp2 | a0003 | c0003 | t0020 | g0122 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02735 | hp2 | a0001 | c0007 | t0001 | g0046 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02809 | hp1 | a0003 | c0003 | t0003 | g0140 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02818 | hp1 | a0002 | c0002 | t0010 | g0141 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02818 | hp2 | a0003 | c0003 | t0003 | g0004 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02896 | hp2 | a0003 | c0003 | t0003 | g0029 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02922 | hp1 | a0002 | c0008 | t0015 | g0262 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02965 | hp1 | a0002 | c0004 | t0002 | g0160 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02965 | hp2 | a0001 | c0010 | t0005 | g0161 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02976 | hp1 | a0003 | c0003 | t0003 | g0033 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02976 | hp2 | a0001 | c0009 | t0022 | g0263 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03017 | hp1 | a0003 | c0003 | t0003 | g0110 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03041 | hp1 | a0002 | c0002 | t0007 | g0003 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03041 | hp2 | a0003 | c0003 | t0003 | g0028 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03098 | hp1 | a0003 | c0003 | t0003 | g0149 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0127 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03195 | hp1 | a0004 | c0013 | t0013 | g0264 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03195 | hp2 | a0003 | c0003 | t0003 | g0148 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0259 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03239 | hp1 | a0002 | c0002 | t0012 | g0143 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03239 | hp2 | a0003 | c0003 | t0003 | g0105 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0260 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0057 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03490 | hp2 | a0003 | c0003 | t0003 | g0206 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0058 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03516 | hp1 | a0002 | c0002 | t0004 | g0137 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0082 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03669 | hp2 | a0006 | c0014 | t0003 | g0249 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0061 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0062 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0084 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0060 | SAS | STU | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0223 | SAS | STU | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG04228 | hp2 | a0003 | c0003 | t0003 | g0250 | SAS | STU | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0036 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18522 | hp2 | a0002 | c0004 | t0002 | g0030 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0157 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18939 | hp2 | a0003 | c0003 | t0003 | g0115 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18940 | hp2 | a0002 | c0002 | t0008 | g0056 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18943 | hp1 | a0001 | c0001 | t0025 | g0009 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18943 | hp2 | a0001 | c0001 | t0024 | g0150 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18946 | hp1 | a0003 | c0003 | t0003 | g0209 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18946 | hp2 | a0001 | c0001 | t0007 | g0080 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18949 | hp1 | a0001 | c0001 | t0017 | g0247 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18950 | hp1 | a0003 | c0003 | t0003 | g0111 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18951 | hp2 | a0003 | c0003 | t0003 | g0218 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18960 | hp1 | a0003 | c0003 | t0021 | g0208 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18960 | hp2 | a0001 | c0001 | t0009 | g0186 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18968 | hp2 | a0002 | c0002 | t0008 | g0066 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18972 | hp2 | a0003 | c0003 | t0003 | g0078 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18973 | hp1 | a0003 | c0003 | t0003 | g0118 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18978 | hp1 | a0004 | c0005 | t0003 | g0026 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0266 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18995 | hp1 | a0003 | c0003 | t0003 | g0125 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19000 | hp2 | a0003 | c0003 | t0003 | g0257 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19003 | hp1 | a0002 | c0002 | t0008 | g0052 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19003 | hp2 | a0001 | c0001 | t0009 | g0173 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19010 | hp1 | a0003 | c0003 | t0003 | g0117 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19010 | hp2 | a0002 | c0002 | t0008 | g0089 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19011 | hp2 | a0003 | c0003 | t0003 | g0207 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19055 | hp2 | a0003 | c0003 | t0003 | g0227 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19060 | hp2 | a0003 | c0003 | t0003 | g0112 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19062 | hp2 | a0002 | c0002 | t0004 | g0205 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19070 | hp2 | a0004 | c0005 | t0003 | g0020 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19077 | hp1 | a0003 | c0003 | t0003 | g0123 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19078 | hp1 | a0001 | c0001 | t0009 | g0188 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19078 | hp2 | a0003 | c0003 | t0003 | g0126 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19084 | hp2 | a0003 | c0003 | t0003 | g0252 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19240 | hp1 | a0003 | c0003 | t0003 | g0106 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0070 | AFR | ASW | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20129 | hp2 | a0003 | c0003 | t0018 | g0128 | AFR | ASW | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | TSI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20805 | hp1 | a0003 | c0003 | t0003 | g0120 | EUR | TSI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | TSI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0235 | SAS | GIH | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | GIH | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0049 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02109 | hp2 | a0003 | c0003 | t0003 | g0114 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02486 | hp1 | a0003 | c0003 | t0003 | g0018 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0232 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20300 | hp1 | a0002 | c0002 | t0014 | g0014 | AFR | USA | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20300 | hp2 | a0002 | c0002 | t0011 | g0047 | AFR | USA | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA21309 | hp1 | a0003 | c0003 | t0003 | g0142 | AFR | LWK | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0254 | AFR | LWK | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0094 | REF | REF | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0051 | REF | REF | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125815403
|
C | T | 1 | a0006 | 1 | HG03669.hp2 | stop_gained&splice_region_variant | HIGH | c.49C>T | p.Arg17* | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/16 | 221/6264 | 49/2829 | 17/942 | chr6 | 125815403 | ||
| chr6:125882430
|
C | T | 1 | a0008 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.578C>T | p.Ala193Val | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/16 | 750/6264 | 578/2829 | 193/942 | chr6 | 125882430 | ||
| chr6:125889039
|
A | C | 1 | a0007 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.985A>C | p.Asn329His | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/16 | 1157/6264 | 985/2829 | 329/942 | chr6 | 125889039 | ||
| chr6:125889249
|
T | G | 2 | a0001a0004 | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
missense_variant | MODERATE | c.1195T>G | p.Ser399Ala | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/16 | 1367/6264 | 1195/2829 | 399/942 | chr6 | 125889249 | ||
| chr6:125889651
|
G | A | 1 | a0005 | 2 | HG00738.hp1 HG01071.hp2 |
missense_variant | MODERATE | c.1597G>A | p.Gly533Arg | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/16 | 1769/6264 | 1597/2829 | 533/942 | chr6 | 125889651 | ||
| chr6:125928768
|
T | G | 5 | a0003a0004a0006others(2): Show | 53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
missense_variant | MODERATE | c.2826T>G | p.Asp942Glu | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 2998/6264 | 2826/2829 | 942/942 | chr6 | 125928768 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125855023
|
G | C | 1 | a0001c0007 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.54G>C | p.Leu18Leu | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/16 | 226/6264 | 54/2829 | 18/942 | chr6 | 125855023 | ||
| chr6:125881137
|
A | G | 1 | a0004c0013 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.507A>G | p.Leu169Leu | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/16 | 679/6264 | 507/2829 | 169/942 | chr6 | 125881137 | ||
| chr6:125885332
|
T | C | 1 | a0002c0008 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.873T>C | p.Asp291Asp | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/16 | 1045/6264 | 873/2829 | 291/942 | chr6 | 125885332 | ||
| chr6:125889140
|
C | T | 1 | a0001c0010 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.1086C>T | p.Pro362Pro | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/16 | 1258/6264 | 1086/2829 | 362/942 | chr6 | 125889140 | ||
| chr6:125920999
|
C | T | 1 | a0002c0004 | 4 | HG02615.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.2301C>T | p.Asp767Asp | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/16 | 2473/6264 | 2301/2829 | 767/942 | chr6 | 125920999 | ||
| chr6:125922720
|
A | G | 1 | a0001c0009 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.2409A>G | p.Pro803Pro | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/16 | 2581/6264 | 2409/2829 | 803/942 | chr6 | 125922720 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125790994
|
G | A | 1 | a0002c0002t0012 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-138G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/16 | 24361 | chr6 | 125790994 | |||||
| chr6:125815296
|
C | T | 4 | a0001c0001t0006a0001c0001t0011a0001c0001t0026others(1): Show | 8 | HG01891.hp2 HG02257.hp2 HG02723.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-59C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/16 | chr6 | 125815296 | ||||||
| chr6:125928810
|
G | A | 1 | a0004c0013t0013 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 39 | chr6 | 125928810 | |||||
| chr6:125929249
|
T | A | 2 | a0002c0002t0014a0002c0008t0015 | 2 | HG02922.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*478T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 478 | chr6 | 125929249 | |||||
| chr6:125929249
|
T | TA | 1 | a0001c0001t0009 | 3 | NA18960.hp2 NA19003.hp2 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*478_*479insA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 479 | chr6 | 125929249 | |||||
| chr6:125929250
|
T | A | 9 | a0001c0001t0001a0001c0001t0009a0001c0001t0016others(6): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*479T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 479 | chr6 | 125929250 | |||||
| chr6:125929250
|
T | TA | 13 | a0001c0001t0005a0001c0010t0005a0002c0002t0005others(10): Show | 60 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*479_*480insA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 480 | chr6 | 125929250 | |||||
| chr6:125929251
|
T | A | 27 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(24): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*480T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 480 | chr6 | 125929251 | |||||
| chr6:125929252
|
T | A | 28 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(25): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*481T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 481 | chr6 | 125929252 | |||||
| chr6:125929253
|
A | T | 1 | a0002c0002t0008 | 4 | NA18940.hp2 NA18968.hp2 NA19003.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*482A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 482 | chr6 | 125929253 | |||||
| chr6:125929285
|
A | T | 1 | a0001c0001t0017 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*514A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 514 | chr6 | 125929285 | |||||
| chr6:125929301
|
C | T | 1 | a0001c0001t0016 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*530C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 530 | chr6 | 125929301 | |||||
| chr6:125929306
|
G | GT | 5 | a0001c0001t0004a0001c0001t0011a0001c0001t0025others(2): Show | 24 | HG00597.hp2 HG00639.hp2 HG02055.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*543dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 544 | INFO_REALIGN_3_PRIME | chr6 | 125929306 | ||||
| chr6:125929435
|
G | A | 1 | a0003c0003t0018 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*664G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 664 | chr6 | 125929435 | |||||
| chr6:125929436
|
ATAGGTCT others(5): Show |
A | 10 | a0003c0003t0003a0003c0003t0018a0003c0003t0019others(7): Show | 53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*666_*677delTAGGTC others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 666 | chr6 | 125929436 | |||||
| chr6:125929581
|
C | G | 1 | a0003c0003t0021 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*810C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 810 | chr6 | 125929581 | |||||
| chr6:125929894
|
T | A | 1 | a0001c0001t0025 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1123T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 1123 | chr6 | 125929894 | |||||
| chr6:125930124
|
G | A | 1 | a0001c0009t0022 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1353G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 1353 | chr6 | 125930124 | |||||
| chr6:125930267
|
G | A | 1 | a0003c0003t0019 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1496G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 1496 | chr6 | 125930267 | |||||
| chr6:125931308
|
T | A | 1 | a0002c0002t0010 | 2 | HG02572.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2537T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 2537 | chr6 | 125931308 | |||||
| chr6:125931487
|
T | C | 27 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(24): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*2716T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 2716 | chr6 | 125931487 | |||||
| chr6:125931531
|
C | A | 9 | a0001c0001t0024a0003c0003t0003a0003c0003t0018others(6): Show | 52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2760C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 2760 | chr6 | 125931531 | |||||
| chr6:125931739
|
G | C | 1 | a0002c0002t0014 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2968G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 2968 | chr6 | 125931739 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125791120
|
C | T | 1 | a0001c0001t0006g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+53C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791120 | ||||||
| chr6:125791178
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-65+111C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791178 | ||||||
| chr6:125791238
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0005g0266 | 2 | NA18961.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-65+171C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791238 | ||||||
| chr6:125791303
|
T | C | 44 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(41): Show | 44 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-65+236T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791303 | ||||||
| chr6:125791309
|
G | A | 3 | a0001c0001t0006g0048a0001c0001t0007g0049a0002c0002t0011g0047 | 3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-65+242G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791309 | ||||||
| chr6:125791810
|
C | T | 1 | a0001c0001t0006g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+743C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791810 | ||||||
| chr6:125791974
|
G | A | 2 | a0001c0001t0006g0048a0002c0002t0011g0047 | 2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-65+907G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791974 | ||||||
| chr6:125792009
|
G | GTA | 44 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(41): Show | 44 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-65+945_-65+946dup others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125792009 | |||||
| chr6:125792078
|
A | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(9): Show | 12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-65+1011A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792078 | ||||||
| chr6:125792205
|
G | C | 1 | a0001c0001t0007g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-65+1138G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792205 | ||||||
| chr6:125792245
|
A | C | 6 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0026g0261others(3): Show | 6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+1178A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792245 | ||||||
| chr6:125792309
|
A | G | 1 | a0001c0001t0006g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+1242A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792309 | ||||||
| chr6:125792327
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-65+1260A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792327 | ||||||
| chr6:125792446
|
A | G | 32 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(29): Show | 32 | HG00639.hp2 HG00741.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-65+1379A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792446 | ||||||
| chr6:125792578
|
A | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(41): Show | 44 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-65+1511A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792578 | ||||||
| chr6:125792676
|
G | A | 54 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(51): Show | 54 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.-65+1609G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792676 | ||||||
| chr6:125792725
|
A | T | 2 | a0002c0002t0001g0256a0003c0003t0003g0257 | 2 | NA18985.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-65+1658A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792725 | ||||||
| chr6:125792778
|
GA | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0041others(41): Show | 44 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-65+1722delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125792778 | |||||
| chr6:125793106
|
A | G | 20 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(17): Show | 20 | HG00741.hp2 HG02055.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-65+2039A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125793106 | ||||||
| chr6:125793151
|
GA | G | 6 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0026g0261others(3): Show | 6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+2091delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125793151 | |||||
| chr6:125793507
|
C | T | 2 | a0002c0002t0002g0254a0002c0002t0005g0253 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-65+2440C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125793507 | ||||||
| chr6:125793527
|
T | A | 29 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(26): Show | 29 | HG00639.hp2 HG00741.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-65+2460T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125793527 | ||||||
| chr6:125793575
|
C | G | 1 | a0003c0003t0003g0252 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-65+2508C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125793575 | ||||||
| chr6:125794006
|
A | G | 1 | a0001c0001t0007g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-65+2939A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794006 | ||||||
| chr6:125794072
|
C | A | 4 | a0002c0002t0002g0015a0002c0002t0002g0032a0003c0003t0003g0033others(1): Show | 4 | HG02615.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-65+3005C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794072 | ||||||
| chr6:125794098
|
C | G | 32 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(29): Show | 32 | HG00639.hp2 HG00741.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-65+3031C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794098 | ||||||
| chr6:125794237
|
A | C | 101 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0165others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.-65+3170A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794237 | ||||||
| chr6:125794675
|
T | C | 101 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0165others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.-65+3608T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794675 | ||||||
| chr6:125794949
|
A | G | 1 | a0001c0001t0004g0031 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-65+3882A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794949 | ||||||
| chr6:125794984
|
C | CAT | 156 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-65+3918_-65+3919i others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125794984 | |||||
| chr6:125795131
|
G | T | 32 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(29): Show | 32 | HG00639.hp2 HG00741.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-65+4064G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795131 | ||||||
| chr6:125795267
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0258 | 2 | HG01175.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-65+4200G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795267 | ||||||
| chr6:125795285
|
G | C | 1 | a0001c0001t0006g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+4218G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795285 | ||||||
| chr6:125795422
|
TC | T | 4 | a0001c0001t0004g0154a0001c0001t0004g0155a0002c0002t0002g0002others(1): Show | 5 | NA18949.hp2 NA18957.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-65+4359delC | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125795422 | |||||
| chr6:125795608
|
G | C | 44 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(41): Show | 44 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-65+4541G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795608 | ||||||
| chr6:125795718
|
G | A | 1 | a0001c0001t0011g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-65+4651G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795718 | ||||||
| chr6:125795722
|
G | A | 1 | a0003c0003t0003g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-65+4655G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795722 | ||||||
| chr6:125795726
|
C | T | 1 | a0002c0002t0002g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-65+4659C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795726 | ||||||
| chr6:125795742
|
G | C | 1 | a0001c0001t0002g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-65+4675G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795742 | ||||||
| chr6:125795807
|
A | G | 98 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0165others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.-65+4740A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795807 | ||||||
| chr6:125795819
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(29): Show | 32 | HG00639.hp2 HG00741.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-65+4752C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795819 | ||||||
| chr6:125796028
|
G | C | 1 | a0001c0001t0006g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-65+4961G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796028 | ||||||
| chr6:125796038
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA19000.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-65+4971T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796038 | ||||||
| chr6:125796081
|
C | T | 1 | a0002c0004t0002g0151 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-65+5014C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796081 | ||||||
| chr6:125796095
|
T | C | 13 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 13 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-65+5028T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796095 | ||||||
| chr6:125796097
|
C | G | 13 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 13 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-65+5030C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796097 | ||||||
| chr6:125796106
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-65+5039C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796106 | ||||||
| chr6:125796146
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-65+5079C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796146 | ||||||
| chr6:125796187
|
A | G | 1 | a0001c0001t0006g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+5120A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796187 | ||||||
| chr6:125796230
|
G | A | 20 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(17): Show | 20 | HG00741.hp2 HG02055.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-65+5163G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796230 | ||||||
| chr6:125796337
|
C | T | 13 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 13 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-65+5270C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796337 | ||||||
| chr6:125796362
|
A | T | 13 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 13 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-65+5295A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796362 | ||||||
| chr6:125796364
|
T | A | 3 | a0001c0001t0002g0038a0001c0001t0004g0037a0001c0001t0004g0039 | 3 | HG01243.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-65+5297T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796364 | ||||||
| chr6:125796375
|
CG | C | 267 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(264): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-65+5309delG | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796375 | ||||||
| chr6:125796457
|
C | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-65+5390C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796457 | ||||||
| chr6:125796608
|
C | A | 2 | a0001c0010t0005g0161a0002c0004t0002g0160 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-65+5541C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796608 | ||||||
| chr6:125796633
|
C | A | 7 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0007g0049others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-65+5566C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796633 | ||||||
| chr6:125796656
|
A | AT | 12 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0039others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-65+5605dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125796656 | |||||
| chr6:125796656
|
A | ATT | 10 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(7): Show | 10 | HG02630.hp1 HG02809.hp2 NA18978.hp1 others(7): Show |
intron_variant | MODIFIER | c.-65+5604_-65+5605d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125796656 | |||||
| chr6:125796656
|
A | G | 1 | a0001c0001t0024g0150 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-65+5589A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796656 | ||||||
| chr6:125796656
|
AT | A | 14 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(11): Show | 14 | HG00639.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-65+5605delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125796656 | |||||
| chr6:125796694
|
G | A | 214 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(211): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.-65+5627G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796694 | ||||||
| chr6:125796739
|
C | T | 1 | a0001c0001t0006g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+5672C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796739 | ||||||
| chr6:125796841
|
G | C | 14 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-65+5774G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796841 | ||||||
| chr6:125797066
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-65+5999G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797066 | ||||||
| chr6:125797131
|
C | G | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | NA18949.hp1 NA18957.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.-65+6064C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797131 | ||||||
| chr6:125797265
|
T | C | 1 | a0003c0003t0003g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-65+6198T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797265 | ||||||
| chr6:125797272
|
T | C | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+6205T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797272 | ||||||
| chr6:125797395
|
A | T | 6 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0026g0261others(3): Show | 6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+6328A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797395 | ||||||
| chr6:125797717
|
A | G | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+6650A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797717 | ||||||
| chr6:125797748
|
G | A | 41 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(38): Show | 41 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.-65+6681G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797748 | ||||||
| chr6:125797795
|
A | T | 6 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0026g0261others(3): Show | 6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+6728A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797795 | ||||||
| chr6:125797938
|
A | G | 6 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(3): Show | 6 | HG02027.hp1 HG02080.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+6871A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797938 | ||||||
| chr6:125798393
|
T | C | 1 | a0003c0003t0003g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-65+7326T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125798393 | ||||||
| chr6:125798615
|
T | G | 9 | a0001c0001t0006g0048a0001c0001t0006g0259a0001c0001t0006g0260others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-65+7548T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125798615 | ||||||
| chr6:125798676
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-65+7609G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125798676 | ||||||
| chr6:125798786
|
T | C | 2 | a0001c0001t0006g0048a0002c0002t0011g0047 | 2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-65+7719T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125798786 | ||||||
| chr6:125798922
|
C | T | 2 | a0001c0001t0001g0239a0001c0001t0005g0238 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-65+7855C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125798922 | ||||||
| chr6:125799089
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-65+8022C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799089 | ||||||
| chr6:125799260
|
C | CT | 9 | a0001c0001t0006g0048a0001c0001t0006g0259a0001c0001t0006g0260others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-65+8195dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125799260 | |||||
| chr6:125799282
|
C | T | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+8215C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799282 | ||||||
| chr6:125799366
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-65+8299G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799366 | ||||||
| chr6:125799443
|
CT | C | 172 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(169): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.-65+8392delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125799443 | |||||
| chr6:125799479
|
G | A | 2 | a0001c0001t0004g0037a0001c0001t0004g0039 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-65+8412G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799479 | ||||||
| chr6:125799567
|
A | G | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+8500A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799567 | ||||||
| chr6:125799568
|
T | G | 1 | a0001c0010t0005g0161 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-65+8501T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799568 | ||||||
| chr6:125799643
|
G | T | 1 | a0001c0007t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-65+8576G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799643 | ||||||
| chr6:125799684
|
C | T | 67 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0083others(64): Show | 69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.-65+8617C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799684 | ||||||
| chr6:125799844
|
G | A | 158 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(155): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.-65+8777G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799844 | ||||||
| chr6:125799882
|
A | G | 1 | a0002c0002t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-65+8815A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799882 | ||||||
| chr6:125800201
|
A | G | 1 | a0001c0001t0011g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-65+9134A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800201 | ||||||
| chr6:125800228
|
C | T | 5 | a0001c0001t0004g0017a0001c0001t0004g0019a0002c0004t0002g0030others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-65+9161C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800228 | ||||||
| chr6:125800384
|
G | A | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+9317G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800384 | ||||||
| chr6:125800441
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-65+9374T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800441 | ||||||
| chr6:125800458
|
T | C | 1 | a0002c0002t0002g0108 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-65+9391T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800458 | ||||||
| chr6:125800516
|
C | T | 1 | a0002c0002t0002g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-65+9449C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800516 | ||||||
| chr6:125800598
|
G | C | 1 | a0002c0002t0002g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-65+9531G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800598 | ||||||
| chr6:125800704
|
A | G | 1 | a0001c0001t0016g0232 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-65+9637A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800704 | ||||||
| chr6:125800730
|
T | G | 201 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.-65+9663T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800730 | ||||||
| chr6:125800843
|
A | G | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+9776A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800843 | ||||||
| chr6:125800886
|
G | A | 1 | a0001c0001t0016g0232 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-65+9819G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800886 | ||||||
| chr6:125801082
|
C | T | 1 | a0001c0001t0006g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+10015C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801082 | ||||||
| chr6:125801083
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-65+10016G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801083 | ||||||
| chr6:125801134
|
C | T | 88 | a0001c0001t0001g0054a0001c0001t0001g0158a0001c0001t0001g0164others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.-65+10067C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801134 | ||||||
| chr6:125801418
|
A | G | 13 | a0002c0002t0002g0108a0002c0002t0002g0144a0002c0002t0002g0145others(10): Show | 13 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.-65+10351A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801418 | ||||||
| chr6:125801471
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-65+10404G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801471 | ||||||
| chr6:125801731
|
T | G | 2 | a0003c0003t0003g0147a0003c0003t0003g0148 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-65+10664T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801731 | ||||||
| chr6:125801819
|
A | C | 1 | a0001c0001t0006g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-65+10752A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801819 | ||||||
| chr6:125801887
|
C | T | 9 | a0002c0002t0002g0096a0002c0002t0002g0097a0002c0002t0002g0098others(6): Show | 9 | NA18944.hp1 NA18978.hp2 NA18982.hp2 others(6): Show |
intron_variant | MODIFIER | c.-65+10820C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801887 | ||||||
| chr6:125802157
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-65+11090A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802157 | ||||||
| chr6:125802187
|
A | G | 6 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0026g0261others(3): Show | 6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+11120A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802187 | ||||||
| chr6:125802270
|
G | A | 1 | a0001c0001t0006g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-65+11203G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802270 | ||||||
| chr6:125802338
|
C | G | 1 | a0002c0002t0001g0095 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-65+11271C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802338 | ||||||
| chr6:125802658
|
T | G | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-65+11591T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802658 | ||||||
| chr6:125802742
|
A | C | 1 | a0002c0002t0001g0094 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-65+11675A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802742 | ||||||
| chr6:125802875
|
T | A | 1 | a0001c0001t0011g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-65+11808T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802875 | ||||||
| chr6:125802890
|
A | G | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+11823A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802890 | ||||||
| chr6:125803012
|
A | G | 1 | a0001c0001t0006g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+11945A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125803012 | ||||||
| chr6:125803024
|
G | C | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+11957G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125803024 | ||||||
| chr6:125803359
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-64-11932T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125803359 | ||||||
| chr6:125803648
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-64-11643A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125803648 | ||||||
| chr6:125803826
|
C | T | 24 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(21): Show | 24 | HG00323.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.-64-11465C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125803826 | ||||||
| chr6:125803944
|
AT | A | 24 | a0001c0001t0004g0017a0001c0001t0004g0021a0001c0001t0004g0022others(21): Show | 24 | HG01884.hp1 HG02486.hp1 HG02615.hp1 others(21): Show |
intron_variant | MODIFIER | c.-64-11335delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125803944 | |||||
| chr6:125804075
|
G | T | 1 | a0002c0002t0001g0229 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-64-11216G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804075 | ||||||
| chr6:125804388
|
A | G | 9 | a0001c0001t0006g0048a0001c0001t0006g0259a0001c0001t0006g0260others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-64-10903A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804388 | ||||||
| chr6:125804443
|
A | T | 1 | a0002c0002t0004g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-64-10848A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804443 | ||||||
| chr6:125804547
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-64-10744A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804547 | ||||||
| chr6:125804672
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-64-10619T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804672 | ||||||
| chr6:125804880
|
G | A | 1 | a0001c0001t0006g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-64-10411G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804880 | ||||||
| chr6:125805087
|
C | CT | 100 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0092others(97): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.-64-10176dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | |||||
| chr6:125805087
|
C | CTT | 19 | a0001c0001t0001g0158a0001c0001t0001g0167a0001c0001t0001g0171others(16): Show | 19 | HG00544.hp2 HG01192.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-64-10177_-64-1017 others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | |||||
| chr6:125805087
|
C | CTTT | 11 | a0001c0001t0001g0005a0001c0001t0004g0008a0001c0001t0004g0010others(8): Show | 11 | HG00639.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-64-10178_-64-1017 others(7): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | |||||
| chr6:125805087
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0002g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-64-10194_-64-1017 others(23): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | |||||
| chr6:125805087
|
CT | C | 5 | a0001c0001t0001g0040a0001c0007t0001g0046a0002c0002t0007g0003others(2): Show | 5 | HG00323.hp2 HG02735.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-10176delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | |||||
| chr6:125805087
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0006g0048a0002c0002t0011g0047 | 2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-64-10185_-64-1017 others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | |||||
| chr6:125805470
|
G | A | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-9821G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125805470 | ||||||
| chr6:125805537
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-64-9754G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125805537 | ||||||
| chr6:125805606
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-64-9685A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125805606 | ||||||
| chr6:125805837
|
A | G | 1 | a0002c0002t0002g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-64-9454A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125805837 | ||||||
| chr6:125805866
|
T | C | 1 | a0001c0001t0001g0265 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-64-9425T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125805866 | ||||||
| chr6:125806036
|
G | A | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-9255G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806036 | ||||||
| chr6:125806055
|
T | C | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-9236T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806055 | ||||||
| chr6:125806109
|
G | C | 1 | a0002c0002t0002g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-64-9182G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806109 | ||||||
| chr6:125806138
|
C | G | 2 | a0002c0002t0007g0003a0003c0003t0003g0004 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-64-9153C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806138 | ||||||
| chr6:125806147
|
C | T | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-9144C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806147 | ||||||
| chr6:125806270
|
G | C | 1 | a0003c0003t0003g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-64-9021G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806270 | ||||||
| chr6:125806592
|
C | T | 1 | a0001c0001t0011g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-8699C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806592 | ||||||
| chr6:125806975
|
G | A | 1 | a0002c0002t0002g0002 | 2 | NA19079.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-64-8316G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806975 | ||||||
| chr6:125807106
|
C | G | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-8185C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807106 | ||||||
| chr6:125807358
|
T | C | 1 | a0002c0002t0002g0108 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-64-7933T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807358 | ||||||
| chr6:125807378
|
G | A | 1 | a0002c0002t0002g0255 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-64-7913G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807378 | ||||||
| chr6:125807464
|
T | G | 1 | a0002c0002t0002g0255 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-64-7827T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807464 | ||||||
| chr6:125807576
|
A | C | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-7715A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807576 | ||||||
| chr6:125807619
|
T | G | 3 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0026g0261 | 3 | HG01891.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-64-7672T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807619 | ||||||
| chr6:125807670
|
A | G | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0002c0002t0010g0133 | 3 | HG01891.hp1 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-64-7621A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807670 | ||||||
| chr6:125807727
|
T | A | 7 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0010others(4): Show | 7 | HG00639.hp2 NA18940.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.-64-7564T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807727 | ||||||
| chr6:125807951
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-64-7340C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807951 | ||||||
| chr6:125807983
|
A | G | 1 | a0001c0001t0002g0228 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-64-7308A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807983 | ||||||
| chr6:125808207
|
A | T | 3 | a0001c0001t0001g0083a0002c0002t0002g0053a0002c0002t0002g0082 | 3 | HG02698.hp1 HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-64-7084A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808207 | ||||||
| chr6:125808389
|
C | G | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-64-6902C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808389 | ||||||
| chr6:125808577
|
T | G | 2 | a0002c0002t0002g0057a0002c0002t0002g0058 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-64-6714T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808577 | ||||||
| chr6:125808779
|
G | A | 3 | a0002c0002t0002g0057a0002c0002t0002g0058a0002c0002t0002g0084 | 3 | HG03490.hp1 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-64-6512G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808779 | ||||||
| chr6:125808825
|
C | T | 1 | a0003c0003t0003g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-64-6466C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808825 | ||||||
| chr6:125808968
|
G | T | 1 | a0001c0001t0011g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-6323G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808968 | ||||||
| chr6:125809022
|
G | A | 10 | a0001c0001t0006g0048a0001c0001t0006g0259a0001c0001t0006g0260others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-64-6269G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809022 | ||||||
| chr6:125809159
|
G | C | 1 | a0001c0001t0011g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-6132G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809159 | ||||||
| chr6:125809171
|
G | C | 1 | a0001c0001t0011g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-6120G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809171 | ||||||
| chr6:125809309
|
C | T | 1 | a0002c0002t0010g0133 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-64-5982C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809309 | ||||||
| chr6:125809502
|
A | G | 5 | a0001c0001t0004g0017a0001c0001t0004g0019a0002c0004t0002g0030others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-5789A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809502 | ||||||
| chr6:125809506
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-64-5785G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809506 | ||||||
| chr6:125809671
|
A | G | 1 | a0001c0001t0016g0232 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-64-5620A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809671 | ||||||
| chr6:125810009
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-64-5282C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810009 | ||||||
| chr6:125810217
|
G | A | 10 | a0001c0001t0006g0048a0001c0001t0006g0259a0001c0001t0006g0260others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-64-5074G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810217 | ||||||
| chr6:125810466
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-64-4825C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810466 | ||||||
| chr6:125810504
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-64-4787G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810504 | ||||||
| chr6:125810561
|
A | G | 3 | a0002c0002t0001g0180a0002c0002t0002g0179a0002c0002t0002g0219 | 3 | HG00099.hp1 HG01109.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-64-4730A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810561 | ||||||
| chr6:125810636
|
T | C | 2 | a0002c0002t0002g0096a0002c0002t0002g0097 | 2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-64-4655T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810636 | ||||||
| chr6:125810792
|
G | A | 35 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(32): Show | 35 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.-64-4499G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810792 | ||||||
| chr6:125811071
|
A | C | 1 | a0004c0005t0003g0026 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-64-4220A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811071 | ||||||
| chr6:125811193
|
C | T | 2 | a0001c0001t0006g0259a0001c0001t0006g0260 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-64-4098C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811193 | ||||||
| chr6:125811323
|
G | A | 10 | a0001c0001t0006g0048a0001c0001t0006g0259a0001c0001t0006g0260others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-64-3968G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811323 | ||||||
| chr6:125811538
|
G | A | 25 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(22): Show | 25 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(22): Show |
intron_variant | MODIFIER | c.-64-3753G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811538 | ||||||
| chr6:125811672
|
G | C | 25 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(22): Show | 25 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(22): Show |
intron_variant | MODIFIER | c.-64-3619G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811672 | ||||||
| chr6:125811859
|
G | A | 1 | a0003c0003t0020g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-64-3432G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811859 | ||||||
| chr6:125811877
|
T | C | 1 | a0002c0002t0004g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-64-3414T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811877 | ||||||
| chr6:125811895
|
G | A | 25 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(22): Show | 25 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(22): Show |
intron_variant | MODIFIER | c.-64-3396G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811895 | ||||||
| chr6:125812243
|
A | G | 194 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.-64-3048A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812243 | ||||||
| chr6:125812335
|
C | G | 1 | a0002c0002t0002g0108 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-64-2956C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812335 | ||||||
| chr6:125812493
|
T | C | 2 | a0001c0009t0022g0263a0002c0008t0015g0262 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-64-2798T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812493 | ||||||
| chr6:125812667
|
C | T | 1 | a0001c0001t0011g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-2624C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812667 | ||||||
| chr6:125812677
|
A | G | 10 | a0001c0001t0006g0048a0001c0001t0006g0259a0001c0001t0006g0260others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-64-2614A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812677 | ||||||
| chr6:125812734
|
T | C | 24 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(21): Show | 24 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.-64-2557T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812734 | ||||||
| chr6:125812816
|
C | T | 1 | a0003c0003t0003g0130 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-64-2475C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812816 | ||||||
| chr6:125812918
|
A | G | 1 | a0003c0003t0003g0218 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-64-2373A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812918 | ||||||
| chr6:125812941
|
C | G | 1 | a0002c0002t0001g0256 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-64-2350C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812941 | ||||||
| chr6:125813204
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-64-2087C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813204 | ||||||
| chr6:125813228
|
A | G | 6 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(3): Show | 6 | NA18982.hp1 NA18985.hp2 NA19068.hp1 others(3): Show |
intron_variant | MODIFIER | c.-64-2063A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813228 | ||||||
| chr6:125813449
|
A | AT | 13 | a0001c0001t0002g0217a0001c0001t0006g0048a0001c0001t0006g0259others(10): Show | 13 | HG01891.hp2 HG01981.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-64-1822dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125813449 | |||||
| chr6:125813449
|
AT | A | 8 | a0001c0001t0001g0236a0001c0001t0004g0017a0001c0001t0004g0019others(5): Show | 8 | HG01517.hp2 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-64-1822delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125813449 | |||||
| chr6:125813458
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-64-1833T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813458 | ||||||
| chr6:125813669
|
C | T | 1 | a0001c0001t0011g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-1622C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813669 | ||||||
| chr6:125813755
|
T | G | 1 | a0002c0002t0002g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-64-1536T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813755 | ||||||
| chr6:125813790
|
G | A | 157 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.-64-1501G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813790 | ||||||
| chr6:125813923
|
A | ATTT | 203 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(200): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-64-1366_-64-1365i others(5): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125813923 | |||||
| chr6:125814223
|
T | C | 204 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-64-1068T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814223 | ||||||
| chr6:125814278
|
C | T | 1 | a0001c0010t0005g0161 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-64-1013C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814278 | ||||||
| chr6:125814301
|
T | C | 203 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(200): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-64-990T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814301 | ||||||
| chr6:125814370
|
G | A | 5 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-921G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814370 | ||||||
| chr6:125814424
|
G | A | 5 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0026g0261others(2): Show | 5 | HG01891.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-867G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814424 | ||||||
| chr6:125814434
|
G | T | 1 | a0001c0001t0001g0216 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-64-857G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814434 | ||||||
| chr6:125814452
|
C | G | 1 | a0002c0004t0002g0151 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-64-839C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814452 | ||||||
| chr6:125814591
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-64-700C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814591 | ||||||
| chr6:125814681
|
A | G | 27 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(24): Show | 27 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-64-610A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814681 | ||||||
| chr6:125814702
|
G | T | 26 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(23): Show | 26 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-64-589G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814702 | ||||||
| chr6:125814736
|
A | G | 1 | a0002c0002t0001g0081 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-64-555A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814736 | ||||||
| chr6:125814747
|
C | G | 73 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0083others(70): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-64-544C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814747 | ||||||
| chr6:125814856
|
A | G | 4 | a0001c0001t0004g0154a0001c0001t0004g0155a0002c0002t0002g0002others(1): Show | 5 | NA18949.hp2 NA18957.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-435A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814856 | ||||||
| chr6:125814963
|
T | A | 1 | a0001c0001t0001g0041 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-64-328T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814963 | ||||||
| chr6:125815031
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-64-260G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125815031 | ||||||
| chr6:125815127
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-64-164T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125815127 | ||||||
| chr6:125815137
|
A | G | 1 | a0002c0002t0004g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-64-154A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125815137 | ||||||
| chr6:125815279
|
C | T | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-12C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125815279 | ||||||
| chr6:125815967
|
A | C | 4 | a0001c0001t0004g0154a0001c0001t0004g0155a0002c0002t0002g0002others(1): Show | 5 | NA18949.hp2 NA18957.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.50+563A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125815967 | ||||||
| chr6:125816686
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.50+1282G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816686 | ||||||
| chr6:125816768
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.50+1364A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816768 | ||||||
| chr6:125816778
|
C | A | 1 | a0002c0002t0002g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.50+1374C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816778 | ||||||
| chr6:125816861
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0007g0080 | 2 | NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.50+1457C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816861 | ||||||
| chr6:125816886
|
C | T | 3 | a0002c0004t0002g0030a0002c0004t0002g0160a0003c0003t0003g0018 | 3 | HG02486.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.50+1482C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816886 | ||||||
| chr6:125816933
|
T | A | 10 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(7): Show | 10 | HG00639.hp2 HG01884.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.50+1529T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816933 | ||||||
| chr6:125816935
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0043others(1): Show | 4 | HG00323.hp2 HG00738.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.50+1531C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816935 | ||||||
| chr6:125816998
|
A | G | 23 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.50+1594A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816998 | ||||||
| chr6:125817201
|
G | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0136 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.50+1797G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817201 | ||||||
| chr6:125817472
|
G | A | 1 | a0002c0002t0002g0108 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.50+2068G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817472 | ||||||
| chr6:125817835
|
T | C | 1 | a0001c0001t0004g0154 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.50+2431T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817835 | ||||||
| chr6:125817936
|
G | A | 1 | a0002c0002t0002g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.50+2532G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817936 | ||||||
| chr6:125817941
|
G | C | 3 | a0001c0001t0002g0038a0001c0001t0004g0037a0001c0001t0004g0039 | 3 | HG01243.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.50+2537G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817941 | ||||||
| chr6:125817975
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.50+2571C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817975 | ||||||
| chr6:125817980
|
C | T | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50+2576C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817980 | ||||||
| chr6:125818022
|
C | G | 1 | a0002c0002t0004g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.50+2618C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818022 | ||||||
| chr6:125818062
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50+2658G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818062 | ||||||
| chr6:125818098
|
T | C | 2 | a0001c0001t0004g0017a0001c0001t0004g0019 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.50+2694T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818098 | ||||||
| chr6:125818589
|
G | A | 2 | a0002c0002t0010g0133a0002c0002t0010g0141 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.50+3185G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818589 | ||||||
| chr6:125818594
|
AG | A | 4 | a0001c0001t0002g0159a0002c0002t0007g0003a0002c0008t0015g0262others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.50+3191delG | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818594 | ||||||
| chr6:125818715
|
A | G | 6 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0011g0157others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.50+3311A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818715 | ||||||
| chr6:125818871
|
T | C | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.50+3467T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818871 | ||||||
| chr6:125818873
|
C | A | 1 | a0002c0002t0002g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50+3469C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818873 | ||||||
| chr6:125818919
|
A | T | 1 | a0003c0003t0003g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.50+3515A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818919 | ||||||
| chr6:125819046
|
A | G | 1 | a0005c0006t0002g0001 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.50+3642A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819046 | ||||||
| chr6:125819141
|
A | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0136 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.50+3737A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819141 | ||||||
| chr6:125819239
|
C | T | 157 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.50+3835C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819239 | ||||||
| chr6:125819255
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(6): Show | 9 | HG00639.hp2 HG02922.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.50+3851A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819255 | ||||||
| chr6:125819341
|
A | G | 1 | a0002c0002t0002g0235 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.50+3937A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819341 | ||||||
| chr6:125819551
|
A | G | 162 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(159): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.50+4147A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819551 | ||||||
| chr6:125819896
|
C | G | 1 | a0001c0001t0007g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.50+4492C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819896 | ||||||
| chr6:125820055
|
T | C | 206 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.50+4651T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820055 | ||||||
| chr6:125820198
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0136 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.50+4794A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820198 | ||||||
| chr6:125820297
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.50+4893G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820297 | ||||||
| chr6:125820424
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(16): Show | 19 | HG00639.hp2 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.50+5020A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820424 | ||||||
| chr6:125820814
|
A | G | 2 | a0003c0003t0003g0028a0003c0003t0003g0029 | 2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.50+5410A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820814 | ||||||
| chr6:125820877
|
G | T | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50+5473G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820877 | ||||||
| chr6:125820914
|
T | C | 203 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(200): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.50+5510T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820914 | ||||||
| chr6:125820958
|
T | C | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.50+5554T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820958 | ||||||
| chr6:125821108
|
T | C | 10 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.50+5704T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821108 | ||||||
| chr6:125821199
|
G | C | 7 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(4): Show | 7 | NA18978.hp1 NA18982.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.50+5795G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821199 | ||||||
| chr6:125821340
|
G | A | 2 | a0002c0002t0007g0003a0003c0003t0003g0004 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.50+5936G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821340 | ||||||
| chr6:125821430
|
T | G | 204 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.50+6026T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821430 | ||||||
| chr6:125821504
|
G | C | 1 | a0003c0003t0003g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.50+6100G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821504 | ||||||
| chr6:125821507
|
C | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0136 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.50+6103C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821507 | ||||||
| chr6:125821640
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.50+6236T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821640 | ||||||
| chr6:125821700
|
A | G | 3 | a0003c0003t0003g0127a0003c0003t0003g0130a0003c0003t0018g0128 | 3 | HG02647.hp1 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.50+6296A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821700 | ||||||
| chr6:125821713
|
C | A | 1 | a0002c0002t0002g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.50+6309C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821713 | ||||||
| chr6:125821755
|
C | T | 2 | a0002c0002t0007g0003a0003c0003t0003g0004 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.50+6351C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821755 | ||||||
| chr6:125822158
|
C | T | 3 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0026g0261 | 3 | HG01891.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.50+6754C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822158 | ||||||
| chr6:125822225
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.50+6821T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822225 | ||||||
| chr6:125822535
|
A | G | 218 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(215): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.50+7131A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822535 | ||||||
| chr6:125822612
|
T | C | 4 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.50+7208T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822612 | ||||||
| chr6:125822619
|
T | G | 2 | a0003c0003t0003g0028a0003c0003t0003g0029 | 2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.50+7215T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822619 | ||||||
| chr6:125822641
|
A | G | 1 | a0002c0002t0014g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+7237A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822641 | ||||||
| chr6:125822898
|
G | A | 16 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(13): Show | 16 | HG01884.hp1 HG02630.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.50+7494G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822898 | ||||||
| chr6:125822935
|
C | CA | 10 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0171others(7): Show | 10 | HG00544.hp1 HG00544.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.50+7546dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125822935 | |||||
| chr6:125822937
|
A | G | 15 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(12): Show | 15 | HG01884.hp1 HG02630.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.50+7533A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822937 | ||||||
| chr6:125822954
|
C | A | 1 | a0001c0001t0001g0230 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.50+7550C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822954 | ||||||
| chr6:125822994
|
GA | G | 202 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.50+7600delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125822994 | |||||
| chr6:125823178
|
C | CG | 5 | a0003c0003t0003g0117a0003c0003t0003g0118a0003c0003t0003g0123others(2): Show | 5 | NA18973.hp1 NA18995.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.50+7775dupG | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125823178 | |||||
| chr6:125823244
|
A | G | 10 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.50+7840A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125823244 | ||||||
| chr6:125823803
|
T | C | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0004g0225 | 3 | NA18961.hp2 NA18987.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.50+8399T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125823803 | ||||||
| chr6:125824071
|
T | A | 2 | a0003c0003t0003g0147a0003c0003t0003g0148 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.50+8667T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824071 | ||||||
| chr6:125824213
|
T | A | 2 | a0001c0001t0004g0154a0001c0001t0004g0155 | 2 | NA18949.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.50+8809T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824213 | ||||||
| chr6:125824221
|
A | G | 2 | a0001c0001t0004g0154a0001c0001t0004g0155 | 2 | NA18949.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.50+8817A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824221 | ||||||
| chr6:125824238
|
C | A | 1 | a0001c0001t0001g0172 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.50+8834C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824238 | ||||||
| chr6:125824255
|
A | T | 1 | a0002c0002t0002g0079 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.50+8851A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824255 | ||||||
| chr6:125824303
|
A | T | 1 | a0003c0003t0003g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.50+8899A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824303 | ||||||
| chr6:125824332
|
C | T | 2 | a0002c0002t0007g0003a0003c0003t0003g0004 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.50+8928C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824332 | ||||||
| chr6:125824751
|
A | C | 203 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(200): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.50+9347A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824751 | ||||||
| chr6:125824820
|
G | C | 159 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.50+9416G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824820 | ||||||
| chr6:125824851
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.50+9447C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824851 | ||||||
| chr6:125824877
|
G | A | 1 | a0001c0001t0016g0232 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.50+9473G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824877 | ||||||
| chr6:125824918
|
C | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0007t0001g0046 | 3 | HG01074.hp2 HG01123.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.50+9514C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824918 | ||||||
| chr6:125824934
|
G | C | 1 | a0002c0002t0001g0256 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.50+9530G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824934 | ||||||
| chr6:125825174
|
C | CA | 21 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(18): Show | 21 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.50+9789dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125825174 | |||||
| chr6:125825174
|
C | CAA | 7 | a0001c0001t0001g0043a0001c0001t0004g0017a0001c0001t0004g0019others(4): Show | 7 | HG02055.hp2 HG02486.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.50+9788_50+9789dup others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125825174 | |||||
| chr6:125825174
|
C | CAAA | 17 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(14): Show | 17 | HG01884.hp1 HG02630.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.50+9787_50+9789dup others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125825174 | |||||
| chr6:125825209
|
A | C | 184 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.50+9805A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125825209 | ||||||
| chr6:125825239
|
G | A | 172 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0073others(169): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.50+9835G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125825239 | ||||||
| chr6:125825293
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | NA18995.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.50+9889G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125825293 | ||||||
| chr6:125825565
|
A | G | 81 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0083others(78): Show | 83 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.50+10161A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125825565 | ||||||
| chr6:125826051
|
C | T | 86 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.50+10647C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826051 | ||||||
| chr6:125826091
|
C | T | 1 | a0002c0002t0002g0215 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.50+10687C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826091 | ||||||
| chr6:125826130
|
A | T | 1 | a0001c0001t0002g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.50+10726A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826130 | ||||||
| chr6:125826336
|
G | GA | 15 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(12): Show | 15 | HG02615.hp1 HG02630.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.50+10945dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125826336 | |||||
| chr6:125826336
|
GA | G | 83 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(80): Show | 85 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.50+10945delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125826336 | |||||
| chr6:125826350
|
G | A | 1 | a0003c0003t0003g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.50+10946G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826350 | ||||||
| chr6:125826369
|
C | T | 1 | a0003c0003t0003g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.50+10965C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826369 | ||||||
| chr6:125826413
|
A | G | 15 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.50+11009A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826413 | ||||||
| chr6:125826459
|
A | C | 1 | a0003c0003t0003g0115 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.50+11055A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826459 | ||||||
| chr6:125826771
|
G | A | 1 | a0002c0002t0002g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.50+11367G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826771 | ||||||
| chr6:125826839
|
G | T | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.50+11435G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826839 | ||||||
| chr6:125826926
|
G | A | 1 | a0001c0001t0009g0186 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.50+11522G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826926 | ||||||
| chr6:125826928
|
T | G | 84 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(81): Show | 86 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.50+11524T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826928 | ||||||
| chr6:125826972
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.50+11568C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826972 | ||||||
| chr6:125827172
|
G | A | 133 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.50+11768G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827172 | ||||||
| chr6:125827188
|
C | CA | 20 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0026g0261others(17): Show | 20 | HG00738.hp2 HG01517.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.50+11812dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | |||||
| chr6:125827188
|
CA | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(89): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.50+11812delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | |||||
| chr6:125827188
|
CAA | C | 6 | a0001c0001t0001g0177a0001c0001t0002g0132a0001c0001t0002g0136others(3): Show | 6 | HG00741.hp2 HG01891.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.50+11811_50+11812d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | |||||
| chr6:125827188
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0187 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.50+11801_50+11812d others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | |||||
| chr6:125827188
|
CAAAAAAA others(6): Show |
C | 70 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0109others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.50+11800_50+11812d others(15): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | |||||
| chr6:125827188
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0221 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.50+11799_50+11812d others(16): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | |||||
| chr6:125827294
|
A | G | 1 | a0002c0002t0010g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.50+11890A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827294 | ||||||
| chr6:125827475
|
G | A | 1 | a0005c0006t0002g0001 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.50+12071G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827475 | ||||||
| chr6:125827583
|
A | G | 1 | a0002c0002t0014g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+12179A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827583 | ||||||
| chr6:125827686
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.50+12282G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827686 | ||||||
| chr6:125827828
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0044 | 2 | HG00738.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.50+12424A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827828 | ||||||
| chr6:125827922
|
T | A | 205 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.50+12518T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827922 | ||||||
| chr6:125827981
|
C | T | 133 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.50+12577C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827981 | ||||||
| chr6:125828058
|
C | T | 2 | a0001c0001t0006g0259a0001c0001t0006g0260 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.50+12654C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828058 | ||||||
| chr6:125828101
|
G | A | 1 | a0003c0003t0003g0029 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.50+12697G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828101 | ||||||
| chr6:125828163
|
G | A | 4 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.50+12759G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828163 | ||||||
| chr6:125828281
|
G | T | 2 | a0002c0002t0002g0087a0002c0002t0002g0234 | 2 | HG00735.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.50+12877G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828281 | ||||||
| chr6:125828478
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.50+13074G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828478 | ||||||
| chr6:125828506
|
C | A | 1 | a0002c0002t0014g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+13102C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828506 | ||||||
| chr6:125828691
|
G | A | 2 | a0002c0002t0001g0152a0002c0002t0007g0153 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.50+13287G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828691 | ||||||
| chr6:125828804
|
T | C | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.50+13400T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828804 | ||||||
| chr6:125828846
|
C | T | 2 | a0003c0003t0003g0033a0003c0003t0003g0034 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.50+13442C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828846 | ||||||
| chr6:125829024
|
A | G | 2 | a0002c0002t0007g0003a0003c0003t0003g0004 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.50+13620A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829024 | ||||||
| chr6:125829350
|
T | C | 6 | a0002c0002t0002g0144a0002c0002t0002g0145a0002c0002t0012g0143others(3): Show | 6 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.50+13946T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829350 | ||||||
| chr6:125829414
|
C | A | 1 | a0001c0001t0016g0232 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.50+14010C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829414 | ||||||
| chr6:125829766
|
C | CT | 71 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0109others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.50+14362_50+14363i others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829766 | ||||||
| chr6:125829767
|
A | T | 71 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0109others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.50+14363A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829767 | ||||||
| chr6:125829789
|
C | T | 1 | a0002c0002t0002g0077 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.50+14385C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829789 | ||||||
| chr6:125829854
|
T | G | 71 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0109others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.50+14450T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829854 | ||||||
| chr6:125829912
|
C | G | 3 | a0002c0002t0002g0015a0003c0003t0003g0033a0003c0003t0003g0034 | 3 | HG02615.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.50+14508C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829912 | ||||||
| chr6:125829954
|
G | A | 7 | a0001c0001t0004g0065a0002c0002t0002g0067a0002c0002t0002g0068others(4): Show | 7 | HG00597.hp2 HG02132.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.50+14550G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829954 | ||||||
| chr6:125829959
|
A | T | 1 | a0002c0002t0014g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+14555A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829959 | ||||||
| chr6:125830258
|
C | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50+14854C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830258 | ||||||
| chr6:125830472
|
T | C | 2 | a0002c0002t0002g0057a0002c0002t0002g0058 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.50+15068T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830472 | ||||||
| chr6:125830721
|
T | TTA | 3 | a0001c0001t0004g0037a0001c0001t0004g0039a0003c0003t0003g0110 | 3 | HG03017.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.50+15333_50+15334d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830721 | |||||
| chr6:125830721
|
TTA | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0164a0001c0001t0001g0165others(13): Show | 16 | HG00639.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.50+15333_50+15334d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830721 | |||||
| chr6:125830733
|
A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0236 | 3 | HG03491.hp1 HG03492.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.50+15330_50+15331i others(12): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830733 | |||||
| chr6:125830733
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.50+15329A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830733 | ||||||
| chr6:125830735
|
A | ATG | 10 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0184others(7): Show | 10 | HG01109.hp2 HG01256.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | |||||
| chr6:125830735
|
A | ATGTG | 12 | a0001c0001t0001g0054a0001c0001t0001g0182a0001c0001t0001g0191others(9): Show | 12 | HG00140.hp2 HG01069.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | |||||
| chr6:125830735
|
A | ATGTGTG | 11 | a0001c0001t0001g0109a0001c0001t0001g0170a0001c0001t0001g0185others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(8): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | |||||
| chr6:125830735
|
A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0086a0001c0001t0001g0169a0001c0001t0001g0171others(2): Show | 5 | HG00642.hp2 HG01192.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(10): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | |||||
| chr6:125830735
|
A | ATGTGTGT others(3): Show |
5 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0001g0216others(2): Show | 5 | HG00735.hp2 HG01243.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(12): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | |||||
| chr6:125830735
|
A | ATGTGTGT others(5): Show |
7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 7 | HG00544.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | |||||
| chr6:125830735
|
A | ATGTGTGT others(7): Show |
2 | a0001c0001t0001g0202a0001c0001t0001g0246 | 2 | HG03927.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.50+15332_50+15333i others(16): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | |||||
| chr6:125830735
|
A | G | 7 | a0001c0001t0001g0121a0001c0001t0001g0167a0001c0001t0001g0187others(4): Show | 7 | HG00597.hp1 HG01106.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.50+15331A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830735 | ||||||
| chr6:125830735
|
ATATGTGT others(5): Show |
A | 1 | a0001c0001t0016g0232 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.50+15333_50+15344d others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | |||||
| chr6:125830737
|
A | ATG | 3 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0011g0157 | 3 | HG02055.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.50+15355_50+15356d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830737 | |||||
| chr6:125830737
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0009g0186 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.50+15341_50+15356d others(18): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830737 | |||||
| chr6:125830737
|
A | G | 173 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.50+15333A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830737 | ||||||
| chr6:125830739
|
G | A | 1 | a0001c0001t0005g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.50+15335G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830739 | ||||||
| chr6:125830751
|
G | GTGTGTGT others(1): Show |
3 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0026g0261 | 3 | HG01891.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.50+15354_50+15355i others(10): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830751 | |||||
| chr6:125830753
|
G | GTGTGTA | 11 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.50+15354_50+15355i others(8): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830753 | |||||
| chr6:125830757
|
G | GTA | 15 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(12): Show | 15 | HG02109.hp1 HG02615.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.50+15354_50+15355i others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830757 | |||||
| chr6:125830759
|
G | A | 77 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0083others(74): Show | 79 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.50+15355G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830759 | ||||||
| chr6:125830759
|
GTA | G | 4 | a0001c0001t0001g0239a0001c0001t0005g0006a0001c0001t0005g0238others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.50+15357_50+15358d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830759 | |||||
| chr6:125830761
|
A | G | 183 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.50+15357A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830761 | ||||||
| chr6:125831218
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.50+15814C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831218 | ||||||
| chr6:125831338
|
A | G | 12 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(9): Show | 12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.50+15934A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831338 | ||||||
| chr6:125831388
|
T | A | 14 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(11): Show | 14 | HG02615.hp1 HG02630.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.50+15984T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831388 | ||||||
| chr6:125831430
|
T | C | 5 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178others(2): Show | 5 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.50+16026T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831430 | ||||||
| chr6:125831526
|
C | A | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.50+16122C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831526 | ||||||
| chr6:125831649
|
A | G | 103 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(100): Show | 105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.50+16245A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831649 | ||||||
| chr6:125831666
|
TA | T | 9 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(6): Show | 9 | HG00639.hp2 HG03225.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.50+16267delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125831666 | |||||
| chr6:125831708
|
C | T | 2 | a0003c0003t0003g0147a0003c0003t0003g0148 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.50+16304C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831708 | ||||||
| chr6:125831975
|
A | G | 1 | a0002c0002t0014g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+16571A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831975 | ||||||
| chr6:125832107
|
T | C | 71 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0083others(68): Show | 73 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.50+16703T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832107 | ||||||
| chr6:125832333
|
C | T | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.50+16929C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832333 | ||||||
| chr6:125832337
|
A | G | 4 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.50+16933A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832337 | ||||||
| chr6:125832461
|
A | G | 1 | a0002c0002t0002g0234 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.50+17057A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832461 | ||||||
| chr6:125832470
|
C | A | 1 | a0001c0001t0004g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.50+17066C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832470 | ||||||
| chr6:125832647
|
G | T | 1 | a0002c0002t0001g0135 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.50+17243G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832647 | ||||||
| chr6:125832664
|
A | G | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.50+17260A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832664 | ||||||
| chr6:125833018
|
A | G | 12 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(9): Show | 12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.50+17614A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833018 | ||||||
| chr6:125833094
|
G | C | 2 | a0002c0002t0002g0162a0002c0002t0002g0255 | 2 | NA18963.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.50+17690G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833094 | ||||||
| chr6:125833158
|
T | C | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.50+17754T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833158 | ||||||
| chr6:125833208
|
A | G | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.50+17804A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833208 | ||||||
| chr6:125833329
|
G | A | 71 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0109others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.50+17925G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833329 | ||||||
| chr6:125833592
|
G | A | 1 | a0003c0003t0019g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.50+18188G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833592 | ||||||
| chr6:125833593
|
A | AG | 122 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0042others(119): Show | 123 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.50+18196dupG | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125833593 | |||||
| chr6:125833601
|
A | G | 1 | a0001c0001t0009g0188 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.50+18197A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833601 | ||||||
| chr6:125833799
|
G | A | 1 | a0002c0002t0014g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+18395G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833799 | ||||||
| chr6:125834088
|
AT | A | 72 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0109others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.50+18685delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834088 | ||||||
| chr6:125834091
|
A | G | 72 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0109others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.50+18687A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834091 | ||||||
| chr6:125834156
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.50+18752T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834156 | ||||||
| chr6:125834170
|
CAA | C | 15 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.50+18768_50+18769d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125834170 | |||||
| chr6:125834367
|
A | G | 1 | a0001c0001t0009g0188 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.50+18963A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834367 | ||||||
| chr6:125834381
|
A | G | 1 | a0001c0001t0005g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.50+18977A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834381 | ||||||
| chr6:125834433
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(6): Show | 9 | HG00639.hp2 HG03225.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.50+19029G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834433 | ||||||
| chr6:125834843
|
G | C | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.50+19439G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834843 | ||||||
| chr6:125834848
|
A | G | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.50+19444A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834848 | ||||||
| chr6:125835203
|
A | G | 3 | a0002c0002t0002g0162a0002c0002t0002g0163a0002c0002t0002g0255 | 3 | NA18951.hp1 NA18963.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.50+19799A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835203 | ||||||
| chr6:125835307
|
C | T | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51-19713C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835307 | ||||||
| chr6:125835353
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.51-19667A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835353 | ||||||
| chr6:125835426
|
T | C | 14 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(11): Show | 14 | HG02615.hp1 HG02630.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.51-19594T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835426 | ||||||
| chr6:125835464
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.51-19556G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835464 | ||||||
| chr6:125835601
|
G | A | 1 | a0002c0002t0014g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.51-19419G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835601 | ||||||
| chr6:125835797
|
G | A | 71 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0109others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.51-19223G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835797 | ||||||
| chr6:125835807
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51-19213G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835807 | ||||||
| chr6:125835811
|
G | A | 4 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-19209G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835811 | ||||||
| chr6:125835893
|
G | A | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-19127G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835893 | ||||||
| chr6:125836032
|
C | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.51-18988C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125836032 | ||||||
| chr6:125836082
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.51-18938G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125836082 | ||||||
| chr6:125836410
|
A | G | 2 | a0003c0003t0003g0114a0007c0011t0003g0129 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.51-18610A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125836410 | ||||||
| chr6:125836682
|
G | A | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-18338G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125836682 | ||||||
| chr6:125836863
|
G | T | 2 | a0001c0001t0001g0231a0001c0001t0009g0173 | 2 | NA18964.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.51-18157G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125836863 | ||||||
| chr6:125837111
|
G | C | 26 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(23): Show | 26 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.51-17909G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837111 | ||||||
| chr6:125837210
|
CT | C | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-17809delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837210 | ||||||
| chr6:125837305
|
G | A | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51-17715G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837305 | ||||||
| chr6:125837332
|
G | A | 1 | a0003c0003t0003g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.51-17688G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837332 | ||||||
| chr6:125837449
|
C | T | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-17571C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837449 | ||||||
| chr6:125837604
|
T | G | 1 | a0002c0002t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.51-17416T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837604 | ||||||
| chr6:125837813
|
C | T | 1 | a0003c0003t0003g0227 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.51-17207C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837813 | ||||||
| chr6:125837971
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.51-17049T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837971 | ||||||
| chr6:125838017
|
C | G | 106 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(103): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.51-17003C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838017 | ||||||
| chr6:125838038
|
G | T | 2 | a0002c0002t0007g0003a0003c0003t0003g0004 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.51-16982G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838038 | ||||||
| chr6:125838506
|
G | A | 15 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.51-16514G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838506 | ||||||
| chr6:125838595
|
A | C | 1 | a0001c0001t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51-16425A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838595 | ||||||
| chr6:125838604
|
G | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0196a0001c0001t0001g0251 | 3 | HG02132.hp2 NA18939.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.51-16416G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838604 | ||||||
| chr6:125838924
|
G | A | 1 | a0002c0002t0002g0255 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.51-16096G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838924 | ||||||
| chr6:125839101
|
C | T | 1 | a0002c0002t0005g0253 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.51-15919C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839101 | ||||||
| chr6:125839188
|
G | A | 15 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.51-15832G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839188 | ||||||
| chr6:125839447
|
G | C | 12 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(9): Show | 12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.51-15573G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839447 | ||||||
| chr6:125839472
|
C | T | 6 | a0002c0002t0001g0135a0003c0003t0003g0134a0003c0003t0003g0139others(3): Show | 6 | HG01192.hp2 HG01884.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.51-15548C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839472 | ||||||
| chr6:125839537
|
C | T | 1 | a0002c0002t0002g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.51-15483C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839537 | ||||||
| chr6:125839570
|
C | T | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.51-15450C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839570 | ||||||
| chr6:125839682
|
A | C | 222 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.51-15338A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839682 | ||||||
| chr6:125839749
|
A | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.51-15271A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839749 | ||||||
| chr6:125839988
|
C | G | 2 | a0003c0003t0003g0209a0003c0003t0021g0208 | 2 | NA18946.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.51-15032C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839988 | ||||||
| chr6:125840027
|
G | A | 1 | a0002c0002t0002g0219 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.51-14993G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840027 | ||||||
| chr6:125840230
|
G | T | 1 | a0001c0001t0001g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.51-14790G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840230 | ||||||
| chr6:125840366
|
GA | G | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.51-14648delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840366 | |||||
| chr6:125840488
|
T | C | 15 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.51-14532T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840488 | ||||||
| chr6:125840576
|
T | A | 1 | a0002c0002t0002g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.51-14444T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840576 | ||||||
| chr6:125840867
|
GGTTTTTT others(10): Show |
G | 3 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0010t0005g0161 | 3 | HG02055.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.51-14152_51-14136d others(19): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840867 | ||||||
| chr6:125840867
|
GGTTTTTT others(11): Show |
G | 7 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0037others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.51-14152_51-14135d others(20): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840867 | ||||||
| chr6:125840867
|
GGTTTTTT others(14): Show |
G | 1 | a0001c0001t0005g0016 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.51-14152_51-14132d others(23): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840867 | ||||||
| chr6:125840868
|
G | GTT | 5 | a0001c0001t0004g0007a0001c0001t0004g0012a0002c0002t0004g0137others(2): Show | 5 | HG02080.hp1 HG03516.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.51-14111_51-14110d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTT | 9 | a0002c0002t0001g0256a0002c0002t0002g0055a0002c0002t0002g0057others(6): Show | 10 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.51-14114_51-14110d others(7): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTT | 17 | a0001c0001t0001g0073a0001c0001t0001g0092a0001c0001t0001g0210others(14): Show | 17 | HG00544.hp1 HG01257.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.51-14115_51-14110d others(8): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT | 9 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0004g0155others(6): Show | 9 | HG02004.hp1 HG02293.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.51-14116_51-14110d others(9): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(2): Show |
5 | a0002c0002t0002g0015a0002c0002t0002g0082a0002c0002t0002g0102others(2): Show | 5 | HG03098.hp2 HG03669.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.51-14118_51-14110d others(11): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0004g0008a0001c0001t0005g0085 | 2 | HG02647.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.51-14119_51-14110d others(12): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(4): Show |
3 | a0001c0001t0024g0150a0002c0002t0002g0076a0002c0002t0002g0215 | 3 | HG00642.hp1 HG01261.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.51-14120_51-14110d others(13): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(5): Show |
6 | a0002c0002t0001g0229a0002c0002t0002g0061a0002c0002t0002g0062others(3): Show | 6 | HG00323.hp1 HG02293.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.51-14121_51-14110d others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(6): Show |
5 | a0002c0002t0002g0060a0002c0002t0002g0068a0002c0002t0002g0087others(2): Show | 5 | HG00735.hp1 HG01981.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.51-14122_51-14110d others(15): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(8): Show |
3 | a0002c0002t0002g0053a0002c0002t0007g0003a0003c0003t0003g0004 | 3 | HG02698.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.51-14124_51-14110d others(17): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(9): Show |
1 | a0002c0002t0002g0079 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.51-14125_51-14110d others(18): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(10): Show |
1 | a0002c0002t0001g0094 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.51-14126_51-14110d others(19): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(11): Show |
3 | a0001c0001t0006g0036a0002c0002t0002g0096a0002c0002t0002g0097 | 3 | NA18522.hp1 NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.51-14127_51-14110d others(20): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(12): Show |
1 | a0002c0002t0007g0153 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.51-14128_51-14110d others(21): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(13): Show |
1 | a0002c0002t0001g0152 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.51-14129_51-14110d others(22): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
G | GTTTTTTT others(22): Show |
1 | a0002c0002t0002g0099 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.51-14138_51-14110d others(31): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GT | G | 23 | a0001c0001t0004g0010a0001c0009t0022g0263a0002c0002t0001g0180others(20): Show | 23 | HG00099.hp1 HG00639.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.51-14110delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTT | G | 15 | a0001c0001t0001g0005a0002c0002t0001g0059a0002c0002t0001g0135others(12): Show | 15 | HG00280.hp2 HG01192.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.51-14111_51-14110d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTT | G | 13 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0025g0009others(10): Show | 13 | HG01891.hp1 HG02145.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.51-14112_51-14110d others(5): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTT | G | 8 | a0001c0001t0002g0159a0001c0001t0004g0065a0001c0001t0004g0225others(5): Show | 8 | HG00597.hp2 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.51-14113_51-14110d others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTTTTT others(5): Show |
G | 2 | a0002c0002t0002g0063a0002c0002t0005g0253 | 2 | HG00639.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.51-14121_51-14110d others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTTTTT others(6): Show |
G | 3 | a0001c0001t0001g0043a0003c0003t0003g0111a0003c0003t0003g0115 | 3 | HG03831.hp1 NA18939.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.51-14122_51-14110d others(15): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTTTTT others(7): Show |
G | 11 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.51-14123_51-14110d others(16): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTTTTT others(8): Show |
G | 2 | a0001c0001t0006g0268a0001c0001t0007g0049 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.51-14124_51-14110d others(17): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTTTTT others(9): Show |
G | 2 | a0001c0001t0002g0038a0001c0001t0026g0261 | 2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.51-14125_51-14110d others(18): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTTTTT others(10): Show |
G | 4 | a0001c0001t0006g0259a0001c0001t0006g0260a0003c0003t0003g0139others(1): Show | 4 | HG02717.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-14126_51-14110d others(19): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTTTTT others(11): Show |
G | 1 | a0004c0005t0003g0026 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.51-14127_51-14110d others(20): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTTTTT others(12): Show |
G | 7 | a0001c0001t0004g0021a0001c0001t0004g0023a0001c0001t0004g0024others(4): Show | 7 | HG03490.hp2 NA18982.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.51-14128_51-14110d others(21): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTTTTT others(13): Show |
G | 17 | a0001c0001t0001g0086a0001c0001t0001g0158a0001c0001t0001g0167others(14): Show | 17 | HG00642.hp2 HG01106.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.51-14129_51-14110d others(22): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTTTTT others(14): Show |
G | 56 | a0001c0001t0001g0054a0001c0001t0001g0109a0001c0001t0001g0121others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.51-14130_51-14110d others(23): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840868
|
GTTTTTTT others(15): Show |
G | 1 | a0002c0002t0014g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.51-14131_51-14110d others(24): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | |||||
| chr6:125840997
|
A | G | 123 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(120): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.51-14023A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840997 | ||||||
| chr6:125841026
|
G | A | 1 | a0003c0003t0003g0029 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.51-13994G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841026 | ||||||
| chr6:125841136
|
T | C | 151 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(148): Show | 153 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.51-13884T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841136 | ||||||
| chr6:125841137
|
G | A | 14 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(11): Show | 14 | HG02615.hp1 HG02630.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.51-13883G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841137 | ||||||
| chr6:125841153
|
G | A | 2 | a0003c0003t0003g0124a0003c0003t0003g0149 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.51-13867G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841153 | ||||||
| chr6:125841179
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51-13841C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841179 | ||||||
| chr6:125841186
|
GGCC | G | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-13833_51-13831d others(5): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841186 | ||||||
| chr6:125841191
|
A | AT | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-13829_51-13828i others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841191 | ||||||
| chr6:125841192
|
C | G | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-13828C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841192 | ||||||
| chr6:125841193
|
C | T | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-13827C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841193 | ||||||
| chr6:125841212
|
G | A | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.51-13808G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841212 | ||||||
| chr6:125841510
|
G | A | 2 | a0001c0001t0004g0037a0001c0001t0004g0039 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.51-13510G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841510 | ||||||
| chr6:125841551
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.51-13469C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841551 | ||||||
| chr6:125841991
|
G | A | 1 | a0002c0002t0008g0066 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.51-13029G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841991 | ||||||
| chr6:125842030
|
TAA | T | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-12989_51-12988d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842030 | ||||||
| chr6:125842262
|
C | T | 3 | a0002c0002t0001g0180a0002c0002t0002g0179a0002c0002t0002g0219 | 3 | HG00099.hp1 HG01109.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.51-12758C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842262 | ||||||
| chr6:125842294
|
C | T | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-12726C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842294 | ||||||
| chr6:125842295
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.51-12725G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842295 | ||||||
| chr6:125842321
|
T | C | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.51-12699T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842321 | ||||||
| chr6:125842391
|
C | T | 94 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0083others(91): Show | 96 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.51-12629C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842391 | ||||||
| chr6:125842444
|
C | T | 1 | a0002c0002t0012g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.51-12576C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842444 | ||||||
| chr6:125842453
|
A | G | 11 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.51-12567A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842453 | ||||||
| chr6:125842496
|
G | A | 1 | a0002c0002t0002g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.51-12524G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842496 | ||||||
| chr6:125842649
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.51-12371C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842649 | ||||||
| chr6:125842711
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.51-12309T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842711 | ||||||
| chr6:125842736
|
C | T | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-12284C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842736 | ||||||
| chr6:125842794
|
A | C | 2 | a0003c0003t0003g0124a0003c0003t0003g0149 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.51-12226A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842794 | ||||||
| chr6:125843030
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.51-11990G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843030 | ||||||
| chr6:125843438
|
G | C | 4 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-11582G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843438 | ||||||
| chr6:125843458
|
T | C | 1 | a0001c0001t0017g0247 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.51-11562T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843458 | ||||||
| chr6:125843558
|
T | C | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-11462T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843558 | ||||||
| chr6:125843674
|
A | G | 1 | a0002c0002t0007g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.51-11346A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843674 | ||||||
| chr6:125843721
|
G | A | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-11299G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843721 | ||||||
| chr6:125843787
|
C | G | 1 | a0002c0002t0002g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.51-11233C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843787 | ||||||
| chr6:125843857
|
G | A | 134 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(131): Show | 136 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.51-11163G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843857 | ||||||
| chr6:125843914
|
C | T | 1 | a0002c0002t0014g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.51-11106C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843914 | ||||||
| chr6:125844122
|
A | C | 1 | a0002c0002t0005g0253 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.51-10898A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125844122 | ||||||
| chr6:125844254
|
T | C | 1 | a0003c0003t0003g0142 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.51-10766T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125844254 | ||||||
| chr6:125844319
|
G | A | 216 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(213): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.51-10701G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125844319 | ||||||
| chr6:125844574
|
G | T | 132 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(129): Show | 134 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.51-10446G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125844574 | ||||||
| chr6:125844775
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.51-10245C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125844775 | ||||||
| chr6:125845166
|
A | G | 1 | a0004c0005t0003g0026 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.51-9854A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845166 | ||||||
| chr6:125845239
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.51-9781C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845239 | ||||||
| chr6:125845272
|
T | A | 1 | a0002c0002t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51-9748T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845272 | ||||||
| chr6:125845504
|
G | A | 12 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(9): Show | 12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.51-9516G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845504 | ||||||
| chr6:125845721
|
C | T | 73 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0086others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.51-9299C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845721 | ||||||
| chr6:125845786
|
G | A | 2 | a0002c0002t0002g0087a0002c0002t0002g0234 | 2 | HG00735.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.51-9234G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845786 | ||||||
| chr6:125845833
|
C | T | 4 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-9187C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845833 | ||||||
| chr6:125845983
|
A | G | 16 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(13): Show | 16 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.51-9037A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845983 | ||||||
| chr6:125846305
|
T | C | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.51-8715T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846305 | ||||||
| chr6:125846326
|
G | T | 76 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0092others(73): Show | 78 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.51-8694G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846326 | ||||||
| chr6:125846361
|
A | T | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.51-8659A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846361 | ||||||
| chr6:125846361
|
AT | A | 6 | a0001c0001t0006g0260a0002c0002t0002g0145a0002c0002t0007g0003others(3): Show | 6 | HG01515.hp1 HG02109.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.51-8641delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125846361 | |||||
| chr6:125846361
|
ATT | A | 33 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(30): Show | 33 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.51-8642_51-8641del others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125846361 | |||||
| chr6:125846361
|
ATTT | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0075a0001c0001t0001g0083others(90): Show | 95 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.51-8643_51-8641del others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125846361 | |||||
| chr6:125846361
|
ATTTT | A | 76 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0086others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.51-8644_51-8641del others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125846361 | |||||
| chr6:125846363
|
T | A | 3 | a0001c0001t0006g0260a0002c0002t0007g0003a0003c0003t0003g0004 | 3 | HG02818.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.51-8657T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846363 | ||||||
| chr6:125846364
|
T | A | 26 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(23): Show | 26 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.51-8656T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846364 | ||||||
| chr6:125846365
|
T | A | 18 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(15): Show | 18 | HG00639.hp2 HG02280.hp1 HG03225.hp1 others(15): Show |
intron_variant | MODIFIER | c.51-8655T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846365 | ||||||
| chr6:125847078
|
A | G | 2 | a0001c0001t0026g0261a0004c0013t0013g0264 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.51-7942A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847078 | ||||||
| chr6:125847113
|
T | A | 1 | a0001c0001t0001g0190 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.51-7907T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847113 | ||||||
| chr6:125847154
|
A | G | 1 | a0008c0012t0003g0113 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.51-7866A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847154 | ||||||
| chr6:125847355
|
T | C | 1 | a0002c0002t0002g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.51-7665T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847355 | ||||||
| chr6:125847459
|
C | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.51-7561C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847459 | ||||||
| chr6:125847590
|
G | A | 1 | a0001c0001t0007g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.51-7430G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847590 | ||||||
| chr6:125847792
|
A | G | 4 | a0001c0001t0001g0073a0001c0001t0001g0167a0001c0001t0001g0226others(1): Show | 4 | NA18943.hp2 NA18950.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-7228A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847792 | ||||||
| chr6:125848093
|
C | A | 2 | a0001c0001t0006g0259a0001c0001t0006g0260 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.51-6927C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848093 | ||||||
| chr6:125848102
|
AC | A | 4 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-6916delC | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125848102 | |||||
| chr6:125848443
|
G | A | 4 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.51-6577G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848443 | ||||||
| chr6:125848488
|
A | G | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.51-6532A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848488 | ||||||
| chr6:125848549
|
G | C | 16 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(13): Show | 16 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.51-6471G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848549 | ||||||
| chr6:125848592
|
T | C | 1 | a0002c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.51-6428T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848592 | ||||||
| chr6:125848855
|
A | G | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-6165A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848855 | ||||||
| chr6:125849471
|
G | A | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-5549G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125849471 | ||||||
| chr6:125849607
|
A | G | 1 | a0002c0002t0002g0098 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.51-5413A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125849607 | ||||||
| chr6:125849622
|
G | A | 10 | a0002c0002t0001g0059a0002c0002t0002g0108a0002c0002t0002g0144others(7): Show | 10 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.51-5398G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125849622 | ||||||
| chr6:125849717
|
T | C | 4 | a0002c0002t0008g0052a0002c0002t0008g0056a0002c0002t0008g0066others(1): Show | 4 | NA18940.hp2 NA18968.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-5303T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125849717 | ||||||
| chr6:125849963
|
T | G | 2 | a0001c0001t0026g0261a0004c0013t0013g0264 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.51-5057T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125849963 | ||||||
| chr6:125850064
|
G | A | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-4956G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125850064 | ||||||
| chr6:125851216
|
A | G | 62 | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.51-3804A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851216 | ||||||
| chr6:125851335
|
C | T | 17 | a0002c0002t0001g0135a0002c0002t0010g0133a0002c0002t0010g0141others(14): Show | 17 | HG01192.hp2 HG01884.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.51-3685C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851335 | ||||||
| chr6:125851489
|
C | T | 1 | a0002c0004t0002g0151 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.51-3531C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851489 | ||||||
| chr6:125851679
|
G | T | 16 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(13): Show | 16 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.51-3341G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851679 | ||||||
| chr6:125851835
|
C | T | 4 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.51-3185C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851835 | ||||||
| chr6:125851850
|
T | C | 10 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 10 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.51-3170T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851850 | ||||||
| chr6:125851890
|
C | CT | 14 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.51-3119dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125851890 | |||||
| chr6:125852131
|
G | A | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51-2889G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125852131 | ||||||
| chr6:125852884
|
T | A | 2 | a0001c0001t0026g0261a0004c0013t0013g0264 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.51-2136T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125852884 | ||||||
| chr6:125852896
|
C | T | 1 | a0002c0002t0002g0179 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.51-2124C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125852896 | ||||||
| chr6:125853069
|
T | C | 135 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0086others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.51-1951T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853069 | ||||||
| chr6:125853482
|
G | A | 16 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(13): Show | 16 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.51-1538G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853482 | ||||||
| chr6:125853528
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.51-1492T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853528 | ||||||
| chr6:125853568
|
C | G | 135 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0086others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.51-1452C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853568 | ||||||
| chr6:125853601
|
A | G | 173 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(170): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.51-1419A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853601 | ||||||
| chr6:125853620
|
A | G | 3 | a0002c0002t0001g0180a0002c0002t0002g0179a0002c0002t0002g0219 | 3 | HG00099.hp1 HG01109.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.51-1400A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853620 | ||||||
| chr6:125853673
|
G | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG00280.hp1 HG00733.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.51-1347G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853673 | ||||||
| chr6:125853713
|
A | C | 135 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0086others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.51-1307A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853713 | ||||||
| chr6:125853939
|
A | G | 198 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(195): Show | 198 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.51-1081A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853939 | ||||||
| chr6:125853947
|
G | C | 135 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0086others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.51-1073G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853947 | ||||||
| chr6:125853954
|
A | G | 5 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.51-1066A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853954 | ||||||
| chr6:125854039
|
A | T | 73 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0086others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.51-981A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125854039 | ||||||
| chr6:125854339
|
C | G | 1 | a0003c0003t0003g0029 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.51-681C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125854339 | ||||||
| chr6:125854447
|
C | T | 1 | a0002c0002t0001g0095 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.51-573C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125854447 | ||||||
| chr6:125854737
|
A | G | 4 | a0001c0001t0001g0073a0001c0001t0001g0167a0001c0001t0001g0226others(1): Show | 4 | NA18943.hp2 NA18950.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-283A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125854737 | ||||||
| chr6:125854948
|
C | T | 2 | a0001c0009t0022g0263a0002c0002t0014g0014 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.51-72C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125854948 | ||||||
| chr6:125855281
|
A | T | 1 | a0001c0001t0002g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.271+41A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855281 | ||||||
| chr6:125855424
|
T | C | 1 | a0008c0012t0003g0113 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.271+184T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855424 | ||||||
| chr6:125855544
|
C | A | 23 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(20): Show | 23 | HG00639.hp2 HG01891.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.271+304C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855544 | ||||||
| chr6:125855646
|
G | T | 1 | a0002c0002t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.271+406G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855646 | ||||||
| chr6:125855650
|
AAAAAAC | A | 4 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+426_271+431del others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125855650 | |||||
| chr6:125855651
|
A | C | 1 | a0002c0002t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.271+411A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855651 | ||||||
| chr6:125855672
|
C | CA | 6 | a0001c0001t0001g0258a0001c0001t0002g0217a0001c0001t0017g0247others(3): Show | 6 | HG01175.hp2 HG01981.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.271+441dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125855672 | |||||
| chr6:125855673
|
A | C | 1 | a0001c0001t0009g0188 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.271+433A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855673 | ||||||
| chr6:125855828
|
T | C | 4 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+588T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855828 | ||||||
| chr6:125855874
|
G | A | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.271+634G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855874 | ||||||
| chr6:125856189
|
G | A | 1 | a0001c0001t0007g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.271+949G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856189 | ||||||
| chr6:125856261
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.271+1021A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856261 | ||||||
| chr6:125856298
|
A | G | 162 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.271+1058A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856298 | ||||||
| chr6:125856362
|
GT | G | 100 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.271+1130delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125856362 | |||||
| chr6:125856454
|
A | G | 2 | a0003c0003t0003g0139a0003c0003t0003g0140 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.271+1214A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856454 | ||||||
| chr6:125856609
|
C | T | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.271+1369C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856609 | ||||||
| chr6:125856786
|
C | G | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.271+1546C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856786 | ||||||
| chr6:125856831
|
T | C | 11 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.271+1591T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856831 | ||||||
| chr6:125856882
|
G | A | 2 | a0003c0003t0003g0147a0003c0003t0003g0148 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.271+1642G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856882 | ||||||
| chr6:125857000
|
G | A | 62 | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.271+1760G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857000 | ||||||
| chr6:125857288
|
A | T | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.271+2048A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857288 | ||||||
| chr6:125857292
|
C | T | 11 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.271+2052C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857292 | ||||||
| chr6:125857428
|
CAT | C | 12 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0004g0017others(9): Show | 12 | HG00741.hp2 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+2201_271+2202d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125857428 | |||||
| chr6:125857439
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.271+2199A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857439 | ||||||
| chr6:125857439
|
ATAT | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.271+2201_271+2203d others(5): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125857439 | |||||
| chr6:125857441
|
A | T | 77 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0086others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.271+2201A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857441 | ||||||
| chr6:125857441
|
AT | A | 61 | a0001c0001t0001g0005a0001c0001t0004g0007a0001c0001t0004g0008others(58): Show | 61 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.271+2212delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125857441 | |||||
| chr6:125857441
|
ATT | A | 6 | a0002c0002t0001g0146a0002c0002t0007g0003a0003c0003t0003g0004others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.271+2211_271+2212d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125857441 | |||||
| chr6:125857443
|
T | A | 26 | a0001c0009t0022g0263a0002c0002t0001g0256a0002c0002t0002g0068others(23): Show | 26 | HG00280.hp2 HG00544.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.271+2203T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857443 | ||||||
| chr6:125857545
|
C | T | 3 | a0002c0002t0001g0091a0002c0002t0001g0095a0002c0002t0002g0076 | 3 | HG01123.hp1 HG01261.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.271+2305C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857545 | ||||||
| chr6:125857859
|
T | G | 28 | a0002c0002t0001g0256a0002c0002t0004g0205a0003c0003t0003g0050others(25): Show | 28 | HG00280.hp2 HG01106.hp2 HG02027.hp2 others(25): Show |
intron_variant | MODIFIER | c.271+2619T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857859 | ||||||
| chr6:125857878
|
A | G | 1 | a0002c0002t0008g0052 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.271+2638A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857878 | ||||||
| chr6:125857924
|
G | A | 1 | a0001c0001t0002g0228 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.271+2684G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857924 | ||||||
| chr6:125857963
|
G | A | 1 | a0003c0003t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.271+2723G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857963 | ||||||
| chr6:125857965
|
G | A | 73 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0086others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.271+2725G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857965 | ||||||
| chr6:125858213
|
A | G | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.271+2973A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125858213 | ||||||
| chr6:125858231
|
T | C | 1 | a0001c0010t0005g0161 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271+2991T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125858231 | ||||||
| chr6:125858416
|
A | T | 2 | a0003c0003t0003g0139a0003c0003t0003g0140 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.271+3176A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125858416 | ||||||
| chr6:125858698
|
T | C | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.271+3458T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125858698 | ||||||
| chr6:125859061
|
A | C | 1 | a0001c0010t0005g0161 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271+3821A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125859061 | ||||||
| chr6:125859485
|
G | T | 89 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.271+4245G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125859485 | ||||||
| chr6:125859787
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.271+4547T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125859787 | ||||||
| chr6:125860114
|
G | A | 1 | a0001c0001t0006g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.271+4874G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860114 | ||||||
| chr6:125860145
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.271+4905G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860145 | ||||||
| chr6:125860473
|
G | A | 1 | a0002c0002t0005g0253 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.271+5233G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860473 | ||||||
| chr6:125860559
|
G | A | 1 | a0002c0002t0005g0253 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.271+5319G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860559 | ||||||
| chr6:125860701
|
C | T | 2 | a0001c0001t0026g0261a0004c0013t0013g0264 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+5461C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860701 | ||||||
| chr6:125860714
|
A | G | 2 | a0002c0002t0007g0003a0003c0003t0003g0004 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.271+5474A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860714 | ||||||
| chr6:125860810
|
T | C | 88 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.271+5570T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860810 | ||||||
| chr6:125861081
|
T | A | 2 | a0002c0002t0001g0152a0002c0002t0007g0153 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.271+5841T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861081 | ||||||
| chr6:125861265
|
A | G | 1 | a0002c0002t0005g0253 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.271+6025A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861265 | ||||||
| chr6:125861416
|
G | A | 4 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+6176G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861416 | ||||||
| chr6:125861464
|
T | A | 4 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+6224T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861464 | ||||||
| chr6:125861898
|
G | A | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.271+6658G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861898 | ||||||
| chr6:125861898
|
GTGGTGGC others(4285): Show |
G | 62 | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.271+6679_272-8679d others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125861898 | |||||
| chr6:125861901
|
G | A | 2 | a0001c0001t0001g0045a0001c0007t0001g0046 | 2 | HG01074.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.271+6661G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861901 | ||||||
| chr6:125862037
|
C | CA | 22 | a0001c0001t0004g0010a0002c0002t0001g0081a0002c0002t0001g0091others(19): Show | 22 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.271+6824dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125862037 | |||||
| chr6:125862037
|
CA | C | 23 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0002g0132others(20): Show | 23 | HG00323.hp1 HG00741.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.271+6824delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125862037 | |||||
| chr6:125862037
|
CAAAAAA | C | 16 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(13): Show | 16 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.271+6819_271+6824d others(8): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125862037 | |||||
| chr6:125862037
|
CAAAAAAA others(2): Show |
C | 70 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0086others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.271+6816_271+6824d others(11): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125862037 | |||||
| chr6:125862037
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0178 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.271+6815_271+6824d others(12): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125862037 | |||||
| chr6:125862059
|
A | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.271+6819A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125862059 | ||||||
| chr6:125862093
|
A | G | 3 | a0002c0002t0002g0162a0002c0002t0002g0163a0002c0002t0002g0255 | 3 | NA18951.hp1 NA18963.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.271+6853A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125862093 | ||||||
| chr6:125862539
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.271+7299G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125862539 | ||||||
| chr6:125862597
|
T | C | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.271+7357T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125862597 | ||||||
| chr6:125862638
|
T | C | 1 | a0001c0001t0004g0039 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.271+7398T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125862638 | ||||||
| chr6:125863076
|
G | T | 2 | a0001c0001t0026g0261a0004c0013t0013g0264 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+7836G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125863076 | ||||||
| chr6:125863205
|
C | T | 1 | a0002c0002t0011g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.271+7965C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125863205 | ||||||
| chr6:125863265
|
G | A | 2 | a0001c0001t0006g0259a0001c0001t0006g0260 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.271+8025G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125863265 | ||||||
| chr6:125863610
|
GGAAAAAT others(20): Show |
G | 1 | a0001c0001t0004g0013 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.271+8371_271+8397d others(29): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125863610 | ||||||
| chr6:125864013
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0251 | 2 | NA18939.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.271+8773G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864013 | ||||||
| chr6:125864039
|
T | C | 174 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.271+8799T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864039 | ||||||
| chr6:125864063
|
A | G | 4 | a0002c0002t0001g0094a0002c0002t0001g0152a0002c0002t0001g0229others(1): Show | 4 | HG00323.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+8823A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864063 | ||||||
| chr6:125864171
|
G | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.271+8931G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864171 | ||||||
| chr6:125864391
|
T | G | 2 | a0001c0001t0026g0261a0004c0013t0013g0264 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+9151T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864391 | ||||||
| chr6:125864702
|
G | A | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.271+9462G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864702 | ||||||
| chr6:125865328
|
G | C | 25 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(22): Show | 25 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.272-9561G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125865328 | ||||||
| chr6:125865488
|
C | T | 2 | a0001c0001t0006g0259a0001c0001t0006g0260 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.272-9401C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125865488 | ||||||
| chr6:125865694
|
C | G | 1 | a0002c0002t0002g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.272-9195C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125865694 | ||||||
| chr6:125865839
|
T | TTTTCTTT others(5): Show |
1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.272-9038_272-9027d others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125865839 | |||||
| chr6:125865942
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.272-8947C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125865942 | ||||||
| chr6:125866011
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG00140.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.272-8878A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866011 | ||||||
| chr6:125866062
|
T | G | 32 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(29): Show | 32 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.272-8827T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866062 | ||||||
| chr6:125866338
|
GA | G | 6 | a0002c0002t0007g0003a0002c0002t0014g0014a0002c0008t0015g0262others(3): Show | 6 | HG02615.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.272-8541delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125866338 | |||||
| chr6:125866439
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.272-8450A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866439 | ||||||
| chr6:125866487
|
T | C | 7 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0005g0006others(4): Show | 7 | HG00741.hp2 HG01884.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.272-8402T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866487 | ||||||
| chr6:125866550
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.272-8339G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866550 | ||||||
| chr6:125866610
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.272-8279A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866610 | ||||||
| chr6:125866712
|
A | T | 1 | a0001c0001t0004g0013 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.272-8177A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866712 | ||||||
| chr6:125866973
|
T | A | 31 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(28): Show | 31 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.272-7916T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866973 | ||||||
| chr6:125867098
|
A | T | 31 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(28): Show | 31 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.272-7791A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867098 | ||||||
| chr6:125867099
|
T | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0177a0001c0001t0001g0239others(29): Show | 32 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.272-7790T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867099 | ||||||
| chr6:125867157
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0005g0016 | 2 | HG00741.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.272-7732C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867157 | ||||||
| chr6:125867284
|
C | T | 1 | a0001c0001t0004g0013 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.272-7605C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867284 | ||||||
| chr6:125867342
|
G | C | 62 | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.272-7547G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867342 | ||||||
| chr6:125867396
|
A | G | 6 | a0002c0002t0007g0003a0002c0002t0014g0014a0002c0008t0015g0262others(3): Show | 6 | HG02615.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.272-7493A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867396 | ||||||
| chr6:125867406
|
T | C | 1 | a0002c0002t0005g0253 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.272-7483T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867406 | ||||||
| chr6:125867407
|
T | A | 1 | a0002c0002t0005g0253 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.272-7482T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867407 | ||||||
| chr6:125867511
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0017g0247 | 2 | NA18949.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.272-7378G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867511 | ||||||
| chr6:125867747
|
G | A | 1 | a0001c0001t0006g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.272-7142G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867747 | ||||||
| chr6:125867843
|
G | T | 1 | a0001c0001t0007g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.272-7046G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867843 | ||||||
| chr6:125868002
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.272-6887T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868002 | ||||||
| chr6:125868026
|
C | T | 5 | a0002c0002t0007g0003a0002c0002t0014g0014a0003c0003t0003g0004others(2): Show | 5 | HG02615.hp1 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.272-6863C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868026 | ||||||
| chr6:125868102
|
A | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0043others(1): Show | 4 | HG00323.hp2 HG00738.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-6787A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868102 | ||||||
| chr6:125868155
|
A | T | 3 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0011g0157 | 3 | HG02055.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.272-6734A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868155 | ||||||
| chr6:125868188
|
A | C | 3 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0024 | 3 | NA18985.hp2 NA19068.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.272-6701A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868188 | ||||||
| chr6:125868295
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.272-6594G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868295 | ||||||
| chr6:125868501
|
A | G | 8 | a0002c0002t0002g0062a0002c0002t0002g0063a0002c0002t0002g0064others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.272-6388A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868501 | ||||||
| chr6:125868513
|
A | G | 4 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.272-6376A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868513 | ||||||
| chr6:125868751
|
A | G | 2 | a0002c0002t0002g0015a0002c0002t0002g0032 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.272-6138A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868751 | ||||||
| chr6:125868841
|
T | A | 1 | a0001c0001t0001g0216 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.272-6048T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868841 | ||||||
| chr6:125868857
|
T | A | 7 | a0002c0002t0002g0108a0002c0002t0002g0144a0002c0002t0002g0145others(4): Show | 7 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.272-6032T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868857 | ||||||
| chr6:125868914
|
G | A | 1 | a0001c0001t0024g0150 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.272-5975G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868914 | ||||||
| chr6:125869061
|
C | T | 25 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(22): Show | 25 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.272-5828C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869061 | ||||||
| chr6:125869207
|
C | G | 1 | a0008c0012t0003g0113 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.272-5682C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869207 | ||||||
| chr6:125869280
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.272-5609C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869280 | ||||||
| chr6:125869329
|
C | A | 1 | a0002c0002t0005g0253 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.272-5560C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869329 | ||||||
| chr6:125869407
|
T | C | 3 | a0002c0002t0014g0014a0003c0003t0003g0033a0003c0003t0003g0034 | 3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.272-5482T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869407 | ||||||
| chr6:125869442
|
C | G | 88 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(85): Show | 88 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.272-5447C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869442 | ||||||
| chr6:125869748
|
A | G | 74 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.272-5141A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869748 | ||||||
| chr6:125869794
|
C | T | 3 | a0001c0001t0006g0048a0001c0001t0006g0268a0002c0002t0011g0047 | 3 | HG02257.hp2 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.272-5095C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869794 | ||||||
| chr6:125870057
|
C | T | 25 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(22): Show | 25 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.272-4832C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870057 | ||||||
| chr6:125870074
|
A | G | 25 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(22): Show | 25 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.272-4815A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870074 | ||||||
| chr6:125870122
|
G | A | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.272-4767G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870122 | ||||||
| chr6:125870248
|
C | T | 93 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(90): Show | 93 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.272-4641C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870248 | ||||||
| chr6:125870587
|
T | C | 200 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(197): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.272-4302T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870587 | ||||||
| chr6:125870650
|
C | G | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.272-4239C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870650 | ||||||
| chr6:125870888
|
C | T | 74 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.272-4001C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870888 | ||||||
| chr6:125870890
|
C | T | 1 | a0002c0002t0001g0081 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.272-3999C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870890 | ||||||
| chr6:125871014
|
A | G | 32 | a0001c0001t0001g0005a0001c0001t0001g0177a0001c0001t0001g0239others(29): Show | 32 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.272-3875A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125871014 | ||||||
| chr6:125871277
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.272-3612G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125871277 | ||||||
| chr6:125871281
|
GAGCACCA others(6): Show |
G | 93 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(90): Show | 93 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.272-3602_272-3590d others(15): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125871281 | |||||
| chr6:125871336
|
G | A | 2 | a0002c0002t0007g0003a0003c0003t0003g0004 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.272-3553G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125871336 | ||||||
| chr6:125871448
|
C | G | 1 | a0002c0002t0002g0069 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.272-3441C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125871448 | ||||||
| chr6:125871998
|
GA | G | 84 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(81): Show | 84 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.272-2871delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125871998 | |||||
| chr6:125871999
|
A | G | 1 | a0002c0002t0002g0215 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.272-2890A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125871999 | ||||||
| chr6:125872066
|
A | G | 1 | a0002c0002t0002g0099 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.272-2823A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872066 | ||||||
| chr6:125872273
|
C | T | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.272-2616C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872273 | ||||||
| chr6:125872343
|
A | G | 3 | a0002c0002t0014g0014a0003c0003t0003g0033a0003c0003t0003g0034 | 3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.272-2546A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872343 | ||||||
| chr6:125872413
|
C | G | 1 | a0002c0002t0002g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.272-2476C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872413 | ||||||
| chr6:125872673
|
A | G | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.272-2216A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872673 | ||||||
| chr6:125872962
|
G | C | 2 | a0001c0001t0004g0037a0001c0001t0004g0039 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.272-1927G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872962 | ||||||
| chr6:125872963
|
T | C | 5 | a0002c0002t0007g0003a0002c0002t0014g0014a0003c0003t0003g0004others(2): Show | 5 | HG02615.hp1 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.272-1926T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872963 | ||||||
| chr6:125873143
|
G | A | 7 | a0002c0002t0002g0108a0002c0002t0002g0144a0002c0002t0002g0145others(4): Show | 7 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.272-1746G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125873143 | ||||||
| chr6:125873626
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.272-1263G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125873626 | ||||||
| chr6:125873688
|
A | G | 1 | a0002c0002t0002g0163 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.272-1201A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125873688 | ||||||
| chr6:125874274
|
G | A | 1 | a0002c0002t0002g0002 | 2 | NA19079.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.272-615G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125874274 | ||||||
| chr6:125874284
|
C | T | 1 | a0003c0003t0003g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.272-605C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125874284 | ||||||
| chr6:125874297
|
C | G | 1 | a0001c0001t0004g0010 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.272-592C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125874297 | ||||||
| chr6:125874354
|
G | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.272-535G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125874354 | ||||||
| chr6:125874996
|
T | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0171a0001c0001t0001g0212others(6): Show | 9 | HG00140.hp2 HG00642.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.351+28T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125874996 | ||||||
| chr6:125875274
|
C | T | 1 | a0002c0002t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.351+306C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125875274 | ||||||
| chr6:125875903
|
C | T | 24 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(21): Show | 24 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.351+935C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125875903 | ||||||
| chr6:125876097
|
G | A | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.351+1129G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876097 | ||||||
| chr6:125876100
|
G | A | 1 | a0002c0002t0002g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.351+1132G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876100 | ||||||
| chr6:125876223
|
C | G | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.351+1255C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876223 | ||||||
| chr6:125876252
|
T | C | 1 | a0001c0001t0007g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.351+1284T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876252 | ||||||
| chr6:125876294
|
A | G | 1 | a0002c0002t0007g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.351+1326A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876294 | ||||||
| chr6:125876333
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0043others(1): Show | 4 | HG00323.hp2 HG00738.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+1365G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876333 | ||||||
| chr6:125876558
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.351+1590A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876558 | ||||||
| chr6:125876601
|
TA | T | 11 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.352-1645delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 125876601 | |||||
| chr6:125876798
|
G | A | 3 | a0002c0002t0002g0098a0002c0002t0002g0101a0002c0002t0002g0103 | 3 | NA18978.hp2 NA18982.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.352-1465G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876798 | ||||||
| chr6:125877178
|
G | C | 24 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(21): Show | 24 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.352-1085G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877178 | ||||||
| chr6:125877462
|
A | C | 1 | a0002c0002t0007g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.352-801A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877462 | ||||||
| chr6:125877536
|
A | AG | 4 | a0002c0002t0007g0003a0002c0002t0014g0014a0003c0003t0003g0033others(1): Show | 4 | HG02615.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-726dupG | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 125877536 | |||||
| chr6:125877592
|
C | T | 2 | a0002c0002t0002g0090a0002c0002t0002g0215 | 2 | HG00642.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.352-671C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877592 | ||||||
| chr6:125877923
|
G | A | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.352-340G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877923 | ||||||
| chr6:125877954
|
C | G | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.352-309C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877954 | ||||||
| chr6:125877994
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.352-269A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877994 | ||||||
| chr6:125878031
|
A | G | 1 | a0001c0001t0005g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-232A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125878031 | ||||||
| chr6:125878234
|
A | G | 1 | a0001c0001t0004g0039 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.352-29A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125878234 | ||||||
| chr6:125878563
|
G | A | 62 | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.459+193G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878563 | ||||||
| chr6:125878683
|
C | A | 1 | a0003c0003t0003g0134 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.459+313C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878683 | ||||||
| chr6:125878686
|
T | C | 1 | a0002c0002t0002g0107 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.459+316T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878686 | ||||||
| chr6:125878716
|
C | T | 62 | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.459+346C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878716 | ||||||
| chr6:125878992
|
T | A | 3 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0009t0022g0263 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.459+622T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878992 | ||||||
| chr6:125878994
|
G | T | 3 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0024 | 3 | NA18985.hp2 NA19068.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.459+624G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878994 | ||||||
| chr6:125879049
|
T | A | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+679T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879049 | ||||||
| chr6:125879129
|
T | C | 1 | a0002c0002t0002g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.459+759T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879129 | ||||||
| chr6:125879174
|
T | C | 3 | a0003c0003t0003g0105a0003c0003t0003g0138a0003c0003t0003g0142 | 3 | HG01175.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+804T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879174 | ||||||
| chr6:125879200
|
CATTGACC others(3): Show |
C | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.459+836_459+845del others(10): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr6 | 125879200 | |||||
| chr6:125879486
|
A | G | 1 | a0003c0003t0003g0117 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.459+1116A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879486 | ||||||
| chr6:125879492
|
T | A | 91 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(88): Show | 91 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.459+1122T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879492 | ||||||
| chr6:125879651
|
T | C | 1 | a0003c0003t0003g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.459+1281T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879651 | ||||||
| chr6:125879740
|
G | A | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202 | 3 | HG01167.hp1 HG01169.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.460-1350G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879740 | ||||||
| chr6:125880012
|
G | A | 197 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(194): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.460-1078G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880012 | ||||||
| chr6:125880079
|
G | T | 8 | a0001c0001t0001g0172a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | NA18944.hp2 NA18963.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-1011G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880079 | ||||||
| chr6:125880176
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.460-914G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880176 | ||||||
| chr6:125880360
|
A | T | 1 | a0005c0006t0002g0001 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.460-730A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880360 | ||||||
| chr6:125880448
|
C | T | 2 | a0001c0001t0006g0259a0001c0001t0006g0260 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.460-642C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880448 | ||||||
| chr6:125880517
|
ATATTTTA others(3): Show |
A | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.460-556_460-547del others(10): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr6 | 125880517 | |||||
| chr6:125880598
|
G | T | 3 | a0002c0002t0014g0014a0003c0003t0003g0033a0003c0003t0003g0034 | 3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.460-492G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880598 | ||||||
| chr6:125880944
|
G | A | 1 | a0002c0002t0002g0082 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.460-146G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880944 | ||||||
| chr6:125880992
|
A | G | 62 | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.460-98A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880992 | ||||||
| chr6:125881229
|
A | T | 1 | a0002c0002t0005g0253 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.573+26A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881229 | ||||||
| chr6:125881337
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.573+134G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881337 | ||||||
| chr6:125881670
|
CA | C | 10 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0240others(7): Show | 10 | HG01106.hp2 HG01243.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.573+487delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr6 | 125881670 | |||||
| chr6:125881670
|
CAA | C | 157 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(154): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.573+486_573+487del others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr6 | 125881670 | |||||
| chr6:125881670
|
CAAA | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0177a0001c0001t0001g0239others(28): Show | 31 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.573+485_573+487del others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr6 | 125881670 | |||||
| chr6:125881736
|
G | A | 197 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(194): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.573+533G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881736 | ||||||
| chr6:125881772
|
T | A | 26 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(23): Show | 26 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.573+569T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881772 | ||||||
| chr6:125881773
|
A | T | 1 | a0003c0003t0003g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.573+570A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881773 | ||||||
| chr6:125881862
|
T | C | 1 | a0002c0002t0002g0108 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.574-564T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881862 | ||||||
| chr6:125881886
|
C | T | 1 | a0002c0002t0002g0156 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.574-540C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881886 | ||||||
| chr6:125882103
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.574-323C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125882103 | ||||||
| chr6:125882105
|
C | T | 1 | a0002c0002t0002g0067 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.574-321C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125882105 | ||||||
| chr6:125882230
|
G | GA | 12 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0006g0268others(9): Show | 12 | HG01192.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.574-186dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr6 | 125882230 | |||||
| chr6:125882277
|
A | G | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.574-149A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125882277 | ||||||
| chr6:125882834
|
A | G | 1 | a0002c0002t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.699+283A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125882834 | ||||||
| chr6:125883057
|
G | C | 192 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(189): Show | 192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.699+506G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883057 | ||||||
| chr6:125883156
|
T | C | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.699+605T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883156 | ||||||
| chr6:125883187
|
C | G | 91 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(88): Show | 91 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.699+636C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883187 | ||||||
| chr6:125883263
|
A | G | 1 | a0001c0001t0005g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.699+712A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883263 | ||||||
| chr6:125883324
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.699+773G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883324 | ||||||
| chr6:125883398
|
A | G | 24 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(21): Show | 24 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.699+847A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883398 | ||||||
| chr6:125883713
|
C | CT | 6 | a0002c0002t0002g0215a0002c0002t0002g0234a0002c0002t0008g0056others(3): Show | 6 | HG00642.hp1 HG02257.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+1185dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr6 | 125883713 | |||||
| chr6:125883713
|
CT | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.699+1185delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr6 | 125883713 | |||||
| chr6:125883753
|
C | G | 1 | a0002c0002t0002g0215 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.699+1202C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883753 | ||||||
| chr6:125883902
|
A | G | 1 | a0002c0002t0010g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.700-1257A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883902 | ||||||
| chr6:125884010
|
C | T | 1 | a0001c0001t0016g0232 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.700-1149C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884010 | ||||||
| chr6:125884171
|
T | C | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.700-988T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884171 | ||||||
| chr6:125884319
|
A | G | 2 | a0002c0002t0002g0063a0002c0002t0002g0079 | 2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.700-840A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884319 | ||||||
| chr6:125884330
|
T | C | 4 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0006g0268others(1): Show | 4 | HG02257.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.700-829T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884330 | ||||||
| chr6:125884443
|
T | G | 74 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.700-716T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884443 | ||||||
| chr6:125884799
|
C | A | 1 | a0001c0001t0001g0240 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.700-360C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884799 | ||||||
| chr6:125884863
|
G | A | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.700-296G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884863 | ||||||
| chr6:125884897
|
A | G | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.700-262A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884897 | ||||||
| chr6:125884898
|
C | G | 3 | a0002c0002t0014g0014a0003c0003t0003g0033a0003c0003t0003g0034 | 3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.700-261C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884898 | ||||||
| chr6:125884921
|
T | C | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.700-238T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884921 | ||||||
| chr6:125885508
|
A | G | 3 | a0002c0002t0014g0014a0003c0003t0003g0033a0003c0003t0003g0034 | 3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.884+165A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885508 | ||||||
| chr6:125885517
|
A | G | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.884+174A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885517 | ||||||
| chr6:125885542
|
A | C | 62 | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.884+199A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885542 | ||||||
| chr6:125885799
|
G | A | 197 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(194): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.884+456G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885799 | ||||||
| chr6:125885871
|
T | C | 1 | a0003c0003t0003g0148 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.884+528T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885871 | ||||||
| chr6:125885917
|
C | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.884+574C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885917 | ||||||
| chr6:125886040
|
C | T | 24 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(21): Show | 24 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.884+697C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886040 | ||||||
| chr6:125886061
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.884+718A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886061 | ||||||
| chr6:125886080
|
A | G | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.884+737A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886080 | ||||||
| chr6:125886144
|
C | T | 1 | a0002c0002t0004g0205 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.884+801C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886144 | ||||||
| chr6:125886160
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG00280.hp1 HG00733.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.884+817A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886160 | ||||||
| chr6:125886164
|
G | GA | 75 | a0001c0001t0001g0083a0001c0001t0001g0202a0001c0001t0005g0006others(72): Show | 75 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.884+839dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 125886164 | |||||
| chr6:125886164
|
G | GAA | 20 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0042others(17): Show | 20 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.884+838_884+839dup others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 125886164 | |||||
| chr6:125886164
|
G | GAAA | 6 | a0001c0001t0001g0041a0001c0001t0001g0168a0001c0001t0002g0038others(3): Show | 6 | HG00741.hp1 HG01243.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.884+837_884+839dup others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 125886164 | |||||
| chr6:125886771
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.884+1428A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886771 | ||||||
| chr6:125886903
|
C | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0177a0001c0001t0001g0239others(28): Show | 31 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.884+1560C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886903 | ||||||
| chr6:125886910
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0044 | 2 | HG00738.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.884+1567A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886910 | ||||||
| chr6:125887112
|
C | T | 1 | a0003c0003t0003g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.884+1769C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125887112 | ||||||
| chr6:125887411
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.885-1528A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125887411 | ||||||
| chr6:125887883
|
A | G | 62 | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.885-1056A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125887883 | ||||||
| chr6:125888099
|
G | A | 90 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(87): Show | 90 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.885-840G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888099 | ||||||
| chr6:125888267
|
A | T | 1 | a0001c0001t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.885-672A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888267 | ||||||
| chr6:125888315
|
G | A | 1 | a0003c0003t0003g0206 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.885-624G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888315 | ||||||
| chr6:125888386
|
A | C | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.885-553A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888386 | ||||||
| chr6:125888442
|
T | G | 1 | a0003c0003t0003g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.885-497T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888442 | ||||||
| chr6:125888505
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0007g0080 | 2 | NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.885-434T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888505 | ||||||
| chr6:125888530
|
ATGTT | A | 62 | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.885-406_885-403del others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 125888530 | |||||
| chr6:125888599
|
T | C | 2 | a0002c0002t0002g0090a0002c0002t0002g0215 | 2 | HG00642.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.885-340T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888599 | ||||||
| chr6:125888680
|
T | C | 1 | a0002c0002t0001g0081 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.885-259T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888680 | ||||||
| chr6:125890040
|
T | G | 1 | a0001c0001t0001g0222 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1927+59T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890040 | ||||||
| chr6:125890168
|
G | A | 266 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1927+187G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890168 | ||||||
| chr6:125890265
|
G | A | 1 | a0004c0005t0003g0020 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1927+284G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890265 | ||||||
| chr6:125890416
|
A | T | 2 | a0002c0002t0002g0144a0002c0002t0002g0145 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1928-226A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890416 | ||||||
| chr6:125890513
|
C | T | 62 | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.1928-129C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890513 | ||||||
| chr6:125890629
|
G | A | 1 | a0002c0002t0001g0180 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1928-13G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890629 | ||||||
| chr6:125891106
|
T | C | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2096+296T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891106 | ||||||
| chr6:125891552
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG00280.hp1 HG00733.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.2096+742A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891552 | ||||||
| chr6:125891768
|
T | G | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2096+958T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891768 | ||||||
| chr6:125891771
|
T | C | 3 | a0002c0002t0014g0014a0003c0003t0003g0033a0003c0003t0003g0034 | 3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2096+961T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891771 | ||||||
| chr6:125891825
|
C | A | 1 | a0001c0001t0007g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2096+1015C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891825 | ||||||
| chr6:125891951
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0005g0238 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2096+1141G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891951 | ||||||
| chr6:125892452
|
C | T | 1 | a0003c0003t0003g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2096+1642C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892452 | ||||||
| chr6:125892566
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2096+1756C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892566 | ||||||
| chr6:125892589
|
G | A | 12 | a0002c0002t0001g0025a0002c0002t0001g0059a0002c0002t0001g0131others(9): Show | 12 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.2096+1779G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892589 | ||||||
| chr6:125892630
|
C | T | 2 | a0002c0002t0002g0162a0002c0002t0002g0255 | 2 | NA18963.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2096+1820C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892630 | ||||||
| chr6:125892653
|
G | A | 1 | a0001c0001t0009g0186 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2096+1843G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892653 | ||||||
| chr6:125892765
|
C | T | 1 | a0003c0003t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2096+1955C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892765 | ||||||
| chr6:125892951
|
C | G | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2096+2141C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892951 | ||||||
| chr6:125892979
|
T | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0177a0001c0001t0001g0239others(28): Show | 31 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.2096+2169T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892979 | ||||||
| chr6:125893263
|
C | T | 3 | a0002c0002t0014g0014a0003c0003t0003g0033a0003c0003t0003g0034 | 3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2096+2453C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893263 | ||||||
| chr6:125893446
|
TA | T | 3 | a0002c0002t0014g0014a0003c0003t0003g0033a0003c0003t0003g0034 | 3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2096+2641delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125893446 | |||||
| chr6:125893478
|
A | C | 74 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.2096+2668A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893478 | ||||||
| chr6:125893589
|
G | T | 1 | a0001c0001t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2096+2779G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893589 | ||||||
| chr6:125893592
|
C | T | 63 | a0002c0002t0001g0025a0002c0002t0001g0059a0002c0002t0001g0131others(60): Show | 63 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(60): Show |
intron_variant | MODIFIER | c.2096+2782C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893592 | ||||||
| chr6:125893666
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2096+2856C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893666 | ||||||
| chr6:125893846
|
C | T | 3 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0006g0268 | 3 | HG02257.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2096+3036C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893846 | ||||||
| chr6:125893859
|
C | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2096+3049C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893859 | ||||||
| chr6:125893903
|
A | G | 3 | a0002c0002t0014g0014a0003c0003t0003g0033a0003c0003t0003g0034 | 3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2096+3093A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893903 | ||||||
| chr6:125893955
|
T | C | 63 | a0002c0002t0001g0025a0002c0002t0001g0059a0002c0002t0001g0131others(60): Show | 63 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(60): Show |
intron_variant | MODIFIER | c.2096+3145T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893955 | ||||||
| chr6:125894004
|
C | T | 1 | a0002c0002t0002g0063 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2096+3194C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894004 | ||||||
| chr6:125894051
|
A | T | 75 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.2096+3241A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894051 | ||||||
| chr6:125894150
|
C | T | 75 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.2096+3340C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894150 | ||||||
| chr6:125894275
|
G | A | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2096+3465G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894275 | ||||||
| chr6:125894329
|
G | A | 1 | a0003c0003t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2096+3519G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894329 | ||||||
| chr6:125894340
|
G | C | 74 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.2096+3530G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894340 | ||||||
| chr6:125894764
|
T | G | 1 | a0001c0001t0006g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2096+3954T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894764 | ||||||
| chr6:125894879
|
G | A | 169 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.2096+4069G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894879 | ||||||
| chr6:125894901
|
C | A | 67 | a0001c0001t0001g0177a0001c0001t0001g0239a0001c0001t0005g0006others(64): Show | 67 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.2096+4091C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894901 | ||||||
| chr6:125894985
|
T | A | 1 | a0001c0001t0005g0085 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2096+4175T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894985 | ||||||
| chr6:125895006
|
G | C | 1 | a0002c0002t0002g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2096+4196G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895006 | ||||||
| chr6:125895043
|
A | G | 4 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2096+4233A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895043 | ||||||
| chr6:125895229
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2096+4419G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895229 | ||||||
| chr6:125895257
|
C | G | 94 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0075others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2096+4447C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895257 | ||||||
| chr6:125895961
|
A | G | 1 | a0001c0001t0016g0232 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2096+5151A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895961 | ||||||
| chr6:125895965
|
A | ATG | 5 | a0001c0001t0002g0038a0002c0002t0001g0091a0002c0002t0001g0095others(2): Show | 5 | HG01123.hp1 HG01243.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.2096+5179_2096+518 others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125895965 | |||||
| chr6:125895965
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0092 | 3 | HG02145.hp2 HG02293.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2096+5155A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895965 | ||||||
| chr6:125895965
|
ATG | A | 53 | a0001c0001t0026g0261a0002c0002t0010g0133a0002c0002t0010g0141others(50): Show | 53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2096+5179_2096+518 others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125895965 | |||||
| chr6:125895965
|
ATGTG | A | 14 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159others(11): Show | 14 | HG01891.hp1 HG02027.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2096+5177_2096+518 others(8): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125895965 | |||||
| chr6:125895981
|
G | C | 1 | a0002c0002t0007g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2096+5171G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895981 | ||||||
| chr6:125896142
|
G | A | 1 | a0002c0002t0004g0205 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2096+5332G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125896142 | ||||||
| chr6:125896176
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2096+5366T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125896176 | ||||||
| chr6:125896446
|
G | T | 1 | a0002c0002t0007g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2096+5636G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125896446 | ||||||
| chr6:125896540
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2096+5730C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125896540 | ||||||
| chr6:125897053
|
A | G | 3 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0006g0268 | 3 | HG02257.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2096+6243A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897053 | ||||||
| chr6:125897454
|
T | C | 209 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(206): Show | 209 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.2096+6644T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897454 | ||||||
| chr6:125897696
|
T | G | 1 | a0003c0003t0018g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2096+6886T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897696 | ||||||
| chr6:125897765
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2096+6955C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897765 | ||||||
| chr6:125897815
|
C | G | 173 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(170): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2096+7005C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897815 | ||||||
| chr6:125897900
|
T | C | 3 | a0002c0002t0010g0133a0002c0002t0010g0141a0003c0003t0003g0004 | 3 | HG02572.hp1 HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2096+7090T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897900 | ||||||
| chr6:125898119
|
C | G | 2 | a0002c0002t0002g0087a0002c0002t0002g0234 | 2 | HG00735.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2096+7309C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125898119 | ||||||
| chr6:125898248
|
G | T | 52 | a0002c0002t0010g0133a0002c0002t0010g0141a0003c0003t0003g0004others(49): Show | 52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2096+7438G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125898248 | ||||||
| chr6:125898582
|
A | G | 10 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(7): Show | 10 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2096+7772A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125898582 | ||||||
| chr6:125898680
|
C | G | 63 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(60): Show | 63 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(60): Show |
intron_variant | MODIFIER | c.2096+7870C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125898680 | ||||||
| chr6:125898850
|
A | G | 3 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0024 | 3 | NA18985.hp2 NA19068.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2096+8040A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125898850 | ||||||
| chr6:125899077
|
A | G | 77 | a0001c0001t0001g0054a0001c0001t0001g0075a0001c0001t0001g0083others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.2096+8267A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125899077 | ||||||
| chr6:125899709
|
C | T | 63 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(60): Show | 63 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(60): Show |
intron_variant | MODIFIER | c.2096+8899C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125899709 | ||||||
| chr6:125899843
|
A | G | 1 | a0002c0002t0002g0077 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2096+9033A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125899843 | ||||||
| chr6:125899862
|
G | A | 91 | a0001c0001t0001g0054a0001c0001t0001g0075a0001c0001t0001g0083others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2096+9052G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125899862 | ||||||
| chr6:125900070
|
G | C | 1 | a0001c0001t0001g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2096+9260G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900070 | ||||||
| chr6:125900373
|
A | G | 1 | a0002c0002t0002g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2096+9563A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900373 | ||||||
| chr6:125900385
|
A | C | 3 | a0002c0002t0010g0133a0002c0002t0010g0141a0003c0003t0003g0004 | 3 | HG02572.hp1 HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2096+9575A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900385 | ||||||
| chr6:125900455
|
G | A | 12 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(9): Show | 12 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2096+9645G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900455 | ||||||
| chr6:125900611
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2096+9801C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900611 | ||||||
| chr6:125900676
|
G | A | 1 | a0002c0002t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2096+9866G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900676 | ||||||
| chr6:125901149
|
C | T | 1 | a0002c0002t0007g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2096+10339C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901149 | ||||||
| chr6:125901286
|
G | A | 1 | a0001c0001t0002g0228 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2096+10476G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901286 | ||||||
| chr6:125901371
|
C | G | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2096+10561C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901371 | ||||||
| chr6:125901440
|
G | A | 2 | a0002c0002t0014g0014a0002c0008t0015g0262 | 2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2096+10630G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901440 | ||||||
| chr6:125901466
|
G | C | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2096+10656G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901466 | ||||||
| chr6:125901541
|
C | G | 1 | a0003c0003t0003g0252 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2096+10731C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901541 | ||||||
| chr6:125901571
|
A | T | 1 | a0001c0001t0007g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2096+10761A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901571 | ||||||
| chr6:125901886
|
G | A | 115 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2096+11076G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901886 | ||||||
| chr6:125901927
|
G | A | 105 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2096+11117G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901927 | ||||||
| chr6:125902412
|
G | A | 54 | a0002c0002t0010g0133a0002c0002t0010g0141a0003c0003t0003g0004others(51): Show | 54 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(51): Show |
intron_variant | MODIFIER | c.2096+11602G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902412 | ||||||
| chr6:125902481
|
G | GT | 6 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2096+11685dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125902481 | |||||
| chr6:125902496
|
A | T | 203 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(200): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.2096+11686A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902496 | ||||||
| chr6:125902508
|
G | T | 1 | a0002c0002t0002g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2096+11698G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902508 | ||||||
| chr6:125902571
|
G | A | 1 | a0001c0001t0004g0031 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2096+11761G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902571 | ||||||
| chr6:125902757
|
G | C | 53 | a0002c0002t0010g0133a0002c0002t0010g0141a0003c0003t0003g0004others(50): Show | 53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2096+11947G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902757 | ||||||
| chr6:125902798
|
G | A | 92 | a0001c0001t0001g0054a0001c0001t0001g0075a0001c0001t0001g0083others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.2096+11988G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902798 | ||||||
| chr6:125902879
|
G | T | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2096+12069G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902879 | ||||||
| chr6:125903125
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2097-12208G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903125 | ||||||
| chr6:125903570
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0092 | 3 | HG02145.hp2 HG02293.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2097-11763A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903570 | ||||||
| chr6:125903709
|
C | CT | 94 | a0001c0001t0001g0054a0001c0001t0001g0075a0001c0001t0001g0083others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2097-11610dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125903709 | |||||
| chr6:125903722
|
T | C | 10 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(7): Show | 10 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2097-11611T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903722 | ||||||
| chr6:125903793
|
C | T | 1 | a0002c0002t0002g0069 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2097-11540C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903793 | ||||||
| chr6:125903825
|
C | T | 6 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2097-11508C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903825 | ||||||
| chr6:125903849
|
G | A | 1 | a0002c0002t0007g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2097-11484G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903849 | ||||||
| chr6:125904153
|
C | G | 1 | a0001c0001t0006g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2097-11180C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125904153 | ||||||
| chr6:125904288
|
G | A | 2 | a0002c0002t0010g0133a0002c0002t0010g0141 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2097-11045G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125904288 | ||||||
| chr6:125904500
|
C | A | 2 | a0003c0003t0003g0117a0003c0003t0003g0125 | 2 | NA18995.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2097-10833C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125904500 | ||||||
| chr6:125904727
|
C | T | 1 | a0003c0003t0003g0207 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2097-10606C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125904727 | ||||||
| chr6:125905136
|
A | C | 2 | a0001c0001t0009g0186a0001c0001t0009g0188 | 2 | NA18960.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2097-10197A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905136 | ||||||
| chr6:125905238
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2097-10095G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905238 | ||||||
| chr6:125905253
|
A | AT | 79 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(76): Show | 79 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.2097-10060dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125905253 | |||||
| chr6:125905253
|
AT | A | 5 | a0001c0001t0004g0012a0001c0001t0006g0048a0002c0002t0002g0102others(2): Show | 5 | HG02723.hp1 HG03239.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.2097-10060delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125905253 | |||||
| chr6:125905330
|
C | A | 54 | a0002c0002t0010g0133a0002c0002t0010g0141a0003c0003t0003g0004others(51): Show | 54 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(51): Show |
intron_variant | MODIFIER | c.2097-10003C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905330 | ||||||
| chr6:125905513
|
C | T | 10 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(7): Show | 10 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2097-9820C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905513 | ||||||
| chr6:125905681
|
A | G | 64 | a0001c0001t0001g0005a0001c0001t0006g0036a0001c0001t0006g0048others(61): Show | 64 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(61): Show |
intron_variant | MODIFIER | c.2097-9652A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905681 | ||||||
| chr6:125905701
|
C | G | 1 | a0003c0003t0003g0126 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2097-9632C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905701 | ||||||
| chr6:125905975
|
G | A | 52 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(49): Show | 52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2097-9358G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905975 | ||||||
| chr6:125906246
|
G | T | 1 | a0001c0001t0004g0065 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2097-9087G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906246 | ||||||
| chr6:125906309
|
C | T | 1 | a0003c0003t0003g0117 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2097-9024C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906309 | ||||||
| chr6:125906314
|
G | A | 1 | a0002c0002t0007g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2097-9019G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906314 | ||||||
| chr6:125906610
|
G | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0159 | 3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2097-8723G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906610 | ||||||
| chr6:125906690
|
T | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2097-8643T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906690 | ||||||
| chr6:125906920
|
C | T | 2 | a0001c0001t0002g0174a0001c0001t0002g0217 | 2 | HG01069.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2097-8413C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906920 | ||||||
| chr6:125906953
|
A | G | 1 | a0001c0001t0007g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2097-8380A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906953 | ||||||
| chr6:125907082
|
A | T | 6 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2097-8251A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907082 | ||||||
| chr6:125907249
|
G | C | 172 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(169): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2097-8084G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907249 | ||||||
| chr6:125907352
|
G | C | 153 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0075others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2097-7981G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907352 | ||||||
| chr6:125907366
|
G | A | 105 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0075others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2097-7967G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907366 | ||||||
| chr6:125907387
|
G | A | 3 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0006g0268 | 3 | HG02257.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2097-7946G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907387 | ||||||
| chr6:125907389
|
C | CT | 106 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0075others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2097-7942dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125907389 | |||||
| chr6:125907399
|
A | G | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2097-7934A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907399 | ||||||
| chr6:125907440
|
C | T | 1 | a0003c0003t0003g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2097-7893C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907440 | ||||||
| chr6:125907521
|
A | G | 1 | a0001c0001t0005g0238 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2097-7812A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907521 | ||||||
| chr6:125907524
|
C | T | 2 | a0002c0002t0014g0014a0002c0008t0015g0262 | 2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2097-7809C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907524 | ||||||
| chr6:125907673
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2097-7660G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907673 | ||||||
| chr6:125907781
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2097-7552C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907781 | ||||||
| chr6:125908434
|
T | C | 172 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(169): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2097-6899T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125908434 | ||||||
| chr6:125908546
|
T | C | 1 | a0001c0001t0006g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2097-6787T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125908546 | ||||||
| chr6:125908668
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2097-6665G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125908668 | ||||||
| chr6:125908983
|
A | G | 1 | a0002c0002t0011g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2097-6350A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125908983 | ||||||
| chr6:125908988
|
GCATTCTC others(4): Show |
G | 1 | a0002c0002t0002g0179 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2097-6340_2097-633 others(15): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125908988 | |||||
| chr6:125909210
|
A | G | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2097-6123A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909210 | ||||||
| chr6:125909299
|
C | T | 199 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(196): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.2097-6034C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909299 | ||||||
| chr6:125909472
|
T | G | 4 | a0003c0003t0003g0078a0003c0003t0003g0116a0003c0003t0003g0209others(1): Show | 4 | HG02080.hp1 NA18946.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2097-5861T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909472 | ||||||
| chr6:125909644
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2097-5689A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909644 | ||||||
| chr6:125909679
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2097-5654G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909679 | ||||||
| chr6:125909740
|
G | A | 2 | a0001c0001t0001g0201a0002c0002t0002g0090 | 2 | HG02572.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2097-5593G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909740 | ||||||
| chr6:125909771
|
C | T | 1 | a0002c0002t0007g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2097-5562C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909771 | ||||||
| chr6:125909937
|
A | G | 1 | a0002c0002t0002g0099 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2097-5396A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909937 | ||||||
| chr6:125910604
|
T | G | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2097-4729T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125910604 | ||||||
| chr6:125910825
|
A | G | 24 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0010others(21): Show | 24 | HG00597.hp2 HG00639.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2097-4508A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125910825 | ||||||
| chr6:125910917
|
G | A | 158 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0075others(155): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.2097-4416G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125910917 | ||||||
| chr6:125910999
|
G | A | 52 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(49): Show | 52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2097-4334G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125910999 | ||||||
| chr6:125911031
|
G | A | 1 | a0002c0002t0002g0156 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2097-4302G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911031 | ||||||
| chr6:125911053
|
A | G | 6 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2097-4280A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911053 | ||||||
| chr6:125911072
|
G | A | 52 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(49): Show | 52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2097-4261G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911072 | ||||||
| chr6:125911302
|
C | T | 4 | a0003c0003t0003g0050a0003c0003t0003g0105a0003c0003t0003g0138others(1): Show | 4 | HG00280.hp2 HG01175.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2097-4031C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911302 | ||||||
| chr6:125911648
|
A | G | 1 | a0002c0008t0015g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2097-3685A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911648 | ||||||
| chr6:125911743
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2097-3590C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911743 | ||||||
| chr6:125911891
|
A | G | 2 | a0002c0002t0002g0053a0002c0002t0002g0082 | 2 | HG02698.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2097-3442A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911891 | ||||||
| chr6:125912186
|
C | A | 1 | a0003c0003t0003g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2097-3147C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912186 | ||||||
| chr6:125912248
|
T | A | 1 | a0001c0007t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2097-3085T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912248 | ||||||
| chr6:125912360
|
CTCCATAT | C | 51 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(48): Show | 51 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(48): Show |
intron_variant | MODIFIER | c.2097-2971_2097-296 others(11): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125912360 | |||||
| chr6:125912399
|
T | A | 1 | a0002c0002t0004g0205 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2097-2934T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912399 | ||||||
| chr6:125912545
|
G | A | 158 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0075others(155): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.2097-2788G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912545 | ||||||
| chr6:125912606
|
A | C | 1 | a0001c0001t0001g0226 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2097-2727A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912606 | ||||||
| chr6:125912651
|
G | A | 1 | a0001c0009t0022g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2097-2682G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912651 | ||||||
| chr6:125912664
|
G | A | 158 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0075others(155): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.2097-2669G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912664 | ||||||
| chr6:125913173
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2097-2160A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913173 | ||||||
| chr6:125913271
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2097-2062G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913271 | ||||||
| chr6:125913489
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2097-1844C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913489 | ||||||
| chr6:125913603
|
C | T | 2 | a0001c0001t0004g0023a0001c0001t0004g0031 | 2 | NA18982.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2097-1730C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913603 | ||||||
| chr6:125913887
|
G | A | 6 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2097-1446G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913887 | ||||||
| chr6:125913921
|
G | A | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2097-1412G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913921 | ||||||
| chr6:125914037
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2097-1296C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914037 | ||||||
| chr6:125914054
|
T | A | 1 | a0003c0003t0003g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2097-1279T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914054 | ||||||
| chr6:125914111
|
T | C | 2 | a0002c0002t0014g0014a0002c0008t0015g0262 | 2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2097-1222T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914111 | ||||||
| chr6:125914170
|
G | A | 266 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2097-1163G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914170 | ||||||
| chr6:125914275
|
T | C | 1 | a0002c0002t0001g0094 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2097-1058T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914275 | ||||||
| chr6:125914281
|
C | T | 53 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(50): Show | 53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2097-1052C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914281 | ||||||
| chr6:125914708
|
A | G | 52 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(49): Show | 52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2097-625A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914708 | ||||||
| chr6:125914720
|
A | G | 53 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(50): Show | 53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2097-613A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914720 | ||||||
| chr6:125914778
|
G | A | 2 | a0001c0001t0001g0177a0002c0002t0005g0253 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2097-555G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914778 | ||||||
| chr6:125915538
|
G | C | 5 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(2): Show | 5 | HG02257.hp2 HG02723.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244+58G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125915538 | ||||||
| chr6:125915585
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2244+105G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125915585 | ||||||
| chr6:125915660
|
A | G | 53 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(50): Show | 53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2244+180A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125915660 | ||||||
| chr6:125915978
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2244+498G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125915978 | ||||||
| chr6:125915981
|
A | G | 53 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(50): Show | 53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2244+501A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125915981 | ||||||
| chr6:125916339
|
A | G | 7 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0011others(4): Show | 7 | NA18940.hp1 NA18943.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.2244+859A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125916339 | ||||||
| chr6:125916374
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2244+894G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125916374 | ||||||
| chr6:125916428
|
G | A | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2244+948G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125916428 | ||||||
| chr6:125916759
|
A | G | 55 | a0001c0001t0001g0185a0002c0002t0001g0059a0003c0003t0003g0004others(52): Show | 55 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.2244+1279A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125916759 | ||||||
| chr6:125916837
|
A | G | 1 | a0001c0001t0001g0265 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2244+1357A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125916837 | ||||||
| chr6:125917164
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.2244+1684C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125917164 | ||||||
| chr6:125917196
|
T | TAGAATCT others(3390): Show |
1 | a0001c0001t0006g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(3401): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | |||||
| chr6:125917196
|
T | TAGAATCT others(3394): Show |
1 | a0001c0001t0006g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(3405): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | |||||
| chr6:125917196
|
T | TAGAATCT others(3393): Show |
1 | a0001c0001t0006g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(3404): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | |||||
| chr6:125917196
|
T | TAGAATCT others(3444): Show |
1 | a0001c0001t0006g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(3455): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | |||||
| chr6:125917196
|
T | TAGAATCT others(2634): Show |
1 | a0001c0001t0007g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(2645): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | |||||
| chr6:125917196
|
T | TAGAATCT others(3495): Show |
1 | a0001c0001t0006g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(3506): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | |||||
| chr6:125917400
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2244+1920A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125917400 | ||||||
| chr6:125917521
|
A | G | 12 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(9): Show | 12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.2244+2041A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125917521 | ||||||
| chr6:125917871
|
A | G | 53 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(50): Show | 53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2244+2391A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125917871 | ||||||
| chr6:125918050
|
C | T | 1 | a0002c0002t0007g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2244+2570C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918050 | ||||||
| chr6:125918246
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2245-2697T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918246 | ||||||
| chr6:125918270
|
T | C | 1 | a0003c0003t0003g0125 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2245-2673T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918270 | ||||||
| chr6:125918438
|
A | G | 1 | a0002c0002t0007g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2245-2505A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918438 | ||||||
| chr6:125918814
|
G | A | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2245-2129G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918814 | ||||||
| chr6:125918946
|
G | A | 6 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0259others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2245-1997G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918946 | ||||||
| chr6:125919094
|
G | A | 4 | a0002c0004t0002g0027a0002c0004t0002g0030a0002c0004t0002g0151others(1): Show | 4 | HG02615.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-1849G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125919094 | ||||||
| chr6:125919664
|
AAC | A | 52 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(49): Show | 52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2245-1275_2245-127 others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125919664 | |||||
| chr6:125919748
|
G | A | 52 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(49): Show | 52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2245-1195G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125919748 | ||||||
| chr6:125920588
|
G | A | 266 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2245-355G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125920588 | ||||||
| chr6:125920837
|
G | A | 1 | a0001c0001t0016g0232 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2245-106G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125920837 | ||||||
| chr6:125920858
|
C | G | 267 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(264): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2245-85C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125920858 | ||||||
| chr6:125920859
|
G | C | 267 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(264): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2245-84G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125920859 | ||||||
| chr6:125920860
|
G | A | 2 | a0001c0001t0009g0186a0001c0001t0009g0188 | 2 | NA18960.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2245-83G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125920860 | ||||||
| chr6:125921129
|
G | C | 1 | a0001c0001t0004g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2370+61G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921129 | ||||||
| chr6:125921131
|
C | G | 1 | a0001c0001t0004g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2370+63C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921131 | ||||||
| chr6:125921171
|
A | G | 1 | a0001c0001t0004g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2370+103A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921171 | ||||||
| chr6:125921327
|
T | G | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2370+259T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921327 | ||||||
| chr6:125921920
|
A | G | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2371-762A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921920 | ||||||
| chr6:125921921
|
T | A | 1 | a0001c0001t0004g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2371-761T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921921 | ||||||
| chr6:125921924
|
C | T | 1 | a0001c0001t0004g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2371-758C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921924 | ||||||
| chr6:125921982
|
G | T | 1 | a0001c0001t0004g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2371-700G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921982 | ||||||
| chr6:125922009
|
A | T | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2371-673A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125922009 | ||||||
| chr6:125922114
|
G | A | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2371-568G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125922114 | ||||||
| chr6:125922197
|
T | C | 1 | a0003c0003t0018g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2371-485T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125922197 | ||||||
| chr6:125922241
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2371-441G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125922241 | ||||||
| chr6:125922445
|
C | G | 116 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2371-237C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125922445 | ||||||
| chr6:125922839
|
G | A | 1 | a0003c0003t0003g0004 | 1 | HG02818.hp2 | splice_region_variant&intron_variant | LOW | c.2523+5G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125922839 | ||||||
| chr6:125923217
|
C | G | 1 | a0002c0002t0002g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2523+383C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923217 | ||||||
| chr6:125923362
|
G | A | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2523+528G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923362 | ||||||
| chr6:125923481
|
G | T | 2 | a0001c0009t0022g0263a0002c0002t0007g0003 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2523+647G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923481 | ||||||
| chr6:125923507
|
G | A | 2 | a0002c0002t0002g0090a0002c0002t0002g0215 | 2 | HG00642.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2523+673G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923507 | ||||||
| chr6:125923535
|
A | G | 1 | a0002c0002t0002g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2523+701A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923535 | ||||||
| chr6:125923536
|
T | C | 171 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2523+702T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923536 | ||||||
| chr6:125924301
|
A | G | 53 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(50): Show | 53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2523+1467A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125924301 | ||||||
| chr6:125924498
|
C | A | 52 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(49): Show | 52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2523+1664C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125924498 | ||||||
| chr6:125924699
|
C | A | 52 | a0003c0003t0003g0004a0003c0003t0003g0018a0003c0003t0003g0028others(49): Show | 52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2523+1865C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125924699 | ||||||
| chr6:125924772
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2523+1938G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125924772 | ||||||
| chr6:125924825
|
ACT | A | 3 | a0001c0001t0006g0259a0001c0001t0006g0260a0001c0001t0006g0268 | 3 | HG02257.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2523+1996_2523+199 others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 125924825 | |||||
| chr6:125924914
|
G | C | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2523+2080G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125924914 | ||||||
| chr6:125925005
|
C | T | 1 | a0001c0001t0026g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2523+2171C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125925005 | ||||||
| chr6:125925572
|
A | G | 25 | a0002c0002t0002g0067a0002c0002t0002g0068a0002c0002t0002g0069others(22): Show | 25 | HG00544.hp1 HG02132.hp1 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.2524-2091A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125925572 | ||||||
| chr6:125925778
|
C | G | 1 | a0003c0003t0003g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2524-1885C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125925778 | ||||||
| chr6:125926132
|
G | A | 2 | a0002c0002t0010g0133a0002c0002t0010g0141 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2524-1531G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926132 | ||||||
| chr6:125926139
|
C | T | 1 | a0002c0002t0002g0104 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2524-1524C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926139 | ||||||
| chr6:125926204
|
G | A | 7 | a0002c0002t0002g0015a0002c0002t0002g0032a0002c0002t0002g0254others(4): Show | 7 | HG02615.hp2 HG02630.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2524-1459G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926204 | ||||||
| chr6:125926260
|
T | C | 266 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2524-1403T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926260 | ||||||
| chr6:125926311
|
CA | C | 54 | a0001c0001t0001g0169a0002c0002t0001g0094a0002c0002t0001g0229others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.2524-1339delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 125926311 | |||||
| chr6:125926324
|
A | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0214 | 2 | HG01106.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2524-1339A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926324 | ||||||
| chr6:125926404
|
T | C | 1 | a0001c0001t0004g0065 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2524-1259T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926404 | ||||||
| chr6:125926865
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG00280.hp1 HG00733.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.2524-798A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926865 | ||||||
| chr6:125926971
|
C | T | 1 | a0004c0013t0013g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2524-692C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926971 | ||||||
| chr6:125927073
|
C | T | 2 | a0001c0001t0004g0037a0001c0001t0004g0039 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2524-590C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125927073 | ||||||
| chr6:125927228
|
T | C | 114 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.2524-435T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125927228 | ||||||
| chr6:125927450
|
G | A | 195 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0040others(192): Show | 195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2524-213G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125927450 | ||||||
| chr6:125927799
|
G | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0242 | 2 | HG00597.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.2619+41G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 14/15 | chr6 | 125927799 | ||||||
| chr6:125927878
|
G | A | 12 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(9): Show | 12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.2619+120G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 14/15 | chr6 | 125927878 | ||||||
| chr6:125927999
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2620-175T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 14/15 | chr6 | 125927999 | ||||||
| chr6:125928393
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2693+146C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 15/15 | chr6 | 125928393 | ||||||
| chr6:125928448
|
T | C | 1 | a0001c0001t0005g0016 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2694-188T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 15/15 | chr6 | 125928448 |