| geneid | 26054 |
|---|---|
| ensemblid | ENSG00000112701.18 |
| hgncid | 20944 |
| symbol | SENP6 |
| name | SUMO specific peptidase 6 |
| refseq_nuc | NM_015571.4 |
| refseq_prot | NP_056386.2 |
| ensembl_nuc | ENST00000447266.7 |
| ensembl_prot | ENSP00000402527.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 75601880 |
| end | 75718281 |
| strand | + |
| ver | v1.2 |
| region | chr6:75601880-75718281 |
| region5000 | chr6:75596880-75723281 |
| regionname0 | SENP6_chr6_75601880_75718281 |
| regionname5000 | SENP6_chr6_75596880_75723281 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1112 | 321 | 81 | 37 | 163 | 12 | 27 | 127 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0002 | 0/1 | 1112 | 26 | 2 | 7 | 7 | 4 | 5 | 5 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0003 | 0/0 | 1112 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0004 | 0/0 | 1112 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0005 | 0/0 | 1112 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0006 | 0/0 | 1112 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0007 | 0/0 | 1112 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0008 | 0/0 | 1112 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0009 | 0/0 | 1112 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0010 | 0/0 | 1112 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0011 | 0/0 | 1112 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0012 | 0/0 | 1112 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| 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 | 3339 | 257 | 43 | 36 | 140 | 12 | 26 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0002 | 1/0 | 3339 | 45 | 19 | 1 | 23 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0003 | 0/1 | 3339 | 26 | 2 | 7 | 7 | 4 | 5 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0004 | 0/0 | 3339 | 10 | 10 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0005 | 0/0 | 3339 | 5 | 5 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0006 | 0/0 | 3339 | 3 | 0 | 0 | 3 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0007 | 0/0 | 3339 | 3 | 3 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0008 | 0/0 | 3339 | 2 | 2 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0009 | 0/0 | 3339 | 2 | 0 | 0 | 2 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0010 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0011 | 0/0 | 3339 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0012 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0013 | 0/0 | 3339 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0014 | 0/0 | 3339 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0015 | 0/0 | 3339 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0016 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0017 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| c0018 | 0/0 | 3339 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| 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 | 0/0 | 3331 | 93 | 6 | 20 | 51 | 6 | 10 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0002 | 1/0 | 3333 | 87 | 23 | 8 | 40 | 2 | 13 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0003 | 0/0 | 3333 | 79 | 30 | 9 | 30 | 4 | 6 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0004 | 0/0 | 3333 | 29 | 0 | 2 | 26 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0005 | 0/0 | 3333 | 24 | 4 | 6 | 9 | 3 | 2 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0006 | 0/0 | 3333 | 9 | 9 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0007 | 0/0 | 3333 | 9 | 0 | 1 | 8 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0008 | 0/0 | 3327 | 8 | 0 | 0 | 8 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0009 | 0/0 | 3333 | 6 | 6 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0010 | 0/0 | 3333 | 3 | 3 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0011 | 0/0 | 3333 | 2 | 2 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0012 | 0/0 | 3333 | 2 | 0 | 0 | 2 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0013 | 0/0 | 3333 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0014 | 0/0 | 3333 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0015 | 0/0 | 3333 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0016 | 0/0 | 3331 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0017 | 0/0 | 3333 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0018 | 0/0 | 3333 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0019 | 0/1 | 3333 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0020 | 0/0 | 3331 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0021 | 0/0 | 3333 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0022 | 0/0 | 3333 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| t0023 | 0/0 | 3331 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| 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 | 3339 | 257 | 43 | 36 | 140 | 12 | 26 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0002 | 1/0 | 3339 | 45 | 19 | 1 | 23 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0004 | 0/0 | 3339 | 10 | 10 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0005 | 0/0 | 3339 | 5 | 5 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0008 | 0/0 | 3339 | 2 | 2 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0016 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0017 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0002c0003 | 0/1 | 3339 | 26 | 2 | 7 | 7 | 4 | 5 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0003c0007 | 0/0 | 3339 | 3 | 3 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0004c0006 | 0/0 | 3339 | 3 | 0 | 0 | 3 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0005c0009 | 0/0 | 3339 | 2 | 0 | 0 | 2 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0006c0010 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0007c0014 | 0/0 | 3339 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0008c0011 | 0/0 | 3339 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0009c0013 | 0/0 | 3339 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0010c0012 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0011c0015 | 0/0 | 3339 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0012c0018 | 0/0 | 3339 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6669 | 89 | 6 | 19 | 49 | 6 | 9 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0002 | 0/0 | 6671 | 84 | 22 | 8 | 40 | 2 | 12 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0003 | 0/0 | 6671 | 6 | 5 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0004 | 0/0 | 6671 | 29 | 0 | 2 | 26 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0005 | 0/0 | 6671 | 20 | 4 | 5 | 6 | 3 | 2 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0007 | 0/0 | 6671 | 9 | 0 | 1 | 8 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0008 | 0/0 | 6665 | 8 | 0 | 0 | 8 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0010 | 0/0 | 6671 | 3 | 3 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0012 | 0/0 | 6671 | 2 | 0 | 0 | 2 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0013 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0015 | 0/0 | 6671 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0016 | 0/0 | 6669 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0017 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0018 | 0/0 | 6671 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0020 | 0/0 | 6669 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0001t0023 | 0/0 | 6669 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0002t0002 | 1/0 | 6671 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0002t0003 | 0/0 | 6671 | 35 | 11 | 1 | 22 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0002t0009 | 0/0 | 6671 | 5 | 5 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0002t0011 | 0/0 | 6671 | 2 | 2 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0002t0021 | 0/0 | 6671 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0002t0022 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0004t0003 | 0/0 | 6671 | 9 | 9 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0004t0014 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0005t0006 | 0/0 | 6671 | 5 | 5 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0008t0003 | 0/0 | 6671 | 2 | 2 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0016t0006 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0001c0017t0002 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0002c0003t0003 | 0/0 | 6671 | 25 | 2 | 7 | 7 | 4 | 5 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0002c0003t0019 | 0/1 | 6671 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0003c0007t0006 | 0/0 | 6671 | 3 | 3 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0004c0006t0005 | 0/0 | 6671 | 3 | 0 | 0 | 3 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0005c0009t0001 | 0/0 | 6669 | 2 | 0 | 0 | 2 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0006c0010t0009 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0007c0014t0002 | 0/0 | 6671 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0008c0011t0003 | 0/0 | 6671 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0009c0013t0005 | 0/0 | 6671 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0010c0012t0003 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0011c0015t0001 | 0/0 | 6669 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| a0012c0018t0001 | 0/0 | 6669 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | copy fasta | chr6 | 75596880 | 75723281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0007g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0007g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0007g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0007g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0007g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0007g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0007g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0008g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0008g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0008g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0010g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0012g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0012g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0013g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0015g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0016g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0017g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0018g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0020g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0001t0023g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0002g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0011g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0021g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0002t0022g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0004t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0004t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0004t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0004t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0004t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0004t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0004t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0004t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0004t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0004t0014g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0005t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0005t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0005t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0005t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0005t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0008t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0008t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0016t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0001c0017t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0002c0003t0019g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0003c0007t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0003c0007t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0003c0007t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0004c0006t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0004c0006t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0004c0006t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0005c0009t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0005c0009t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0006c0010t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0007c0014t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0008c0011t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0009c0013t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0010c0012t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0011c0015t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| a0012c0018t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | GBR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00099 | hp2 | a0001 | c0001 | t0018 | g0060 | EUR | GBR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | GBR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | GBR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0136 | EUR | FIN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0157 | EUR | FIN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0322 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0357 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00423 | hp2 | a0001 | c0001 | t0008 | g0258 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0323 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0346 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0152 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0314 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00738 | hp1 | a0002 | c0003 | t0003 | g0044 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00741 | hp1 | a0002 | c0003 | t0003 | g0026 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0164 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01074 | hp1 | a0011 | c0015 | t0001 | g0287 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01074 | hp2 | a0002 | c0003 | t0003 | g0046 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01081 | hp2 | a0002 | c0003 | t0003 | g0038 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0169 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0163 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01168 | hp1 | a0002 | c0003 | t0003 | g0036 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01169 | hp2 | a0002 | c0003 | t0003 | g0042 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01243 | hp2 | a0002 | c0003 | t0003 | g0039 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0154 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01346 | hp1 | a0009 | c0013 | t0005 | g0140 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0156 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01516 | hp1 | a0002 | c0003 | t0003 | g0051 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01517 | hp1 | a0002 | c0003 | t0003 | g0052 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0011 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0305 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01975 | hp2 | a0001 | c0001 | t0007 | g0307 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0304 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02015 | hp2 | a0005 | c0009 | t0001 | g0191 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0358 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02040 | hp2 | a0005 | c0009 | t0001 | g0193 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02055 | hp2 | a0001 | c0004 | t0003 | g0181 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02056 | hp1 | a0002 | c0003 | t0003 | g0031 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0335 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0349 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0310 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02132 | hp1 | a0001 | c0001 | t0008 | g0228 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02132 | hp2 | a0002 | c0003 | t0003 | g0028 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02145 | hp1 | a0001 | c0001 | t0017 | g0073 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02145 | hp2 | a0002 | c0003 | t0003 | g0048 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02155 | hp1 | a0001 | c0001 | t0008 | g0220 | EAS | CDX | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CDX | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CDX | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | CDX | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0005 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02257 | hp2 | a0001 | c0005 | t0006 | g0296 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02280 | hp1 | a0001 | c0004 | t0003 | g0174 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02280 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02451 | hp1 | a0002 | c0003 | t0003 | g0045 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02451 | hp2 | a0003 | c0007 | t0006 | g0294 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02572 | hp2 | a0001 | c0004 | t0003 | g0180 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0182 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02622 | hp2 | a0001 | c0002 | t0009 | g0171 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02630 | hp1 | a0001 | c0002 | t0022 | g0017 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02647 | hp1 | a0003 | c0007 | t0006 | g0290 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02698 | hp1 | a0002 | c0003 | t0003 | g0043 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0318 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02717 | hp1 | a0001 | c0004 | t0003 | g0178 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02717 | hp2 | a0001 | c0017 | t0002 | g0108 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02723 | hp2 | a0001 | c0002 | t0009 | g0170 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02735 | hp1 | a0002 | c0003 | t0003 | g0027 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02735 | hp2 | a0001 | c0001 | t0020 | g0249 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02738 | hp1 | a0002 | c0003 | t0003 | g0047 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02738 | hp2 | a0001 | c0001 | t0015 | g0131 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0298 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02886 | hp2 | a0001 | c0001 | t0016 | g0121 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02895 | hp2 | a0001 | c0004 | t0003 | g0176 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02897 | hp1 | a0001 | c0004 | t0003 | g0175 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0019 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02965 | hp1 | a0001 | c0002 | t0011 | g0012 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0184 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03098 | hp1 | a0001 | c0008 | t0003 | g0185 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0187 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03130 | hp1 | a0001 | c0002 | t0003 | g0003 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03130 | hp2 | a0001 | c0002 | t0009 | g0008 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0183 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03209 | hp2 | a0006 | c0010 | t0009 | g0010 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03225 | hp1 | a0001 | c0004 | t0014 | g0049 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0020 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03453 | hp1 | a0001 | c0005 | t0006 | g0291 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03453 | hp2 | a0001 | c0004 | t0003 | g0177 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0299 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03516 | hp1 | a0001 | c0004 | t0003 | g0179 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03516 | hp2 | a0001 | c0008 | t0003 | g0186 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03540 | hp1 | a0001 | c0005 | t0006 | g0295 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0021 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0158 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0155 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03831 | hp1 | a0002 | c0003 | t0003 | g0037 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03831 | hp2 | a0012 | c0018 | t0001 | g0239 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03834 | hp1 | a0007 | c0014 | t0002 | g0096 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0341 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG04115 | hp1 | a0002 | c0003 | t0003 | g0035 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18522 | hp1 | a0001 | c0005 | t0006 | g0293 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18522 | hp2 | a0001 | c0002 | t0009 | g0009 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CHB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0344 | EAS | CHB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CHB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18906 | hp2 | a0001 | c0004 | t0003 | g0173 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0348 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18940 | hp1 | a0002 | c0003 | t0003 | g0030 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18940 | hp2 | a0001 | c0002 | t0003 | g0356 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18941 | hp2 | a0002 | c0003 | t0003 | g0032 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0337 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0331 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18947 | hp2 | a0001 | c0002 | t0003 | g0359 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18949 | hp2 | a0002 | c0003 | t0003 | g0034 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18962 | hp1 | a0001 | c0001 | t0007 | g0308 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18962 | hp2 | a0002 | c0003 | t0003 | g0033 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18964 | hp2 | a0001 | c0002 | t0003 | g0360 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18965 | hp1 | a0001 | c0002 | t0003 | g0351 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0352 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0332 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0338 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0303 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0339 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0361 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0313 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18980 | hp1 | a0004 | c0006 | t0005 | g0160 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0350 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0353 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18984 | hp2 | a0001 | c0001 | t0008 | g0195 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18988 | hp2 | a0001 | c0001 | t0012 | g0149 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18991 | hp1 | a0001 | c0002 | t0021 | g0342 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18993 | hp1 | a0001 | c0002 | t0003 | g0362 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18994 | hp1 | a0001 | c0001 | t0023 | g0142 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18994 | hp2 | a0004 | c0006 | t0005 | g0150 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0340 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0317 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0327 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19004 | hp2 | a0001 | c0002 | t0003 | g0345 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19005 | hp1 | a0008 | c0011 | t0003 | g0347 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19006 | hp2 | a0001 | c0001 | t0008 | g0253 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19054 | hp1 | a0001 | c0001 | t0012 | g0148 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0209 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19057 | hp1 | a0001 | c0002 | t0003 | g0355 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19062 | hp2 | a0001 | c0002 | t0003 | g0354 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19066 | hp1 | a0001 | c0001 | t0008 | g0259 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0315 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0343 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0302 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19087 | hp1 | a0002 | c0003 | t0003 | g0029 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19088 | hp1 | a0004 | c0006 | t0005 | g0151 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19090 | hp2 | a0001 | c0001 | t0008 | g0254 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19240 | hp1 | a0010 | c0012 | t0003 | g0166 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0018 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA20129 | hp1 | a0001 | c0005 | t0006 | g0292 | AFR | ASW | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ASW | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA20752 | hp1 | a0002 | c0003 | t0003 | g0041 | EUR | TSI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0153 | EUR | TSI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA20805 | hp2 | a0002 | c0003 | t0003 | g0050 | EUR | TSI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | GIH | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | GIH | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02109 | hp2 | a0003 | c0007 | t0006 | g0167 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02486 | hp2 | a0001 | c0002 | t0009 | g0007 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG06807 | hp1 | a0001 | c0002 | t0011 | g0016 | AFR | USA | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| HG06807 | hp2 | a0001 | c0016 | t0006 | g0297 | AFR | USA | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | USA | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | USA | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0019 | g0040 | REF | REF | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0015 | REF | REF | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:75621591
|
C | T | 1 | a0012 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.112C>T | p.His38Tyr | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/24 | 757/6671 | 112/3339 | 38/1112 | chr6 | 75621591 | ||
| chr6:75634715
|
C | T | 2 | a0002a0005 | 28 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(25): Show |
missense_variant | MODERATE | c.362C>T | p.Thr121Met | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/24 | 1007/6671 | 362/3339 | 121/1112 | chr6 | 75634715 | ||
| chr6:75659265
|
G | A | 1 | a0006 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.554G>A | p.Arg185His | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/24 | 1199/6671 | 554/3339 | 185/1112 | chr6 | 75659265 | ||
| chr6:75659328
|
A | G | 1 | a0011 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.617A>G | p.Gln206Arg | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/24 | 1262/6671 | 617/3339 | 206/1112 | chr6 | 75659328 | ||
| chr6:75670644
|
C | T | 1 | a0007 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1316C>T | p.Ser439Phe | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/24 | 1961/6671 | 1316/3339 | 439/1112 | chr6 | 75670644 | ||
| chr6:75678608
|
T | C | 1 | a0004 | 3 | NA18980.hp1 NA18994.hp2 NA19088.hp1 |
missense_variant | MODERATE | c.1874T>C | p.Leu625Pro | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 15/24 | 2519/6671 | 1874/3339 | 625/1112 | chr6 | 75678608 | ||
| chr6:75678611
|
G | A | 1 | a0008 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.1877G>A | p.Arg626Lys | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 15/24 | 2522/6671 | 1877/3339 | 626/1112 | chr6 | 75678611 | ||
| chr6:75702739
|
A | G | 1 | a0009 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2383A>G | p.Lys795Glu | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/24 | 3028/6671 | 2383/3339 | 795/1112 | chr6 | 75702739 | ||
| chr6:75702815
|
C | T | 1 | a0003 | 3 | HG02109.hp2 HG02451.hp2 HG02647.hp1 |
missense_variant | MODERATE | c.2459C>T | p.Ala820Val | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/24 | 3104/6671 | 2459/3339 | 820/1112 | chr6 | 75702815 | ||
| chr6:75715470
|
G | A | 1 | a0010 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.3215G>A | p.Arg1072Gln | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 3860/6671 | 3215/3339 | 1072/1112 | chr6 | 75715470 | ||
| chr6:75715572
|
A | G | 1 | a0002 | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
missense_variant | MODERATE | c.3317A>G | p.Tyr1106Cys | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 3962/6671 | 3317/3339 | 1106/1112 | chr6 | 75715572 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:75634788
|
A | T | 1 | a0001c0017 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.435A>T | p.Pro145Pro | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/24 | 1080/6671 | 435/3339 | 145/1112 | chr6 | 75634788 | ||
| chr6:75647788
|
G | T | 3 | a0001c0005a0001c0016a0003c0007 | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
synonymous_variant | LOW | c.537G>T | p.Arg179Arg | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/24 | 1182/6671 | 537/3339 | 179/1112 | chr6 | 75647788 | ||
| chr6:75659338
|
A | G | 15 | a0001c0001a0001c0004a0001c0005others(12): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
synonymous_variant | LOW | c.627A>G | p.Arg209Arg | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/24 | 1272/6671 | 627/3339 | 209/1112 | chr6 | 75659338 | ||
| chr6:75663286
|
G | A | 2 | a0001c0005a0003c0007 | 8 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
synonymous_variant | LOW | c.762G>A | p.Thr254Thr | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/24 | 1407/6671 | 762/3339 | 254/1112 | chr6 | 75663286 | ||
| chr6:75666836
|
G | A | 2 | a0001c0004a0002c0003 | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
synonymous_variant | LOW | c.1119G>A | p.Ala373Ala | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/24 | 1764/6671 | 1119/3339 | 373/1112 | chr6 | 75666836 | ||
| chr6:75678820
|
A | G | 1 | a0001c0008 | 2 | HG03098.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1968A>G | p.Val656Val | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/24 | 2613/6671 | 1968/3339 | 656/1112 | chr6 | 75678820 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:75601899
|
G | A | 1 | a0001c0001t0013 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-626G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/24 | 626 | chr6 | 75601899 | |||||
| chr6:75602002
|
C | T | 5 | a0001c0001t0005a0001c0001t0012a0001c0001t0023others(2): Show | 27 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-523C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/24 | 523 | chr6 | 75602002 | |||||
| chr6:75602033
|
G | T | 2 | a0001c0001t0004a0001c0001t0007 | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-492G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/24 | 492 | chr6 | 75602033 | |||||
| chr6:75602205
|
G | C | 1 | a0001c0004t0014 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-320G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/24 | 320 | chr6 | 75602205 | |||||
| chr6:75602443
|
C | T | 1 | a0001c0002t0022 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/24 | 82 | chr6 | 75602443 | |||||
| chr6:75715657
|
A | T | 2 | a0001c0002t0011a0001c0002t0022 | 3 | HG02630.hp1 HG02965.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*63A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 63 | chr6 | 75715657 | |||||
| chr6:75715825
|
A | G | 1 | a0001c0002t0021 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*231A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 231 | chr6 | 75715825 | |||||
| chr6:75715878
|
A | C | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 236 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*284A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 284 | chr6 | 75715878 | |||||
| chr6:75716048
|
A | G | 1 | a0001c0001t0018 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 454 | chr6 | 75716048 | |||||
| chr6:75716056
|
T | C | 1 | a0001c0001t0007 | 9 | HG01975.hp2 NA18946.hp1 NA18962.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*462T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 462 | chr6 | 75716056 | |||||
| chr6:75716253
|
C | A | 1 | a0001c0001t0015 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*659C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 659 | chr6 | 75716253 | |||||
| chr6:75716295
|
G | C | 1 | a0002c0003t0019 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*701G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 701 | chr6 | 75716295 | |||||
| chr6:75716465
|
T | A | 1 | a0001c0001t0012 | 2 | NA18988.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*871T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 871 | chr6 | 75716465 | |||||
| chr6:75716686
|
G | A | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 236 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*1092G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 1092 | chr6 | 75716686 | |||||
| chr6:75717088
|
C | G | 2 | a0001c0002t0009a0006c0010t0009 | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1494C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 1494 | chr6 | 75717088 | |||||
| chr6:75717205
|
A | T | 1 | a0001c0001t0017 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1611A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 1611 | chr6 | 75717205 | |||||
| chr6:75717349
|
A | G | 32 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(29): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*1755A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 1755 | chr6 | 75717349 | |||||
| chr6:75717401
|
A | C | 1 | a0001c0001t0020 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1807A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 1807 | chr6 | 75717401 | |||||
| chr6:75717795
|
TTAGA | T | 1 | a0001c0001t0008 | 8 | HG00423.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2207_*2210delAGAT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 2207 | INFO_REALIGN_3_PRIME | chr6 | 75717795 | ||||
| chr6:75717805
|
C | A | 2 | a0001c0001t0010a0001c0001t0013 | 4 | HG02622.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2211C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 2211 | chr6 | 75717805 | |||||
| chr6:75718107
|
CTT | C | 8 | a0001c0001t0001a0001c0001t0008a0001c0001t0016others(5): Show | 104 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2514_*2515delTT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 2514 | chr6 | 75718107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:75602599
|
C | T | 25 | a0001c0002t0003g0338a0001c0002t0003g0339a0001c0002t0003g0340others(22): Show | 25 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.52+23C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75602599 | ||||||
| chr6:75602930
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.52+354A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75602930 | ||||||
| chr6:75603047
|
A | G | 2 | a0001c0001t0005g0298a0001c0001t0005g0299 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.52+471A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603047 | ||||||
| chr6:75603071
|
C | T | 8 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(5): Show | 8 | HG02257.hp2 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.52+495C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603071 | ||||||
| chr6:75603086
|
C | T | 102 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.52+510C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603086 | ||||||
| chr6:75603128
|
C | T | 6 | a0001c0001t0010g0182a0001c0001t0010g0183a0001c0001t0010g0187others(3): Show | 6 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+552C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603128 | ||||||
| chr6:75603194
|
C | G | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+618C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603194 | ||||||
| chr6:75603208
|
T | G | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.52+632T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603208 | ||||||
| chr6:75603256
|
G | A | 1 | a0001c0001t0004g0300 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.52+680G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603256 | ||||||
| chr6:75603261
|
A | G | 1 | a0001c0001t0004g0337 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.52+685A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603261 | ||||||
| chr6:75603297
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.52+721G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603297 | ||||||
| chr6:75603322
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.52+746G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603322 | ||||||
| chr6:75603334
|
C | T | 1 | a0001c0001t0002g0172 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.52+758C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603334 | ||||||
| chr6:75603342
|
A | G | 2 | a0001c0002t0009g0170a0001c0002t0009g0171 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.52+766A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603342 | ||||||
| chr6:75603646
|
C | T | 1 | a0001c0002t0003g0169 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.52+1070C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603646 | ||||||
| chr6:75603753
|
G | T | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.52+1177G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603753 | ||||||
| chr6:75603843
|
C | G | 1 | a0001c0001t0001g0289 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.52+1267C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603843 | ||||||
| chr6:75604058
|
A | G | 1 | a0001c0016t0006g0297 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.52+1482A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604058 | ||||||
| chr6:75604262
|
A | G | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.52+1686A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604262 | ||||||
| chr6:75604282
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.52+1706C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604282 | ||||||
| chr6:75604379
|
C | T | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+1803C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604379 | ||||||
| chr6:75604452
|
C | T | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+1876C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604452 | ||||||
| chr6:75604482
|
T | G | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+1906T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604482 | ||||||
| chr6:75604625
|
C | CA | 43 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0001g0194others(40): Show | 43 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.52+2060dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75604625 | |||||
| chr6:75604711
|
G | C | 1 | a0001c0001t0008g0195 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.52+2135G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604711 | ||||||
| chr6:75604804
|
G | A | 1 | a0002c0003t0003g0026 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.52+2228G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604804 | ||||||
| chr6:75604811
|
G | A | 1 | a0001c0001t0003g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.52+2235G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604811 | ||||||
| chr6:75604941
|
C | T | 3 | a0002c0003t0003g0050a0002c0003t0003g0051a0002c0003t0003g0052 | 3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.52+2365C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604941 | ||||||
| chr6:75604966
|
G | T | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.52+2390G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604966 | ||||||
| chr6:75605126
|
T | C | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.52+2550T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605126 | ||||||
| chr6:75605680
|
T | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.52+3104T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605680 | ||||||
| chr6:75605829
|
TAGG | T | 22 | a0001c0001t0005g0143a0001c0001t0005g0144a0001c0001t0005g0145others(19): Show | 22 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.52+3254_52+3256del others(3): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605829 | ||||||
| chr6:75605910
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.52+3334G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605910 | ||||||
| chr6:75605917
|
G | A | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.52+3341G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605917 | ||||||
| chr6:75605950
|
T | C | 1 | a0002c0003t0003g0027 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.52+3374T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605950 | ||||||
| chr6:75605969
|
T | A | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.52+3393T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605969 | ||||||
| chr6:75606054
|
G | T | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+3478G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606054 | ||||||
| chr6:75606156
|
C | G | 3 | a0001c0001t0001g0286a0001c0001t0001g0288a0011c0015t0001g0287 | 3 | HG01074.hp1 HG01975.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.52+3580C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606156 | ||||||
| chr6:75606292
|
G | A | 3 | a0001c0001t0003g0053a0001c0001t0003g0165a0010c0012t0003g0166 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+3716G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606292 | ||||||
| chr6:75606350
|
A | G | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.52+3774A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606350 | ||||||
| chr6:75606693
|
C | T | 1 | a0001c0001t0004g0336 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.52+4117C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606693 | ||||||
| chr6:75606791
|
AAAAATCT | A | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.52+4216_52+4222del others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606791 | ||||||
| chr6:75606897
|
G | A | 1 | a0001c0001t0002g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.52+4321G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606897 | ||||||
| chr6:75606987
|
G | A | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+4411G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606987 | ||||||
| chr6:75607254
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.52+4678G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607254 | ||||||
| chr6:75607286
|
C | G | 1 | a0001c0001t0005g0299 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.52+4710C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607286 | ||||||
| chr6:75607302
|
A | C | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+4726A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607302 | ||||||
| chr6:75607497
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.52+4921T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607497 | ||||||
| chr6:75607529
|
A | G | 1 | a0001c0001t0023g0142 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.52+4953A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607529 | ||||||
| chr6:75607547
|
C | CT | 37 | a0001c0001t0001g0284a0001c0001t0004g0300a0001c0001t0004g0301others(34): Show | 37 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.52+4981dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75607547 | |||||
| chr6:75607580
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.52+5004A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607580 | ||||||
| chr6:75607622
|
C | T | 1 | a0001c0001t0002g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.52+5046C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607622 | ||||||
| chr6:75607758
|
C | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0282 | 2 | HG02027.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.52+5182C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607758 | ||||||
| chr6:75607912
|
C | CA | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.52+5337dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75607912 | |||||
| chr6:75608119
|
T | C | 2 | a0001c0001t0004g0304a0001c0001t0004g0305 | 2 | HG01928.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.52+5543T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608119 | ||||||
| chr6:75608276
|
C | A | 3 | a0002c0003t0003g0028a0002c0003t0003g0029a0002c0003t0003g0030 | 3 | HG02132.hp2 NA18940.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.52+5700C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608276 | ||||||
| chr6:75608386
|
C | G | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.52+5810C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608386 | ||||||
| chr6:75608550
|
A | G | 314 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(311): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.52+5974A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608550 | ||||||
| chr6:75608679
|
TACTTA | T | 91 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.52+6108_52+6112del others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75608679 | |||||
| chr6:75608837
|
A | G | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.52+6261A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608837 | ||||||
| chr6:75608916
|
G | A | 1 | a0001c0001t0002g0057 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.52+6340G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608916 | ||||||
| chr6:75609077
|
T | G | 5 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+6501T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609077 | ||||||
| chr6:75609126
|
T | TG | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.52+6554dupG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75609126 | |||||
| chr6:75609206
|
C | G | 8 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(5): Show | 8 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+6630C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609206 | ||||||
| chr6:75609207
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.52+6631G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609207 | ||||||
| chr6:75609520
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.52+6944G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609520 | ||||||
| chr6:75609618
|
G | A | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.52+7042G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609618 | ||||||
| chr6:75609773
|
T | G | 3 | a0002c0003t0003g0050a0002c0003t0003g0051a0002c0003t0003g0052 | 3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.52+7197T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609773 | ||||||
| chr6:75609791
|
A | G | 2 | a0001c0001t0001g0281a0001c0001t0002g0130 | 2 | HG02897.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.52+7215A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609791 | ||||||
| chr6:75609816
|
G | T | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.52+7240G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609816 | ||||||
| chr6:75609932
|
C | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG00741.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.52+7356C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609932 | ||||||
| chr6:75609945
|
G | A | 1 | a0001c0001t0004g0306 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.52+7369G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609945 | ||||||
| chr6:75610047
|
C | T | 1 | a0001c0002t0003g0169 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.52+7471C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610047 | ||||||
| chr6:75610071
|
A | C | 2 | a0002c0003t0003g0051a0002c0003t0003g0052 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.52+7495A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610071 | ||||||
| chr6:75610141
|
C | T | 1 | a0009c0013t0005g0140 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.52+7565C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610141 | ||||||
| chr6:75610383
|
A | T | 34 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(31): Show | 34 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.52+7807A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610383 | ||||||
| chr6:75610671
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.52+8095C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610671 | ||||||
| chr6:75610764
|
A | G | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.52+8188A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610764 | ||||||
| chr6:75610906
|
T | TGAAACAG others(80): Show |
26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.52+8333_52+8419dup others(87): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75610906 | |||||
| chr6:75610917
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.52+8341G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610917 | ||||||
| chr6:75611081
|
T | C | 5 | a0001c0001t0002g0059a0001c0001t0002g0061a0001c0001t0002g0168others(2): Show | 5 | HG00099.hp2 HG02486.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+8505T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611081 | ||||||
| chr6:75611130
|
C | T | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.52+8554C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611130 | ||||||
| chr6:75611190
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.52+8614A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611190 | ||||||
| chr6:75611383
|
G | A | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.52+8807G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611383 | ||||||
| chr6:75611666
|
T | G | 1 | a0001c0001t0004g0336 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.52+9090T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611666 | ||||||
| chr6:75611835
|
C | T | 5 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+9259C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611835 | ||||||
| chr6:75612229
|
G | A | 4 | a0001c0001t0010g0182a0001c0001t0010g0183a0001c0001t0013g0184others(1): Show | 4 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-9303G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612229 | ||||||
| chr6:75612306
|
A | G | 3 | a0001c0001t0005g0162a0001c0001t0005g0163a0001c0001t0005g0164 | 3 | HG01069.hp1 HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-9226A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612306 | ||||||
| chr6:75612378
|
C | T | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-9154C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612378 | ||||||
| chr6:75612542
|
G | T | 1 | a0001c0001t0002g0129 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.53-8990G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612542 | ||||||
| chr6:75612584
|
C | G | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.53-8948C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612584 | ||||||
| chr6:75612597
|
T | C | 1 | a0001c0002t0003g0169 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.53-8935T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612597 | ||||||
| chr6:75612674
|
A | G | 3 | a0001c0001t0003g0053a0001c0001t0003g0165a0010c0012t0003g0166 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-8858A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612674 | ||||||
| chr6:75612824
|
A | G | 1 | a0001c0001t0002g0061 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.53-8708A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612824 | ||||||
| chr6:75613114
|
T | TA | 123 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.53-8405dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75613114 | |||||
| chr6:75613459
|
T | C | 354 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(351): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.53-8073T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613459 | ||||||
| chr6:75613464
|
A | C | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.53-8068A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613464 | ||||||
| chr6:75613651
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.53-7881G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613651 | ||||||
| chr6:75613683
|
G | T | 6 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(3): Show | 6 | NA18970.hp1 NA18981.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-7849G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613683 | ||||||
| chr6:75613717
|
G | A | 7 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(4): Show | 7 | HG02056.hp1 HG03139.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-7815G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613717 | ||||||
| chr6:75613833
|
A | G | 1 | a0002c0003t0003g0027 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.53-7699A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613833 | ||||||
| chr6:75613952
|
T | A | 1 | a0001c0001t0002g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-7580T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613952 | ||||||
| chr6:75613954
|
G | T | 1 | a0001c0001t0002g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-7578G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613954 | ||||||
| chr6:75614009
|
A | G | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.53-7523A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614009 | ||||||
| chr6:75614055
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.53-7477C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614055 | ||||||
| chr6:75614056
|
G | A | 6 | a0001c0002t0009g0007a0001c0002t0009g0008a0001c0002t0009g0009others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-7476G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614056 | ||||||
| chr6:75614064
|
G | T | 1 | a0001c0002t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53-7468G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614064 | ||||||
| chr6:75614089
|
G | T | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | NA18612.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.53-7443G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614089 | ||||||
| chr6:75614102
|
T | A | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.53-7430T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614102 | ||||||
| chr6:75614208
|
G | A | 1 | a0001c0002t0003g0338 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.53-7324G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614208 | ||||||
| chr6:75614260
|
C | CT | 13 | a0001c0001t0001g0194a0001c0001t0001g0272a0001c0001t0001g0273others(10): Show | 13 | HG01517.hp2 HG02027.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-7253dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75614260 | |||||
| chr6:75614272
|
T | G | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.53-7260T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614272 | ||||||
| chr6:75614274
|
T | G | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.53-7258T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614274 | ||||||
| chr6:75614276
|
T | G | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.53-7256T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614276 | ||||||
| chr6:75614280
|
G | T | 1 | a0001c0001t0002g0061 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.53-7252G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614280 | ||||||
| chr6:75614353
|
C | T | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.53-7179C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614353 | ||||||
| chr6:75614682
|
A | C | 354 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(351): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.53-6850A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614682 | ||||||
| chr6:75614913
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.53-6619T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614913 | ||||||
| chr6:75614969
|
C | T | 1 | a0001c0008t0003g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.53-6563C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614969 | ||||||
| chr6:75615262
|
C | T | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-6270C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615262 | ||||||
| chr6:75615328
|
C | T | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.53-6204C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615328 | ||||||
| chr6:75615380
|
G | A | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.53-6152G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615380 | ||||||
| chr6:75615417
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.53-6115T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615417 | ||||||
| chr6:75615528
|
T | C | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.53-6004T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615528 | ||||||
| chr6:75615938
|
T | G | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(3): Show | 6 | HG00642.hp2 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-5594T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615938 | ||||||
| chr6:75615959
|
C | G | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.53-5573C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615959 | ||||||
| chr6:75615974
|
T | C | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.53-5558T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615974 | ||||||
| chr6:75615980
|
A | G | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG00738.hp2 HG01169.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5552A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615980 | ||||||
| chr6:75615984
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.53-5548C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615984 | ||||||
| chr6:75615997
|
C | T | 1 | a0001c0001t0003g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.53-5535C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615997 | ||||||
| chr6:75616452
|
G | A | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.53-5080G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75616452 | ||||||
| chr6:75616516
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-5016A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75616516 | ||||||
| chr6:75616540
|
G | A | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.53-4992G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75616540 | ||||||
| chr6:75616745
|
C | CA | 49 | a0001c0001t0001g0190a0001c0001t0001g0202a0001c0001t0001g0203others(46): Show | 49 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.53-4768dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75616745 | |||||
| chr6:75616851
|
A | C | 2 | a0001c0001t0002g0130a0001c0001t0016g0121 | 2 | HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.53-4681A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75616851 | ||||||
| chr6:75616875
|
T | C | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-4657T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75616875 | ||||||
| chr6:75617023
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-4509G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617023 | ||||||
| chr6:75617223
|
T | C | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.53-4309T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617223 | ||||||
| chr6:75617236
|
A | T | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-4296A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617236 | ||||||
| chr6:75617263
|
C | CT | 37 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(34): Show | 37 | HG00423.hp2 HG00544.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.53-4242dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617263 | |||||
| chr6:75617263
|
C | CTT | 8 | a0002c0003t0003g0026a0002c0003t0003g0030a0002c0003t0003g0034others(5): Show | 8 | HG00741.hp1 HG01074.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.53-4243_53-4242dup others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617263 | |||||
| chr6:75617263
|
CT | C | 107 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0267others(104): Show | 107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.53-4242delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617263 | |||||
| chr6:75617263
|
CTT | C | 87 | a0001c0001t0001g0204a0001c0001t0002g0054a0001c0001t0002g0055others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.53-4243_53-4242del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617263 | |||||
| chr6:75617263
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0017g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53-4258_53-4242del others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617263 | |||||
| chr6:75617265
|
T | TTC | 7 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0066others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-4266_53-4265ins others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617265 | |||||
| chr6:75617268
|
T | C | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.53-4264T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617268 | ||||||
| chr6:75617330
|
A | G | 1 | a0001c0001t0003g0025 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53-4202A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617330 | ||||||
| chr6:75617514
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.53-4018C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617514 | ||||||
| chr6:75617553
|
C | T | 1 | a0001c0001t0003g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.53-3979C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617553 | ||||||
| chr6:75617972
|
A | G | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.53-3560A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617972 | ||||||
| chr6:75618070
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-3462G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618070 | ||||||
| chr6:75618135
|
C | T | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.53-3397C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618135 | ||||||
| chr6:75618240
|
A | C | 1 | a0001c0001t0002g0127 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.53-3292A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618240 | ||||||
| chr6:75618272
|
C | T | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-3260C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618272 | ||||||
| chr6:75618303
|
GTTTAT | G | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.53-3221_53-3217del others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75618303 | |||||
| chr6:75618377
|
T | C | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.53-3155T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618377 | ||||||
| chr6:75618733
|
T | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-2799T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618733 | ||||||
| chr6:75618787
|
C | G | 1 | a0001c0004t0003g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-2745C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618787 | ||||||
| chr6:75618819
|
C | T | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.53-2713C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618819 | ||||||
| chr6:75618824
|
TCTA | T | 4 | a0001c0002t0003g0340a0001c0002t0003g0353a0001c0002t0003g0354others(1): Show | 4 | NA18983.hp1 NA18995.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2704_53-2702del others(3): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75618824 | |||||
| chr6:75618879
|
T | C | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.53-2653T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618879 | ||||||
| chr6:75618904
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.53-2628G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618904 | ||||||
| chr6:75619018
|
C | CT | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.53-2502dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619018 | |||||
| chr6:75619018
|
CT | C | 102 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.53-2502delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619018 | |||||
| chr6:75619239
|
C | T | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.53-2293C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75619239 | ||||||
| chr6:75619392
|
A | G | 4 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(1): Show | 4 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2140A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75619392 | ||||||
| chr6:75619443
|
CTA | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-2087_53-2086del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619443 | |||||
| chr6:75619445
|
A | ATG | 32 | a0001c0001t0001g0201a0001c0001t0003g0053a0001c0002t0003g0018others(29): Show | 32 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.53-2059_53-2058dup others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619445 | |||||
| chr6:75619445
|
A | ATGTGTGT others(5): Show |
3 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0021 | 3 | HG03041.hp2 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.53-2069_53-2058dup others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619445 | |||||
| chr6:75619445
|
A | ATGTGTGT others(7): Show |
2 | a0001c0002t0003g0005a0001c0002t0003g0006 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.53-2071_53-2058dup others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619445 | |||||
| chr6:75619445
|
ATG | A | 166 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(163): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.53-2059_53-2058del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619445 | |||||
| chr6:75619445
|
ATGTG | A | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.53-2061_53-2058del others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619445 | |||||
| chr6:75619582
|
A | T | 1 | a0001c0002t0009g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.53-1950A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75619582 | ||||||
| chr6:75619650
|
G | T | 3 | a0001c0001t0003g0053a0001c0001t0003g0165a0010c0012t0003g0166 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-1882G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75619650 | ||||||
| chr6:75619747
|
C | G | 1 | a0001c0001t0003g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.53-1785C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75619747 | ||||||
| chr6:75620007
|
C | A | 1 | a0001c0001t0003g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.53-1525C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620007 | ||||||
| chr6:75620007
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.53-1525C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620007 | ||||||
| chr6:75620082
|
C | CA | 27 | a0001c0004t0014g0049a0001c0008t0003g0186a0002c0003t0003g0026others(24): Show | 27 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.53-1429dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | |||||
| chr6:75620082
|
C | CAA | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-1430_53-1429dup others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | |||||
| chr6:75620082
|
CA | C | 134 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(131): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.53-1429delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | |||||
| chr6:75620082
|
CAA | C | 6 | a0001c0001t0001g0248a0001c0001t0001g0263a0001c0001t0001g0264others(3): Show | 6 | HG01928.hp1 HG02735.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-1430_53-1429del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | |||||
| chr6:75620082
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0017g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53-1438_53-1429del others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | |||||
| chr6:75620082
|
CAAAAAAA others(4): Show |
C | 124 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.53-1439_53-1429del others(11): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | |||||
| chr6:75620267
|
A | C | 1 | a0001c0001t0003g0025 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53-1265A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620267 | ||||||
| chr6:75620635
|
G | T | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.53-897G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620635 | ||||||
| chr6:75620718
|
G | C | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.53-814G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620718 | ||||||
| chr6:75620768
|
C | T | 2 | a0002c0003t0003g0045a0002c0003t0003g0046 | 2 | HG01074.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.53-764C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620768 | ||||||
| chr6:75621032
|
T | C | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.53-500T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75621032 | ||||||
| chr6:75621123
|
T | G | 1 | a0001c0001t0002g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.53-409T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75621123 | ||||||
| chr6:75621126
|
C | T | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-406C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75621126 | ||||||
| chr6:75621155
|
T | C | 1 | a0001c0002t0009g0170 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.53-377T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75621155 | ||||||
| chr6:75621741
|
ACT | A | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.146+119_146+120del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr6 | 75621741 | |||||
| chr6:75622268
|
A | G | 1 | a0001c0002t0009g0007 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146+643A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622268 | ||||||
| chr6:75622329
|
A | G | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.146+704A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622329 | ||||||
| chr6:75622429
|
T | C | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.146+804T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622429 | ||||||
| chr6:75622483
|
C | T | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.146+858C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622483 | ||||||
| chr6:75622500
|
A | G | 1 | a0001c0001t0002g0129 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.146+875A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622500 | ||||||
| chr6:75622662
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.146+1037A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622662 | ||||||
| chr6:75622664
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.146+1039A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622664 | ||||||
| chr6:75622716
|
G | T | 1 | a0001c0001t0004g0329 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.146+1091G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622716 | ||||||
| chr6:75622863
|
G | A | 1 | a0005c0009t0001g0191 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.147-1037G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622863 | ||||||
| chr6:75622947
|
A | C | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064 | 3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.147-953A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622947 | ||||||
| chr6:75623087
|
A | G | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.147-813A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75623087 | ||||||
| chr6:75623166
|
CGTT | C | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.147-731_147-729del others(3): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr6 | 75623166 | |||||
| chr6:75623218
|
A | G | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.147-682A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75623218 | ||||||
| chr6:75623546
|
A | G | 1 | a0009c0013t0005g0140 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.147-354A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75623546 | ||||||
| chr6:75623770
|
G | A | 348 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(345): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.147-130G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75623770 | ||||||
| chr6:75623999
|
A | G | 1 | a0001c0001t0002g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.207+39A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75623999 | ||||||
| chr6:75624078
|
G | T | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.207+118G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624078 | ||||||
| chr6:75624220
|
T | G | 1 | a0002c0003t0003g0027 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.207+260T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624220 | ||||||
| chr6:75624227
|
G | A | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.207+267G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624227 | ||||||
| chr6:75624319
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.207+359C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624319 | ||||||
| chr6:75624425
|
G | C | 1 | a0001c0001t0001g0208 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.207+465G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624425 | ||||||
| chr6:75624515
|
T | C | 11 | a0001c0001t0002g0055a0001c0001t0002g0078a0001c0001t0002g0079others(8): Show | 11 | HG01123.hp2 HG01192.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+555T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624515 | ||||||
| chr6:75624705
|
A | G | 1 | a0001c0001t0005g0164 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.207+745A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624705 | ||||||
| chr6:75625060
|
T | C | 1 | a0001c0001t0008g0209 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.207+1100T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625060 | ||||||
| chr6:75625112
|
C | CT | 171 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(168): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.207+1171dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75625112 | |||||
| chr6:75625112
|
C | CTT | 81 | a0001c0001t0001g0266a0001c0001t0002g0075a0001c0001t0002g0076others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.207+1170_207+1171d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75625112 | |||||
| chr6:75625112
|
C | CTTT | 20 | a0001c0001t0003g0053a0001c0001t0003g0165a0001c0001t0004g0301others(17): Show | 20 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.207+1169_207+1171d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75625112 | |||||
| chr6:75625112
|
CT | C | 8 | a0001c0001t0002g0061a0001c0002t0003g0003a0001c0002t0003g0004others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+1171delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75625112 | |||||
| chr6:75625136
|
C | T | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.207+1176C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625136 | ||||||
| chr6:75625172
|
C | T | 1 | a0001c0001t0017g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.207+1212C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625172 | ||||||
| chr6:75625216
|
A | T | 1 | a0001c0001t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.207+1256A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625216 | ||||||
| chr6:75625532
|
G | C | 1 | a0001c0001t0001g0288 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.207+1572G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625532 | ||||||
| chr6:75625566
|
T | G | 1 | a0001c0001t0002g0126 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.207+1606T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625566 | ||||||
| chr6:75625617
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.207+1657C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625617 | ||||||
| chr6:75625636
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.207+1676A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625636 | ||||||
| chr6:75625693
|
A | G | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.207+1733A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625693 | ||||||
| chr6:75625825
|
C | T | 1 | a0006c0010t0009g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.207+1865C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625825 | ||||||
| chr6:75625855
|
C | A | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+1895C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625855 | ||||||
| chr6:75625856
|
G | A | 1 | a0001c0002t0003g0018 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.207+1896G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625856 | ||||||
| chr6:75625997
|
G | C | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.207+2037G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625997 | ||||||
| chr6:75626025
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.207+2065A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626025 | ||||||
| chr6:75626125
|
T | G | 27 | a0001c0001t0005g0157a0002c0003t0003g0026a0002c0003t0003g0027others(24): Show | 27 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.207+2165T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626125 | ||||||
| chr6:75626125
|
T | TTTG | 278 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.207+2183_207+2185d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75626125 | |||||
| chr6:75626143
|
G | T | 1 | a0002c0003t0003g0044 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.207+2183G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626143 | ||||||
| chr6:75626188
|
C | A | 1 | a0001c0001t0002g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.207+2228C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626188 | ||||||
| chr6:75626189
|
A | G | 3 | a0001c0001t0003g0053a0001c0001t0003g0165a0010c0012t0003g0166 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+2229A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626189 | ||||||
| chr6:75626339
|
T | TTA | 17 | a0001c0001t0001g0211a0001c0001t0001g0247a0001c0001t0001g0263others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.207+2395_207+2396d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75626339 | |||||
| chr6:75626339
|
T | TTATA | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.207+2393_207+2396d others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75626339 | |||||
| chr6:75626673
|
T | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0212 | 2 | HG01081.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.207+2713T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626673 | ||||||
| chr6:75626719
|
C | T | 2 | a0001c0001t0005g0156a0001c0001t0005g0161 | 2 | HG01168.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.207+2759C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626719 | ||||||
| chr6:75626796
|
G | A | 1 | a0001c0001t0003g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.207+2836G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626796 | ||||||
| chr6:75626841
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.207+2881A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626841 | ||||||
| chr6:75627543
|
C | T | 3 | a0001c0001t0010g0182a0001c0001t0010g0183a0001c0001t0013g0184 | 3 | HG02622.hp1 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.207+3583C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75627543 | ||||||
| chr6:75627783
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.207+3823C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75627783 | ||||||
| chr6:75627859
|
G | T | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.207+3899G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75627859 | ||||||
| chr6:75627920
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.207+3960C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75627920 | ||||||
| chr6:75627952
|
G | A | 6 | a0001c0002t0009g0007a0001c0002t0009g0008a0001c0002t0009g0009others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+3992G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75627952 | ||||||
| chr6:75628161
|
A | G | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.207+4201A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75628161 | ||||||
| chr6:75628526
|
T | G | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+4566T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75628526 | ||||||
| chr6:75628795
|
C | G | 1 | a0001c0001t0001g0262 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.208-4786C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75628795 | ||||||
| chr6:75628829
|
A | C | 348 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(345): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.208-4752A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75628829 | ||||||
| chr6:75628832
|
G | A | 16 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(13): Show | 16 | HG02293.hp2 HG02486.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.208-4749G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75628832 | ||||||
| chr6:75629060
|
A | G | 3 | a0003c0007t0006g0167a0003c0007t0006g0290a0003c0007t0006g0294 | 3 | HG02109.hp2 HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.208-4521A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629060 | ||||||
| chr6:75629154
|
T | G | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.208-4427T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629154 | ||||||
| chr6:75629326
|
G | T | 1 | a0001c0001t0001g0266 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-4255G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629326 | ||||||
| chr6:75629437
|
C | A | 1 | a0001c0001t0001g0266 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-4144C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629437 | ||||||
| chr6:75629728
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.208-3853G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629728 | ||||||
| chr6:75629894
|
A | T | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.208-3687A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629894 | ||||||
| chr6:75630068
|
CT | C | 33 | a0001c0001t0002g0001a0001c0001t0002g0078a0001c0001t0004g0309others(30): Show | 33 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.208-3495delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75630068 | |||||
| chr6:75630111
|
C | G | 102 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.208-3470C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630111 | ||||||
| chr6:75630244
|
A | T | 1 | a0001c0001t0001g0266 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-3337A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630244 | ||||||
| chr6:75630245
|
T | A | 1 | a0001c0001t0001g0266 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-3336T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630245 | ||||||
| chr6:75630250
|
A | T | 1 | a0001c0001t0001g0266 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-3331A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630250 | ||||||
| chr6:75630350
|
T | G | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.208-3231T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630350 | ||||||
| chr6:75630576
|
T | A | 1 | a0001c0001t0001g0266 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-3005T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630576 | ||||||
| chr6:75630580
|
A | G | 1 | a0001c0001t0015g0131 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.208-3001A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630580 | ||||||
| chr6:75630730
|
T | G | 1 | a0001c0002t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-2851T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630730 | ||||||
| chr6:75630848
|
T | TA | 8 | a0001c0002t0003g0011a0001c0002t0009g0007a0001c0002t0009g0008others(5): Show | 8 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-2722dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75630848 | |||||
| chr6:75630848
|
TA | T | 102 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.208-2722delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75630848 | |||||
| chr6:75630928
|
ATC | A | 22 | a0001c0001t0005g0143a0001c0001t0005g0144a0001c0001t0005g0145others(19): Show | 22 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.208-2649_208-2648d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75630928 | |||||
| chr6:75630946
|
G | T | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.208-2635G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630946 | ||||||
| chr6:75631206
|
C | G | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.208-2375C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631206 | ||||||
| chr6:75631222
|
T | A | 1 | a0001c0001t0001g0266 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-2359T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631222 | ||||||
| chr6:75631584
|
CAT | C | 3 | a0001c0001t0010g0182a0001c0001t0010g0183a0001c0001t0013g0184 | 3 | HG02622.hp1 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.208-1996_208-1995d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631584 | ||||||
| chr6:75631755
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.208-1826A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631755 | ||||||
| chr6:75631787
|
G | A | 2 | a0001c0001t0002g0133a0001c0001t0002g0134 | 2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.208-1794G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631787 | ||||||
| chr6:75631942
|
A | G | 1 | a0001c0002t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-1639A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631942 | ||||||
| chr6:75632010
|
C | G | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.208-1571C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632010 | ||||||
| chr6:75632122
|
C | T | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.208-1459C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632122 | ||||||
| chr6:75632144
|
G | C | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.208-1437G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632144 | ||||||
| chr6:75632381
|
A | G | 1 | a0001c0002t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-1200A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632381 | ||||||
| chr6:75632415
|
G | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.208-1166G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632415 | ||||||
| chr6:75632456
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.208-1125G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632456 | ||||||
| chr6:75632653
|
G | A | 1 | a0001c0002t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-928G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632653 | ||||||
| chr6:75632673
|
C | CT | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.208-906dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75632673 | |||||
| chr6:75632730
|
A | G | 3 | a0001c0001t0001g0206a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG00609.hp1 NA19058.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.208-851A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632730 | ||||||
| chr6:75633346
|
A | G | 11 | a0001c0001t0002g0055a0001c0001t0002g0078a0001c0001t0002g0079others(8): Show | 11 | HG01123.hp2 HG01192.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-235A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75633346 | ||||||
| chr6:75633374
|
A | T | 1 | a0001c0002t0003g0360 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.208-207A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75633374 | ||||||
| chr6:75633456
|
A | G | 1 | a0001c0002t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-125A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75633456 | ||||||
| chr6:75633930
|
A | G | 1 | a0001c0002t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.353+204A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75633930 | ||||||
| chr6:75634067
|
A | G | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.353+341A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634067 | ||||||
| chr6:75634200
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.353+474A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634200 | ||||||
| chr6:75634488
|
T | C | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.354-219T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634488 | ||||||
| chr6:75634551
|
G | A | 25 | a0001c0002t0003g0338a0001c0002t0003g0339a0001c0002t0003g0340others(22): Show | 25 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.354-156G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634551 | ||||||
| chr6:75634639
|
G | T | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.354-68G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634639 | ||||||
| chr6:75634690
|
G | A | 1 | a0001c0002t0022g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.354-17G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634690 | ||||||
| chr6:75634827
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+16G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75634827 | ||||||
| chr6:75634968
|
T | C | 1 | a0001c0001t0005g0299 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.458+157T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75634968 | ||||||
| chr6:75635078
|
T | G | 1 | a0001c0002t0003g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.458+267T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75635078 | ||||||
| chr6:75635159
|
C | T | 5 | a0001c0001t0002g0074a0001c0001t0002g0115a0001c0001t0002g0116others(2): Show | 5 | HG00544.hp1 HG00558.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+348C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75635159 | ||||||
| chr6:75635160
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.458+349C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75635160 | ||||||
| chr6:75635282
|
A | C | 1 | a0001c0001t0002g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.458+471A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75635282 | ||||||
| chr6:75635374
|
C | G | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.458+563C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75635374 | ||||||
| chr6:75636046
|
T | TA | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+1244dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75636046 | |||||
| chr6:75636058
|
A | G | 3 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0161 | 3 | HG00280.hp2 HG01168.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.458+1247A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636058 | ||||||
| chr6:75636062
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.458+1251G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636062 | ||||||
| chr6:75636245
|
T | A | 1 | a0001c0001t0002g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.458+1434T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636245 | ||||||
| chr6:75636296
|
T | A | 4 | a0001c0001t0005g0143a0001c0001t0005g0144a0001c0001t0005g0145others(1): Show | 4 | NA18995.hp1 NA19057.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+1485T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636296 | ||||||
| chr6:75636323
|
C | T | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.458+1512C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636323 | ||||||
| chr6:75636378
|
C | T | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.458+1567C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636378 | ||||||
| chr6:75636430
|
C | T | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.458+1619C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636430 | ||||||
| chr6:75636434
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+1623G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636434 | ||||||
| chr6:75636875
|
A | AT | 143 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(140): Show | 143 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.458+2080dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75636875 | |||||
| chr6:75637140
|
T | G | 1 | a0009c0013t0005g0140 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.458+2329T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637140 | ||||||
| chr6:75637184
|
T | C | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458+2373T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637184 | ||||||
| chr6:75637232
|
T | C | 1 | a0001c0002t0003g0021 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.458+2421T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637232 | ||||||
| chr6:75637304
|
G | A | 38 | a0001c0001t0003g0053a0001c0004t0003g0173a0001c0004t0003g0174others(35): Show | 38 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.458+2493G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637304 | ||||||
| chr6:75637307
|
G | A | 1 | a0001c0002t0003g0169 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.458+2496G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637307 | ||||||
| chr6:75637904
|
A | G | 5 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-2780A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637904 | ||||||
| chr6:75637910
|
G | C | 1 | a0001c0001t0001g0218 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.459-2774G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637910 | ||||||
| chr6:75638242
|
G | GT | 102 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.459-2428dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638242 | |||||
| chr6:75638242
|
G | T | 1 | a0001c0002t0003g0359 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.459-2442G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638242 | ||||||
| chr6:75638242
|
GT | G | 12 | a0001c0001t0002g0097a0001c0001t0002g0116a0001c0001t0004g0310others(9): Show | 12 | HG00544.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.459-2428delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638242 | |||||
| chr6:75638242
|
GTT | G | 97 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.459-2429_459-2428d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638242 | |||||
| chr6:75638242
|
GTTT | G | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.459-2430_459-2428d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638242 | |||||
| chr6:75638385
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0267 | 2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.459-2299C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638385 | ||||||
| chr6:75638488
|
A | G | 1 | a0002c0003t0003g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.459-2196A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638488 | ||||||
| chr6:75638555
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0223 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.459-2102_459-2093d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638555 | |||||
| chr6:75638576
|
GTGTGTGT others(19): Show |
G | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.459-2106_459-2081d others(28): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638576 | |||||
| chr6:75638578
|
GTGTGTGT others(15): Show |
G | 2 | a0001c0001t0001g0208a0001c0001t0003g0053 | 2 | NA18955.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.459-2104_459-2083d others(24): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638578 | |||||
| chr6:75638578
|
GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0004g0311 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.459-2104_459-2081d others(26): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638578 | |||||
| chr6:75638580
|
GTGTGTGT others(5): Show |
G | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.459-2102_459-2091d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638580 | |||||
| chr6:75638580
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0001g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.459-2102_459-2087d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638580 | |||||
| chr6:75638580
|
GTGTGTGT others(11): Show |
G | 20 | a0001c0001t0001g0192a0001c0001t0001g0194a0001c0001t0001g0205others(17): Show | 20 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.459-2102_459-2085d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638580 | |||||
| chr6:75638580
|
GTGTGTGT others(13): Show |
G | 47 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0196others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.459-2102_459-2083d others(22): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638580 | |||||
| chr6:75638580
|
GTGTGTGT others(15): Show |
G | 27 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(24): Show | 27 | HG00642.hp2 HG01070.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.459-2102_459-2081d others(24): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638580 | |||||
| chr6:75638582
|
GTGTGTGT others(7): Show |
G | 2 | a0001c0001t0004g0330a0001c0001t0007g0307 | 2 | HG01975.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.459-2100_459-2087d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638582 | |||||
| chr6:75638582
|
GTGTGTGT others(9): Show |
G | 13 | a0001c0001t0002g0072a0001c0001t0004g0300a0001c0001t0004g0305others(10): Show | 13 | HG00673.hp1 HG01928.hp2 NA18906.hp1 others(10): Show |
intron_variant | MODIFIER | c.459-2100_459-2085d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638582 | |||||
| chr6:75638582
|
GTGTGTGT others(11): Show |
G | 2 | a0001c0001t0004g0304a0001c0001t0007g0327 | 2 | HG02004.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.459-2100_459-2083d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638582 | |||||
| chr6:75638582
|
GTGTGTGT others(13): Show |
G | 7 | a0001c0001t0001g0188a0001c0001t0001g0207a0001c0001t0001g0243others(4): Show | 7 | HG02027.hp2 HG02602.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2100_459-2081d others(22): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638582 | |||||
| chr6:75638582
|
GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0001g0242 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.459-2100_459-2079d others(24): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638582 | |||||
| chr6:75638584
|
GTGTGTGT others(3): Show |
G | 6 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG02040.hp1 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-2098_459-2089d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | |||||
| chr6:75638584
|
GTGTGTGT others(5): Show |
G | 8 | a0001c0001t0002g0117a0001c0001t0002g0139a0001c0001t0004g0301others(5): Show | 8 | HG02109.hp1 NA18941.hp1 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-2098_459-2087d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | |||||
| chr6:75638584
|
GTGTGTGT others(7): Show |
G | 7 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0333others(4): Show | 7 | HG00408.hp2 HG00438.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-2098_459-2085d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | |||||
| chr6:75638584
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.459-2098_459-2083d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | |||||
| chr6:75638584
|
GTGTGTGT others(11): Show |
G | 2 | a0001c0001t0004g0324a0001c0001t0004g0328 | 2 | NA18966.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.459-2098_459-2081d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | |||||
| chr6:75638584
|
GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0005g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.459-2098_459-2075d others(26): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | |||||
| chr6:75638586
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01106.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.459-2098G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638586 | ||||||
| chr6:75638586
|
GTGTGTAT others(1): Show |
G | 6 | a0001c0002t0003g0338a0001c0002t0003g0343a0001c0002t0003g0344others(3): Show | 6 | NA18612.hp2 NA18940.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-2096_459-2089d others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638586 | |||||
| chr6:75638586
|
GTGTGTAT others(3): Show |
G | 13 | a0001c0002t0003g0339a0001c0002t0003g0341a0001c0002t0003g0345others(10): Show | 13 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.459-2096_459-2087d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638586 | |||||
| chr6:75638586
|
GTGTGTAT others(5): Show |
G | 8 | a0001c0001t0004g0309a0001c0001t0004g0325a0001c0001t0004g0334others(5): Show | 8 | HG00597.hp1 HG02723.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-2096_459-2085d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638586 | |||||
| chr6:75638586
|
GTGTGTAT others(7): Show |
G | 2 | a0001c0001t0002g0122a0001c0001t0004g0310 | 2 | HG02129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.459-2096_459-2083d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638586 | |||||
| chr6:75638586
|
GTGTGTAT others(11): Show |
G | 1 | a0001c0001t0002g0086 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.459-2096_459-2079d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638586 | |||||
| chr6:75638588
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01106.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.459-2096G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638588 | ||||||
| chr6:75638588
|
GTGTATAT others(1): Show |
G | 3 | a0001c0001t0002g0079a0001c0002t0003g0011a0001c0002t0003g0351 | 3 | HG01192.hp1 HG01891.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.459-2094_459-2087d others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638588 | |||||
| chr6:75638588
|
GTGTATAT others(3): Show |
G | 1 | a0001c0001t0002g0089 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.459-2094_459-2085d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638588 | |||||
| chr6:75638588
|
GTGTATAT others(5): Show |
G | 18 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0059others(15): Show | 18 | HG00099.hp2 HG01123.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.459-2094_459-2083d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638588 | |||||
| chr6:75638588
|
GTGTATAT others(7): Show |
G | 4 | a0001c0001t0002g0058a0001c0001t0002g0101a0001c0001t0002g0120others(1): Show | 4 | HG01261.hp1 HG02145.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-2094_459-2081d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638588 | |||||
| chr6:75638588
|
GTGTATAT others(9): Show |
G | 5 | a0001c0001t0002g0071a0001c0001t0002g0094a0001c0001t0002g0095others(2): Show | 5 | HG02004.hp1 HG03579.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-2094_459-2079d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638588 | |||||
| chr6:75638590
|
G | A | 19 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.459-2094G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638590 | ||||||
| chr6:75638590
|
GTATATAT others(3): Show |
G | 7 | a0001c0001t0002g0061a0001c0001t0002g0085a0001c0001t0002g0133others(4): Show | 7 | HG00741.hp2 HG02602.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2070_459-2061d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638590 | |||||
| chr6:75638590
|
GTATATAT others(5): Show |
G | 2 | a0001c0001t0002g0068a0001c0001t0002g0097 | 2 | HG02055.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.459-2072_459-2061d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638590 | |||||
| chr6:75638590
|
GTATATAT others(7): Show |
G | 1 | a0001c0001t0002g0107 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.459-2074_459-2061d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638590 | |||||
| chr6:75638592
|
A | G | 91 | a0001c0001t0002g0074a0001c0001t0002g0109a0001c0001t0002g0110others(88): Show | 91 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.459-2092A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638592 | ||||||
| chr6:75638594
|
A | G | 68 | a0001c0001t0002g0114a0001c0001t0003g0022a0001c0001t0003g0023others(65): Show | 68 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.459-2090A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638594 | ||||||
| chr6:75638596
|
A | G | 54 | a0001c0001t0005g0143a0001c0001t0005g0144a0001c0001t0005g0145others(51): Show | 54 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.459-2088A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638596 | ||||||
| chr6:75638598
|
A | G | 35 | a0001c0001t0005g0145a0001c0001t0005g0152a0001c0001t0005g0153others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.459-2086A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638598 | ||||||
| chr6:75638600
|
A | G | 24 | a0001c0001t0002g0134a0001c0001t0005g0156a0001c0001t0005g0157others(21): Show | 24 | HG00280.hp2 HG00738.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.459-2084A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638600 | ||||||
| chr6:75638602
|
A | G | 7 | a0002c0003t0003g0031a0002c0003t0003g0032a0002c0003t0003g0033others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-2082A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638602 | ||||||
| chr6:75638604
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.459-2080A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638604 | ||||||
| chr6:75638606
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0057 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.459-2076_459-2060d others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638606 | |||||
| chr6:75638608
|
ATATATAT others(10): Show |
A | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.459-2074_459-2058d others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638608 | |||||
| chr6:75638608
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0005g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.459-2074_459-2053d others(24): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638608 | |||||
| chr6:75638608
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0005g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.459-2074_459-2051d others(26): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638608 | |||||
| chr6:75638609
|
TATATATA others(6): Show |
T | 1 | a0001c0017t0002g0108 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-2074_459-2062d others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638609 | ||||||
| chr6:75638610
|
ATATATAT others(6): Show |
A | 5 | a0001c0001t0002g0081a0001c0001t0002g0098a0001c0001t0002g0099others(2): Show | 5 | HG02165.hp2 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-2072_459-2060d others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | |||||
| chr6:75638610
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG02523.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.459-2072_459-2059d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | |||||
| chr6:75638610
|
ATATATAT others(9): Show |
A | 2 | a0001c0001t0002g0002a0001c0001t0002g0070 | 2 | HG01071.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.459-2072_459-2057d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | |||||
| chr6:75638610
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0001 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.459-2072_459-2056d others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | |||||
| chr6:75638610
|
ATATATAT others(11): Show |
A | 3 | a0001c0005t0006g0295a0004c0006t0005g0151a0004c0006t0005g0160 | 3 | HG03540.hp1 NA18980.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.459-2072_459-2055d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | |||||
| chr6:75638610
|
ATATATAT others(12): Show |
A | 1 | a0004c0006t0005g0150 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.459-2072_459-2054d others(21): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | |||||
| chr6:75638610
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0012g0148 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.459-2072_459-2052d others(23): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | |||||
| chr6:75638611
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0002g0136 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.459-2072_459-2062d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638611 | ||||||
| chr6:75638612
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0002g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.459-2070_459-2060d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | |||||
| chr6:75638612
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0002g0069a0001c0001t0002g0168 | 2 | HG03927.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.459-2070_459-2059d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | |||||
| chr6:75638612
|
ATATATAT others(6): Show |
A | 3 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113 | 3 | NA18955.hp1 NA18983.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.459-2070_459-2058d others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | |||||
| chr6:75638612
|
ATATATAT others(8): Show |
A | 1 | a0002c0003t0003g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.459-2070_459-2056d others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | |||||
| chr6:75638612
|
ATATATAT others(9): Show |
A | 2 | a0001c0005t0006g0292a0001c0005t0006g0293 | 2 | NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.459-2070_459-2055d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | |||||
| chr6:75638612
|
ATATATAT others(11): Show |
A | 9 | a0001c0001t0005g0143a0001c0001t0005g0144a0001c0001t0005g0159others(6): Show | 9 | HG01109.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-2070_459-2053d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | |||||
| chr6:75638612
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0005g0164 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.459-2070_459-2052d others(21): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | |||||
| chr6:75638612
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0223 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.459-2070_459-2050d others(23): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | |||||
| chr6:75638614
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0002g0114 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.459-2068_459-2059d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | |||||
| chr6:75638614
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0002g0128a0001c0002t0003g0350 | 2 | HG03195.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.459-2068_459-2058d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | |||||
| chr6:75638614
|
ATATATAT others(5): Show |
A | 3 | a0001c0001t0002g0109a0001c0001t0002g0119a0001c0001t0002g0123 | 3 | HG02015.hp1 NA18974.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.459-2068_459-2057d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | |||||
| chr6:75638614
|
ATATATAT others(9): Show |
A | 5 | a0001c0001t0005g0145a0001c0001t0005g0298a0001c0001t0005g0299others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-2068_459-2053d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | |||||
| chr6:75638614
|
ATATATAT others(10): Show |
A | 6 | a0001c0001t0005g0152a0001c0001t0005g0153a0001c0001t0005g0154others(3): Show | 6 | HG00280.hp2 HG00642.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-2068_459-2052d others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | |||||
| chr6:75638614
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0002g0125 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.459-2068_459-2046d others(25): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | |||||
| chr6:75638615
|
TATATATA | T | 3 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0110 | 3 | HG04115.hp2 NA18981.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.459-2068_459-2062d others(9): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638615 | ||||||
| chr6:75638616
|
A | T | 1 | a0001c0002t0003g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.459-2068A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638616 | ||||||
| chr6:75638616
|
ATATATAT others(3): Show |
A | 3 | a0001c0001t0002g0115a0001c0002t0003g0349a0001c0004t0014g0049 | 3 | HG00558.hp2 HG02083.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.459-2066_459-2057d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | |||||
| chr6:75638616
|
ATATATAT others(4): Show |
A | 1 | a0002c0003t0003g0029 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.459-2066_459-2056d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | |||||
| chr6:75638616
|
ATATATAT others(5): Show |
A | 1 | a0001c0016t0006g0297 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.459-2066_459-2055d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | |||||
| chr6:75638616
|
ATATATAT others(8): Show |
A | 2 | a0001c0001t0005g0156a0001c0001t0005g0161 | 2 | HG01168.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.459-2066_459-2052d others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | |||||
| chr6:75638616
|
ATATATAT others(10): Show |
A | 1 | a0009c0013t0005g0140 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.459-2066_459-2050d others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | |||||
| chr6:75638616
|
ATATATAT others(14): Show |
A | 1 | a0001c0002t0003g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459-2066_459-2046d others(23): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | |||||
| chr6:75638618
|
A | T | 4 | a0001c0002t0003g0005a0001c0002t0003g0006a0001c0002t0003g0021others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-2066A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638618 | ||||||
| chr6:75638618
|
ATATATTT others(5): Show |
A | 2 | a0001c0001t0010g0182a0001c0001t0010g0183 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.459-2064_459-2053d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638618 | |||||
| chr6:75638618
|
ATATATTT others(6): Show |
A | 1 | a0001c0001t0003g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.459-2064_459-2052d others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638618 | |||||
| chr6:75638620
|
A | T | 6 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-2064A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638620 | ||||||
| chr6:75638620
|
ATATTTTT others(3): Show |
A | 1 | a0001c0001t0010g0187 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.459-2062_459-2053d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638620 | |||||
| chr6:75638620
|
ATATTTTT others(4): Show |
A | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0013g0184others(1): Show | 4 | HG02145.hp2 HG02293.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-2062_459-2052d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638620 | |||||
| chr6:75638620
|
ATATTTTT others(5): Show |
A | 1 | a0001c0001t0003g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-2062_459-2051d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638620 | |||||
| chr6:75638621
|
TA | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0211a0001c0001t0001g0264others(1): Show | 4 | HG02523.hp2 NA18997.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-2062delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638621 | ||||||
| chr6:75638622
|
A | T | 25 | a0001c0001t0001g0285a0001c0001t0002g0056a0001c0001t0002g0065others(22): Show | 25 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.459-2062A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638622 | ||||||
| chr6:75638622
|
AT | A | 48 | a0001c0001t0001g0189a0001c0001t0001g0196a0001c0001t0001g0202others(45): Show | 48 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.459-2034delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638622 | |||||
| chr6:75638622
|
ATTT | A | 31 | a0001c0001t0001g0192a0001c0001t0001g0215a0001c0001t0001g0219others(28): Show | 31 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.459-2036_459-2034d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638622 | |||||
| chr6:75638622
|
ATTTT | A | 23 | a0001c0001t0001g0205a0001c0001t0001g0214a0001c0001t0002g0063others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.459-2037_459-2034d others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638622 | |||||
| chr6:75638622
|
ATTTTT | A | 18 | a0001c0001t0001g0212a0001c0001t0002g0062a0001c0001t0002g0117others(15): Show | 18 | HG00408.hp2 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.459-2038_459-2034d others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638622 | |||||
| chr6:75638622
|
ATTTTTT | A | 8 | a0001c0001t0002g0072a0001c0001t0004g0301a0001c0001t0004g0306others(5): Show | 8 | HG01516.hp1 HG02040.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-2039_459-2034d others(8): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638622 | |||||
| chr6:75638624
|
T | A | 47 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(44): Show | 47 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.459-2060T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638624 | ||||||
| chr6:75638626
|
T | A | 3 | a0001c0001t0002g0077a0001c0001t0003g0165a0001c0001t0004g0311 | 3 | HG02559.hp1 HG02683.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.459-2058T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638626 | ||||||
| chr6:75638627
|
T | A | 8 | a0002c0003t0003g0031a0002c0003t0003g0032a0002c0003t0003g0034others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-2057T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638627 | ||||||
| chr6:75638628
|
T | A | 2 | a0001c0001t0002g0077a0002c0003t0003g0047 | 2 | HG02683.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.459-2056T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638628 | ||||||
| chr6:75638630
|
T | A | 1 | a0001c0001t0002g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.459-2054T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638630 | ||||||
| chr6:75638631
|
T | A | 1 | a0001c0008t0003g0186 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459-2053T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638631 | ||||||
| chr6:75638632
|
T | A | 1 | a0001c0001t0002g0075 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.459-2052T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638632 | ||||||
| chr6:75638893
|
A | T | 6 | a0001c0002t0009g0007a0001c0002t0009g0008a0001c0002t0009g0009others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-1791A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638893 | ||||||
| chr6:75638947
|
G | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-1737G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638947 | ||||||
| chr6:75639031
|
A | G | 1 | a0001c0001t0020g0249 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.459-1653A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639031 | ||||||
| chr6:75639134
|
A | G | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.459-1550A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639134 | ||||||
| chr6:75639207
|
T | C | 1 | a0001c0001t0002g0090 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.459-1477T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639207 | ||||||
| chr6:75639389
|
T | A | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.459-1295T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639389 | ||||||
| chr6:75639390
|
A | C | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.459-1294A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639390 | ||||||
| chr6:75639452
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.459-1232G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639452 | ||||||
| chr6:75639546
|
C | T | 4 | a0001c0001t0010g0182a0001c0001t0010g0183a0001c0001t0010g0187others(1): Show | 4 | HG02622.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-1138C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639546 | ||||||
| chr6:75639640
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.459-1044A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639640 | ||||||
| chr6:75639733
|
A | G | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.459-951A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639733 | ||||||
| chr6:75639754
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.459-930T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639754 | ||||||
| chr6:75639831
|
T | A | 1 | a0007c0014t0002g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.459-853T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639831 | ||||||
| chr6:75639840
|
T | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-844T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639840 | ||||||
| chr6:75639998
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-686G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639998 | ||||||
| chr6:75640277
|
C | T | 6 | a0001c0002t0009g0007a0001c0002t0009g0008a0001c0002t0009g0009others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-407C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640277 | ||||||
| chr6:75640305
|
A | G | 1 | a0001c0004t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.459-379A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640305 | ||||||
| chr6:75640322
|
A | G | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.459-362A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640322 | ||||||
| chr6:75640415
|
T | C | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.459-269T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640415 | ||||||
| chr6:75640478
|
CCTGTT | C | 102 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.459-205_459-201del others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640478 | ||||||
| chr6:75640561
|
T | G | 1 | a0001c0001t0001g0221 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.459-123T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640561 | ||||||
| chr6:75640597
|
C | G | 2 | a0001c0001t0002g0130a0001c0001t0016g0121 | 2 | HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.459-87C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640597 | ||||||
| chr6:75640924
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.479+220A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75640924 | ||||||
| chr6:75641002
|
T | A | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.479+298T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641002 | ||||||
| chr6:75641014
|
T | C | 1 | a0002c0003t0003g0027 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.479+310T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641014 | ||||||
| chr6:75641241
|
A | C | 1 | a0001c0001t0005g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.479+537A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641241 | ||||||
| chr6:75641258
|
A | G | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.479+554A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641258 | ||||||
| chr6:75641259
|
T | C | 1 | a0002c0003t0003g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.479+555T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641259 | ||||||
| chr6:75641345
|
T | C | 4 | a0001c0001t0005g0141a0001c0001t0005g0298a0001c0001t0005g0299others(1): Show | 4 | HG01346.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+641T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641345 | ||||||
| chr6:75641456
|
T | G | 1 | a0011c0015t0001g0287 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.479+752T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641456 | ||||||
| chr6:75641484
|
T | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.479+780T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641484 | ||||||
| chr6:75641694
|
T | G | 1 | a0001c0002t0022g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.479+990T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641694 | ||||||
| chr6:75641745
|
A | G | 1 | a0002c0003t0003g0038 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.479+1041A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641745 | ||||||
| chr6:75641904
|
G | C | 1 | a0001c0002t0009g0007 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+1200G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641904 | ||||||
| chr6:75641924
|
C | T | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.479+1220C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641924 | ||||||
| chr6:75642162
|
G | A | 1 | a0001c0001t0017g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.479+1458G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642162 | ||||||
| chr6:75642266
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.479+1562T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642266 | ||||||
| chr6:75642283
|
C | G | 153 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(150): Show | 153 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.479+1579C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642283 | ||||||
| chr6:75642314
|
C | T | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064 | 3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.479+1610C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642314 | ||||||
| chr6:75642333
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.479+1629G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642333 | ||||||
| chr6:75642342
|
G | A | 3 | a0001c0001t0003g0053a0001c0001t0003g0165a0010c0012t0003g0166 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.479+1638G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642342 | ||||||
| chr6:75642794
|
A | G | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.479+2090A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642794 | ||||||
| chr6:75643264
|
T | A | 2 | a0001c0002t0003g0018a0001c0002t0003g0019 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.479+2560T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643264 | ||||||
| chr6:75643336
|
A | G | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.479+2632A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643336 | ||||||
| chr6:75643367
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.479+2663G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643367 | ||||||
| chr6:75643605
|
C | G | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.479+2901C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643605 | ||||||
| chr6:75643649
|
G | A | 1 | a0001c0002t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.479+2945G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643649 | ||||||
| chr6:75643765
|
A | G | 2 | a0001c0001t0004g0310a0001c0001t0004g0323 | 2 | HG00438.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.479+3061A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643765 | ||||||
| chr6:75643876
|
A | G | 1 | a0001c0002t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.479+3172A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643876 | ||||||
| chr6:75644001
|
A | G | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.479+3297A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644001 | ||||||
| chr6:75644081
|
A | G | 1 | a0002c0003t0003g0045 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.479+3377A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644081 | ||||||
| chr6:75644154
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.479+3450A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644154 | ||||||
| chr6:75644210
|
G | T | 1 | a0001c0001t0001g0240 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.479+3506G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644210 | ||||||
| chr6:75644227
|
A | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.480-3504A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644227 | ||||||
| chr6:75644253
|
C | T | 1 | a0001c0001t0017g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.480-3478C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644253 | ||||||
| chr6:75644291
|
A | G | 1 | a0001c0001t0003g0024 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.480-3440A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644291 | ||||||
| chr6:75644317
|
G | A | 19 | a0001c0001t0005g0143a0001c0001t0005g0144a0001c0001t0005g0145others(16): Show | 19 | HG00280.hp2 HG00642.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.480-3414G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644317 | ||||||
| chr6:75644475
|
C | CT | 156 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.480-3242dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 75644475 | |||||
| chr6:75644559
|
A | C | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.480-3172A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644559 | ||||||
| chr6:75644682
|
G | T | 1 | a0001c0001t0002g0125 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.480-3049G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644682 | ||||||
| chr6:75644728
|
G | T | 1 | a0001c0001t0002g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.480-3003G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644728 | ||||||
| chr6:75644738
|
G | A | 6 | a0001c0001t0001g0208a0001c0001t0001g0229a0001c0001t0001g0230others(3): Show | 6 | HG02027.hp2 NA18944.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.480-2993G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644738 | ||||||
| chr6:75644913
|
C | T | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.480-2818C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644913 | ||||||
| chr6:75645381
|
C | T | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.480-2350C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75645381 | ||||||
| chr6:75645573
|
C | T | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.480-2158C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75645573 | ||||||
| chr6:75645766
|
ACT | A | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.480-1962_480-1961d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 75645766 | |||||
| chr6:75645802
|
C | A | 2 | a0001c0002t0003g0338a0001c0002t0003g0345 | 2 | NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.480-1929C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75645802 | ||||||
| chr6:75645980
|
C | T | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.480-1751C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75645980 | ||||||
| chr6:75646013
|
A | G | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.480-1718A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646013 | ||||||
| chr6:75646034
|
A | G | 1 | a0001c0002t0003g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.480-1697A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646034 | ||||||
| chr6:75646042
|
A | T | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.480-1689A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646042 | ||||||
| chr6:75646215
|
C | A | 1 | a0001c0001t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.480-1516C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646215 | ||||||
| chr6:75646427
|
A | G | 2 | a0001c0001t0001g0204a0001c0002t0003g0011 | 2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.480-1304A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646427 | ||||||
| chr6:75646466
|
T | G | 4 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(1): Show | 4 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-1265T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646466 | ||||||
| chr6:75646497
|
A | C | 25 | a0001c0002t0003g0338a0001c0002t0003g0339a0001c0002t0003g0340others(22): Show | 25 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.480-1234A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646497 | ||||||
| chr6:75646565
|
G | A | 2 | a0001c0002t0003g0018a0001c0002t0003g0019 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.480-1166G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646565 | ||||||
| chr6:75646619
|
G | A | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.480-1112G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646619 | ||||||
| chr6:75646708
|
C | T | 38 | a0001c0001t0003g0053a0001c0004t0003g0173a0001c0004t0003g0174others(35): Show | 38 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.480-1023C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646708 | ||||||
| chr6:75646729
|
G | T | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.480-1002G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646729 | ||||||
| chr6:75646814
|
C | T | 1 | a0002c0003t0003g0030 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.480-917C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646814 | ||||||
| chr6:75647130
|
C | G | 87 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(84): Show | 87 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.480-601C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647130 | ||||||
| chr6:75647145
|
T | C | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.480-586T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647145 | ||||||
| chr6:75647167
|
T | G | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.480-564T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647167 | ||||||
| chr6:75647176
|
A | G | 1 | a0001c0002t0009g0009 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.480-555A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647176 | ||||||
| chr6:75647204
|
C | T | 1 | a0001c0004t0003g0177 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.480-527C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647204 | ||||||
| chr6:75647320
|
A | G | 1 | a0001c0001t0004g0322 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.480-411A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647320 | ||||||
| chr6:75647463
|
T | C | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.480-268T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647463 | ||||||
| chr6:75647652
|
T | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.480-79T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647652 | ||||||
| chr6:75647710
|
C | T | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.480-21C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647710 | ||||||
| chr6:75647877
|
G | A | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.550+76G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75647877 | ||||||
| chr6:75647911
|
A | G | 1 | a0001c0001t0010g0187 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.550+110A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75647911 | ||||||
| chr6:75647941
|
T | A | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.550+140T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75647941 | ||||||
| chr6:75647984
|
C | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.550+183C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75647984 | ||||||
| chr6:75648119
|
T | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.550+318T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648119 | ||||||
| chr6:75648142
|
G | A | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+341G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648142 | ||||||
| chr6:75648196
|
C | G | 1 | a0001c0005t0006g0296 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.550+395C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648196 | ||||||
| chr6:75648204
|
C | G | 1 | a0001c0001t0001g0247 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.550+403C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648204 | ||||||
| chr6:75648513
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.550+712C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648513 | ||||||
| chr6:75648572
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.550+771T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648572 | ||||||
| chr6:75648597
|
T | G | 1 | a0001c0001t0002g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.550+796T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648597 | ||||||
| chr6:75648657
|
T | C | 39 | a0001c0001t0003g0053a0001c0001t0003g0165a0001c0004t0003g0173others(36): Show | 39 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.550+856T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648657 | ||||||
| chr6:75649049
|
A | C | 1 | a0001c0002t0009g0007 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.550+1248A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649049 | ||||||
| chr6:75649085
|
C | T | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.550+1284C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649085 | ||||||
| chr6:75649137
|
C | T | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.550+1336C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649137 | ||||||
| chr6:75649172
|
G | C | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.550+1371G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649172 | ||||||
| chr6:75649307
|
T | A | 2 | a0002c0003t0003g0045a0002c0003t0003g0046 | 2 | HG01074.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.550+1506T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649307 | ||||||
| chr6:75649598
|
A | G | 4 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(1): Show | 4 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+1797A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649598 | ||||||
| chr6:75649674
|
G | A | 1 | a0001c0001t0002g0105 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.550+1873G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649674 | ||||||
| chr6:75649706
|
G | T | 1 | a0001c0002t0003g0018 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.550+1905G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649706 | ||||||
| chr6:75649732
|
G | C | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.550+1931G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649732 | ||||||
| chr6:75649767
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.550+1966G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649767 | ||||||
| chr6:75649797
|
C | T | 2 | a0001c0002t0011g0012a0001c0002t0011g0016 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.550+1996C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649797 | ||||||
| chr6:75649816
|
T | C | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.550+2015T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649816 | ||||||
| chr6:75649925
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.550+2124A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649925 | ||||||
| chr6:75650146
|
T | C | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+2345T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75650146 | ||||||
| chr6:75650327
|
G | A | 1 | a0002c0003t0003g0033 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.550+2526G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75650327 | ||||||
| chr6:75650541
|
C | T | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+2740C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75650541 | ||||||
| chr6:75650962
|
G | C | 1 | a0001c0001t0002g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.550+3161G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75650962 | ||||||
| chr6:75651343
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.550+3542A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75651343 | ||||||
| chr6:75651380
|
G | T | 1 | a0001c0016t0006g0297 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.550+3579G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75651380 | ||||||
| chr6:75651431
|
T | C | 1 | a0001c0001t0004g0300 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.550+3630T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75651431 | ||||||
| chr6:75651447
|
T | G | 39 | a0001c0001t0003g0053a0001c0001t0003g0165a0001c0004t0003g0173others(36): Show | 39 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.550+3646T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75651447 | ||||||
| chr6:75651450
|
T | G | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.550+3649T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75651450 | ||||||
| chr6:75652134
|
G | A | 4 | a0001c0001t0001g0216a0001c0001t0001g0226a0001c0001t0001g0232others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+4333G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652134 | ||||||
| chr6:75652140
|
G | C | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.550+4339G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652140 | ||||||
| chr6:75652158
|
C | T | 1 | a0001c0001t0005g0143 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.550+4357C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652158 | ||||||
| chr6:75652162
|
G | A | 2 | a0002c0003t0003g0051a0002c0003t0003g0052 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.550+4361G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652162 | ||||||
| chr6:75652253
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.550+4452C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652253 | ||||||
| chr6:75652254
|
G | T | 1 | a0001c0001t0001g0274 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.550+4453G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652254 | ||||||
| chr6:75652302
|
C | T | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.550+4501C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652302 | ||||||
| chr6:75652330
|
T | C | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.550+4529T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652330 | ||||||
| chr6:75652487
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.550+4686A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652487 | ||||||
| chr6:75652600
|
G | C | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.550+4799G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652600 | ||||||
| chr6:75652683
|
C | CAAAA | 17 | a0001c0002t0009g0007a0001c0002t0009g0008a0001c0002t0009g0009others(14): Show | 17 | HG01081.hp2 HG02055.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.550+4899_550+4902d others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | |||||
| chr6:75652683
|
C | CAAAAA | 24 | a0001c0004t0003g0177a0002c0003t0003g0026a0002c0003t0003g0027others(21): Show | 24 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.550+4898_550+4902d others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | |||||
| chr6:75652683
|
C | CAAAAAAA others(1): Show |
25 | a0001c0001t0002g0093a0001c0001t0002g0127a0001c0001t0002g0168others(22): Show | 25 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.550+4895_550+4902d others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | |||||
| chr6:75652683
|
C | CAAAAAAA others(2): Show |
83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.550+4894_550+4902d others(11): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | |||||
| chr6:75652683
|
C | CAAAAAAA others(3): Show |
13 | a0001c0001t0002g0056a0001c0001t0002g0071a0001c0001t0002g0082others(10): Show | 13 | HG00140.hp1 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.550+4893_550+4902d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | |||||
| chr6:75652683
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0016g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.550+4892_550+4902d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | |||||
| chr6:75652683
|
C | CAAGAAAA others(3): Show |
1 | a0001c0001t0002g0058 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.550+4884_550+4885i others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | |||||
| chr6:75652683
|
CA | C | 101 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.550+4902delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | |||||
| chr6:75652696
|
A | AAAAAAAA others(4): Show |
3 | a0001c0001t0004g0320a0001c0001t0004g0336a0001c0001t0007g0313 | 3 | NA18941.hp1 NA18977.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.550+4902_550+4903i others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652696 | |||||
| chr6:75652696
|
A | AAAAAAAA others(3): Show |
35 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(32): Show | 35 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.550+4902_550+4903i others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652696 | |||||
| chr6:75652698
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0003g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.550+4902_550+4903i others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652698 | |||||
| chr6:75652698
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.550+4902_550+4903i others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652698 | |||||
| chr6:75652698
|
A | G | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.550+4897A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652698 | ||||||
| chr6:75652700
|
A | AAG | 9 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(6): Show | 9 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+4900_550+4901i others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652700 | |||||
| chr6:75652709
|
A | G | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.550+4908A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652709 | ||||||
| chr6:75652827
|
G | C | 3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093 | 3 | NA18747.hp2 NA18945.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.550+5026G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652827 | ||||||
| chr6:75653025
|
TTTTCTTT others(2): Show |
T | 25 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(22): Show | 25 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.550+5228_550+5236d others(11): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75653025 | |||||
| chr6:75653092
|
G | T | 2 | a0002c0003t0003g0036a0002c0003t0003g0042 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.550+5291G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653092 | ||||||
| chr6:75653139
|
T | C | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.550+5338T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653139 | ||||||
| chr6:75653433
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0267 | 2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.550+5632A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653433 | ||||||
| chr6:75653549
|
T | G | 1 | a0001c0001t0005g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.551-5713T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653549 | ||||||
| chr6:75653653
|
A | G | 1 | a0001c0002t0003g0169 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.551-5609A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653653 | ||||||
| chr6:75653660
|
G | GT | 188 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.551-5590dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75653660 | |||||
| chr6:75653660
|
GT | G | 44 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(41): Show | 44 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.551-5590delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75653660 | |||||
| chr6:75653675
|
CTA | C | 3 | a0001c0001t0001g0205a0001c0001t0001g0214a0001c0001t0001g0219 | 3 | HG01884.hp2 HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.551-5586_551-5585d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653675 | ||||||
| chr6:75653822
|
A | G | 39 | a0001c0001t0003g0053a0001c0001t0003g0165a0001c0004t0003g0173others(36): Show | 39 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.551-5440A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653822 | ||||||
| chr6:75654038
|
G | A | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.551-5224G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654038 | ||||||
| chr6:75654053
|
G | A | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.551-5209G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654053 | ||||||
| chr6:75654148
|
C | T | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.551-5114C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654148 | ||||||
| chr6:75654472
|
C | T | 3 | a0001c0001t0001g0256a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | NA18947.hp1 NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.551-4790C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654472 | ||||||
| chr6:75654556
|
T | C | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.551-4706T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654556 | ||||||
| chr6:75654604
|
A | G | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.551-4658A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654604 | ||||||
| chr6:75654708
|
G | A | 2 | a0001c0004t0003g0173a0001c0004t0003g0179 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.551-4554G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654708 | ||||||
| chr6:75654884
|
T | G | 1 | a0001c0001t0001g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.551-4378T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654884 | ||||||
| chr6:75655034
|
C | G | 1 | a0001c0001t0017g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.551-4228C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655034 | ||||||
| chr6:75655040
|
T | G | 4 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0070others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-4222T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655040 | ||||||
| chr6:75655187
|
C | T | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.551-4075C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655187 | ||||||
| chr6:75655509
|
T | C | 1 | a0011c0015t0001g0287 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.551-3753T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655509 | ||||||
| chr6:75655523
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.551-3739C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655523 | ||||||
| chr6:75655526
|
T | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.551-3736T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655526 | ||||||
| chr6:75655690
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.551-3572C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655690 | ||||||
| chr6:75655779
|
C | G | 36 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057others(33): Show | 36 | HG00099.hp2 HG01123.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.551-3483C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655779 | ||||||
| chr6:75655834
|
C | G | 5 | a0001c0001t0001g0216a0001c0001t0001g0226a0001c0001t0001g0232others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.551-3428C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655834 | ||||||
| chr6:75655899
|
T | C | 2 | a0001c0001t0010g0182a0001c0001t0013g0184 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.551-3363T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655899 | ||||||
| chr6:75656053
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0267 | 2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.551-3209A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656053 | ||||||
| chr6:75656104
|
A | T | 1 | a0001c0002t0011g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.551-3158A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656104 | ||||||
| chr6:75656193
|
G | A | 6 | a0001c0002t0009g0007a0001c0002t0009g0008a0001c0002t0009g0009others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.551-3069G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656193 | ||||||
| chr6:75656208
|
C | T | 1 | a0002c0003t0003g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.551-3054C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656208 | ||||||
| chr6:75656213
|
CA | C | 53 | a0001c0001t0001g0203a0001c0001t0002g0074a0001c0001t0002g0103others(50): Show | 53 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.551-3030delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75656213 | |||||
| chr6:75656213
|
CAA | C | 287 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.551-3031_551-3030d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75656213 | |||||
| chr6:75656295
|
G | A | 4 | a0001c0001t0010g0182a0001c0001t0010g0183a0001c0001t0010g0187others(1): Show | 4 | HG02622.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-2967G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656295 | ||||||
| chr6:75656308
|
T | A | 4 | a0001c0001t0002g0054a0001c0001t0002g0098a0001c0001t0002g0099others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-2954T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656308 | ||||||
| chr6:75656441
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.551-2821G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656441 | ||||||
| chr6:75656531
|
G | A | 4 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(1): Show | 4 | NA18981.hp2 NA19056.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.551-2731G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656531 | ||||||
| chr6:75656540
|
G | A | 1 | a0009c0013t0005g0140 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.551-2722G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656540 | ||||||
| chr6:75656550
|
A | G | 5 | a0002c0003t0003g0035a0002c0003t0003g0039a0002c0003t0003g0050others(2): Show | 5 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.551-2712A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656550 | ||||||
| chr6:75657008
|
T | C | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.551-2254T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657008 | ||||||
| chr6:75657140
|
C | G | 1 | a0006c0010t0009g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.551-2122C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657140 | ||||||
| chr6:75657342
|
A | T | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.551-1920A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657342 | ||||||
| chr6:75657482
|
A | G | 3 | a0001c0001t0002g0069a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG02165.hp2 NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.551-1780A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657482 | ||||||
| chr6:75657485
|
A | G | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.551-1777A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657485 | ||||||
| chr6:75657708
|
A | G | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.551-1554A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657708 | ||||||
| chr6:75657801
|
A | G | 1 | a0001c0001t0002g0061 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.551-1461A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657801 | ||||||
| chr6:75658124
|
G | C | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.551-1138G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658124 | ||||||
| chr6:75658179
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.551-1083G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658179 | ||||||
| chr6:75658219
|
C | T | 1 | a0001c0001t0018g0060 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.551-1043C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658219 | ||||||
| chr6:75658225
|
A | G | 2 | a0001c0001t0002g0130a0001c0001t0016g0121 | 2 | HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.551-1037A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658225 | ||||||
| chr6:75658405
|
A | G | 2 | a0001c0002t0009g0170a0001c0002t0009g0171 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.551-857A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658405 | ||||||
| chr6:75658417
|
C | T | 1 | a0001c0001t0008g0209 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.551-845C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658417 | ||||||
| chr6:75658614
|
A | T | 3 | a0001c0001t0001g0256a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | NA18947.hp1 NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.551-648A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658614 | ||||||
| chr6:75658689
|
G | A | 3 | a0001c0001t0002g0101a0001c0001t0003g0053a0010c0012t0003g0166 | 3 | HG02809.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.551-573G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658689 | ||||||
| chr6:75658721
|
G | A | 315 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.551-541G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658721 | ||||||
| chr6:75658801
|
G | A | 2 | a0001c0001t0005g0298a0001c0001t0005g0299 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.551-461G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658801 | ||||||
| chr6:75658947
|
A | G | 1 | a0001c0001t0005g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.551-315A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658947 | ||||||
| chr6:75658970
|
TC | T | 20 | a0001c0001t0002g0056a0001c0001t0002g0065a0001c0001t0002g0068others(17): Show | 20 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.551-288delC | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658970 | |||||
| chr6:75658973
|
C | CA | 3 | a0001c0001t0005g0146a0001c0001t0005g0298a0009c0013t0005g0140 | 3 | HG01346.hp1 HG02809.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.551-289_551-288ins others(1): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658973 | ||||||
| chr6:75658973
|
CCA | C | 77 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(74): Show | 77 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.551-288_551-287del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658973 | ||||||
| chr6:75658974
|
C | A | 24 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(21): Show | 24 | HG00280.hp2 HG00642.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.551-288C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658974 | ||||||
| chr6:75658974
|
C | CA | 34 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0025others(31): Show | 34 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.551-262dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658974 | |||||
| chr6:75658974
|
C | CAA | 6 | a0001c0001t0003g0023a0001c0001t0010g0187a0001c0008t0003g0185others(3): Show | 6 | HG02145.hp2 HG02723.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-263_551-262dup others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658974 | |||||
| chr6:75658974
|
CA | C | 15 | a0001c0001t0001g0197a0001c0001t0001g0224a0001c0001t0001g0231others(12): Show | 15 | HG00423.hp1 HG00597.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.551-262delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658974 | |||||
| chr6:75658974
|
CAA | C | 116 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.551-263_551-262del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658974 | |||||
| chr6:75658974
|
CAAA | C | 6 | a0001c0001t0001g0217a0001c0001t0001g0226a0001c0001t0001g0230others(3): Show | 6 | HG01515.hp2 NA18522.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.551-264_551-262del others(3): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658974 | |||||
| chr6:75658977
|
A | C | 1 | a0001c0001t0001g0213 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.551-285A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658977 | ||||||
| chr6:75658999
|
AAG | A | 34 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(31): Show | 34 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.551-262_551-261del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658999 | ||||||
| chr6:75659000
|
A | G | 2 | a0001c0002t0003g0356a0001c0002t0011g0012 | 2 | HG02965.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.551-262A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75659000 | ||||||
| chr6:75659000
|
AG | A | 4 | a0001c0001t0003g0165a0001c0001t0007g0327a0001c0001t0007g0332others(1): Show | 4 | HG02559.hp1 HG03225.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.551-258delG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75659000 | |||||
| chr6:75659001
|
G | A | 172 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.551-261G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75659001 | ||||||
| chr6:75659034
|
G | C | 6 | a0001c0002t0009g0007a0001c0002t0009g0008a0001c0002t0009g0009others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.551-228G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75659034 | ||||||
| chr6:75659141
|
TAAGAG | T | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.551-115_551-111del others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75659141 | |||||
| chr6:75659173
|
G | A | 2 | a0001c0001t0002g0133a0001c0001t0002g0134 | 2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.551-89G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75659173 | ||||||
| chr6:75659476
|
T | C | 11 | a0001c0001t0005g0143a0001c0001t0005g0144a0001c0001t0005g0145others(8): Show | 11 | NA18960.hp1 NA18980.hp1 NA18988.hp2 others(8): Show |
intron_variant | MODIFIER | c.696+69T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75659476 | ||||||
| chr6:75659784
|
C | T | 1 | a0001c0002t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.696+377C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75659784 | ||||||
| chr6:75659842
|
G | T | 1 | a0001c0001t0003g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.696+435G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75659842 | ||||||
| chr6:75660057
|
G | A | 1 | a0001c0002t0003g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.696+650G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660057 | ||||||
| chr6:75660057
|
G | C | 2 | a0001c0001t0004g0312a0001c0001t0004g0315 | 2 | NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.696+650G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660057 | ||||||
| chr6:75660269
|
A | G | 347 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(344): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.696+862A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660269 | ||||||
| chr6:75660414
|
G | T | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.696+1007G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660414 | ||||||
| chr6:75660504
|
G | C | 33 | a0001c0002t0003g0020a0001c0002t0003g0169a0001c0002t0003g0338others(30): Show | 33 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.696+1097G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660504 | ||||||
| chr6:75660679
|
C | G | 3 | a0001c0001t0003g0053a0001c0001t0003g0165a0010c0012t0003g0166 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.696+1272C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660679 | ||||||
| chr6:75660695
|
C | T | 6 | a0001c0002t0009g0007a0001c0002t0009g0008a0001c0002t0009g0009others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.696+1288C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660695 | ||||||
| chr6:75660696
|
G | C | 2 | a0001c0001t0002g0058a0001c0017t0002g0108 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.696+1289G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660696 | ||||||
| chr6:75660751
|
C | T | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.696+1344C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660751 | ||||||
| chr6:75660782
|
C | A | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.696+1375C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660782 | ||||||
| chr6:75660790
|
C | T | 1 | a0001c0001t0005g0145 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.696+1383C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660790 | ||||||
| chr6:75660853
|
A | T | 1 | a0001c0001t0001g0247 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.696+1446A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660853 | ||||||
| chr6:75660870
|
G | A | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.696+1463G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660870 | ||||||
| chr6:75660910
|
C | T | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.696+1503C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660910 | ||||||
| chr6:75660997
|
G | A | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+1590G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660997 | ||||||
| chr6:75661070
|
T | C | 1 | a0001c0001t0007g0317 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.696+1663T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661070 | ||||||
| chr6:75661076
|
C | G | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.696+1669C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661076 | ||||||
| chr6:75661204
|
C | A | 5 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+1797C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661204 | ||||||
| chr6:75661230
|
C | T | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.696+1823C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661230 | ||||||
| chr6:75661295
|
T | C | 1 | a0001c0002t0003g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.696+1888T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661295 | ||||||
| chr6:75661405
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.697-1816A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661405 | ||||||
| chr6:75661666
|
T | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0241 | 2 | NA18939.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.697-1555T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661666 | ||||||
| chr6:75661697
|
G | C | 1 | a0002c0003t0003g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.697-1524G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661697 | ||||||
| chr6:75662053
|
A | AAAAT | 8 | a0001c0001t0001g0270a0001c0002t0009g0007a0001c0002t0009g0008others(5): Show | 8 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.697-1144_697-1141d others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr6 | 75662053 | |||||
| chr6:75662053
|
AAAATAAA others(5): Show |
A | 5 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG01070.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-1152_697-1141d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr6 | 75662053 | |||||
| chr6:75662265
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.697-956A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662265 | ||||||
| chr6:75662466
|
CA | C | 4 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0070others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.697-754delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662466 | ||||||
| chr6:75662782
|
G | A | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.697-439G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662782 | ||||||
| chr6:75662839
|
T | C | 1 | a0001c0001t0001g0238 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.697-382T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662839 | ||||||
| chr6:75662964
|
A | G | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.697-257A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662964 | ||||||
| chr6:75662985
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.697-236G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662985 | ||||||
| chr6:75663064
|
T | G | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.697-157T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75663064 | ||||||
| chr6:75663216
|
C | T | 1 | a0002c0003t0003g0039 | 1 | HG01243.hp2 | splice_region_variant&intron_variant | LOW | c.697-5C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75663216 | ||||||
| chr6:75663558
|
C | T | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.994+40C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663558 | ||||||
| chr6:75663727
|
G | GT | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.994+211dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75663727 | |||||
| chr6:75663797
|
G | A | 4 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(1): Show | 4 | NA18981.hp2 NA19056.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+279G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663797 | ||||||
| chr6:75663805
|
TG | T | 213 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(210): Show | 213 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.994+290delG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75663805 | |||||
| chr6:75663807
|
G | GTT | 9 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(6): Show | 9 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.994+289_994+290ins others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663807 | ||||||
| chr6:75663808
|
G | T | 58 | a0001c0001t0001g0234a0001c0001t0001g0237a0001c0001t0001g0274others(55): Show | 58 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.994+290G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663808 | ||||||
| chr6:75663818
|
T | TG | 3 | a0002c0003t0003g0043a0002c0003t0019g0040a0010c0012t0003g0166 | 3 | HG02698.hp1 NA19240.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.994+300_994+301ins others(1): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663818 | ||||||
| chr6:75663820
|
G | T | 2 | a0001c0008t0003g0186a0004c0006t0005g0150 | 2 | HG03516.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.994+302G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663820 | ||||||
| chr6:75663820
|
GT | G | 13 | a0001c0001t0005g0143a0001c0001t0005g0144a0001c0001t0005g0146others(10): Show | 13 | HG00280.hp2 HG01168.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.994+303delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663820 | ||||||
| chr6:75663821
|
T | G | 19 | a0001c0001t0003g0165a0001c0001t0005g0141a0001c0001t0005g0145others(16): Show | 19 | HG00642.hp1 HG01069.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.994+303T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663821 | ||||||
| chr6:75663821
|
T | TG | 38 | a0001c0001t0001g0256a0001c0001t0001g0266a0001c0001t0001g0270others(35): Show | 38 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.994+314dupG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75663821 | |||||
| chr6:75663821
|
TG | T | 150 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0192others(147): Show | 150 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.994+314delG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75663821 | |||||
| chr6:75663821
|
TGG | T | 33 | a0001c0002t0003g0020a0001c0002t0003g0169a0001c0002t0003g0338others(30): Show | 33 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.994+313_994+314del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75663821 | |||||
| chr6:75663827
|
G | C | 1 | a0001c0001t0001g0233 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.994+309G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663827 | ||||||
| chr6:75663830
|
G | T | 1 | a0001c0001t0005g0161 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.994+312G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663830 | ||||||
| chr6:75663851
|
G | A | 271 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(268): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.994+333G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663851 | ||||||
| chr6:75663884
|
A | G | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.994+366A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663884 | ||||||
| chr6:75664023
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.994+505G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664023 | ||||||
| chr6:75664115
|
A | G | 5 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG01070.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.994+597A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664115 | ||||||
| chr6:75664155
|
A | G | 13 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.994+637A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664155 | ||||||
| chr6:75664215
|
C | T | 38 | a0001c0001t0003g0053a0001c0004t0003g0173a0001c0004t0003g0174others(35): Show | 38 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.994+697C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664215 | ||||||
| chr6:75664260
|
T | TG | 25 | a0001c0002t0003g0338a0001c0002t0003g0339a0001c0002t0003g0340others(22): Show | 25 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.994+742_994+743ins others(1): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664260 | ||||||
| chr6:75664261
|
A | G | 21 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(18): Show | 21 | HG01109.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.994+743A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664261 | ||||||
| chr6:75664375
|
TATAC | T | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.994+860_994+863del others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75664375 | |||||
| chr6:75664482
|
AAT | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.994+966_994+967del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75664482 | |||||
| chr6:75664805
|
T | A | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.994+1287T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664805 | ||||||
| chr6:75664921
|
C | T | 1 | a0002c0003t0003g0044 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.994+1403C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664921 | ||||||
| chr6:75664998
|
A | G | 1 | a0001c0001t0002g0081 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.994+1480A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664998 | ||||||
| chr6:75665057
|
C | T | 5 | a0001c0001t0002g0109a0001c0001t0002g0112a0001c0001t0002g0113others(2): Show | 5 | NA18955.hp1 NA18974.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.994+1539C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665057 | ||||||
| chr6:75665069
|
G | A | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.994+1551G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665069 | ||||||
| chr6:75665280
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.995-1432C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665280 | ||||||
| chr6:75665285
|
C | CA | 45 | a0001c0001t0001g0231a0001c0001t0001g0240a0001c0001t0001g0261others(42): Show | 45 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.995-1411dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75665285 | |||||
| chr6:75665285
|
CA | C | 38 | a0001c0001t0001g0216a0001c0001t0005g0141a0001c0001t0005g0143others(35): Show | 38 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.995-1411delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75665285 | |||||
| chr6:75665448
|
G | C | 6 | a0001c0002t0009g0007a0001c0002t0009g0008a0001c0002t0009g0009others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-1264G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665448 | ||||||
| chr6:75665523
|
A | G | 13 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.995-1189A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665523 | ||||||
| chr6:75665605
|
A | G | 149 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.995-1107A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665605 | ||||||
| chr6:75665820
|
A | G | 1 | a0001c0001t0004g0314 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.995-892A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665820 | ||||||
| chr6:75665824
|
C | T | 150 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(147): Show | 150 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.995-888C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665824 | ||||||
| chr6:75665902
|
A | G | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064 | 3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.995-810A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665902 | ||||||
| chr6:75665914
|
G | A | 5 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-798G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665914 | ||||||
| chr6:75665930
|
G | A | 2 | a0001c0001t0005g0298a0001c0001t0005g0299 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.995-782G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665930 | ||||||
| chr6:75665950
|
C | T | 4 | a0001c0001t0002g0058a0001c0001t0002g0065a0001c0001t0002g0120others(1): Show | 4 | HG01261.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-762C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665950 | ||||||
| chr6:75665967
|
A | G | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.995-745A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665967 | ||||||
| chr6:75666053
|
G | GATATATA others(15): Show |
1 | a0001c0001t0002g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.995-626_995-605dup others(22): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666053 | |||||
| chr6:75666073
|
GAT | G | 11 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(8): Show | 11 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.995-631_995-630del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666073 | |||||
| chr6:75666086
|
CGT | C | 146 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(143): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.995-625_995-624del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666086 | ||||||
| chr6:75666086
|
CGTAT | C | 3 | a0001c0001t0001g0211a0001c0001t0001g0223a0001c0001t0001g0264 | 3 | NA18998.hp2 NA19065.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.995-625_995-622del others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666086 | ||||||
| chr6:75666108
|
T | C | 3 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0161 | 3 | HG00280.hp2 HG01168.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.995-604T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666108 | ||||||
| chr6:75666126
|
A | G | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.995-586A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666126 | ||||||
| chr6:75666152
|
CAT | C | 149 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.995-555_995-554del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666152 | |||||
| chr6:75666159
|
GAT | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.995-543_995-542del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666159 | |||||
| chr6:75666161
|
TATATATA others(15): Show |
T | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.995-518_995-497del others(22): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666161 | |||||
| chr6:75666197
|
G | A | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.995-515G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666197 | ||||||
| chr6:75666233
|
TATG | T | 65 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.995-476_995-474del others(3): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666233 | |||||
| chr6:75666255
|
C | T | 1 | a0001c0002t0009g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.995-457C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666255 | ||||||
| chr6:75666320
|
A | G | 1 | a0001c0001t0016g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.995-392A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666320 | ||||||
| chr6:75666398
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.995-314A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666398 | ||||||
| chr6:75666413
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.995-299A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666413 | ||||||
| chr6:75667116
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1224+175T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667116 | ||||||
| chr6:75667262
|
A | G | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1224+321A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667262 | ||||||
| chr6:75667317
|
A | G | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1224+376A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667317 | ||||||
| chr6:75667340
|
T | C | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1224+399T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667340 | ||||||
| chr6:75667386
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1224+445C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667386 | ||||||
| chr6:75667434
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1224+493G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667434 | ||||||
| chr6:75667500
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1224+559A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667500 | ||||||
| chr6:75667510
|
C | A | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1224+569C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667510 | ||||||
| chr6:75667591
|
A | G | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1224+650A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667591 | ||||||
| chr6:75667633
|
A | G | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1224+692A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667633 | ||||||
| chr6:75667789
|
G | A | 149 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1224+848G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667789 | ||||||
| chr6:75668055
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1224+1114T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668055 | ||||||
| chr6:75668282
|
G | A | 271 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(268): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.1224+1341G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668282 | ||||||
| chr6:75668307
|
T | A | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1224+1366T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668307 | ||||||
| chr6:75668345
|
C | T | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1224+1404C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668345 | ||||||
| chr6:75668420
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1224+1479A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668420 | ||||||
| chr6:75668449
|
T | C | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1224+1508T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668449 | ||||||
| chr6:75668671
|
A | G | 1 | a0001c0001t0007g0313 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1224+1730A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668671 | ||||||
| chr6:75668727
|
C | T | 5 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG01070.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1224+1786C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668727 | ||||||
| chr6:75668816
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1225-1737C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668816 | ||||||
| chr6:75668898
|
A | T | 4 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(1): Show | 4 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225-1655A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668898 | ||||||
| chr6:75669023
|
C | T | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1225-1530C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669023 | ||||||
| chr6:75669148
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1225-1405G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669148 | ||||||
| chr6:75669526
|
C | T | 2 | a0001c0001t0004g0320a0001c0001t0004g0321 | 2 | NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1225-1027C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669526 | ||||||
| chr6:75669570
|
A | G | 1 | a0007c0014t0002g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1225-983A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669570 | ||||||
| chr6:75669938
|
A | T | 1 | a0001c0001t0002g0089 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1225-615A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669938 | ||||||
| chr6:75669938
|
AT | A | 271 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(268): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.1225-603delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 75669938 | |||||
| chr6:75669973
|
G | A | 1 | a0012c0018t0001g0239 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1225-580G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669973 | ||||||
| chr6:75669989
|
G | A | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1225-564G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669989 | ||||||
| chr6:75670050
|
CAGCCTCC others(5): Show |
C | 1 | a0001c0001t0017g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1225-486_1225-475d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 75670050 | |||||
| chr6:75670166
|
C | T | 1 | a0001c0002t0003g0356 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1225-387C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75670166 | ||||||
| chr6:75670287
|
A | T | 33 | a0001c0002t0003g0020a0001c0002t0003g0169a0001c0002t0003g0338others(30): Show | 33 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1225-266A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75670287 | ||||||
| chr6:75670319
|
A | C | 271 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(268): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.1225-234A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75670319 | ||||||
| chr6:75670373
|
A | G | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1225-180A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75670373 | ||||||
| chr6:75670752
|
A | G | 3 | a0001c0001t0001g0210a0001c0001t0001g0221a0001c0001t0001g0222 | 3 | HG02129.hp2 HG02165.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1392+32A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75670752 | ||||||
| chr6:75670850
|
C | T | 1 | a0007c0014t0002g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1392+130C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75670850 | ||||||
| chr6:75670874
|
G | A | 1 | a0001c0002t0003g0356 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1392+154G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75670874 | ||||||
| chr6:75670891
|
AAATGAGT others(60): Show |
A | 1 | a0001c0001t0001g0235 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1392+201_1392+267d others(69): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75670891 | |||||
| chr6:75670960
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1392+240A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75670960 | ||||||
| chr6:75670961
|
T | A | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1392+241T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75670961 | ||||||
| chr6:75671014
|
A | G | 1 | a0001c0001t0002g0172 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1392+294A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671014 | ||||||
| chr6:75671152
|
G | A | 2 | a0001c0001t0002g0098a0001c0001t0002g0122 | 2 | HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1392+432G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671152 | ||||||
| chr6:75671168
|
A | G | 1 | a0001c0008t0003g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1392+448A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671168 | ||||||
| chr6:75671172
|
T | TA | 3 | a0001c0001t0001g0256a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | NA18947.hp1 NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1392+453dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75671172 | |||||
| chr6:75671317
|
C | T | 2 | a0001c0002t0003g0018a0001c0002t0003g0019 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1392+597C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671317 | ||||||
| chr6:75671330
|
G | T | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1392+610G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671330 | ||||||
| chr6:75671449
|
C | T | 1 | a0001c0001t0003g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1392+729C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671449 | ||||||
| chr6:75671451
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1392+731C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671451 | ||||||
| chr6:75671578
|
C | T | 4 | a0001c0001t0005g0147a0004c0006t0005g0150a0004c0006t0005g0151others(1): Show | 4 | NA18960.hp1 NA18980.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+858C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671578 | ||||||
| chr6:75671614
|
C | T | 1 | a0001c0002t0009g0170 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1392+894C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671614 | ||||||
| chr6:75672029
|
G | T | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1392+1309G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672029 | ||||||
| chr6:75672349
|
T | C | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1392+1629T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672349 | ||||||
| chr6:75672357
|
T | C | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1392+1637T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672357 | ||||||
| chr6:75672399
|
T | G | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1392+1679T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672399 | ||||||
| chr6:75672418
|
AT | A | 3 | a0001c0001t0013g0184a0001c0008t0003g0185a0001c0008t0003g0186 | 3 | HG03041.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1392+1699delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672418 | ||||||
| chr6:75672419
|
T | A | 7 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(4): Show | 7 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1392+1699T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672419 | ||||||
| chr6:75672444
|
A | G | 1 | a0001c0002t0011g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1392+1724A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672444 | ||||||
| chr6:75672532
|
C | A | 3 | a0001c0001t0003g0053a0001c0001t0003g0165a0010c0012t0003g0166 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1392+1812C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672532 | ||||||
| chr6:75672824
|
G | T | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1392+2104G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672824 | ||||||
| chr6:75672852
|
G | T | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1392+2132G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672852 | ||||||
| chr6:75673028
|
T | C | 8 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1392+2308T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673028 | ||||||
| chr6:75673123
|
G | C | 6 | a0001c0002t0009g0007a0001c0002t0009g0008a0001c0002t0009g0009others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1393-2312G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673123 | ||||||
| chr6:75673146
|
C | T | 26 | a0001c0001t0002g0111a0001c0002t0003g0338a0001c0002t0003g0339others(23): Show | 26 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.1393-2289C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673146 | ||||||
| chr6:75673147
|
G | A | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1393-2288G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673147 | ||||||
| chr6:75673171
|
C | G | 2 | a0001c0001t0001g0197a0001c0001t0001g0201 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1393-2264C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673171 | ||||||
| chr6:75673280
|
A | G | 7 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0018others(4): Show | 7 | HG02630.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1393-2155A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673280 | ||||||
| chr6:75673319
|
C | CT | 46 | a0001c0001t0001g0212a0001c0001t0001g0266a0001c0001t0001g0277others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.1393-2096dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75673319 | |||||
| chr6:75673319
|
C | CTT | 161 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(158): Show | 161 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1393-2097_1393-209 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75673319 | |||||
| chr6:75673319
|
C | CTTT | 22 | a0001c0001t0001g0201a0001c0001t0001g0237a0001c0001t0001g0285others(19): Show | 22 | HG00423.hp2 HG01346.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1393-2098_1393-209 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75673319 | |||||
| chr6:75673339
|
T | G | 1 | a0001c0002t0022g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1393-2096T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673339 | ||||||
| chr6:75673339
|
T | TG | 6 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0018others(3): Show | 6 | HG02922.hp1 HG02965.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1393-2095dupG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75673339 | |||||
| chr6:75673418
|
G | C | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1393-2017G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673418 | ||||||
| chr6:75673460
|
A | T | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.1393-1975A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673460 | ||||||
| chr6:75673600
|
A | G | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1393-1835A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673600 | ||||||
| chr6:75673678
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1393-1757A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673678 | ||||||
| chr6:75673726
|
T | G | 1 | a0001c0001t0007g0302 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1393-1709T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673726 | ||||||
| chr6:75674107
|
T | C | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1393-1328T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674107 | ||||||
| chr6:75674108
|
C | G | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1393-1327C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674108 | ||||||
| chr6:75674146
|
CT | C | 24 | a0001c0001t0001g0194a0001c0001t0001g0230a0001c0001t0001g0238others(21): Show | 24 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1393-1265delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75674146 | |||||
| chr6:75674167
|
T | A | 5 | a0001c0001t0001g0205a0001c0001t0001g0214a0001c0001t0001g0219others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1393-1268T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674167 | ||||||
| chr6:75674167
|
T | TA | 33 | a0001c0001t0001g0250a0001c0001t0004g0300a0001c0001t0004g0304others(30): Show | 33 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.1393-1268_1393-126 others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674167 | ||||||
| chr6:75674168
|
T | A | 146 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(143): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1393-1267T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674168 | ||||||
| chr6:75674168
|
T | TA | 11 | a0001c0001t0001g0226a0001c0001t0001g0232a0001c0001t0001g0246others(8): Show | 11 | HG01071.hp1 HG01256.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1393-1267_1393-126 others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674168 | ||||||
| chr6:75674168
|
T | TAA | 5 | a0001c0001t0004g0301a0001c0001t0004g0325a0001c0001t0004g0333others(2): Show | 5 | HG00597.hp1 HG02083.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1393-1267_1393-126 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674168 | ||||||
| chr6:75674169
|
T | A | 198 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(195): Show | 198 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1393-1266T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674169 | ||||||
| chr6:75674170
|
T | A | 226 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(223): Show | 226 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1393-1265T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674170 | ||||||
| chr6:75674170
|
T | TA | 10 | a0001c0001t0003g0053a0001c0004t0003g0173a0001c0004t0003g0176others(7): Show | 10 | HG02055.hp2 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1393-1260dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75674170 | |||||
| chr6:75674171
|
A | T | 1 | a0001c0001t0002g0126 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1393-1264A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674171 | ||||||
| chr6:75674208
|
G | C | 102 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1393-1227G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674208 | ||||||
| chr6:75674255
|
C | G | 2 | a0001c0001t0002g0130a0001c0001t0016g0121 | 2 | HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1393-1180C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674255 | ||||||
| chr6:75674261
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1393-1174A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674261 | ||||||
| chr6:75674447
|
G | C | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1393-988G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674447 | ||||||
| chr6:75674570
|
A | C | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1393-865A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674570 | ||||||
| chr6:75674695
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1393-740A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674695 | ||||||
| chr6:75674762
|
T | C | 6 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(3): Show | 6 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1393-673T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674762 | ||||||
| chr6:75675076
|
G | T | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1393-359G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75675076 | ||||||
| chr6:75675196
|
A | T | 3 | a0001c0001t0001g0256a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | NA18947.hp1 NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1393-239A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75675196 | ||||||
| chr6:75675614
|
G | C | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1426+146G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 12/23 | chr6 | 75675614 | ||||||
| chr6:75675795
|
A | G | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1427-65A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 12/23 | chr6 | 75675795 | ||||||
| chr6:75676157
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1621+103G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676157 | ||||||
| chr6:75676168
|
A | G | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064 | 3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1621+114A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676168 | ||||||
| chr6:75676336
|
A | G | 1 | a0001c0001t0005g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1621+282A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676336 | ||||||
| chr6:75676558
|
T | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1622-472T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676558 | ||||||
| chr6:75676758
|
A | G | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1622-272A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676758 | ||||||
| chr6:75676940
|
C | T | 1 | a0001c0001t0002g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1622-90C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676940 | ||||||
| chr6:75676996
|
GT | G | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1622-25delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr6 | 75676996 | |||||
| chr6:75677282
|
T | C | 1 | a0002c0003t0003g0027 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1848+26T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75677282 | ||||||
| chr6:75677321
|
T | G | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1848+65T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75677321 | ||||||
| chr6:75677386
|
A | T | 39 | a0001c0001t0003g0053a0001c0001t0003g0165a0001c0004t0003g0173others(36): Show | 39 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.1848+130A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75677386 | ||||||
| chr6:75677786
|
A | G | 1 | a0001c0001t0004g0311 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1848+530A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75677786 | ||||||
| chr6:75677894
|
A | G | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1848+638A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75677894 | ||||||
| chr6:75678154
|
CCT | C | 5 | a0001c0001t0001g0289a0001c0001t0010g0182a0001c0001t0010g0183others(2): Show | 5 | HG02622.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1849-428_1849-427d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678154 | ||||||
| chr6:75678220
|
A | G | 2 | a0001c0001t0001g0274a0001c0002t0003g0360 | 2 | NA18964.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1849-363A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678220 | ||||||
| chr6:75678221
|
C | T | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1849-362C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678221 | ||||||
| chr6:75678227
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1849-356A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678227 | ||||||
| chr6:75678265
|
C | G | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1849-318C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678265 | ||||||
| chr6:75678325
|
G | C | 1 | a0001c0001t0007g0332 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1849-258G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678325 | ||||||
| chr6:75678328
|
G | C | 1 | a0001c0001t0001g0274 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1849-255G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678328 | ||||||
| chr6:75678333
|
A | T | 1 | a0001c0001t0007g0332 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1849-250A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678333 | ||||||
| chr6:75678384
|
A | G | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1849-199A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678384 | ||||||
| chr6:75678409
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1849-174A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678409 | ||||||
| chr6:75678807
|
A | T | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.1959-4A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 15/23 | chr6 | 75678807 | ||||||
| chr6:75679186
|
G | A | 1 | a0001c0001t0003g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2075+259G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679186 | ||||||
| chr6:75679273
|
T | G | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2075+346T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679273 | ||||||
| chr6:75679316
|
A | C | 25 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(22): Show | 25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2075+389A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679316 | ||||||
| chr6:75679355
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2075+428A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679355 | ||||||
| chr6:75679693
|
A | G | 1 | a0001c0002t0003g0358 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2075+766A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679693 | ||||||
| chr6:75679974
|
T | C | 1 | a0001c0002t0003g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2075+1047T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679974 | ||||||
| chr6:75680060
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2075+1133A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680060 | ||||||
| chr6:75680182
|
G | C | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2075+1255G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680182 | ||||||
| chr6:75680290
|
G | A | 1 | a0001c0001t0017g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2075+1363G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680290 | ||||||
| chr6:75680361
|
C | T | 258 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(255): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.2075+1434C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680361 | ||||||
| chr6:75680372
|
G | C | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+1445G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680372 | ||||||
| chr6:75680399
|
A | G | 5 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2075+1472A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680399 | ||||||
| chr6:75680525
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2075+1598A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680525 | ||||||
| chr6:75680763
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0267 | 2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.2075+1836C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680763 | ||||||
| chr6:75680869
|
C | T | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2075+1942C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680869 | ||||||
| chr6:75680872
|
C | T | 2 | a0001c0001t0007g0302a0001c0001t0007g0303 | 2 | NA18972.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2075+1945C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680872 | ||||||
| chr6:75680968
|
C | G | 1 | a0001c0001t0002g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2075+2041C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680968 | ||||||
| chr6:75681043
|
A | G | 1 | a0001c0001t0004g0314 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2075+2116A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681043 | ||||||
| chr6:75681129
|
C | T | 1 | a0001c0002t0009g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2075+2202C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681129 | ||||||
| chr6:75681221
|
C | T | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2075+2294C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681221 | ||||||
| chr6:75681446
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0267 | 2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.2075+2519C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681446 | ||||||
| chr6:75681462
|
CT | C | 28 | a0001c0001t0002g0057a0001c0001t0004g0326a0001c0001t0005g0141others(25): Show | 28 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.2075+2548delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75681462 | |||||
| chr6:75681519
|
C | G | 1 | a0001c0001t0002g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2075+2592C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681519 | ||||||
| chr6:75681521
|
C | T | 1 | a0001c0002t0003g0349 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2075+2594C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681521 | ||||||
| chr6:75681532
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2075+2605C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681532 | ||||||
| chr6:75681652
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2075+2725A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681652 | ||||||
| chr6:75681663
|
T | G | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2075+2736T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681663 | ||||||
| chr6:75681679
|
A | C | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2075+2752A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681679 | ||||||
| chr6:75681856
|
C | G | 6 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(3): Show | 6 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2075+2929C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681856 | ||||||
| chr6:75681978
|
G | A | 3 | a0004c0006t0005g0150a0004c0006t0005g0151a0004c0006t0005g0160 | 3 | NA18980.hp1 NA18994.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2075+3051G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681978 | ||||||
| chr6:75681985
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2075+3058G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681985 | ||||||
| chr6:75682114
|
C | G | 3 | a0001c0001t0001g0210a0001c0001t0001g0221a0001c0001t0001g0222 | 3 | HG02129.hp2 HG02165.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2075+3187C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682114 | ||||||
| chr6:75682140
|
A | T | 3 | a0001c0001t0001g0210a0001c0001t0001g0221a0001c0001t0001g0222 | 3 | HG02129.hp2 HG02165.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2075+3213A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682140 | ||||||
| chr6:75682154
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2075+3227G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682154 | ||||||
| chr6:75682199
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2075+3272G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682199 | ||||||
| chr6:75682391
|
A | G | 6 | a0001c0002t0009g0007a0001c0002t0009g0008a0001c0002t0009g0009others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2075+3464A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682391 | ||||||
| chr6:75682405
|
C | CT | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2075+3490dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75682405 | |||||
| chr6:75682602
|
G | A | 2 | a0002c0003t0003g0051a0002c0003t0003g0052 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2075+3675G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682602 | ||||||
| chr6:75682626
|
G | A | 256 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(253): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.2075+3699G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682626 | ||||||
| chr6:75682626
|
G | C | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2075+3699G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682626 | ||||||
| chr6:75682634
|
C | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2075+3707C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682634 | ||||||
| chr6:75682854
|
C | T | 1 | a0001c0005t0006g0293 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2075+3927C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682854 | ||||||
| chr6:75682857
|
A | C | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.2075+3930A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682857 | ||||||
| chr6:75682888
|
T | C | 1 | a0002c0003t0003g0044 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2075+3961T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682888 | ||||||
| chr6:75682916
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2075+3989T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682916 | ||||||
| chr6:75682920
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2075+3993A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682920 | ||||||
| chr6:75682921
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2075+3994G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682921 | ||||||
| chr6:75682929
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2075+4002G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682929 | ||||||
| chr6:75683067
|
G | A | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2075+4140G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683067 | ||||||
| chr6:75683106
|
C | T | 2 | a0001c0001t0004g0320a0001c0001t0004g0321 | 2 | NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2075+4179C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683106 | ||||||
| chr6:75683114
|
G | A | 1 | a0002c0003t0003g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2075+4187G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683114 | ||||||
| chr6:75683123
|
A | C | 3 | a0001c0002t0009g0007a0001c0002t0009g0170a0001c0002t0009g0171 | 3 | HG02486.hp2 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2075+4196A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683123 | ||||||
| chr6:75683246
|
G | C | 1 | a0001c0001t0002g0081 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2075+4319G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683246 | ||||||
| chr6:75683545
|
C | T | 1 | a0001c0001t0008g0253 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2075+4618C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683545 | ||||||
| chr6:75683569
|
T | C | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2075+4642T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683569 | ||||||
| chr6:75683666
|
TTTC | T | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2075+4742_2075+474 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75683666 | |||||
| chr6:75683741
|
G | A | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+4814G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683741 | ||||||
| chr6:75683795
|
T | C | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2075+4868T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683795 | ||||||
| chr6:75683878
|
G | A | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2075+4951G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683878 | ||||||
| chr6:75684029
|
G | T | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2075+5102G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684029 | ||||||
| chr6:75684113
|
A | G | 3 | a0001c0001t0005g0162a0001c0001t0005g0163a0001c0001t0005g0164 | 3 | HG01069.hp1 HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2075+5186A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684113 | ||||||
| chr6:75684143
|
T | G | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.2075+5216T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684143 | ||||||
| chr6:75684148
|
T | C | 1 | a0001c0001t0005g0164 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2075+5221T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684148 | ||||||
| chr6:75684365
|
A | G | 4 | a0001c0001t0002g0058a0001c0001t0002g0065a0001c0001t0002g0120others(1): Show | 4 | HG01261.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2075+5438A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684365 | ||||||
| chr6:75684438
|
A | C | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.2075+5511A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684438 | ||||||
| chr6:75684612
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2075+5685T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684612 | ||||||
| chr6:75684626
|
A | C | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.2075+5699A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684626 | ||||||
| chr6:75684656
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0267 | 2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.2075+5729C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684656 | ||||||
| chr6:75685003
|
A | G | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.2075+6076A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685003 | ||||||
| chr6:75685013
|
G | A | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+6086G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685013 | ||||||
| chr6:75685062
|
A | G | 1 | a0001c0004t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2075+6135A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685062 | ||||||
| chr6:75685074
|
G | A | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+6147G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685074 | ||||||
| chr6:75685301
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2075+6374A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685301 | ||||||
| chr6:75685302
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2075+6375G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685302 | ||||||
| chr6:75685348
|
A | AT | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+6429dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75685348 | |||||
| chr6:75685362
|
G | GT | 7 | a0001c0001t0002g0090a0001c0001t0002g0168a0001c0001t0003g0053others(4): Show | 7 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2075+6443dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75685362 | |||||
| chr6:75685377
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2075+6450A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685377 | ||||||
| chr6:75685382
|
C | T | 4 | a0001c0002t0003g0340a0001c0002t0003g0353a0001c0002t0003g0354others(1): Show | 4 | NA18983.hp1 NA18995.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.2075+6455C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685382 | ||||||
| chr6:75685404
|
G | A | 1 | a0001c0001t0018g0060 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2075+6477G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685404 | ||||||
| chr6:75685507
|
T | C | 1 | a0001c0001t0004g0316 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2075+6580T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685507 | ||||||
| chr6:75685636
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2075+6709C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685636 | ||||||
| chr6:75685648
|
C | T | 1 | a0002c0003t0003g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2075+6721C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685648 | ||||||
| chr6:75685667
|
A | G | 2 | a0002c0003t0003g0051a0002c0003t0003g0052 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2075+6740A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685667 | ||||||
| chr6:75685846
|
T | C | 1 | a0001c0001t0002g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2075+6919T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685846 | ||||||
| chr6:75685951
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2075+7024C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685951 | ||||||
| chr6:75685954
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2075+7027C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685954 | ||||||
| chr6:75686476
|
G | C | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+7549G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75686476 | ||||||
| chr6:75686491
|
C | T | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2075+7564C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75686491 | ||||||
| chr6:75686653
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2075+7726T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75686653 | ||||||
| chr6:75686729
|
C | A | 1 | a0001c0001t0005g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2075+7802C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75686729 | ||||||
| chr6:75687155
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2075+8228A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687155 | ||||||
| chr6:75687184
|
G | T | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2075+8257G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687184 | ||||||
| chr6:75687236
|
A | G | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2075+8309A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687236 | ||||||
| chr6:75687343
|
A | G | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2075+8416A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687343 | ||||||
| chr6:75687360
|
A | G | 8 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2075+8433A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687360 | ||||||
| chr6:75687372
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2076-8432T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687372 | ||||||
| chr6:75687436
|
C | T | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-8368C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687436 | ||||||
| chr6:75687457
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2076-8347A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687457 | ||||||
| chr6:75687540
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2076-8264C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687540 | ||||||
| chr6:75687554
|
T | C | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(3): Show | 6 | HG00642.hp2 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.2076-8250T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687554 | ||||||
| chr6:75687770
|
C | T | 3 | a0002c0003t0003g0037a0002c0003t0003g0038a0002c0003t0003g0047 | 3 | HG01081.hp2 HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2076-8034C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687770 | ||||||
| chr6:75687960
|
C | CAGA | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-7842_2076-784 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75687960 | |||||
| chr6:75688125
|
G | T | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.2076-7679G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688125 | ||||||
| chr6:75688427
|
T | C | 73 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.2076-7377T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688427 | ||||||
| chr6:75688477
|
G | A | 3 | a0003c0007t0006g0167a0003c0007t0006g0290a0003c0007t0006g0294 | 3 | HG02109.hp2 HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2076-7327G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688477 | ||||||
| chr6:75688493
|
G | A | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2076-7311G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688493 | ||||||
| chr6:75688507
|
T | A | 1 | a0001c0001t0007g0331 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2076-7297T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688507 | ||||||
| chr6:75688509
|
C | T | 1 | a0001c0001t0007g0331 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2076-7295C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688509 | ||||||
| chr6:75688538
|
C | A | 1 | a0001c0001t0007g0331 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2076-7266C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688538 | ||||||
| chr6:75688539
|
A | C | 1 | a0001c0001t0007g0331 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2076-7265A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688539 | ||||||
| chr6:75688656
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02293.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2076-7148A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688656 | ||||||
| chr6:75688757
|
C | T | 1 | a0001c0001t0013g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2076-7047C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688757 | ||||||
| chr6:75688806
|
G | A | 2 | a0001c0002t0011g0012a0001c0002t0011g0016 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2076-6998G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688806 | ||||||
| chr6:75689079
|
C | T | 1 | a0001c0001t0005g0161 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2076-6725C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689079 | ||||||
| chr6:75689085
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2076-6719G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689085 | ||||||
| chr6:75689149
|
C | G | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2076-6655C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689149 | ||||||
| chr6:75689215
|
CAG | C | 8 | a0001c0001t0008g0195a0001c0001t0008g0209a0001c0001t0008g0220others(5): Show | 8 | HG00423.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.2076-6586_2076-658 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75689215 | |||||
| chr6:75689323
|
G | T | 1 | a0001c0002t0003g0356 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2076-6481G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689323 | ||||||
| chr6:75689423
|
A | C | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-6381A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689423 | ||||||
| chr6:75689439
|
T | C | 1 | a0001c0001t0002g0095 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2076-6365T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689439 | ||||||
| chr6:75689448
|
A | G | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.2076-6356A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689448 | ||||||
| chr6:75689581
|
G | A | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-6223G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689581 | ||||||
| chr6:75689613
|
A | G | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2076-6191A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689613 | ||||||
| chr6:75689722
|
G | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.2076-6082G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689722 | ||||||
| chr6:75689733
|
A | G | 1 | a0002c0003t0003g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2076-6071A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689733 | ||||||
| chr6:75689823
|
G | T | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2076-5981G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689823 | ||||||
| chr6:75689830
|
C | CACAACTT others(21): Show |
1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2076-5973_2076-594 others(32): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75689830 | |||||
| chr6:75689872
|
C | A | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2076-5932C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689872 | ||||||
| chr6:75690005
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2076-5799G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690005 | ||||||
| chr6:75690172
|
A | G | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-5632A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690172 | ||||||
| chr6:75690218
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2076-5586A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690218 | ||||||
| chr6:75690683
|
G | T | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.2076-5121G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690683 | ||||||
| chr6:75690699
|
G | GT | 87 | a0001c0001t0001g0224a0001c0001t0002g0106a0001c0001t0003g0022others(84): Show | 87 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.2076-5094dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75690699 | |||||
| chr6:75690729
|
T | TGTCACCC others(10): Show |
4 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(1): Show | 4 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2076-5072_2076-505 others(21): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75690729 | |||||
| chr6:75690730
|
G | GT | 45 | a0001c0001t0005g0141a0001c0002t0003g0003a0001c0002t0003g0004others(42): Show | 45 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.2076-5073dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75690730 | |||||
| chr6:75690843
|
T | C | 3 | a0001c0001t0001g0275a0001c0001t0002g0135a0001c0001t0004g0314 | 3 | HG00673.hp1 HG03017.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.2076-4961T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690843 | ||||||
| chr6:75690845
|
A | G | 2 | a0001c0001t0002g0135a0001c0001t0004g0314 | 2 | HG00673.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2076-4959A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690845 | ||||||
| chr6:75690851
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2076-4953A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690851 | ||||||
| chr6:75690853
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2076-4951A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690853 | ||||||
| chr6:75690865
|
G | T | 1 | a0001c0001t0002g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2076-4939G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690865 | ||||||
| chr6:75691006
|
A | AT | 51 | a0001c0001t0001g0234a0001c0001t0001g0256a0001c0001t0001g0257others(48): Show | 51 | HG00423.hp1 HG00609.hp2 HG01891.hp2 others(48): Show |
intron_variant | MODIFIER | c.2076-4780dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75691006 | |||||
| chr6:75691081
|
C | T | 1 | a0001c0002t0003g0350 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2076-4723C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691081 | ||||||
| chr6:75691143
|
A | AT | 8 | a0001c0001t0001g0237a0001c0001t0001g0279a0001c0002t0003g0343others(5): Show | 8 | HG02622.hp2 HG02723.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.2076-4646dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75691143 | |||||
| chr6:75691143
|
A | ATT | 29 | a0001c0001t0001g0256a0001c0002t0003g0003a0001c0002t0003g0020others(26): Show | 29 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2076-4647_2076-464 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75691143 | |||||
| chr6:75691143
|
A | ATTT | 11 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0006others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2076-4648_2076-464 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75691143 | |||||
| chr6:75691144
|
T | A | 122 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2076-4660T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691144 | ||||||
| chr6:75691145
|
T | A | 3 | a0001c0001t0002g0102a0001c0001t0002g0111a0001c0001t0002g0112 | 3 | HG02004.hp1 NA18983.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2076-4659T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691145 | ||||||
| chr6:75691158
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2076-4646T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691158 | ||||||
| chr6:75691163
|
G | A | 1 | a0001c0005t0006g0296 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2076-4641G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691163 | ||||||
| chr6:75691494
|
A | G | 39 | a0001c0001t0003g0053a0001c0001t0003g0165a0001c0004t0003g0173others(36): Show | 39 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.2076-4310A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691494 | ||||||
| chr6:75691559
|
T | C | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2076-4245T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691559 | ||||||
| chr6:75691607
|
GT | G | 28 | a0001c0001t0004g0310a0001c0001t0004g0323a0001c0001t0004g0324others(25): Show | 28 | HG00438.hp1 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.2076-4187delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75691607 | |||||
| chr6:75691610
|
T | C | 1 | a0001c0002t0003g0340 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2076-4194T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691610 | ||||||
| chr6:75691627
|
C | T | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2076-4177C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691627 | ||||||
| chr6:75691660
|
C | T | 1 | a0001c0001t0023g0142 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2076-4144C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691660 | ||||||
| chr6:75691744
|
G | A | 1 | a0006c0010t0009g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2076-4060G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691744 | ||||||
| chr6:75691796
|
G | A | 91 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2076-4008G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691796 | ||||||
| chr6:75691837
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0135 | 2 | HG00140.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2076-3967G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691837 | ||||||
| chr6:75692006
|
G | A | 3 | a0003c0007t0006g0167a0003c0007t0006g0290a0003c0007t0006g0294 | 3 | HG02109.hp2 HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2076-3798G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692006 | ||||||
| chr6:75692145
|
C | T | 1 | a0001c0001t0007g0331 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2076-3659C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692145 | ||||||
| chr6:75692385
|
C | T | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.2076-3419C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692385 | ||||||
| chr6:75692467
|
C | CA | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-3327dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75692467 | |||||
| chr6:75692508
|
T | C | 1 | a0001c0005t0006g0293 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2076-3296T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692508 | ||||||
| chr6:75692510
|
C | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2076-3294C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692510 | ||||||
| chr6:75692516
|
A | G | 1 | a0001c0002t0011g0016 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2076-3288A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692516 | ||||||
| chr6:75692561
|
G | C | 1 | a0001c0004t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2076-3243G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692561 | ||||||
| chr6:75692617
|
CT | C | 3 | a0001c0001t0002g0069a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG02165.hp2 NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2076-3184delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75692617 | |||||
| chr6:75692625
|
C | T | 1 | a0001c0001t0005g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2076-3179C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692625 | ||||||
| chr6:75692717
|
G | A | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.2076-3087G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692717 | ||||||
| chr6:75692723
|
C | T | 3 | a0001c0001t0003g0053a0001c0001t0003g0165a0010c0012t0003g0166 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2076-3081C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692723 | ||||||
| chr6:75692746
|
C | A | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.2076-3058C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692746 | ||||||
| chr6:75692791
|
C | CA | 20 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(17): Show | 20 | HG02055.hp2 HG02280.hp1 HG02293.hp2 others(17): Show |
intron_variant | MODIFIER | c.2076-3001dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75692791 | |||||
| chr6:75692791
|
CA | C | 9 | a0001c0001t0002g0139a0001c0005t0006g0291a0001c0005t0006g0292others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-3001delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75692791 | |||||
| chr6:75692812
|
C | G | 1 | a0001c0001t0008g0209 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2076-2992C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692812 | ||||||
| chr6:75692880
|
A | G | 39 | a0001c0001t0003g0053a0001c0001t0003g0165a0001c0004t0003g0173others(36): Show | 39 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.2076-2924A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692880 | ||||||
| chr6:75693044
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2076-2760T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693044 | ||||||
| chr6:75693060
|
C | A | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2076-2744C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693060 | ||||||
| chr6:75693130
|
T | G | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064 | 3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2076-2674T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693130 | ||||||
| chr6:75693189
|
A | G | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 49 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.2076-2615A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693189 | ||||||
| chr6:75693398
|
A | G | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2076-2406A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693398 | ||||||
| chr6:75693409
|
T | A | 1 | a0006c0010t0009g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2076-2395T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693409 | ||||||
| chr6:75693409
|
T | TA | 31 | a0001c0001t0001g0190a0001c0001t0002g0066a0001c0001t0002g0086others(28): Show | 31 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2076-2375dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75693409 | |||||
| chr6:75693409
|
T | TAA | 44 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(41): Show | 44 | HG00423.hp1 HG00609.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.2076-2376_2076-237 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75693409 | |||||
| chr6:75693409
|
TA | T | 9 | a0001c0001t0001g0217a0001c0001t0001g0257a0001c0001t0001g0279others(6): Show | 9 | HG01069.hp1 HG01109.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-2375delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75693409 | |||||
| chr6:75693426
|
A | G | 1 | a0001c0001t0002g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2076-2378A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693426 | ||||||
| chr6:75693428
|
A | AC | 8 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2076-2376_2076-237 others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693428 | ||||||
| chr6:75693429
|
A | C | 1 | a0001c0001t0020g0249 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2076-2375A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693429 | ||||||
| chr6:75693541
|
A | G | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2076-2263A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693541 | ||||||
| chr6:75693568
|
CTG | C | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2076-2232_2076-223 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75693568 | |||||
| chr6:75693592
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2076-2212C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693592 | ||||||
| chr6:75693838
|
A | G | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2076-1966A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693838 | ||||||
| chr6:75693946
|
AT | A | 4 | a0001c0001t0008g0195a0001c0001t0008g0220a0001c0001t0008g0254others(1): Show | 4 | HG00423.hp2 HG02155.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.2076-1857delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693946 | ||||||
| chr6:75693958
|
A | G | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2076-1846A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693958 | ||||||
| chr6:75693965
|
C | A | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2076-1839C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693965 | ||||||
| chr6:75693994
|
C | T | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2076-1810C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693994 | ||||||
| chr6:75694040
|
T | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2076-1764T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694040 | ||||||
| chr6:75694074
|
T | C | 1 | a0001c0001t0002g0123 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2076-1730T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694074 | ||||||
| chr6:75694171
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0273 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2076-1633G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694171 | ||||||
| chr6:75694314
|
T | C | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-1490T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694314 | ||||||
| chr6:75694344
|
T | G | 1 | a0001c0001t0004g0311 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2076-1460T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694344 | ||||||
| chr6:75694486
|
T | G | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-1318T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694486 | ||||||
| chr6:75694987
|
A | G | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-817A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694987 | ||||||
| chr6:75694989
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0214a0001c0001t0001g0219 | 3 | HG01884.hp2 HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2076-815C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694989 | ||||||
| chr6:75695032
|
A | G | 258 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(255): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.2076-772A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695032 | ||||||
| chr6:75695095
|
T | C | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-709T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695095 | ||||||
| chr6:75695125
|
C | T | 2 | a0001c0001t0004g0304a0001c0001t0004g0305 | 2 | HG01928.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2076-679C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695125 | ||||||
| chr6:75695231
|
C | T | 1 | a0001c0001t0003g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2076-573C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695231 | ||||||
| chr6:75695238
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2076-566G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695238 | ||||||
| chr6:75695512
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2076-292G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695512 | ||||||
| chr6:75695589
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0200 | 2 | HG00642.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2076-215T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695589 | ||||||
| chr6:75695644
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2076-160G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695644 | ||||||
| chr6:75695984
|
A | G | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2195+61A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75695984 | ||||||
| chr6:75696098
|
G | C | 1 | a0001c0001t0023g0142 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2195+175G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696098 | ||||||
| chr6:75696284
|
G | A | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2195+361G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696284 | ||||||
| chr6:75696285
|
T | G | 1 | a0001c0001t0001g0233 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2195+362T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696285 | ||||||
| chr6:75696315
|
T | A | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2195+392T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696315 | ||||||
| chr6:75696316
|
A | T | 3 | a0001c0001t0002g0122a0001c0002t0003g0350a0001c0002t0003g0359 | 3 | NA18947.hp2 NA18982.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2195+393A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696316 | ||||||
| chr6:75696370
|
C | T | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2195+447C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696370 | ||||||
| chr6:75696626
|
G | A | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG00738.hp2 HG01169.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.2195+703G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696626 | ||||||
| chr6:75696835
|
T | A | 1 | a0001c0001t0001g0274 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2196-590T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696835 | ||||||
| chr6:75696836
|
A | C | 1 | a0001c0001t0001g0274 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2196-589A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696836 | ||||||
| chr6:75696837
|
A | ACTAGATC others(5): Show |
1 | a0001c0001t0001g0274 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2196-588_2196-587i others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696837 | ||||||
| chr6:75697041
|
C | T | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2196-384C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75697041 | ||||||
| chr6:75697375
|
T | G | 1 | a0001c0001t0010g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2196-50T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75697375 | ||||||
| chr6:75697566
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2288+49T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75697566 | ||||||
| chr6:75697641
|
C | T | 7 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0018others(4): Show | 7 | HG02630.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2288+124C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75697641 | ||||||
| chr6:75697808
|
C | T | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2288+291C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75697808 | ||||||
| chr6:75697897
|
G | A | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2288+380G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75697897 | ||||||
| chr6:75697904
|
A | G | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.2288+387A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75697904 | ||||||
| chr6:75698341
|
A | G | 1 | a0002c0003t0003g0044 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2288+824A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698341 | ||||||
| chr6:75698407
|
C | T | 4 | a0001c0002t0003g0338a0001c0002t0003g0345a0001c0002t0003g0350others(1): Show | 4 | NA18947.hp2 NA18968.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2288+890C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698407 | ||||||
| chr6:75698452
|
T | G | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2288+935T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698452 | ||||||
| chr6:75698473
|
G | A | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2288+956G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698473 | ||||||
| chr6:75698485
|
T | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+968T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698485 | ||||||
| chr6:75698495
|
A | AT | 27 | a0001c0001t0001g0275a0001c0001t0005g0141a0001c0001t0005g0143others(24): Show | 27 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.2288+990dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75698495 | |||||
| chr6:75698529
|
C | T | 26 | a0001c0002t0003g0169a0001c0002t0003g0338a0001c0002t0003g0339others(23): Show | 26 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2288+1012C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698529 | ||||||
| chr6:75698581
|
A | C | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2288+1064A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698581 | ||||||
| chr6:75698767
|
T | C | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2288+1250T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698767 | ||||||
| chr6:75698785
|
C | T | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2288+1268C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698785 | ||||||
| chr6:75699006
|
A | G | 1 | a0001c0001t0002g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2288+1489A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699006 | ||||||
| chr6:75699010
|
C | CA | 11 | a0001c0001t0001g0224a0001c0001t0004g0334a0001c0004t0003g0173others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.2288+1506dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699010 | |||||
| chr6:75699072
|
A | G | 1 | a0001c0001t0004g0324 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2288+1555A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699072 | ||||||
| chr6:75699095
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+1578G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699095 | ||||||
| chr6:75699212
|
G | C | 3 | a0001c0001t0003g0053a0001c0001t0003g0165a0010c0012t0003g0166 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2288+1695G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699212 | ||||||
| chr6:75699221
|
C | CTAAGTGA others(7): Show |
38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+1704_2288+170 others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699221 | ||||||
| chr6:75699222
|
C | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+1705C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699222 | ||||||
| chr6:75699224
|
C | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+1707C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699224 | ||||||
| chr6:75699234
|
G | A | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2288+1717G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699234 | ||||||
| chr6:75699259
|
T | C | 1 | a0001c0001t0004g0324 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2288+1742T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699259 | ||||||
| chr6:75699269
|
G | A | 25 | a0001c0002t0003g0338a0001c0002t0003g0339a0001c0002t0003g0340others(22): Show | 25 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.2288+1752G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699269 | ||||||
| chr6:75699354
|
C | CT | 14 | a0001c0001t0001g0260a0001c0001t0001g0272a0001c0001t0008g0253others(11): Show | 14 | HG00741.hp1 HG01106.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2288+1857dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | |||||
| chr6:75699354
|
C | CTT | 43 | a0001c0001t0002g0001a0001c0001t0002g0059a0001c0001t0002g0091others(40): Show | 43 | HG00738.hp1 HG01069.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.2288+1856_2288+185 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | |||||
| chr6:75699354
|
C | CTTT | 89 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0055others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.2288+1855_2288+185 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | |||||
| chr6:75699354
|
C | CTTTT | 33 | a0001c0001t0002g0066a0001c0001t0002g0081a0001c0001t0002g0087others(30): Show | 33 | HG00609.hp2 HG00741.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.2288+1854_2288+185 others(8): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | |||||
| chr6:75699354
|
CT | C | 6 | a0001c0001t0001g0208a0001c0001t0001g0210a0001c0001t0001g0215others(3): Show | 6 | HG00438.hp2 HG01070.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2288+1857delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | |||||
| chr6:75699354
|
CTTT | C | 38 | a0001c0001t0002g0137a0001c0001t0004g0300a0001c0001t0004g0301others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+1855_2288+185 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | |||||
| chr6:75699354
|
CTTTTT | C | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2288+1853_2288+185 others(9): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | |||||
| chr6:75699354
|
CTTTTTT | C | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2288+1852_2288+185 others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | |||||
| chr6:75699396
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2288+1879C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699396 | ||||||
| chr6:75699645
|
G | A | 1 | a0001c0002t0003g0021 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2288+2128G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699645 | ||||||
| chr6:75699660
|
G | A | 10 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2288+2143G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699660 | ||||||
| chr6:75700082
|
T | A | 15 | a0001c0001t0004g0301a0001c0001t0004g0306a0001c0001t0004g0309others(12): Show | 15 | HG00408.hp2 HG00597.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.2289-2563T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700082 | ||||||
| chr6:75700099
|
T | C | 1 | a0001c0001t0002g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2289-2546T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700099 | ||||||
| chr6:75700171
|
A | AT | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2289-2473dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75700171 | |||||
| chr6:75700203
|
G | A | 1 | a0008c0011t0003g0347 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2289-2442G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700203 | ||||||
| chr6:75700525
|
C | T | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2289-2120C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700525 | ||||||
| chr6:75700546
|
G | A | 3 | a0001c0001t0005g0162a0001c0001t0005g0163a0001c0001t0005g0164 | 3 | HG01069.hp1 HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2289-2099G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700546 | ||||||
| chr6:75700611
|
A | C | 1 | a0001c0001t0002g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2289-2034A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700611 | ||||||
| chr6:75700637
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2289-2008C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700637 | ||||||
| chr6:75701217
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2289-1428C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701217 | ||||||
| chr6:75701232
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2289-1413A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701232 | ||||||
| chr6:75701259
|
A | G | 1 | a0001c0001t0010g0187 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2289-1386A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701259 | ||||||
| chr6:75701315
|
G | A | 3 | a0001c0001t0002g0069a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG02165.hp2 NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2289-1330G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701315 | ||||||
| chr6:75701362
|
G | T | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2289-1283G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701362 | ||||||
| chr6:75701589
|
GA | G | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2289-1050delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701589 | |||||
| chr6:75701633
|
C | CT | 162 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0192others(159): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.2289-989dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | |||||
| chr6:75701633
|
C | CTT | 33 | a0001c0001t0001g0190a0001c0001t0001g0202a0001c0001t0001g0218others(30): Show | 33 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.2289-990_2289-989d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | |||||
| chr6:75701633
|
C | CTTT | 80 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.2289-991_2289-989d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | |||||
| chr6:75701633
|
C | CTTTT | 30 | a0001c0001t0002g0064a0001c0001t0002g0068a0001c0001t0002g0084others(27): Show | 30 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.2289-992_2289-989d others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | |||||
| chr6:75701633
|
C | CTTTTT | 11 | a0001c0001t0004g0309a0001c0001t0004g0319a0001c0001t0004g0321others(8): Show | 11 | HG00597.hp1 HG02040.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.2289-993_2289-989d others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | |||||
| chr6:75701633
|
C | CTTTTTT | 9 | a0001c0001t0004g0301a0001c0001t0004g0306a0001c0001t0004g0320others(6): Show | 9 | HG00408.hp2 NA18941.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.2289-994_2289-989d others(8): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | |||||
| chr6:75701633
|
CT | C | 7 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0018others(4): Show | 7 | HG02630.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2289-989delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | |||||
| chr6:75701660
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2289-985G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701660 | ||||||
| chr6:75701670
|
C | T | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2289-975C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701670 | ||||||
| chr6:75701678
|
C | T | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2289-967C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701678 | ||||||
| chr6:75701733
|
G | A | 14 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2289-912G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701733 | ||||||
| chr6:75701765
|
A | G | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2289-880A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701765 | ||||||
| chr6:75701929
|
C | T | 27 | a0001c0001t0002g0059a0001c0001t0005g0141a0001c0001t0005g0143others(24): Show | 27 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.2289-716C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701929 | ||||||
| chr6:75702007
|
C | T | 5 | a0001c0001t0005g0152a0001c0001t0005g0153a0001c0001t0005g0154others(2): Show | 5 | HG00642.hp1 HG01256.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.2289-638C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702007 | ||||||
| chr6:75702064
|
CAAG | C | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2289-578_2289-576d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75702064 | |||||
| chr6:75702084
|
G | A | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2289-561G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702084 | ||||||
| chr6:75702127
|
G | A | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2289-518G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702127 | ||||||
| chr6:75702218
|
C | CT | 104 | a0001c0001t0001g0274a0001c0001t0001g0284a0001c0001t0002g0001others(101): Show | 104 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.2289-412dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75702218 | |||||
| chr6:75702218
|
CT | C | 50 | a0001c0001t0001g0194a0001c0001t0004g0300a0001c0001t0004g0301others(47): Show | 50 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.2289-412delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75702218 | |||||
| chr6:75702359
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2289-286G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702359 | ||||||
| chr6:75702456
|
G | A | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2289-189G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702456 | ||||||
| chr6:75702513
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2289-132C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702513 | ||||||
| chr6:75703122
|
A | AT | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2716+56dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75703122 | |||||
| chr6:75703180
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0214a0001c0001t0001g0219 | 3 | HG01884.hp2 HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2716+108G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703180 | ||||||
| chr6:75703182
|
G | A | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2716+110G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703182 | ||||||
| chr6:75703226
|
C | T | 1 | a0001c0001t0002g0082 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2716+154C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703226 | ||||||
| chr6:75703243
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2716+171G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703243 | ||||||
| chr6:75703263
|
G | A | 1 | a0001c0001t0013g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2716+191G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703263 | ||||||
| chr6:75703276
|
C | G | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2716+204C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703276 | ||||||
| chr6:75703276
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2716+204C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703276 | ||||||
| chr6:75703293
|
C | CA | 39 | a0001c0001t0002g0127a0001c0001t0004g0300a0001c0001t0004g0301others(36): Show | 39 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2716+230dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75703293 | |||||
| chr6:75703362
|
A | G | 22 | a0001c0001t0002g0074a0001c0001t0002g0103a0001c0001t0002g0104others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.2716+290A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703362 | ||||||
| chr6:75703638
|
G | T | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2716+566G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703638 | ||||||
| chr6:75703738
|
G | A | 3 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0021 | 3 | HG03041.hp2 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2716+666G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703738 | ||||||
| chr6:75703781
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2716+709A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703781 | ||||||
| chr6:75703962
|
T | A | 1 | a0001c0001t0002g0123 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2716+890T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703962 | ||||||
| chr6:75703993
|
A | G | 37 | a0001c0001t0001g0275a0001c0004t0003g0173a0001c0004t0003g0174others(34): Show | 37 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.2716+921A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703993 | ||||||
| chr6:75704101
|
A | G | 1 | a0012c0018t0001g0239 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2716+1029A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704101 | ||||||
| chr6:75704115
|
G | A | 258 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(255): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.2716+1043G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704115 | ||||||
| chr6:75704407
|
G | A | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064 | 3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2716+1335G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704407 | ||||||
| chr6:75704434
|
A | G | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2716+1362A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704434 | ||||||
| chr6:75704465
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2716+1393A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704465 | ||||||
| chr6:75704543
|
G | A | 26 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2716+1471G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704543 | ||||||
| chr6:75704617
|
G | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2716+1545G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704617 | ||||||
| chr6:75704787
|
C | T | 1 | a0001c0002t0003g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2716+1715C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704787 | ||||||
| chr6:75704939
|
G | T | 1 | a0001c0001t0002g0082 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2716+1867G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704939 | ||||||
| chr6:75704950
|
A | G | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2716+1878A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704950 | ||||||
| chr6:75705027
|
G | A | 1 | a0001c0002t0003g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2716+1955G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705027 | ||||||
| chr6:75705232
|
C | G | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2716+2160C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705232 | ||||||
| chr6:75705279
|
G | A | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2716+2207G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705279 | ||||||
| chr6:75705285
|
G | A | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2716+2213G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705285 | ||||||
| chr6:75705416
|
C | A | 1 | a0001c0001t0002g0127 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2716+2344C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705416 | ||||||
| chr6:75705440
|
G | A | 8 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2716+2368G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705440 | ||||||
| chr6:75705492
|
T | C | 258 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(255): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.2716+2420T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705492 | ||||||
| chr6:75705530
|
C | T | 39 | a0001c0001t0001g0199a0001c0001t0004g0300a0001c0001t0004g0301others(36): Show | 39 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2716+2458C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705530 | ||||||
| chr6:75705554
|
A | T | 3 | a0001c0002t0003g0011a0001c0002t0003g0338a0001c0002t0003g0345 | 3 | HG01891.hp2 NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2716+2482A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705554 | ||||||
| chr6:75705558
|
A | T | 93 | a0001c0001t0001g0247a0001c0001t0001g0274a0001c0001t0002g0055others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.2716+2486A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705558 | ||||||
| chr6:75705562
|
T | A | 32 | a0001c0001t0001g0212a0001c0001t0002g0117a0001c0004t0014g0049others(29): Show | 32 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.2716+2490T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705562 | ||||||
| chr6:75705566
|
T | A | 2 | a0001c0004t0014g0049a0010c0012t0003g0166 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2716+2494T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705566 | ||||||
| chr6:75705652
|
A | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2716+2580A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705652 | ||||||
| chr6:75705731
|
ATTTTTC | A | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2716+2662_2716+266 others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75705731 | |||||
| chr6:75705923
|
GC | G | 36 | a0001c0001t0010g0182a0001c0001t0010g0183a0001c0001t0013g0184others(33): Show | 36 | HG00609.hp2 HG01891.hp2 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.2716+2853delC | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75705923 | |||||
| chr6:75705924
|
C | CT | 12 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0002t0003g0013others(9): Show | 12 | HG02056.hp1 HG02132.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTT | 5 | a0001c0002t0003g0014a0001c0002t0009g0170a0001c0002t0011g0016others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTTT | 3 | a0001c0002t0009g0007a0001c0002t0009g0009a0001c0002t0009g0171 | 3 | HG02486.hp2 HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTTTTTTT others(5): Show |
1 | a0002c0003t0003g0050 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTTTTTTT others(6): Show |
2 | a0002c0003t0003g0036a0002c0003t0003g0042 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTTTTTTT others(10): Show |
1 | a0002c0003t0003g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(21): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTTTTTTT others(12): Show |
4 | a0002c0003t0003g0026a0002c0003t0003g0043a0002c0003t0003g0046others(1): Show | 4 | HG00741.hp1 HG01074.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(23): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTTTTTTT others(13): Show |
1 | a0002c0003t0003g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(24): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTTTTTTT others(14): Show |
1 | a0001c0004t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(25): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTTTTTTT others(16): Show |
3 | a0002c0003t0003g0039a0002c0003t0003g0051a0002c0003t0003g0052 | 3 | HG01243.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(27): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTTTTTTT others(17): Show |
1 | a0002c0003t0019g0040 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(28): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
C | CTTTTTTT others(22): Show |
1 | a0002c0003t0003g0044 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(33): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
CCT | C | 13 | a0001c0001t0005g0146a0001c0001t0005g0157a0001c0001t0005g0158others(10): Show | 13 | HG00280.hp2 HG01109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2716+2853_2716+285 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
CCTT | C | 19 | a0001c0001t0003g0053a0001c0001t0005g0141a0001c0001t0005g0143others(16): Show | 19 | HG00642.hp1 HG01069.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.2716+2853_2716+285 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
CCTTTTTT others(2): Show |
C | 11 | a0001c0001t0002g0066a0001c0001t0002g0083a0001c0001t0002g0110others(8): Show | 11 | HG02572.hp1 HG02738.hp2 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.2716+2853_2716+286 others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
CCTTTTTT others(3): Show |
C | 115 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2716+2853_2716+286 others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
CCTTTTTT others(4): Show |
C | 2 | a0001c0001t0002g0057a0001c0001t0002g0127 | 2 | NA18954.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2716+2853_2716+286 others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
CCTTTTTT others(5): Show |
C | 2 | a0001c0008t0003g0185a0001c0008t0003g0186 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2716+2853_2716+286 others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705924
|
CCTTTTTT others(11): Show |
C | 2 | a0001c0002t0003g0352a0001c0002t0021g0342 | 2 | NA18966.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.2716+2853_2716+287 others(22): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | ||||||
| chr6:75705925
|
C | CT | 25 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0198others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.2716+2882dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75705925 | |||||
| chr6:75705925
|
C | T | 53 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(50): Show | 53 | HG00423.hp1 HG00738.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.2716+2853C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705925 | ||||||
| chr6:75705925
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2716+2870_2716+288 others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75705925 | |||||
| chr6:75705933
|
T | G | 1 | a0001c0004t0014g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2716+2861T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705933 | ||||||
| chr6:75705957
|
G | A | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2716+2885G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705957 | ||||||
| chr6:75705958
|
A | G | 1 | a0001c0002t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2716+2886A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705958 | ||||||
| chr6:75705961
|
G | A | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2716+2889G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705961 | ||||||
| chr6:75705967
|
C | T | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2716+2895C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705967 | ||||||
| chr6:75706019
|
C | T | 1 | a0001c0004t0003g0180 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2716+2947C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706019 | ||||||
| chr6:75706099
|
A | C | 4 | a0001c0001t0002g0109a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | NA18955.hp1 NA18974.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2716+3027A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706099 | ||||||
| chr6:75706256
|
G | C | 1 | a0001c0001t0001g0211 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2716+3184G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706256 | ||||||
| chr6:75706419
|
T | C | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2717-3108T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706419 | ||||||
| chr6:75706570
|
A | G | 3 | a0001c0001t0002g0069a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG02165.hp2 NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2717-2957A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706570 | ||||||
| chr6:75706600
|
T | C | 9 | a0001c0001t0001g0189a0001c0001t0001g0204a0001c0001t0001g0216others(6): Show | 9 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.2717-2927T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706600 | ||||||
| chr6:75706678
|
T | TAA | 19 | a0001c0001t0005g0143a0001c0001t0005g0144a0001c0001t0005g0145others(16): Show | 19 | HG00280.hp2 HG00642.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.2717-2849_2717-284 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706678 | ||||||
| chr6:75706939
|
G | A | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2717-2588G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706939 | ||||||
| chr6:75707023
|
C | A | 9 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2717-2504C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707023 | ||||||
| chr6:75707027
|
TG | T | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2717-2499delG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707027 | ||||||
| chr6:75707355
|
C | CT | 57 | a0001c0001t0001g0196a0001c0001t0001g0215a0001c0001t0001g0234others(54): Show | 57 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.2717-2146dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | |||||
| chr6:75707355
|
C | CTT | 10 | a0001c0001t0001g0217a0001c0001t0001g0262a0001c0001t0003g0053others(7): Show | 10 | HG02056.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2717-2147_2717-214 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | |||||
| chr6:75707355
|
C | CTTT | 8 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(5): Show | 8 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2717-2148_2717-214 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | |||||
| chr6:75707355
|
CT | C | 68 | a0001c0001t0001g0204a0001c0001t0001g0212a0001c0001t0001g0267others(65): Show | 68 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.2717-2146delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | |||||
| chr6:75707355
|
CTT | C | 23 | a0001c0002t0003g0338a0001c0002t0003g0339a0001c0002t0003g0343others(20): Show | 23 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.2717-2147_2717-214 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | |||||
| chr6:75707355
|
CTTTTTT | C | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2717-2151_2717-214 others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | |||||
| chr6:75707597
|
A | G | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2717-1930A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707597 | ||||||
| chr6:75707677
|
T | G | 1 | a0001c0001t0020g0249 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2717-1850T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707677 | ||||||
| chr6:75707724
|
GAAGTT | G | 3 | a0001c0001t0002g0069a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG02165.hp2 NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2717-1799_2717-179 others(9): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707724 | |||||
| chr6:75707924
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2717-1603C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707924 | ||||||
| chr6:75707988
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2717-1539A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707988 | ||||||
| chr6:75708029
|
T | G | 38 | a0001c0001t0004g0300a0001c0001t0004g0301a0001c0001t0004g0304others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2717-1498T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708029 | ||||||
| chr6:75708070
|
C | A | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2717-1457C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708070 | ||||||
| chr6:75708101
|
C | T | 1 | a0001c0002t0003g0348 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2717-1426C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708101 | ||||||
| chr6:75708270
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2717-1257C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708270 | ||||||
| chr6:75708333
|
A | G | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2717-1194A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708333 | ||||||
| chr6:75708350
|
TATTAACT others(4): Show |
T | 9 | a0001c0001t0007g0302a0001c0001t0007g0303a0001c0001t0007g0307others(6): Show | 9 | HG01975.hp2 NA18946.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.2717-1176_2717-116 others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708350 | ||||||
| chr6:75708362
|
C | G | 9 | a0001c0001t0007g0302a0001c0001t0007g0303a0001c0001t0007g0307others(6): Show | 9 | HG01975.hp2 NA18946.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.2717-1165C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708362 | ||||||
| chr6:75708630
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2717-897C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708630 | ||||||
| chr6:75708812
|
C | T | 1 | a0001c0001t0004g0311 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2717-715C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708812 | ||||||
| chr6:75708872
|
C | T | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2717-655C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708872 | ||||||
| chr6:75709061
|
A | G | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2717-466A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709061 | ||||||
| chr6:75709073
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2717-454A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709073 | ||||||
| chr6:75709123
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2717-404G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709123 | ||||||
| chr6:75709245
|
T | C | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2717-282T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709245 | ||||||
| chr6:75709283
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2717-244G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709283 | ||||||
| chr6:75709337
|
A | T | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2717-190A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709337 | ||||||
| chr6:75709471
|
T | G | 4 | a0002c0003t0003g0031a0002c0003t0003g0032a0002c0003t0003g0033others(1): Show | 4 | HG02056.hp1 NA18941.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.2717-56T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709471 | ||||||
| chr6:75709873
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2820+243G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75709873 | ||||||
| chr6:75709932
|
G | T | 1 | a0001c0016t0006g0297 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2820+302G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75709932 | ||||||
| chr6:75710008
|
C | T | 360 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(357): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.2820+378C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710008 | ||||||
| chr6:75710020
|
C | T | 35 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2820+390C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710020 | ||||||
| chr6:75710196
|
T | TC | 46 | a0001c0002t0003g0003a0001c0002t0003g0004a0001c0002t0003g0005others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2820+567dupC | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr6 | 75710196 | |||||
| chr6:75710256
|
T | A | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2820+626T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710256 | ||||||
| chr6:75710563
|
T | C | 1 | a0001c0001t0002g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2821-765T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710563 | ||||||
| chr6:75710702
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | NA18975.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2821-626A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710702 | ||||||
| chr6:75710721
|
A | G | 1 | a0002c0003t0003g0030 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2821-607A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710721 | ||||||
| chr6:75710895
|
C | T | 1 | a0001c0002t0003g0169 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2821-433C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710895 | ||||||
| chr6:75711187
|
T | C | 2 | a0001c0001t0004g0324a0001c0001t0004g0328 | 2 | NA18966.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2821-141T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75711187 | ||||||
| chr6:75711192
|
AGT | A | 4 | a0001c0001t0010g0182a0001c0001t0010g0183a0001c0001t0010g0187others(1): Show | 4 | HG02622.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2821-133_2821-132d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr6 | 75711192 | |||||
| chr6:75711287
|
A | G | 36 | a0001c0004t0003g0173a0001c0004t0003g0174a0001c0004t0003g0175others(33): Show | 36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.2821-41A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75711287 | ||||||
| chr6:75711496
|
A | T | 1 | a0001c0002t0009g0009 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2909+80A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75711496 | ||||||
| chr6:75711819
|
C | T | 26 | a0001c0001t0005g0141a0001c0001t0005g0143a0001c0001t0005g0144others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2909+403C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75711819 | ||||||
| chr6:75711924
|
G | C | 212 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0054others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2909+508G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75711924 | ||||||
| chr6:75712094
|
A | G | 1 | a0003c0007t0006g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2909+678A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712094 | ||||||
| chr6:75712102
|
G | GAGT | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2909+688_2909+690d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr6 | 75712102 | |||||
| chr6:75712140
|
G | A | 1 | a0001c0001t0004g0336 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2909+724G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712140 | ||||||
| chr6:75712327
|
T | C | 1 | a0001c0001t0004g0311 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2909+911T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712327 | ||||||
| chr6:75712521
|
T | TA | 12 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(9): Show | 12 | HG02293.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2910-980dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr6 | 75712521 | |||||
| chr6:75712531
|
A | T | 9 | a0001c0005t0006g0291a0001c0005t0006g0292a0001c0005t0006g0293others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2910-982A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712531 | ||||||
| chr6:75712569
|
A | AT | 6 | a0002c0003t0003g0026a0002c0003t0003g0036a0002c0003t0003g0041others(3): Show | 6 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2910-936dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr6 | 75712569 | |||||
| chr6:75712678
|
A | G | 1 | a0001c0004t0003g0180 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2910-835A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712678 | ||||||
| chr6:75712700
|
G | C | 1 | a0001c0001t0004g0323 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2910-813G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712700 | ||||||
| chr6:75712735
|
GA | G | 8 | a0001c0001t0004g0309a0001c0001t0004g0322a0001c0001t0004g0325others(5): Show | 8 | HG00408.hp2 HG00597.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.2910-768delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr6 | 75712735 | |||||
| chr6:75712756
|
A | G | 1 | a0001c0017t0002g0108 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2910-757A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712756 | ||||||
| chr6:75712952
|
C | A | 25 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(22): Show | 25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2910-561C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712952 | ||||||
| chr6:75713028
|
G | A | 8 | a0001c0001t0001g0189a0001c0001t0001g0204a0001c0001t0001g0216others(5): Show | 8 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2910-485G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75713028 | ||||||
| chr6:75713348
|
C | T | 2 | a0001c0001t0003g0053a0010c0012t0003g0166 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2910-165C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75713348 | ||||||
| chr6:75713349
|
G | A | 1 | a0001c0001t0002g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2910-164G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75713349 | ||||||
| chr6:75713487
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0223 | 2 | NA19065.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2910-26G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75713487 | ||||||
| chr6:75713638
|
A | G | 2 | a0001c0001t0004g0304a0001c0001t0004g0305 | 2 | HG01928.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2979-37A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 22/23 | chr6 | 75713638 | ||||||
| chr6:75713878
|
G | A | 2 | a0001c0008t0003g0185a0001c0008t0003g0186 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3129+53G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75713878 | ||||||
| chr6:75714585
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3129+760A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714585 | ||||||
| chr6:75714658
|
A | T | 103 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.3130-727A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714658 | ||||||
| chr6:75714802
|
TG | T | 27 | a0001c0002t0003g0020a0001c0002t0003g0169a0001c0002t0003g0338others(24): Show | 27 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.3130-582delG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714802 | ||||||
| chr6:75714803
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3130-582G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714803 | ||||||
| chr6:75714809
|
T | G | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3130-576T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714809 | ||||||
| chr6:75714818
|
C | A | 1 | a0010c0012t0003g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3130-567C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714818 | ||||||
| chr6:75714847
|
C | T | 1 | a0001c0016t0006g0297 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3130-538C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714847 | ||||||
| chr6:75714972
|
G | A | 1 | a0001c0001t0003g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3130-413G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714972 | ||||||
| chr6:75715141
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3130-244G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75715141 | ||||||
| chr6:75715312
|
C | T | 2 | a0002c0003t0003g0045a0002c0003t0003g0046 | 2 | HG01074.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3130-73C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75715312 |