Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 29843 |
|---|---|
| ensemblid | ENSG00000079387.15 |
| hgncid | 17927 |
| symbol | SENP1 |
| name | SUMO specific peptidase 1 |
| refseq_nuc | NM_001267594.2 |
| refseq_prot | NP_001254523.1 |
| ensembl_nuc | ENST00000549518.6 |
| ensembl_prot | ENSP00000447328.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 48042897 |
| end | 48106079 |
| strand | - |
| ver | v1.2 |
| region | chr12:48042897-48106079 |
| region5000 | chr12:48037897-48111079 |
| regionname0 | SENP1_chr12_48042897_48106079 |
| regionname5000 | SENP1_chr12_48037897_48111079 |
| 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 | 1/1 | 644 | 389 | 95 | 69 | 171 | 14 | 38 | 130 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0002 | 0/0 | 644 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0003 | 0/0 | 644 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0004 | 0/0 | 644 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0005 | 0/0 | 644 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| 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 | 1/1 | 1935 | 306 | 82 | 50 | 130 | 10 | 32 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| c0002 | 0/0 | 1935 | 74 | 9 | 18 | 37 | 4 | 6 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| c0003 | 0/0 | 1935 | 6 | 4 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| c0004 | 0/0 | 1935 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| c0005 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| c0006 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| c0007 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| c0008 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| c0009 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| c0010 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2520 | 150 | 16 | 27 | 92 | 3 | 11 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0002 | 0/0 | 2520 | 74 | 9 | 18 | 37 | 4 | 6 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0003 | 0/0 | 2524 | 58 | 14 | 8 | 26 | 4 | 6 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0004 | 0/0 | 2522 | 39 | 13 | 11 | 1 | 3 | 11 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0005 | 0/0 | 2524 | 22 | 18 | 2 | 0 | 0 | 2 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0006 | 0/0 | 2522 | 10 | 8 | 2 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0007 | 0/0 | 2524 | 10 | 0 | 0 | 10 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0008 | 0/0 | 2520 | 6 | 4 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0009 | 0/0 | 2524 | 4 | 4 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0010 | 0/0 | 2528 | 3 | 3 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0011 | 0/0 | 2524 | 2 | 2 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0012 | 0/0 | 2520 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0013 | 0/0 | 2520 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0014 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0015 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0016 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0017 | 0/0 | 2522 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0018 | 0/0 | 2520 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0019 | 0/0 | 2520 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0020 | 0/0 | 2522 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0021 | 0/0 | 2520 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0022 | 0/0 | 2502 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0023 | 1/0 | 2522 | 1 | 0 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0024 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| t0025 | 0/0 | 2524 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| 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 | 4 | 0 | 3 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0002 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0309 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0383 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| 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 | 1/1 | 1935 | 306 | 82 | 50 | 130 | 10 | 32 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0002 | 0/0 | 1935 | 74 | 9 | 18 | 37 | 4 | 6 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0003 | 0/0 | 1935 | 6 | 4 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0005 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0009 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0010 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0002c0004 | 0/0 | 1935 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0003c0007 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0004c0008 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0005c0006 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4454 | 146 | 16 | 27 | 88 | 3 | 11 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0003 | 0/0 | 4458 | 58 | 14 | 8 | 26 | 4 | 6 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0004 | 0/0 | 4456 | 38 | 13 | 10 | 1 | 3 | 11 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0005 | 0/0 | 4458 | 20 | 17 | 1 | 0 | 0 | 2 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0006 | 0/0 | 4456 | 10 | 8 | 2 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0007 | 0/0 | 4458 | 9 | 0 | 0 | 9 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0009 | 0/0 | 4458 | 4 | 4 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0010 | 0/0 | 4462 | 3 | 3 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0011 | 0/0 | 4458 | 2 | 2 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0012 | 0/0 | 4454 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0013 | 0/0 | 4454 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0014 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0015 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0016 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0017 | 0/0 | 4456 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0018 | 0/0 | 4454 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0019 | 0/0 | 4454 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0020 | 0/0 | 4456 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0021 | 0/0 | 4454 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0022 | 0/0 | 4436 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0023 | 1/0 | 4456 | 1 | 0 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0024 | 0/0 | 4458 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0001t0025 | 0/0 | 4458 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0002t0002 | 0/0 | 4454 | 74 | 9 | 18 | 37 | 4 | 6 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0003t0008 | 0/0 | 4454 | 6 | 4 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0005t0001 | 0/0 | 4454 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0009t0004 | 0/0 | 4456 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0001c0010t0001 | 0/0 | 4454 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0002c0004t0001 | 0/0 | 4454 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0003c0007t0007 | 0/0 | 4458 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0004c0008t0005 | 0/0 | 4458 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| a0005c0006t0005 | 0/0 | 4458 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | copy fasta | chr12 | 48037897 | 48111079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0383 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0007g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0007g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0007g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0007g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0009g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0010g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0010g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0010g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0011g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0012g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0012g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0013g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0013g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0014g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0015g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0016g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0017g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0018g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0019g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0020g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0021g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0022g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0023g0309 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0024g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0025g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0002 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0008g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0008g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0008g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0009t0004g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0010t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0002c0004t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0002c0004t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0003c0007t0007g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0004c0008t0005g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0005c0006t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0213 | EUR | GBR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0277 | EUR | GBR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0381 | EUR | FIN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0144 | EUR | FIN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0181 | EUR | FIN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | FIN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0376 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0327 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0145 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0147 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0329 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00673 | hp1 | a0002 | c0004 | t0001 | g0373 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00673 | hp2 | a0001 | c0001 | t0013 | g0022 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0148 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0334 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0283 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0284 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0325 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0177 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0331 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0296 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01106 | hp1 | a0004 | c0008 | t0005 | g0336 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0166 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0333 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0312 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0287 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0314 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01192 | hp1 | a0001 | c0001 | t0025 | g0237 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0175 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0137 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0282 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0326 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0320 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0288 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01361 | hp2 | a0001 | c0001 | t0017 | g0317 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0139 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0368 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0207 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0322 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0154 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0266 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0272 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0328 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0308 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01884 | hp2 | a0001 | c0001 | t0015 | g0278 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0340 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0323 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0173 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0345 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0374 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0286 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0258 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CDX | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0290 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0171 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0228 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02280 | hp2 | a0001 | c0001 | t0018 | g0053 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02523 | hp1 | a0001 | c0001 | t0013 | g0024 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0230 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02622 | hp2 | a0001 | c0003 | t0008 | g0293 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0291 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0347 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0304 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0330 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0203 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0160 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0335 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0211 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0342 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02723 | hp2 | a0001 | c0003 | t0008 | g0349 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0159 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0321 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0346 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0305 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0343 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02886 | hp2 | a0001 | c0003 | t0008 | g0294 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0255 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0297 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0289 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0243 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0170 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0382 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0324 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0136 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0281 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0348 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0140 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0195 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0341 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0227 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0176 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03225 | hp1 | a0001 | c0001 | t0016 | g0344 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0254 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0316 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0210 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0299 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0273 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03486 | hp1 | a0001 | c0001 | t0024 | g0303 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0298 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0319 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0318 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03516 | hp1 | a0001 | c0003 | t0008 | g0151 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0301 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0295 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0232 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0292 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0285 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03654 | hp2 | a0001 | c0001 | t0020 | g0038 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0205 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0357 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03688 | hp2 | a0001 | c0001 | t0022 | g0132 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0271 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0310 | SAS | BEB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0315 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0380 | SAS | BEB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0338 | SAS | BEB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0313 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0265 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0158 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0311 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0307 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0270 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | CHB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | CHB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18949 | hp1 | a0001 | c0001 | t0021 | g0117 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18952 | hp2 | a0001 | c0001 | t0007 | g0262 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18962 | hp1 | a0001 | c0001 | t0007 | g0245 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18964 | hp1 | a0001 | c0001 | t0007 | g0261 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18966 | hp2 | a0001 | c0001 | t0012 | g0101 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18971 | hp1 | a0002 | c0004 | t0001 | g0369 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18974 | hp1 | a0001 | c0005 | t0001 | g0091 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18984 | hp2 | a0001 | c0001 | t0007 | g0260 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18985 | hp1 | a0003 | c0007 | t0007 | g0246 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0199 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0384 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19006 | hp2 | a0001 | c0001 | t0019 | g0093 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19007 | hp2 | a0001 | c0001 | t0012 | g0102 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19030 | hp2 | a0005 | c0006 | t0005 | g0226 | AFR | LWK | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | LWK | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19057 | hp1 | a0001 | c0001 | t0007 | g0247 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19072 | hp1 | a0001 | c0001 | t0007 | g0267 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19077 | hp1 | a0001 | c0003 | t0008 | g0351 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19077 | hp2 | a0001 | c0010 | t0001 | g0083 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0375 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19084 | hp1 | a0001 | c0001 | t0007 | g0244 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0378 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19091 | hp1 | a0001 | c0003 | t0008 | g0350 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0306 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ASW | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | ASW | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0180 | EUR | TSI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01123 | hp1 | a0001 | c0009 | t0004 | g0337 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0332 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0276 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0172 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0339 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0135 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG06807 | hp1 | a0001 | c0001 | t0010 | g0302 | AFR | USA | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | USA | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | USA | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | USA | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | LWK | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | LWK | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0383 | REF | REF | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0023 | g0309 | REF | REF | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48049029
|
G | C | 1 | a0003 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.1511C>G | p.Ala504Gly | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 14/18 | 1607/4456 | 1511/1935 | 504/644 | chr12 | 48049029 | ||
| chr12:48049030
|
C | G | 1 | a0003 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.1510G>C | p.Ala504Pro | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 14/18 | 1606/4456 | 1510/1935 | 504/644 | chr12 | 48049030 | ||
| chr12:48065113
|
T | A | 1 | a0004 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.1227A>T | p.Lys409Asn | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/18 | 1323/4456 | 1227/1935 | 409/644 | chr12 | 48065113 | ||
| chr12:48065129
|
T | C | 1 | a0002 | 2 | HG00673.hp1 NA18971.hp1 |
missense_variant | MODERATE | c.1211A>G | p.Gln404Arg | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/18 | 1307/4456 | 1211/1935 | 404/644 | chr12 | 48065129 | ||
| chr12:48074426
|
C | T | 1 | a0005 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.838G>A | p.Ala280Thr | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/18 | 934/4456 | 838/1935 | 280/644 | chr12 | 48074426 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48046422
|
G | A | 1 | a0001c0003 | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
synonymous_variant | LOW | c.1806C>T | p.Asp602Asp | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 17/18 | 1902/4456 | 1806/1935 | 602/644 | chr12 | 48046422 | ||
| chr12:48074376
|
G | A | 1 | a0001c0003 | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
synonymous_variant | LOW | c.888C>T | p.His296His | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/18 | 984/4456 | 888/1935 | 296/644 | chr12 | 48074376 | ||
| chr12:48083639
|
A | G | 1 | a0001c0002 | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
synonymous_variant | LOW | c.504T>C | p.Leu168Leu | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/18 | 600/4456 | 504/1935 | 168/644 | chr12 | 48083639 | ||
| chr12:48083669
|
T | C | 1 | a0001c0009 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.474A>G | p.Pro158Pro | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/18 | 570/4456 | 474/1935 | 158/644 | chr12 | 48083669 | ||
| chr12:48088869
|
C | T | 1 | a0001c0005 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.312G>A | p.Ser104Ser | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/18 | 408/4456 | 312/1935 | 104/644 | chr12 | 48088869 | ||
| chr12:48098045
|
G | A | 1 | a0001c0010 | 1 | NA19077.hp2 | synonymous_variant | LOW | c.84C>T | p.Leu28Leu | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 3/18 | 180/4456 | 84/1935 | 28/644 | chr12 | 48098045 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48043009
|
A | G | 1 | a0001c0001t0006 | 10 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2313T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 2313 | chr12 | 48043009 | |||||
| chr12:48043258
|
T | C | 1 | a0001c0001t0016 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2064A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 2064 | chr12 | 48043258 | |||||
| chr12:48043312
|
G | T | 1 | a0001c0003t0008 | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2010C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 2010 | chr12 | 48043312 | |||||
| chr12:48043497
|
A | T | 1 | a0001c0001t0012 | 2 | NA18966.hp2 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1825T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 1825 | chr12 | 48043497 | |||||
| chr12:48043520
|
T | C | 1 | a0001c0001t0017 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1802A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 1802 | chr12 | 48043520 | |||||
| chr12:48043615
|
G | C | 1 | a0001c0001t0021 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1707C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 1707 | chr12 | 48043615 | |||||
| chr12:48043903
|
G | A | 2 | a0001c0001t0011a0001c0002t0002 | 76 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1419C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 1419 | chr12 | 48043903 | |||||
| chr12:48043950
|
A | G | 1 | a0001c0003t0008 | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1372T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 1372 | chr12 | 48043950 | |||||
| chr12:48044050
|
G | A | 2 | a0001c0001t0009a0001c0001t0024 | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1272C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 1272 | chr12 | 48044050 | |||||
| chr12:48044097
|
A | G | 2 | a0001c0001t0006a0001c0001t0015 | 11 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1225T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 1225 | chr12 | 48044097 | |||||
| chr12:48044182
|
A | C | 1 | a0001c0001t0024 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1140T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 1140 | chr12 | 48044182 | |||||
| chr12:48044357
|
C | CAT | 4 | a0001c0001t0005a0001c0001t0011a0004c0008t0005others(1): Show | 24 | HG00741.hp2 HG01106.hp1 HG02145.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*963_*964dupAT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 964 | chr12 | 48044357 | |||||
| chr12:48044357
|
C | CATATAT | 1 | a0001c0001t0010 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*959_*964dupATATAT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 964 | chr12 | 48044357 | |||||
| chr12:48044357
|
CAT | C | 11 | a0001c0001t0001a0001c0001t0012a0001c0001t0013others(8): Show | 237 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*963_*964delAT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 963 | chr12 | 48044357 | |||||
| chr12:48044359
|
T | TAC | 6 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(3): Show | 74 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*962_*963insGT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 962 | chr12 | 48044359 | |||||
| chr12:48044362
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0022 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*940_*959delCACATA others(14): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 940 | chr12 | 48044362 | |||||
| chr12:48044424
|
A | G | 1 | a0001c0001t0014 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*898T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 898 | chr12 | 48044424 | |||||
| chr12:48044471
|
A | T | 1 | a0001c0001t0019 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*851T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 851 | chr12 | 48044471 | |||||
| chr12:48044507
|
T | A | 10 | a0001c0001t0001a0001c0001t0012a0001c0001t0013others(7): Show | 158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*815A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 815 | chr12 | 48044507 | |||||
| chr12:48044625
|
C | T | 31 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(28): Show | 393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
3_prime_UTR_variant | MODIFIER | c.*697G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 697 | chr12 | 48044625 | |||||
| chr12:48044683
|
G | A | 2 | a0001c0001t0009a0001c0001t0024 | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*639C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 639 | chr12 | 48044683 | |||||
| chr12:48044827
|
T | C | 1 | a0001c0001t0013 | 2 | HG00673.hp2 HG02523.hp1 |
3_prime_UTR_variant | MODIFIER | c.*495A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 495 | chr12 | 48044827 | |||||
| chr12:48044970
|
T | C | 1 | a0001c0001t0025 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 352 | chr12 | 48044970 | |||||
| chr12:48045142
|
G | C | 2 | a0001c0001t0007a0003c0007t0007 | 10 | NA18947.hp1 NA18952.hp2 NA18962.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*180C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 180 | chr12 | 48045142 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48045439
|
C | T | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1873-55G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 17/17 | chr12 | 48045439 | ||||||
| chr12:48045591
|
A | C | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1873-207T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 17/17 | chr12 | 48045591 | ||||||
| chr12:48045599
|
T | G | 1 | a0001c0001t0006g0296 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1873-215A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 17/17 | chr12 | 48045599 | ||||||
| chr12:48046339
|
T | C | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1872+17A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 17/17 | chr12 | 48046339 | ||||||
| chr12:48046737
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1776+241G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 16/17 | chr12 | 48046737 | ||||||
| chr12:48046738
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1776+240G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 16/17 | chr12 | 48046738 | ||||||
| chr12:48046822
|
C | A | 1 | a0001c0001t0003g0205 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1776+156G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 16/17 | chr12 | 48046822 | ||||||
| chr12:48046822
|
C | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0025others(8): Show | 11 | HG00735.hp2 HG01123.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1776+156G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 16/17 | chr12 | 48046822 | ||||||
| chr12:48046823
|
G | C | 1 | a0001c0001t0003g0205 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1776+155C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 16/17 | chr12 | 48046823 | ||||||
| chr12:48046875
|
G | A | 1 | a0001c0002t0002g0142 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1776+103C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 16/17 | chr12 | 48046875 | ||||||
| chr12:48047238
|
A | C | 1 | a0001c0001t0001g0371 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1692-176T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047238 | ||||||
| chr12:48047385
|
C | T | 10 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(7): Show | 10 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1692-323G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047385 | ||||||
| chr12:48047491
|
C | T | 1 | a0004c0008t0005g0336 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1692-429G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047491 | ||||||
| chr12:48047499
|
T | A | 2 | a0001c0001t0004g0340a0001c0001t0004g0345 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1692-437A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047499 | ||||||
| chr12:48047548
|
A | C | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1691+453T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047548 | ||||||
| chr12:48047623
|
G | A | 9 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(6): Show | 9 | HG01346.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1691+378C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047623 | ||||||
| chr12:48047696
|
C | G | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1691+305G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047696 | ||||||
| chr12:48047807
|
T | C | 8 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1691+194A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047807 | ||||||
| chr12:48047810
|
T | C | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1691+191A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047810 | ||||||
| chr12:48047833
|
G | T | 1 | a0003c0007t0007g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1691+168C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047833 | ||||||
| chr12:48047895
|
T | G | 1 | a0003c0007t0007g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1691+106A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047895 | ||||||
| chr12:48047909
|
C | G | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1691+92G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047909 | ||||||
| chr12:48047965
|
G | A | 13 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(10): Show | 13 | HG00741.hp2 HG02647.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1691+36C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047965 | ||||||
| chr12:48047993
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02602.hp2 | splice_region_variant&intron_variant | LOW | c.1691+8G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 15/17 | chr12 | 48047993 | ||||||
| chr12:48048116
|
A | G | 1 | a0001c0001t0006g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1612-36T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 14/17 | chr12 | 48048116 | ||||||
| chr12:48048137
|
G | GT | 24 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(21): Show | 24 | HG00741.hp2 HG01099.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1612-58dupA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 14/17 | chr12 | 48048137 | ||||||
| chr12:48048233
|
G | A | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1612-153C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 14/17 | chr12 | 48048233 | ||||||
| chr12:48048322
|
A | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1612-242T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 14/17 | chr12 | 48048322 | ||||||
| chr12:48048464
|
T | A | 1 | a0001c0001t0016g0344 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1612-384A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 14/17 | chr12 | 48048464 | ||||||
| chr12:48048554
|
A | G | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1611+375T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 14/17 | chr12 | 48048554 | ||||||
| chr12:48048662
|
TC | T | 9 | a0001c0001t0004g0340a0001c0001t0004g0345a0001c0001t0016g0344others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1611+266delG | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 14/17 | chr12 | 48048662 | ||||||
| chr12:48048768
|
T | G | 1 | a0003c0007t0007g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1611+161A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 14/17 | chr12 | 48048768 | ||||||
| chr12:48048769
|
G | T | 1 | a0003c0007t0007g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1611+160C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 14/17 | chr12 | 48048769 | ||||||
| chr12:48049174
|
C | T | 4 | a0001c0001t0003g0207a0001c0001t0003g0212a0001c0001t0003g0213others(1): Show | 4 | HG00140.hp1 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1408-42G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48049174 | ||||||
| chr12:48049265
|
T | C | 352 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(349): Show | 362 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(359): Show |
intron_variant | MODIFIER | c.1408-133A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48049265 | ||||||
| chr12:48049456
|
A | G | 1 | a0001c0002t0002g0164 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1408-324T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48049456 | ||||||
| chr12:48049563
|
G | A | 1 | a0001c0001t0004g0332 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1408-431C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48049563 | ||||||
| chr12:48049947
|
G | A | 1 | a0003c0007t0007g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1408-815C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48049947 | ||||||
| chr12:48049949
|
A | C | 1 | a0003c0007t0007g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1408-817T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48049949 | ||||||
| chr12:48050030
|
G | A | 1 | a0001c0001t0006g0296 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1408-898C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48050030 | ||||||
| chr12:48050364
|
G | A | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1408-1232C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48050364 | ||||||
| chr12:48050392
|
T | G | 15 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0003g0196others(12): Show | 15 | NA18965.hp2 NA18968.hp2 NA18972.hp1 others(12): Show |
intron_variant | MODIFIER | c.1408-1260A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48050392 | ||||||
| chr12:48050397
|
A | C | 1 | a0001c0002t0002g0179 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1408-1265T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48050397 | ||||||
| chr12:48050423
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1408-1291G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48050423 | ||||||
| chr12:48050668
|
C | A | 1 | a0001c0001t0004g0311 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1408-1536G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48050668 | ||||||
| chr12:48050705
|
C | T | 255 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(252): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.1408-1573G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48050705 | ||||||
| chr12:48050908
|
G | A | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408-1776C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48050908 | ||||||
| chr12:48050922
|
G | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0240a0001c0001t0003g0242others(2): Show | 6 | HG02055.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408-1790C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48050922 | ||||||
| chr12:48050965
|
C | A | 1 | a0001c0002t0002g0166 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1408-1833G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48050965 | ||||||
| chr12:48051082
|
G | GA | 154 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(151): Show | 154 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1408-1951dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48051082 | ||||||
| chr12:48051449
|
T | G | 8 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1408-2317A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48051449 | ||||||
| chr12:48051575
|
T | C | 1 | a0001c0002t0002g0282 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1408-2443A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48051575 | ||||||
| chr12:48051704
|
A | G | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1408-2572T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48051704 | ||||||
| chr12:48051807
|
T | A | 1 | a0001c0001t0003g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1408-2675A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48051807 | ||||||
| chr12:48051842
|
T | TAAG | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1408-2711_1408-271 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48051842 | ||||||
| chr12:48052325
|
T | G | 8 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1408-3193A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48052325 | ||||||
| chr12:48052358
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1408-3226G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48052358 | ||||||
| chr12:48052522
|
A | C | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1408-3390T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48052522 | ||||||
| chr12:48052535
|
T | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1408-3403A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48052535 | ||||||
| chr12:48052747
|
C | A | 1 | a0001c0001t0006g0296 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1408-3615G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48052747 | ||||||
| chr12:48052909
|
G | A | 3 | a0001c0001t0003g0006a0001c0001t0003g0216a0001c0001t0003g0268 | 4 | NA18963.hp1 NA19010.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408-3777C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48052909 | ||||||
| chr12:48052936
|
CAT | C | 9 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301others(6): Show | 9 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1408-3806_1408-380 others(6): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48052936 | ||||||
| chr12:48052968
|
C | T | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1408-3836G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48052968 | ||||||
| chr12:48053041
|
G | A | 4 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0103others(1): Show | 4 | HG02015.hp2 HG02165.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.1408-3909C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48053041 | ||||||
| chr12:48053081
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1408-3949A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48053081 | ||||||
| chr12:48053199
|
G | A | 5 | a0001c0003t0008g0293a0001c0003t0008g0294a0001c0003t0008g0349others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408-4067C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48053199 | ||||||
| chr12:48053322
|
C | A | 342 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(339): Show | 352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.1408-4190G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48053322 | ||||||
| chr12:48053449
|
G | T | 1 | a0001c0001t0001g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1408-4317C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48053449 | ||||||
| chr12:48053480
|
G | GA | 44 | a0001c0001t0001g0031a0001c0001t0001g0070a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1408-4349dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48053480 | ||||||
| chr12:48053590
|
G | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408-4458C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48053590 | ||||||
| chr12:48053607
|
A | G | 1 | a0001c0001t0005g0270 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1408-4475T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48053607 | ||||||
| chr12:48053654
|
C | T | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1408-4522G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48053654 | ||||||
| chr12:48053875
|
A | G | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1408-4743T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48053875 | ||||||
| chr12:48053907
|
CTAA | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408-4778_1408-477 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48053907 | ||||||
| chr12:48054006
|
G | C | 31 | a0001c0001t0001g0048a0001c0001t0001g0074a0001c0001t0001g0107others(28): Show | 31 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1408-4874C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054006 | ||||||
| chr12:48054011
|
A | G | 4 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0165others(1): Show | 4 | NA18949.hp2 NA18960.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1408-4879T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054011 | ||||||
| chr12:48054044
|
A | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408-4912T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054044 | ||||||
| chr12:48054078
|
G | A | 3 | a0001c0001t0004g0340a0001c0001t0004g0345a0001c0001t0016g0344 | 3 | HG01891.hp2 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1408-4946C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054078 | ||||||
| chr12:48054308
|
A | G | 2 | a0001c0001t0004g0340a0001c0001t0004g0345 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1408-5176T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054308 | ||||||
| chr12:48054351
|
C | G | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1408-5219G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054351 | ||||||
| chr12:48054490
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1408-5358G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054490 | ||||||
| chr12:48054491
|
A | G | 160 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(157): Show | 160 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1408-5359T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054491 | ||||||
| chr12:48054587
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1408-5455G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054587 | ||||||
| chr12:48054683
|
G | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1408-5551C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054683 | ||||||
| chr12:48054791
|
A | G | 1 | a0001c0001t0003g0204 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1408-5659T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054791 | ||||||
| chr12:48054869
|
T | C | 13 | a0001c0001t0003g0005a0001c0001t0003g0204a0001c0001t0003g0234others(10): Show | 14 | HG01192.hp1 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1408-5737A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054869 | ||||||
| chr12:48054917
|
A | G | 5 | a0001c0003t0008g0293a0001c0003t0008g0294a0001c0003t0008g0349others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408-5785T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054917 | ||||||
| chr12:48054989
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1408-5857T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48054989 | ||||||
| chr12:48055133
|
G | A | 24 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(21): Show | 24 | HG00741.hp2 HG01099.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1408-6001C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48055133 | ||||||
| chr12:48055264
|
T | C | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1408-6132A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48055264 | ||||||
| chr12:48055380
|
C | T | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1408-6248G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48055380 | ||||||
| chr12:48055441
|
G | C | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1408-6309C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48055441 | ||||||
| chr12:48055490
|
T | C | 1 | a0001c0002t0002g0152 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1408-6358A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48055490 | ||||||
| chr12:48055598
|
A | G | 1 | a0001c0001t0004g0323 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1408-6466T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48055598 | ||||||
| chr12:48055663
|
T | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG01109.hp2 HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1408-6531A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48055663 | ||||||
| chr12:48055841
|
T | C | 13 | a0001c0001t0003g0005a0001c0001t0003g0204a0001c0001t0003g0234others(10): Show | 14 | HG01192.hp1 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1408-6709A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48055841 | ||||||
| chr12:48055924
|
A | G | 1 | a0001c0001t0017g0317 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1408-6792T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48055924 | ||||||
| chr12:48055985
|
G | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1408-6853C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48055985 | ||||||
| chr12:48056047
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0007g0244a0001c0001t0007g0261 | 3 | NA18964.hp1 NA19058.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1408-6915A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056047 | ||||||
| chr12:48056120
|
A | AATATAGT others(28): Show |
2 | a0001c0001t0004g0321a0001c0009t0004g0337 | 2 | HG01123.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1408-7023_1408-698 others(39): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056120 | ||||||
| chr12:48056120
|
AATATAGT others(28): Show |
A | 254 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(251): Show | 262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.1408-7023_1408-698 others(39): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056120 | ||||||
| chr12:48056140
|
ATATATAT others(49): Show |
A | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1408-7064_1408-700 others(60): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056140 | ||||||
| chr12:48056185
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1408-7053A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056185 | ||||||
| chr12:48056273
|
A | G | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1408-7141T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056273 | ||||||
| chr12:48056280
|
A | G | 1 | a0001c0002t0002g0179 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1408-7148T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056280 | ||||||
| chr12:48056323
|
TATAAATA others(8): Show |
T | 1 | a0001c0002t0002g0152 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1408-7206_1408-719 others(19): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056323 | ||||||
| chr12:48056326
|
AAATATTA others(17): Show |
A | 65 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(62): Show | 73 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1408-7218_1408-719 others(28): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056326 | ||||||
| chr12:48056327
|
A | AAT | 189 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1408-7197_1408-719 others(6): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056327 | ||||||
| chr12:48056346
|
C | T | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1408-7214G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056346 | ||||||
| chr12:48056346
|
CATATA | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0066others(6): Show | 9 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1408-7219_1408-721 others(9): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056346 | ||||||
| chr12:48056381
|
T | A | 2 | a0001c0001t0014g0339a0001c0005t0001g0091 | 2 | HG02559.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1408-7249A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056381 | ||||||
| chr12:48056384
|
A | T | 2 | a0001c0001t0014g0339a0001c0005t0001g0091 | 2 | HG02559.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1408-7252T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056384 | ||||||
| chr12:48056388
|
A | T | 2 | a0001c0001t0014g0339a0001c0005t0001g0091 | 2 | HG02559.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1408-7256T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056388 | ||||||
| chr12:48056389
|
G | T | 2 | a0001c0001t0014g0339a0001c0005t0001g0091 | 2 | HG02559.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1408-7257C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056389 | ||||||
| chr12:48056390
|
T | A | 2 | a0001c0001t0014g0339a0001c0005t0001g0091 | 2 | HG02559.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1408-7258A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056390 | ||||||
| chr12:48056392
|
C | T | 2 | a0001c0001t0014g0339a0001c0005t0001g0091 | 2 | HG02559.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1408-7260G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056392 | ||||||
| chr12:48056406
|
AATT | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1408-7277_1408-727 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056406 | ||||||
| chr12:48056420
|
G | T | 339 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(336): Show | 349 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(346): Show |
intron_variant | MODIFIER | c.1408-7288C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056420 | ||||||
| chr12:48056437
|
A | AAATAT | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+7272_1407+727 others(9): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056437 | ||||||
| chr12:48056451
|
T | G | 6 | a0001c0001t0004g0318a0001c0001t0004g0319a0001c0001t0004g0325others(3): Show | 6 | HG01074.hp1 HG01081.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1407+7259A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056451 | ||||||
| chr12:48056454
|
CATATTAC others(58): Show |
C | 1 | a0001c0002t0002g0191 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1407+7191_1407+725 others(69): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056454 | ||||||
| chr12:48056461
|
C | T | 82 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(79): Show | 82 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1407+7249G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056461 | ||||||
| chr12:48056483
|
TATATTAC | T | 6 | a0001c0001t0004g0340a0001c0001t0004g0341a0001c0001t0004g0342others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1407+7220_1407+722 others(11): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056483 | ||||||
| chr12:48056490
|
C | CATATTAC others(51): Show |
2 | a0001c0001t0004g0318a0001c0001t0004g0319 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1407+7162_1407+721 others(62): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056490 | ||||||
| chr12:48056490
|
C | CATATTAC others(80): Show |
1 | a0004c0008t0005g0336 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1407+7133_1407+721 others(91): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056490 | ||||||
| chr12:48056490
|
CATATTAC others(138): Show |
C | 19 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0042others(16): Show | 19 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.1407+7075_1407+721 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056490 | ||||||
| chr12:48056497
|
C | T | 1 | a0001c0005t0001g0091 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1407+7213G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056497 | ||||||
| chr12:48056508
|
A | AATT | 8 | a0001c0001t0005g0285a0001c0001t0005g0295a0001c0001t0005g0300others(5): Show | 8 | HG01884.hp2 HG03453.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1407+7201_1407+720 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056508 | ||||||
| chr12:48056508
|
ATAT | A | 72 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(69): Show | 74 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1407+7199_1407+720 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056508 | ||||||
| chr12:48056508
|
ATATT | A | 16 | a0001c0001t0005g0284a0001c0001t0006g0281a0001c0001t0006g0286others(13): Show | 16 | HG00741.hp2 HG01099.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.1407+7198_1407+720 others(8): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056508 | ||||||
| chr12:48056511
|
T | A | 8 | a0001c0001t0005g0285a0001c0001t0005g0295a0001c0001t0005g0300others(5): Show | 8 | HG01884.hp2 HG03453.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1407+7199A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056511 | ||||||
| chr12:48056511
|
T | TTTAA | 12 | a0001c0001t0005g0225a0001c0001t0005g0256a0001c0001t0007g0199others(9): Show | 12 | HG02895.hp1 HG02897.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.1407+7198_1407+719 others(8): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056511 | ||||||
| chr12:48056515
|
T | A | 20 | a0001c0001t0005g0225a0001c0001t0005g0256a0001c0001t0005g0285others(17): Show | 20 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(17): Show |
intron_variant | MODIFIER | c.1407+7195A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056515 | ||||||
| chr12:48056517
|
A | T | 20 | a0001c0001t0005g0225a0001c0001t0005g0256a0001c0001t0005g0285others(17): Show | 20 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(17): Show |
intron_variant | MODIFIER | c.1407+7193T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056517 | ||||||
| chr12:48056519
|
T | C | 20 | a0001c0001t0005g0225a0001c0001t0005g0256a0001c0001t0005g0285others(17): Show | 20 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(17): Show |
intron_variant | MODIFIER | c.1407+7191A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056519 | ||||||
| chr12:48056526
|
CATATATA others(15): Show |
C | 13 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0194others(10): Show | 14 | HG01069.hp2 HG01192.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1407+7162_1407+718 others(26): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056526 | ||||||
| chr12:48056526
|
CATATATA others(44): Show |
C | 74 | a0001c0001t0003g0006a0001c0001t0003g0161a0001c0001t0003g0193others(71): Show | 75 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1407+7133_1407+718 others(55): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056526 | ||||||
| chr12:48056526
|
CATATATA others(73): Show |
C | 22 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0045others(19): Show | 22 | HG00423.hp2 HG00741.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1407+7104_1407+718 others(84): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056526 | ||||||
| chr12:48056526
|
CATATATA others(102): Show |
C | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(121): Show | 124 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1407+7075_1407+718 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056526 | ||||||
| chr12:48056534
|
A | C | 2 | a0001c0001t0004g0211a0001c0001t0005g0230 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1407+7176T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056534 | ||||||
| chr12:48056537
|
A | AATT | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1407+7172_1407+717 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056537 | ||||||
| chr12:48056540
|
T | A | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1407+7170A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056540 | ||||||
| chr12:48056544
|
T | A | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1407+7166A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056544 | ||||||
| chr12:48056545
|
T | A | 2 | a0001c0001t0004g0211a0001c0001t0005g0230 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1407+7165A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056545 | ||||||
| chr12:48056546
|
A | T | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1407+7164T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056546 | ||||||
| chr12:48056548
|
T | C | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1407+7162A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056548 | ||||||
| chr12:48056548
|
TATATTAC others(116): Show |
T | 2 | a0001c0003t0008g0350a0001c0003t0008g0351 | 2 | NA19077.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1407+7039_1407+716 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056548 | ||||||
| chr12:48056555
|
CATATATA others(15): Show |
C | 1 | a0001c0001t0010g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1407+7133_1407+715 others(26): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056555 | ||||||
| chr12:48056555
|
CATATATA others(73): Show |
C | 1 | a0001c0001t0016g0344 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1407+7075_1407+715 others(84): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056555 | ||||||
| chr12:48056562
|
A | T | 2 | a0001c0001t0004g0211a0001c0001t0005g0230 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1407+7148T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056562 | ||||||
| chr12:48056577
|
T | C | 2 | a0001c0001t0004g0211a0001c0001t0005g0230 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1407+7133A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056577 | ||||||
| chr12:48056577
|
TATATTAC others(87): Show |
T | 2 | a0001c0001t0005g0285a0001c0002t0002g0283 | 2 | HG00741.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1407+7039_1407+713 others(98): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056577 | ||||||
| chr12:48056584
|
CATATATA others(15): Show |
C | 1 | a0001c0003t0008g0293 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1407+7104_1407+712 others(26): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056584 | ||||||
| chr12:48056584
|
CATATATA others(44): Show |
C | 2 | a0001c0001t0004g0340a0001c0001t0004g0345 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1407+7075_1407+712 others(55): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056584 | ||||||
| chr12:48056602
|
T | A | 1 | a0001c0001t0003g0209 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1407+7108A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056602 | ||||||
| chr12:48056606
|
TATATTAC others(58): Show |
T | 60 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0002t0002g0001others(57): Show | 68 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1407+7039_1407+710 others(69): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056606 | ||||||
| chr12:48056613
|
CATATATA others(15): Show |
C | 12 | a0001c0001t0005g0225a0001c0001t0005g0256a0001c0001t0007g0199others(9): Show | 12 | HG02895.hp1 HG02897.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.1407+7075_1407+709 others(26): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056613 | ||||||
| chr12:48056626
|
A | G | 17 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0045others(14): Show | 17 | HG00423.hp2 HG01243.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1407+7084T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056626 | ||||||
| chr12:48056635
|
T | C | 1 | a0001c0001t0004g0343 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1407+7075A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056635 | ||||||
| chr12:48056635
|
T | TATATTAC others(29): Show |
1 | a0001c0001t0004g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1407+7039_1407+707 others(40): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056635 | ||||||
| chr12:48056650
|
AATATATT others(128): Show |
A | 11 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(8): Show | 11 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1407+6925_1407+705 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056650 | ||||||
| chr12:48056650
|
AATATATT others(191): Show |
A | 1 | a0001c0001t0024g0303 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1407+6862_1407+705 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056650 | ||||||
| chr12:48056655
|
A | G | 122 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(119): Show | 122 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1407+7055T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056655 | ||||||
| chr12:48056661
|
T | C | 1 | a0001c0001t0003g0269 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1407+7049A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056661 | ||||||
| chr12:48056664
|
TATATTAC | T | 134 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(131): Show | 134 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.1407+7039_1407+704 others(11): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056664 | ||||||
| chr12:48056686
|
AATATATT others(92): Show |
A | 15 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0094others(12): Show | 15 | HG00423.hp2 HG01243.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.1407+6925_1407+702 others(103): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056686 | ||||||
| chr12:48056689
|
ATATTATT others(95): Show |
A | 1 | a0001c0001t0001g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1407+6919_1407+702 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056689 | ||||||
| chr12:48056691
|
A | G | 20 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0042others(17): Show | 20 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.1407+7019T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056691 | ||||||
| chr12:48056691
|
ATTATTTA others(96): Show |
A | 1 | a0001c0001t0001g0368 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1407+6916_1407+701 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056691 | ||||||
| chr12:48056700
|
TATATTAC | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0042others(20): Show | 23 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1407+7003_1407+700 others(11): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056700 | ||||||
| chr12:48056707
|
C | A | 6 | a0001c0002t0002g0145a0001c0002t0002g0156a0001c0002t0002g0164others(3): Show | 6 | HG00408.hp1 HG00597.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+7003G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056707 | ||||||
| chr12:48056729
|
TATTTAAT others(234): Show |
T | 7 | a0001c0002t0002g0145a0001c0002t0002g0154a0001c0002t0002g0156others(4): Show | 7 | HG00408.hp1 HG00597.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6740_1407+698 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056729 | ||||||
| chr12:48056730
|
A | G | 4 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(1): Show | 4 | HG02647.hp2 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1407+6980T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056730 | ||||||
| chr12:48056736
|
T | C | 1 | a0001c0003t0008g0349 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1407+6974A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056736 | ||||||
| chr12:48056743
|
C | A | 58 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(55): Show | 66 | HG00323.hp1 HG00438.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1407+6967G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056743 | ||||||
| chr12:48056745
|
TATTACAT others(194): Show |
T | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1407+6764_1407+696 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056745 | ||||||
| chr12:48056745
|
TATTACAT others(309): Show |
T | 1 | a0001c0003t0008g0349 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1407+6649_1407+696 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056745 | ||||||
| chr12:48056758
|
AATATATT others(20): Show |
A | 103 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0042others(100): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1407+6925_1407+695 others(31): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056758 | ||||||
| chr12:48056761
|
A | ATAT | 7 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0004g0341others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6946_1407+694 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056761 | ||||||
| chr12:48056767
|
AACATATT others(128): Show |
A | 1 | a0001c0002t0002g0189 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1407+6808_1407+694 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056767 | ||||||
| chr12:48056767
|
AACATATT others(163): Show |
A | 7 | a0001c0002t0002g0003a0001c0002t0002g0147a0001c0002t0002g0148others(4): Show | 8 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1407+6773_1407+694 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056767 | ||||||
| chr12:48056767
|
AACATATT others(198): Show |
A | 49 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0004others(46): Show | 56 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1407+6738_1407+694 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056767 | ||||||
| chr12:48056767
|
AACATATT others(234): Show |
A | 2 | a0001c0002t0002g0133a0001c0002t0002g0168 | 2 | NA18961.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1407+6702_1407+694 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056767 | ||||||
| chr12:48056769
|
C | T | 7 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0004g0341others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6941G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056769 | ||||||
| chr12:48056778
|
TATTACAT others(240): Show |
T | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1407+6685_1407+693 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056778 | ||||||
| chr12:48056778
|
TATTACAT others(276): Show |
T | 4 | a0001c0003t0008g0293a0001c0003t0008g0294a0001c0003t0008g0350others(1): Show | 4 | HG02622.hp2 HG02886.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1407+6649_1407+693 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056778 | ||||||
| chr12:48056788
|
ATATTATT others(200): Show |
A | 3 | a0001c0001t0003g0264a0001c0001t0003g0266a0001c0001t0003g0272 | 3 | HG01069.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1407+6715_1407+692 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056788 | ||||||
| chr12:48056790
|
A | AAAT | 7 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0004g0341others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6919_1407+692 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056790 | ||||||
| chr12:48056791
|
T | A | 7 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0004g0341others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6919A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056791 | ||||||
| chr12:48056799
|
T | C | 8 | a0001c0001t0001g0027a0001c0001t0004g0322a0001c0001t0004g0328others(5): Show | 8 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1407+6911A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056799 | ||||||
| chr12:48056819
|
TAAATATA others(198): Show |
T | 1 | a0001c0001t0003g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1407+6686_1407+689 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056819 | ||||||
| chr12:48056819
|
TAAATATA others(270): Show |
T | 131 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(128): Show | 131 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.1407+6614_1407+689 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056819 | ||||||
| chr12:48056820
|
AAAT | A | 7 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0004g0341others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6887_1407+688 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056820 | ||||||
| chr12:48056824
|
A | T | 7 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0004g0341others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6886T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056824 | ||||||
| chr12:48056832
|
C | T | 7 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0004g0341others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6878G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056832 | ||||||
| chr12:48056848
|
T | TATATATT others(21): Show |
1 | a0004c0008t0005g0336 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1407+6861_1407+686 others(32): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056848 | ||||||
| chr12:48056848
|
T | TATATATT others(28): Show |
1 | a0001c0001t0004g0334 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1407+6827_1407+686 others(39): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056848 | ||||||
| chr12:48056848
|
TATATATT others(28): Show |
T | 1 | a0001c0001t0004g0343 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1407+6827_1407+686 others(39): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056848 | ||||||
| chr12:48056851
|
ATAT | A | 47 | a0001c0001t0003g0161a0001c0001t0003g0193a0001c0001t0003g0194others(44): Show | 47 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1407+6856_1407+685 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056851 | ||||||
| chr12:48056851
|
ATATTATT others(66): Show |
A | 1 | a0001c0001t0003g0006 | 2 | NA18963.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1407+6786_1407+685 others(77): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056851 | ||||||
| chr12:48056851
|
ATATTATT others(101): Show |
A | 3 | a0001c0001t0003g0008a0001c0001t0003g0220a0001c0001t0003g0269 | 3 | HG01074.hp2 HG02129.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1407+6751_1407+685 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056851 | ||||||
| chr12:48056853
|
A | AAAT | 7 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0004g0341others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6856_1407+685 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056853 | ||||||
| chr12:48056854
|
T | A | 7 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0004g0341others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6856A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056854 | ||||||
| chr12:48056862
|
T | C | 7 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0004g0341others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6848A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056862 | ||||||
| chr12:48056878
|
TATATA | T | 7 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0004g0341others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6827_1407+683 others(9): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056878 | ||||||
| chr12:48056882
|
TAATATAT others(99): Show |
T | 6 | a0001c0001t0003g0215a0001c0001t0003g0221a0001c0001t0003g0274others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1407+6722_1407+682 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056882 | ||||||
| chr12:48056891
|
A | G | 1 | a0001c0001t0024g0303 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1407+6819T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056891 | ||||||
| chr12:48056904
|
CATATTAC others(135): Show |
C | 63 | a0001c0001t0003g0005a0001c0001t0003g0161a0001c0001t0003g0193others(60): Show | 64 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1407+6664_1407+680 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056904 | ||||||
| chr12:48056904
|
CATATTAC others(171): Show |
C | 1 | a0001c0001t0006g0292 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1407+6628_1407+680 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056904 | ||||||
| chr12:48056904
|
CATATTAC others(207): Show |
C | 14 | a0001c0001t0001g0027a0001c0001t0001g0368a0001c0001t0006g0281others(11): Show | 14 | HG01099.hp1 HG01346.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1407+6592_1407+680 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056904 | ||||||
| chr12:48056917
|
T | TA | 10 | a0001c0001t0003g0268a0001c0001t0004g0211a0001c0001t0005g0230others(7): Show | 10 | HG02615.hp2 HG02717.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.1407+6792dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056917 | ||||||
| chr12:48056917
|
TAATATAT others(100): Show |
T | 1 | a0001c0001t0003g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1407+6686_1407+679 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056917 | ||||||
| chr12:48056918
|
AATATATT others(27): Show |
A | 1 | a0001c0001t0003g0216 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1407+6758_1407+679 others(38): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056918 | ||||||
| chr12:48056932
|
T | C | 1 | a0001c0001t0024g0303 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1407+6778A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056932 | ||||||
| chr12:48056939
|
C | T | 1 | a0001c0001t0003g0268 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1407+6771G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056939 | ||||||
| chr12:48056939
|
CATATTAC others(100): Show |
C | 1 | a0001c0001t0003g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1407+6664_1407+677 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056939 | ||||||
| chr12:48056939
|
CATATTAC others(172): Show |
C | 33 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0031others(30): Show | 33 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1407+6592_1407+677 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056939 | ||||||
| chr12:48056951
|
AT | A | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1407+6758delA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056951 | ||||||
| chr12:48056952
|
T | TA | 3 | a0001c0001t0003g0268a0001c0001t0004g0346a0001c0002t0002g0189 | 3 | HG02040.hp2 HG02809.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1407+6757dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056952 | ||||||
| chr12:48056972
|
T | A | 7 | a0001c0002t0002g0145a0001c0002t0002g0154a0001c0002t0002g0156others(4): Show | 7 | HG00408.hp1 HG00597.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+6738A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056972 | ||||||
| chr12:48056974
|
C | T | 3 | a0001c0001t0003g0216a0001c0001t0003g0268a0001c0002t0002g0189 | 3 | HG02040.hp2 NA19055.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1407+6736G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056974 | ||||||
| chr12:48056987
|
TA | T | 62 | a0001c0001t0003g0008a0001c0001t0003g0220a0001c0001t0003g0269others(59): Show | 69 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1407+6722delT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48056987 | ||||||
| chr12:48057010
|
C | CATATTAC others(65): Show |
1 | a0001c0001t0004g0338 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1407+6699_1407+670 others(76): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057010 | ||||||
| chr12:48057010
|
C | T | 9 | a0001c0001t0003g0006a0001c0002t0002g0003a0001c0002t0002g0147others(6): Show | 11 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1407+6700G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057010 | ||||||
| chr12:48057010
|
CATATTAC others(29): Show |
C | 3 | a0001c0001t0003g0216a0001c0001t0004g0310a0001c0001t0004g0327 | 3 | HG00438.hp2 HG03834.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1407+6664_1407+669 others(40): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057010 | ||||||
| chr12:48057010
|
CATATTAC others(65): Show |
C | 1 | a0001c0001t0003g0268 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1407+6628_1407+669 others(76): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057010 | ||||||
| chr12:48057010
|
CATATTAC others(101): Show |
C | 1 | a0001c0001t0024g0303 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1407+6592_1407+669 others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057010 | ||||||
| chr12:48057023
|
TA | T | 5 | a0001c0001t0003g0264a0001c0001t0003g0266a0001c0001t0003g0272others(2): Show | 5 | HG01069.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1407+6686delT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057023 | ||||||
| chr12:48057028
|
ATAT | A | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1407+6679_1407+668 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057028 | ||||||
| chr12:48057034
|
T | A | 1 | a0001c0002t0002g0152 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1407+6676A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057034 | ||||||
| chr12:48057039
|
T | C | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1407+6671A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057039 | ||||||
| chr12:48057046
|
T | C | 16 | a0001c0001t0003g0241a0001c0001t0003g0264a0001c0001t0003g0266others(13): Show | 16 | HG00642.hp1 HG01069.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1407+6664A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057046 | ||||||
| chr12:48057055
|
TATATAA | T | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1407+6649_1407+665 others(10): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057055 | ||||||
| chr12:48057082
|
T | C | 9 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301others(6): Show | 9 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1407+6628A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057082 | ||||||
| chr12:48057095
|
TA | T | 8 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301others(5): Show | 8 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1407+6614delT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057095 | ||||||
| chr12:48057118
|
T | C | 140 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 140 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1407+6592A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057118 | ||||||
| chr12:48057140
|
T | C | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1407+6570A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057140 | ||||||
| chr12:48057154
|
T | C | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1407+6556A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057154 | ||||||
| chr12:48057165
|
TATAA | T | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1407+6541_1407+654 others(8): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057165 | ||||||
| chr12:48057170
|
AT | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1407+6539delA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057170 | ||||||
| chr12:48057205
|
T | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+6505A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057205 | ||||||
| chr12:48057226
|
T | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1407+6484A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057226 | ||||||
| chr12:48057240
|
A | T | 1 | a0001c0001t0001g0372 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1407+6470T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057240 | ||||||
| chr12:48057271
|
C | A | 1 | a0001c0001t0004g0343 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1407+6439G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057271 | ||||||
| chr12:48057281
|
G | A | 1 | a0002c0004t0001g0369 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1407+6429C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057281 | ||||||
| chr12:48057444
|
G | A | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+6266C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057444 | ||||||
| chr12:48057464
|
A | G | 36 | a0001c0001t0001g0048a0001c0001t0001g0074a0001c0001t0001g0107others(33): Show | 36 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1407+6246T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057464 | ||||||
| chr12:48057477
|
G | A | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1407+6233C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057477 | ||||||
| chr12:48057522
|
G | A | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1407+6188C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057522 | ||||||
| chr12:48057525
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1407+6185G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057525 | ||||||
| chr12:48057556
|
ATATAT | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1407+6149_1407+615 others(9): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057556 | ||||||
| chr12:48057592
|
TTATTTTA others(2): Show |
T | 255 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(252): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.1407+6109_1407+611 others(13): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057592 | ||||||
| chr12:48057635
|
C | CAG | 342 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(339): Show | 352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.1407+6073_1407+607 others(6): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057635 | ||||||
| chr12:48057671
|
C | T | 13 | a0001c0001t0004g0340a0001c0001t0004g0345a0001c0001t0007g0199others(10): Show | 13 | HG01891.hp2 HG02055.hp2 HG03225.hp1 others(10): Show |
intron_variant | MODIFIER | c.1407+6039G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057671 | ||||||
| chr12:48057941
|
C | CT | 98 | a0001c0001t0001g0016a0001c0001t0001g0107a0001c0001t0001g0113others(95): Show | 99 | HG00140.hp1 HG00408.hp2 HG01069.hp2 others(96): Show |
intron_variant | MODIFIER | c.1407+5768dupA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057941 | ||||||
| chr12:48057941
|
C | CTT | 55 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(52): Show | 55 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1407+5767_1407+576 others(6): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057941 | ||||||
| chr12:48057941
|
C | CTTT | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1407+5766_1407+576 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057941 | ||||||
| chr12:48057941
|
C | CTTTT | 9 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0069others(6): Show | 9 | HG00735.hp2 HG01070.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1407+5765_1407+576 others(8): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057941 | ||||||
| chr12:48057941
|
CTT | C | 7 | a0001c0001t0004g0341a0001c0001t0004g0343a0001c0001t0004g0346others(4): Show | 7 | HG01175.hp1 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+5767_1407+576 others(6): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057941 | ||||||
| chr12:48057941
|
CTTT | C | 64 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(61): Show | 72 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1407+5766_1407+576 others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057941 | ||||||
| chr12:48058049
|
G | A | 2 | a0001c0001t0004g0211a0001c0001t0004g0236 | 2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1407+5661C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058049 | ||||||
| chr12:48058176
|
C | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1407+5534G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058176 | ||||||
| chr12:48058225
|
C | A | 2 | a0001c0002t0002g0148a0001c0002t0002g0190 | 2 | HG00733.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1407+5485G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058225 | ||||||
| chr12:48058232
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0122 | 2 | HG00597.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1407+5478G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058232 | ||||||
| chr12:48058261
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0079others(1): Show | 4 | NA18948.hp2 NA18960.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1407+5449T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058261 | ||||||
| chr12:48058298
|
A | T | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1407+5412T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058298 | ||||||
| chr12:48058328
|
G | C | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1407+5382C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058328 | ||||||
| chr12:48058454
|
C | T | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1407+5256G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058454 | ||||||
| chr12:48058718
|
G | T | 1 | a0001c0003t0008g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1407+4992C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058718 | ||||||
| chr12:48058810
|
T | C | 2 | a0001c0001t0003g0006a0001c0001t0003g0268 | 3 | NA18963.hp1 NA19010.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1407+4900A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058810 | ||||||
| chr12:48058907
|
T | TACTGACA others(16): Show |
1 | a0001c0001t0001g0384 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1407+4780_1407+480 others(27): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058907 | ||||||
| chr12:48058926
|
T | C | 13 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(10): Show | 13 | HG00741.hp2 HG02647.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1407+4784A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48058926 | ||||||
| chr12:48059124
|
C | A | 1 | a0001c0001t0004g0330 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1407+4586G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48059124 | ||||||
| chr12:48059256
|
T | C | 13 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(10): Show | 13 | HG00741.hp2 HG02647.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1407+4454A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48059256 | ||||||
| chr12:48059345
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1407+4365G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48059345 | ||||||
| chr12:48059406
|
T | C | 10 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(7): Show | 10 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1407+4304A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48059406 | ||||||
| chr12:48059639
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1407+4071A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48059639 | ||||||
| chr12:48060036
|
G | A | 1 | a0001c0002t0002g0139 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1407+3674C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48060036 | ||||||
| chr12:48060037
|
A | G | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1407+3673T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48060037 | ||||||
| chr12:48060099
|
G | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1407+3611C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48060099 | ||||||
| chr12:48060124
|
C | T | 2 | a0001c0001t0003g0220a0001c0001t0003g0221 | 2 | HG02129.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1407+3586G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48060124 | ||||||
| chr12:48060186
|
T | G | 1 | a0001c0002t0002g0137 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1407+3524A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48060186 | ||||||
| chr12:48060333
|
A | T | 1 | a0001c0001t0001g0359 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1407+3377T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48060333 | ||||||
| chr12:48060825
|
T | G | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1407+2885A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48060825 | ||||||
| chr12:48060836
|
C | T | 1 | a0001c0001t0025g0237 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1407+2874G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48060836 | ||||||
| chr12:48060843
|
C | T | 1 | a0001c0001t0001g0378 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1407+2867G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48060843 | ||||||
| chr12:48060847
|
G | A | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1407+2863C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48060847 | ||||||
| chr12:48060898
|
C | T | 10 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(7): Show | 10 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1407+2812G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48060898 | ||||||
| chr12:48061416
|
T | C | 1 | a0001c0001t0001g0354 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1407+2294A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48061416 | ||||||
| chr12:48061421
|
T | C | 19 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(16): Show | 19 | HG00741.hp2 HG02622.hp2 HG02647.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+2289A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48061421 | ||||||
| chr12:48061472
|
G | A | 244 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(241): Show | 252 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.1407+2238C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48061472 | ||||||
| chr12:48061549
|
A | G | 3 | a0001c0001t0004g0340a0001c0001t0004g0345a0001c0001t0016g0344 | 3 | HG01891.hp2 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1407+2161T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48061549 | ||||||
| chr12:48061627
|
T | C | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1407+2083A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48061627 | ||||||
| chr12:48061784
|
G | A | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1407+1926C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48061784 | ||||||
| chr12:48061831
|
G | A | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+1879C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48061831 | ||||||
| chr12:48061867
|
GT | G | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0123others(3): Show | 6 | HG00423.hp2 NA18946.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+1842delA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48061867 | ||||||
| chr12:48061990
|
A | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0121 | 2 | NA19057.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1407+1720T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48061990 | ||||||
| chr12:48061998
|
T | C | 1 | a0001c0001t0004g0348 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1407+1712A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48061998 | ||||||
| chr12:48062005
|
A | C | 1 | a0001c0001t0004g0348 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1407+1705T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48062005 | ||||||
| chr12:48062070
|
A | G | 1 | a0001c0001t0004g0326 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1407+1640T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48062070 | ||||||
| chr12:48062283
|
A | G | 1 | a0001c0001t0003g0269 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1407+1427T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48062283 | ||||||
| chr12:48062371
|
T | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+1339A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48062371 | ||||||
| chr12:48062630
|
A | G | 5 | a0001c0003t0008g0293a0001c0003t0008g0294a0001c0003t0008g0349others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1407+1080T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48062630 | ||||||
| chr12:48062685
|
T | C | 7 | a0001c0002t0002g0138a0001c0002t0002g0145a0001c0002t0002g0167others(4): Show | 7 | HG00597.hp2 HG02132.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1407+1025A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48062685 | ||||||
| chr12:48062718
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1407+992A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48062718 | ||||||
| chr12:48063040
|
C | T | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1407+670G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48063040 | ||||||
| chr12:48063157
|
A | C | 1 | a0001c0001t0010g0299 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1407+553T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48063157 | ||||||
| chr12:48063162
|
C | T | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1407+548G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48063162 | ||||||
| chr12:48063249
|
C | T | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1407+461G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48063249 | ||||||
| chr12:48063277
|
A | G | 3 | a0001c0001t0004g0340a0001c0001t0004g0345a0001c0001t0016g0344 | 3 | HG01891.hp2 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1407+433T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48063277 | ||||||
| chr12:48063351
|
T | C | 2 | a0001c0001t0006g0281a0001c0001t0006g0288 | 2 | HG01346.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1407+359A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48063351 | ||||||
| chr12:48063376
|
G | A | 255 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(252): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.1407+334C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48063376 | ||||||
| chr12:48063556
|
A | C | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1407+154T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48063556 | ||||||
| chr12:48063602
|
C | T | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1407+108G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48063602 | ||||||
| chr12:48063672
|
T | A | 1 | a0001c0001t0007g0262 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1407+38A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48063672 | ||||||
| chr12:48063688
|
G | A | 1 | a0001c0001t0006g0286 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1407+22C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48063688 | ||||||
| chr12:48064366
|
C | T | 158 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(155): Show | 158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.1276-525G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/17 | chr12 | 48064366 | ||||||
| chr12:48064367
|
G | T | 1 | a0001c0001t0001g0086 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1276-526C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/17 | chr12 | 48064367 | ||||||
| chr12:48064626
|
C | G | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1275+439G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/17 | chr12 | 48064626 | ||||||
| chr12:48064662
|
G | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0054others(1): Show | 4 | HG01070.hp2 HG01243.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1275+403C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/17 | chr12 | 48064662 | ||||||
| chr12:48064665
|
T | G | 67 | a0001c0001t0003g0208a0001c0002t0002g0001a0001c0002t0002g0002others(64): Show | 75 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1275+400A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/17 | chr12 | 48064665 | ||||||
| chr12:48064680
|
T | C | 1 | a0001c0001t0004g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1275+385A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/17 | chr12 | 48064680 | ||||||
| chr12:48064705
|
C | T | 1 | a0001c0002t0002g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1275+360G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/17 | chr12 | 48064705 | ||||||
| chr12:48064731
|
C | T | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1275+334G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/17 | chr12 | 48064731 | ||||||
| chr12:48064746
|
G | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1275+319C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/17 | chr12 | 48064746 | ||||||
| chr12:48064967
|
G | A | 1 | a0001c0001t0005g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1275+98C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 12/17 | chr12 | 48064967 | ||||||
| chr12:48065233
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0080 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1120-13T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 11/17 | chr12 | 48065233 | ||||||
| chr12:48065282
|
G | A | 9 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0110others(6): Show | 9 | HG01069.hp1 HG01071.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.1120-62C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 11/17 | chr12 | 48065282 | ||||||
| chr12:48065328
|
T | C | 1 | a0001c0001t0003g0213 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1120-108A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 11/17 | chr12 | 48065328 | ||||||
| chr12:48065514
|
C | T | 1 | a0001c0001t0004g0341 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1119+82G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 11/17 | chr12 | 48065514 | ||||||
| chr12:48065705
|
C | G | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1035-25G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 10/17 | chr12 | 48065705 | ||||||
| chr12:48065782
|
G | A | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1035-102C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 10/17 | chr12 | 48065782 | ||||||
| chr12:48066233
|
T | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1035-553A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 10/17 | chr12 | 48066233 | ||||||
| chr12:48066300
|
G | A | 31 | a0001c0001t0001g0048a0001c0001t0001g0074a0001c0001t0001g0107others(28): Show | 31 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1035-620C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 10/17 | chr12 | 48066300 | ||||||
| chr12:48066432
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1034+495A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 10/17 | chr12 | 48066432 | ||||||
| chr12:48066547
|
T | C | 1 | a0001c0001t0014g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1034+380A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 10/17 | chr12 | 48066547 | ||||||
| chr12:48066780
|
G | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1034+147C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 10/17 | chr12 | 48066780 | ||||||
| chr12:48067121
|
T | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.996-156A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48067121 | ||||||
| chr12:48067179
|
A | C | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.996-214T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48067179 | ||||||
| chr12:48067334
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.996-369A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48067334 | ||||||
| chr12:48067581
|
C | A | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.996-616G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48067581 | ||||||
| chr12:48067632
|
T | C | 9 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(6): Show | 9 | HG01346.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.996-667A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48067632 | ||||||
| chr12:48067668
|
G | A | 31 | a0001c0001t0001g0048a0001c0001t0001g0074a0001c0001t0001g0107others(28): Show | 31 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.996-703C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48067668 | ||||||
| chr12:48067798
|
T | C | 231 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(228): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.996-833A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48067798 | ||||||
| chr12:48067852
|
G | T | 342 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(339): Show | 352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.996-887C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48067852 | ||||||
| chr12:48067855
|
T | C | 1 | a0001c0001t0001g0372 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.996-890A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48067855 | ||||||
| chr12:48068198
|
A | G | 1 | a0001c0001t0014g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.996-1233T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068198 | ||||||
| chr12:48068202
|
A | C | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.996-1237T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068202 | ||||||
| chr12:48068275
|
C | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0032others(3): Show | 6 | HG00735.hp2 HG01361.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.996-1310G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068275 | ||||||
| chr12:48068341
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.996-1376C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068341 | ||||||
| chr12:48068388
|
A | G | 2 | a0001c0001t0007g0247a0001c0001t0007g0262 | 2 | NA18952.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.996-1423T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068388 | ||||||
| chr12:48068414
|
T | C | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.996-1449A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068414 | ||||||
| chr12:48068422
|
C | T | 3 | a0001c0002t0002g0153a0001c0002t0002g0163a0001c0002t0002g0192 | 3 | NA18966.hp1 NA19005.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.996-1457G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068422 | ||||||
| chr12:48068672
|
T | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.996-1707A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068672 | ||||||
| chr12:48068809
|
C | A | 2 | a0001c0001t0003g0220a0001c0001t0003g0221 | 2 | HG02129.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.996-1844G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068809 | ||||||
| chr12:48068862
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.996-1897G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068862 | ||||||
| chr12:48068922
|
G | A | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.996-1957C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068922 | ||||||
| chr12:48068924
|
G | A | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.996-1959C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068924 | ||||||
| chr12:48068958
|
G | A | 8 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.996-1993C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068958 | ||||||
| chr12:48068977
|
A | T | 1 | a0001c0002t0002g0185 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.996-2012T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068977 | ||||||
| chr12:48068998
|
CAAAAA | C | 31 | a0001c0001t0001g0048a0001c0001t0001g0074a0001c0001t0001g0107others(28): Show | 31 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.996-2038_996-2034d others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48068998 | ||||||
| chr12:48069085
|
G | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.996-2120C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069085 | ||||||
| chr12:48069134
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.996-2169A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069134 | ||||||
| chr12:48069152
|
C | CA | 13 | a0001c0001t0001g0360a0001c0001t0001g0365a0001c0001t0001g0367others(10): Show | 13 | HG00423.hp1 HG00741.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.996-2188dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069152 | ||||||
| chr12:48069152
|
C | CAA | 9 | a0001c0001t0005g0301a0001c0001t0006g0288a0001c0001t0006g0289others(6): Show | 9 | HG01346.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.996-2189_996-2188d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069152 | ||||||
| chr12:48069152
|
CA | C | 209 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(206): Show | 217 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.996-2188delT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069152 | ||||||
| chr12:48069152
|
CAA | C | 77 | a0001c0001t0001g0126a0001c0001t0003g0005a0001c0001t0003g0006others(74): Show | 79 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.996-2189_996-2188d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069152 | ||||||
| chr12:48069152
|
CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0003g0251a0001c0001t0003g0264a0001c0001t0003g0266others(1): Show | 4 | HG01069.hp2 HG01257.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.996-2198_996-2188d others(13): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069152 | ||||||
| chr12:48069152
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0003t0008g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.996-2203_996-2188d others(18): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069152 | ||||||
| chr12:48069175
|
A | G | 2 | a0001c0001t0001g0384a0001c0002t0002g0138 | 2 | NA18612.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.996-2210T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069175 | ||||||
| chr12:48069197
|
C | T | 1 | a0001c0002t0002g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.996-2232G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069197 | ||||||
| chr12:48069217
|
T | C | 1 | a0001c0002t0002g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.996-2252A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069217 | ||||||
| chr12:48069264
|
A | T | 1 | a0001c0002t0002g0282 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.996-2299T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069264 | ||||||
| chr12:48069276
|
G | A | 1 | a0001c0001t0016g0344 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.996-2311C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069276 | ||||||
| chr12:48069592
|
T | C | 10 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(7): Show | 10 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.995+2075A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069592 | ||||||
| chr12:48069664
|
AAGGTATC others(3): Show |
A | 1 | a0001c0002t0002g0134 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.995+1993_995+2002d others(12): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069664 | ||||||
| chr12:48069818
|
C | A | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.995+1849G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069818 | ||||||
| chr12:48069950
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.995+1717A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069950 | ||||||
| chr12:48070019
|
A | G | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.995+1648T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48070019 | ||||||
| chr12:48070023
|
T | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.995+1644A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48070023 | ||||||
| chr12:48070237
|
C | T | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.995+1430G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48070237 | ||||||
| chr12:48070412
|
T | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.995+1255A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48070412 | ||||||
| chr12:48070692
|
A | G | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.995+975T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48070692 | ||||||
| chr12:48070779
|
C | T | 1 | a0001c0001t0004g0310 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.995+888G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48070779 | ||||||
| chr12:48070808
|
C | T | 1 | a0001c0003t0008g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.995+859G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48070808 | ||||||
| chr12:48070836
|
G | A | 1 | a0001c0001t0006g0296 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.995+831C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48070836 | ||||||
| chr12:48070885
|
A | T | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.995+782T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48070885 | ||||||
| chr12:48071007
|
C | T | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.995+660G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071007 | ||||||
| chr12:48071138
|
T | G | 1 | a0001c0001t0005g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.995+529A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071138 | ||||||
| chr12:48071240
|
A | T | 1 | a0001c0001t0001g0081 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.995+427T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071240 | ||||||
| chr12:48071278
|
A | G | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.995+389T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071278 | ||||||
| chr12:48071317
|
T | A | 1 | a0001c0001t0001g0279 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.995+350A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071317 | ||||||
| chr12:48071344
|
GGTGGCTC others(6): Show |
G | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.995+310_995+322del others(13): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071344 | ||||||
| chr12:48071382
|
G | A | 1 | a0001c0003t0008g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.995+285C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071382 | ||||||
| chr12:48071403
|
G | A | 1 | a0001c0002t0002g0146 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.995+264C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071403 | ||||||
| chr12:48071408
|
G | A | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.995+259C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071408 | ||||||
| chr12:48071418
|
C | A | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.995+249G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071418 | ||||||
| chr12:48071447
|
C | T | 1 | a0001c0001t0009g0306 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.995+220G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071447 | ||||||
| chr12:48071521
|
CAGA | C | 3 | a0001c0002t0002g0141a0001c0002t0002g0162a0001c0002t0002g0184 | 3 | NA18946.hp1 NA18990.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.995+143_995+145del others(3): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071521 | ||||||
| chr12:48071588
|
C | G | 1 | a0001c0002t0002g0181 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.995+79G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071588 | ||||||
| chr12:48071618
|
A | G | 2 | a0001c0001t0004g0321a0001c0009t0004g0337 | 2 | HG01123.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.995+49T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071618 | ||||||
| chr12:48071642
|
A | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.995+25T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48071642 | ||||||
| chr12:48071733
|
C | G | 1 | a0001c0001t0001g0049 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.941-12G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48071733 | ||||||
| chr12:48071776
|
TC | T | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.941-56delG | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48071776 | ||||||
| chr12:48072404
|
C | T | 4 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0103others(1): Show | 4 | HG02015.hp2 HG02165.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-683G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48072404 | ||||||
| chr12:48072425
|
C | T | 1 | a0001c0001t0006g0292 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.941-704G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48072425 | ||||||
| chr12:48072550
|
C | T | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.941-829G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48072550 | ||||||
| chr12:48072551
|
G | A | 2 | a0001c0002t0002g0141a0001c0002t0002g0184 | 2 | NA18946.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.941-830C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48072551 | ||||||
| chr12:48072558
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.941-837G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48072558 | ||||||
| chr12:48072726
|
T | C | 1 | a0001c0001t0006g0292 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.941-1005A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48072726 | ||||||
| chr12:48072914
|
G | T | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.941-1193C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48072914 | ||||||
| chr12:48073119
|
T | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+1205A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48073119 | ||||||
| chr12:48073185
|
A | C | 1 | a0001c0001t0016g0344 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.940+1139T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48073185 | ||||||
| chr12:48073257
|
G | A | 1 | a0001c0001t0005g0195 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.940+1067C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48073257 | ||||||
| chr12:48073282
|
C | CT | 86 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(83): Show | 88 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.940+1041dupA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48073282 | ||||||
| chr12:48073565
|
A | C | 1 | a0001c0002t0002g0174 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.940+759T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48073565 | ||||||
| chr12:48073612
|
A | T | 1 | a0001c0001t0003g0207 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.940+712T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48073612 | ||||||
| chr12:48073681
|
G | C | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.940+643C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48073681 | ||||||
| chr12:48073710
|
G | A | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+614C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48073710 | ||||||
| chr12:48073799
|
T | C | 1 | a0001c0002t0002g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.940+525A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48073799 | ||||||
| chr12:48073938
|
A | G | 231 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(228): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.940+386T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48073938 | ||||||
| chr12:48074068
|
C | CT | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.940+255dupA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48074068 | ||||||
| chr12:48074194
|
C | T | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.940+130G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48074194 | ||||||
| chr12:48074208
|
TC | T | 4 | a0001c0003t0008g0294a0001c0003t0008g0349a0001c0003t0008g0350others(1): Show | 4 | HG02723.hp2 HG02886.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+115delG | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48074208 | ||||||
| chr12:48074211
|
G | A | 4 | a0001c0003t0008g0294a0001c0003t0008g0349a0001c0003t0008g0350others(1): Show | 4 | HG02723.hp2 HG02886.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+113C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48074211 | ||||||
| chr12:48074215
|
C | T | 1 | a0001c0001t0003g0248 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.940+109G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 8/17 | chr12 | 48074215 | ||||||
| chr12:48074805
|
C | CAA | 8 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.553-14_553-13dupTT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48074805 | ||||||
| chr12:48074819
|
A | G | 11 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(8): Show | 11 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-26T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48074819 | ||||||
| chr12:48074869
|
A | G | 255 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(252): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.553-76T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48074869 | ||||||
| chr12:48075055
|
T | TA | 22 | a0001c0001t0003g0005a0001c0001t0003g0204a0001c0001t0003g0234others(19): Show | 23 | HG00741.hp2 HG01192.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.553-263dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075055 | ||||||
| chr12:48075140
|
T | C | 24 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(21): Show | 24 | HG00741.hp2 HG01099.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.553-347A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075140 | ||||||
| chr12:48075205
|
ACT | A | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.553-414_553-413del others(2): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075205 | ||||||
| chr12:48075216
|
A | AAAAAC | 161 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(158): Show | 161 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.553-428_553-424dup others(5): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075216 | ||||||
| chr12:48075289
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG01167.hp1 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-496A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075289 | ||||||
| chr12:48075324
|
A | G | 1 | a0001c0001t0004g0338 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.553-531T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075324 | ||||||
| chr12:48075410
|
G | T | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.553-617C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075410 | ||||||
| chr12:48075607
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-814G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075607 | ||||||
| chr12:48075612
|
A | C | 1 | a0001c0003t0008g0351 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.553-819T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075612 | ||||||
| chr12:48075781
|
T | C | 11 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(8): Show | 11 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-988A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075781 | ||||||
| chr12:48075790
|
T | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0240a0001c0001t0003g0242others(2): Show | 6 | HG02055.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-997A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075790 | ||||||
| chr12:48075851
|
T | TA | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.553-1059dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075851 | ||||||
| chr12:48075913
|
T | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.553-1120A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075913 | ||||||
| chr12:48075968
|
G | A | 8 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.553-1175C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48075968 | ||||||
| chr12:48076044
|
G | A | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.553-1251C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076044 | ||||||
| chr12:48076125
|
T | C | 8 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.553-1332A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076125 | ||||||
| chr12:48076238
|
G | A | 1 | a0001c0002t0002g0180 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.553-1445C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076238 | ||||||
| chr12:48076255
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0095 | 2 | HG02071.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.553-1462A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076255 | ||||||
| chr12:48076258
|
G | A | 1 | a0001c0001t0006g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.553-1465C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076258 | ||||||
| chr12:48076315
|
G | A | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.553-1522C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076315 | ||||||
| chr12:48076385
|
C | T | 11 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(8): Show | 11 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-1592G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076385 | ||||||
| chr12:48076386
|
G | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.553-1593C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076386 | ||||||
| chr12:48076491
|
AT | A | 8 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0124others(5): Show | 8 | HG00323.hp1 HG01168.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.553-1699delA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076491 | ||||||
| chr12:48076604
|
T | C | 1 | a0001c0001t0005g0230 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.553-1811A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076604 | ||||||
| chr12:48076636
|
G | GT | 4 | a0001c0001t0001g0019a0001c0001t0001g0370a0001c0001t0013g0022others(1): Show | 4 | HG00673.hp2 HG01261.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-1844dupA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076636 | ||||||
| chr12:48076641
|
TG | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0048a0001c0001t0001g0088 | 3 | HG03139.hp2 NA19012.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.553-1849delC | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076641 | ||||||
| chr12:48076642
|
G | T | 156 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(153): Show | 156 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.553-1849C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076642 | ||||||
| chr12:48076642
|
GC | G | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.553-1850delG | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076642 | ||||||
| chr12:48076643
|
C | T | 189 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.553-1850G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076643 | ||||||
| chr12:48076750
|
C | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.553-1957G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076750 | ||||||
| chr12:48076771
|
T | G | 1 | a0001c0001t0013g0024 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.553-1978A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076771 | ||||||
| chr12:48076799
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.553-2006G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076799 | ||||||
| chr12:48076817
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.553-2024A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076817 | ||||||
| chr12:48076897
|
G | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.553-2104C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076897 | ||||||
| chr12:48076933
|
C | T | 1 | a0001c0001t0001g0359 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.553-2140G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076933 | ||||||
| chr12:48076934
|
G | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.553-2141C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076934 | ||||||
| chr12:48076967
|
G | C | 3 | a0001c0001t0001g0362a0001c0001t0001g0363a0001c0001t0001g0374 | 3 | HG00544.hp2 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.553-2174C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48076967 | ||||||
| chr12:48077173
|
T | C | 1 | a0001c0001t0001g0355 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.553-2380A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077173 | ||||||
| chr12:48077177
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.553-2384T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077177 | ||||||
| chr12:48077393
|
T | C | 3 | a0001c0003t0008g0349a0001c0003t0008g0350a0001c0003t0008g0351 | 3 | HG02723.hp2 NA19077.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.553-2600A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077393 | ||||||
| chr12:48077485
|
T | G | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.553-2692A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077485 | ||||||
| chr12:48077565
|
C | T | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.553-2772G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077565 | ||||||
| chr12:48077585
|
CT | C | 8 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.553-2793delA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077585 | ||||||
| chr12:48077666
|
T | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-2873A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077666 | ||||||
| chr12:48077707
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.553-2914A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077707 | ||||||
| chr12:48077759
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.553-2966C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077759 | ||||||
| chr12:48077784
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.553-2991G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077784 | ||||||
| chr12:48077792
|
T | G | 12 | a0001c0001t0003g0241a0001c0001t0006g0281a0001c0001t0006g0286others(9): Show | 12 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.553-2999A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077792 | ||||||
| chr12:48077890
|
C | A | 1 | a0001c0001t0001g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.553-3097G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48077890 | ||||||
| chr12:48078152
|
T | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0103others(1): Show | 4 | HG02015.hp2 HG02165.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-3359A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078152 | ||||||
| chr12:48078251
|
G | A | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.553-3458C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078251 | ||||||
| chr12:48078288
|
A | T | 1 | a0001c0001t0003g0269 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.553-3495T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078288 | ||||||
| chr12:48078317
|
T | A | 8 | a0001c0001t0001g0100a0001c0001t0001g0116a0001c0001t0001g0128others(5): Show | 8 | HG02155.hp1 HG02155.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.553-3524A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TATATATA others(22): Show |
1 | a0001c0001t0001g0060 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.553-3525_553-3524i others(31): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TATATATA others(24): Show |
1 | a0001c0001t0001g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.553-3525_553-3524i others(33): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TATATATA others(32): Show |
1 | a0001c0001t0001g0086 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.553-3525_553-3524i others(41): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTA | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-3526_553-3525d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATA | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.553-3528_553-3525d others(6): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(1): Show |
8 | a0001c0001t0003g0161a0001c0001t0006g0281a0001c0001t0006g0286others(5): Show | 8 | HG00408.hp2 HG01346.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.553-3532_553-3525d others(10): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(11): Show |
5 | a0001c0001t0003g0265a0001c0001t0004g0320a0001c0003t0008g0349others(2): Show | 5 | HG01346.hp1 HG02723.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-3542_553-3525d others(20): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(13): Show |
3 | a0001c0001t0004g0276a0001c0001t0004g0316a0001c0001t0017g0317 | 3 | HG01361.hp2 HG02486.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.553-3525_553-3524i others(22): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(15): Show |
5 | a0001c0001t0004g0277a0001c0001t0004g0314a0001c0001t0004g0325others(2): Show | 5 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-3525_553-3524i others(24): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(17): Show |
7 | a0001c0001t0004g0310a0001c0001t0004g0315a0001c0001t0004g0323others(4): Show | 7 | HG01109.hp1 HG01123.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-3525_553-3524i others(26): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(19): Show |
8 | a0001c0001t0003g0215a0001c0001t0003g0217a0001c0001t0003g0219others(5): Show | 8 | HG01261.hp2 HG02698.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.553-3525_553-3524i others(28): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(21): Show |
14 | a0001c0001t0001g0085a0001c0001t0003g0006a0001c0001t0003g0193others(11): Show | 15 | HG03540.hp1 HG03579.hp1 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.553-3525_553-3524i others(30): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(23): Show |
8 | a0001c0001t0003g0008a0001c0001t0003g0196a0001c0001t0003g0200others(5): Show | 8 | HG00438.hp2 HG01168.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.553-3525_553-3524i others(32): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(25): Show |
4 | a0001c0001t0003g0206a0001c0001t0004g0338a0001c0001t0005g0301others(1): Show | 4 | HG01106.hp1 HG03516.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-3525_553-3524i others(34): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(27): Show |
3 | a0001c0001t0003g0194a0001c0001t0004g0334a0001c0010t0001g0083 | 3 | HG00738.hp2 NA19060.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.553-3525_553-3524i others(36): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(29): Show |
1 | a0001c0001t0003g0220 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.553-3525_553-3524i others(38): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(33): Show |
1 | a0001c0001t0001g0099 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.553-3525_553-3524i others(42): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
T | TTATATAT others(35): Show |
1 | a0001c0001t0003g0248 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.553-3525_553-3524i others(44): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078317
|
TTA | T | 13 | a0001c0001t0003g0005a0001c0001t0003g0204a0001c0001t0003g0234others(10): Show | 14 | HG01192.hp1 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.553-3526_553-3525d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078317 | ||||||
| chr12:48078332
|
T | TACATATA others(51): Show |
1 | a0001c0001t0001g0354 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.553-3540_553-3539i others(60): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078332 | ||||||
| chr12:48078334
|
T | C | 15 | a0001c0001t0001g0055a0001c0001t0001g0354a0001c0001t0003g0005others(12): Show | 16 | HG00738.hp1 HG01192.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.553-3541A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TAC | 3 | a0001c0001t0004g0340a0001c0001t0004g0345a0001c0001t0016g0344 | 3 | HG01891.hp2 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.553-3543_553-3542d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(1): Show |
3 | a0001c0001t0001g0031a0001c0001t0006g0290a0001c0001t0006g0291 | 3 | HG02257.hp1 HG02630.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.553-3542_553-3541i others(10): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(31): Show |
1 | a0001c0001t0005g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.553-3542_553-3541i others(40): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(11): Show |
1 | a0001c0001t0003g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.553-3542_553-3541i others(20): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(13): Show |
4 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0003g0271others(1): Show | 4 | HG02293.hp2 HG02602.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(22): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(17): Show |
1 | a0001c0001t0001g0357 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.553-3542_553-3541i others(26): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(15): Show |
7 | a0001c0001t0001g0023a0001c0001t0001g0070a0001c0001t0001g0089others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(24): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(17): Show |
14 | a0001c0001t0001g0012a0001c0001t0001g0084a0001c0001t0004g0236others(11): Show | 14 | HG00741.hp2 HG02647.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(26): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(19): Show |
20 | a0001c0001t0001g0059a0001c0001t0001g0075a0001c0001t0001g0076others(17): Show | 20 | HG00423.hp2 HG01167.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(28): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(21): Show |
7 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0036others(4): Show | 7 | HG00323.hp2 HG01099.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(30): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(27): Show |
1 | a0001c0001t0001g0367 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.553-3542_553-3541i others(36): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(21): Show |
11 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0049others(8): Show | 11 | HG00597.hp1 HG01109.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(30): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(23): Show |
1 | a0001c0001t0001g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.553-3542_553-3541i others(32): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(25): Show |
1 | a0001c0001t0001g0052 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.553-3542_553-3541i others(34): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(23): Show |
15 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0063others(12): Show | 15 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(32): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(25): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0079others(1): Show | 4 | HG02886.hp2 HG03490.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(34): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(27): Show |
1 | a0001c0001t0001g0358 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.553-3542_553-3541i others(36): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(29): Show |
2 | a0001c0001t0001g0362a0001c0001t0001g0377 | 2 | HG00544.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.553-3542_553-3541i others(38): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(31): Show |
2 | a0001c0001t0001g0365a0001c0001t0001g0374 | 2 | HG02132.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.553-3542_553-3541i others(40): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(25): Show |
17 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0018others(14): Show | 17 | HG01123.hp2 HG01258.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(34): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(27): Show |
7 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0003g0207others(4): Show | 7 | HG00140.hp1 HG01243.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(36): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(31): Show |
5 | a0001c0001t0001g0370a0001c0001t0001g0371a0001c0001t0001g0372others(2): Show | 5 | HG01074.hp2 HG02071.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(40): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(27): Show |
21 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(18): Show | 21 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(36): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(29): Show |
1 | a0001c0001t0001g0046 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.553-3542_553-3541i others(38): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(31): Show |
5 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0355others(2): Show | 5 | HG01167.hp2 HG01169.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(40): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(33): Show |
4 | a0001c0001t0001g0363a0001c0001t0001g0366a0001c0001t0007g0262others(1): Show | 4 | HG00673.hp1 HG02135.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(42): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(29): Show |
10 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0068others(7): Show | 10 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(38): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(33): Show |
7 | a0001c0001t0001g0074a0001c0001t0001g0279a0001c0001t0001g0356others(4): Show | 7 | HG01928.hp1 HG02004.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(42): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(33): Show |
1 | a0001c0001t0001g0069 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.553-3542_553-3541i others(42): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(31): Show |
12 | a0001c0001t0001g0009a0001c0001t0001g0057a0001c0001t0001g0100others(9): Show | 12 | HG00673.hp2 HG01243.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(40): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(33): Show |
1 | a0001c0001t0001g0025 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.553-3542_553-3541i others(42): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(35): Show |
5 | a0001c0001t0001g0048a0001c0001t0001g0360a0001c0001t0001g0368others(2): Show | 5 | HG00423.hp1 HG01496.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(44): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(33): Show |
6 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0047others(3): Show | 6 | HG01069.hp2 HG01928.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(42): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(39): Show |
2 | a0001c0001t0001g0109a0001c0003t0008g0293 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.553-3542_553-3541i others(48): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(35): Show |
6 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0088others(3): Show | 6 | HG02080.hp2 NA18956.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-3542_553-3541i others(44): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(37): Show |
1 | a0001c0001t0001g0384 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.553-3542_553-3541i others(46): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(39): Show |
3 | a0001c0001t0007g0199a0001c0001t0007g0244a0001c0001t0007g0261 | 3 | NA18964.hp1 NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.553-3542_553-3541i others(48): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(37): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0112 | 2 | NA18951.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.553-3542_553-3541i others(46): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(41): Show |
2 | a0001c0001t0007g0245a0001c0001t0007g0247 | 2 | NA18962.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.553-3542_553-3541i others(50): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(39): Show |
1 | a0001c0001t0001g0026 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.553-3542_553-3541i others(48): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(49): Show |
1 | a0001c0001t0007g0260 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.553-3542_553-3541i others(58): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078334
|
T | TATATATA others(53): Show |
1 | a0001c0001t0007g0263 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.553-3542_553-3541i others(62): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078334 | ||||||
| chr12:48078336
|
C | T | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.553-3543G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078336 | ||||||
| chr12:48078338
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0052a0001c0002t0002g0186 | 3 | HG00408.hp1 HG01070.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.553-3545G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078338 | ||||||
| chr12:48078340
|
C | T | 175 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(172): Show | 175 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.553-3547G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078340 | ||||||
| chr12:48078342
|
C | T | 70 | a0001c0001t0001g0030a0001c0001t0001g0052a0001c0001t0005g0295others(67): Show | 78 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.553-3549G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078342 | ||||||
| chr12:48078344
|
T | C | 70 | a0001c0001t0003g0269a0001c0001t0005g0295a0001c0001t0005g0300others(67): Show | 78 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.553-3551A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078344 | ||||||
| chr12:48078344
|
T | TAC | 4 | a0001c0001t0001g0085a0001c0003t0008g0349a0001c0003t0008g0350others(1): Show | 4 | HG02723.hp2 NA18747.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-3552_553-3551i others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078344 | ||||||
| chr12:48078346
|
T | C | 1 | a0001c0002t0002g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.553-3553A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078346 | ||||||
| chr12:48078354
|
C | T | 252 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(249): Show | 260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.553-3561G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078354 | ||||||
| chr12:48078356
|
C | T | 1 | a0001c0002t0002g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.553-3563G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078356 | ||||||
| chr12:48078366
|
T | C | 1 | a0001c0002t0002g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.553-3573A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078366 | ||||||
| chr12:48078366
|
T | G | 65 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(62): Show | 73 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.553-3573A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078366 | ||||||
| chr12:48078368
|
C | G | 1 | a0001c0002t0002g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.553-3575G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078368 | ||||||
| chr12:48078370
|
CAT | C | 65 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(62): Show | 73 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.553-3579_553-3578d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078370 | ||||||
| chr12:48078372
|
T | C | 1 | a0001c0002t0002g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.553-3579A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078372 | ||||||
| chr12:48078560
|
G | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.553-3767C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078560 | ||||||
| chr12:48078583
|
C | T | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.553-3790G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078583 | ||||||
| chr12:48078670
|
G | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.553-3877C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078670 | ||||||
| chr12:48078821
|
C | A | 11 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(8): Show | 11 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-4028G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078821 | ||||||
| chr12:48078854
|
T | TTTG | 4 | a0001c0001t0001g0380a0001c0001t0001g0381a0001c0001t0001g0382others(1): Show | 4 | HG00280.hp1 HG03017.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-4064_553-4062d others(5): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078854 | ||||||
| chr12:48078945
|
T | C | 4 | a0001c0002t0002g0146a0001c0002t0002g0174a0001c0002t0002g0179others(1): Show | 4 | HG02027.hp1 HG02040.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-4152A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078945 | ||||||
| chr12:48078955
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.553-4162G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078955 | ||||||
| chr12:48078977
|
T | C | 2 | a0001c0001t0007g0199a0003c0007t0007g0246 | 2 | NA18985.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.553-4184A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48078977 | ||||||
| chr12:48079036
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.553-4243T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079036 | ||||||
| chr12:48079085
|
G | T | 1 | a0001c0003t0008g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.553-4292C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079085 | ||||||
| chr12:48079276
|
G | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.552+4315C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079276 | ||||||
| chr12:48079455
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18971.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.552+4136G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079455 | ||||||
| chr12:48079456
|
G | A | 2 | a0001c0001t0004g0340a0001c0001t0004g0345 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.552+4135C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079456 | ||||||
| chr12:48079482
|
G | A | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.552+4109C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079482 | ||||||
| chr12:48079586
|
G | A | 255 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(252): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.552+4005C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079586 | ||||||
| chr12:48079616
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0065 | 2 | HG01123.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.552+3975C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079616 | ||||||
| chr12:48079677
|
A | G | 5 | a0001c0003t0008g0293a0001c0003t0008g0294a0001c0003t0008g0349others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+3914T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079677 | ||||||
| chr12:48079748
|
TAGAG | T | 24 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(21): Show | 24 | HG00741.hp2 HG01099.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.552+3839_552+3842d others(6): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079748 | ||||||
| chr12:48079784
|
CTG | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.552+3805_552+3806d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079784 | ||||||
| chr12:48079829
|
C | T | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.552+3762G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079829 | ||||||
| chr12:48079847
|
A | G | 5 | a0001c0003t0008g0293a0001c0003t0008g0294a0001c0003t0008g0349others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+3744T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079847 | ||||||
| chr12:48079956
|
T | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.552+3635A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48079956 | ||||||
| chr12:48080029
|
G | A | 1 | a0001c0001t0003g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.552+3562C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48080029 | ||||||
| chr12:48080173
|
T | G | 1 | a0001c0001t0001g0074 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.552+3418A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48080173 | ||||||
| chr12:48080186
|
T | C | 11 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(8): Show | 11 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.552+3405A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48080186 | ||||||
| chr12:48080400
|
A | C | 1 | a0001c0001t0001g0018 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.552+3191T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48080400 | ||||||
| chr12:48080655
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0079others(1): Show | 4 | NA18948.hp2 NA18960.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+2936C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48080655 | ||||||
| chr12:48080924
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.552+2667A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48080924 | ||||||
| chr12:48081054
|
G | T | 1 | a0002c0004t0001g0369 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.552+2537C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081054 | ||||||
| chr12:48081070
|
A | G | 123 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0042others(120): Show | 125 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.552+2521T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081070 | ||||||
| chr12:48081130
|
G | A | 1 | a0001c0003t0008g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.552+2461C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081130 | ||||||
| chr12:48081392
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG01167.hp1 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+2199A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081392 | ||||||
| chr12:48081450
|
T | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.552+2141A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081450 | ||||||
| chr12:48081518
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.552+2073G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081518 | ||||||
| chr12:48081552
|
G | A | 2 | a0001c0003t0008g0350a0001c0003t0008g0351 | 2 | NA19077.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.552+2039C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081552 | ||||||
| chr12:48081569
|
C | CG | 3 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0066 | 3 | HG01257.hp2 HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.552+2021dupC | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081569 | ||||||
| chr12:48081570
|
G | GT | 283 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(280): Show | 293 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.552+2020dupA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081570 | ||||||
| chr12:48081570
|
G | GTT | 40 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0046others(37): Show | 40 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.552+2019_552+2020d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081570 | ||||||
| chr12:48081576
|
T | G | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.552+2015A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081576 | ||||||
| chr12:48081577
|
T | G | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.552+2014A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081577 | ||||||
| chr12:48081823
|
C | T | 1 | a0001c0001t0004g0341 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.552+1768G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081823 | ||||||
| chr12:48081834
|
G | A | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.552+1757C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081834 | ||||||
| chr12:48081951
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.552+1640G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081951 | ||||||
| chr12:48082020
|
C | G | 1 | a0001c0002t0002g0185 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.552+1571G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082020 | ||||||
| chr12:48082050
|
T | C | 231 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(228): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.552+1541A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082050 | ||||||
| chr12:48082329
|
G | A | 1 | a0001c0003t0008g0293 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.552+1262C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082329 | ||||||
| chr12:48082389
|
T | C | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.552+1202A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082389 | ||||||
| chr12:48082400
|
C | T | 1 | a0001c0001t0005g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.552+1191G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082400 | ||||||
| chr12:48082434
|
C | T | 3 | a0001c0001t0004g0322a0001c0001t0004g0328a0001c0001t0005g0335 | 3 | HG01515.hp2 HG01517.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.552+1157G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082434 | ||||||
| chr12:48082469
|
C | A | 1 | a0001c0001t0003g0275 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.552+1122G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082469 | ||||||
| chr12:48082499
|
C | T | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.552+1092G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082499 | ||||||
| chr12:48082539
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0085 | 2 | HG00544.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.552+1052G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082539 | ||||||
| chr12:48082552
|
C | CTGGAAGC others(12): Show |
6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.552+1020_552+1038d others(21): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082552 | ||||||
| chr12:48082627
|
G | A | 1 | a0001c0001t0001g0354 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.552+964C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082627 | ||||||
| chr12:48082871
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0005g0295a0001c0001t0005g0300others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+720A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48082871 | ||||||
| chr12:48083012
|
C | T | 84 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(81): Show | 84 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.552+579G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48083012 | ||||||
| chr12:48083044
|
A | G | 3 | a0001c0001t0001g0365a0001c0001t0001g0367a0001c0001t0001g0379 | 3 | NA18957.hp2 NA19056.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.552+547T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48083044 | ||||||
| chr12:48083091
|
G | T | 1 | a0001c0001t0013g0022 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.552+500C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48083091 | ||||||
| chr12:48083101
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0122 | 2 | HG00597.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.552+490G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48083101 | ||||||
| chr12:48083265
|
C | T | 8 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(5): Show | 8 | HG01346.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.552+326G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48083265 | ||||||
| chr12:48083266
|
G | A | 1 | a0001c0001t0014g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.552+325C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48083266 | ||||||
| chr12:48083293
|
AAG | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG01167.hp1 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+296_552+297del others(2): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48083293 | ||||||
| chr12:48083303
|
C | G | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.552+288G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48083303 | ||||||
| chr12:48083380
|
A | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG01109.hp2 HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.552+211T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48083380 | ||||||
| chr12:48083414
|
C | T | 231 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(228): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.552+177G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48083414 | ||||||
| chr12:48083501
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.552+90G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48083501 | ||||||
| chr12:48083794
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0051others(5): Show | 8 | HG00323.hp2 HG01070.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.381-32G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48083794 | ||||||
| chr12:48083847
|
T | C | 11 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(8): Show | 11 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.381-85A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48083847 | ||||||
| chr12:48083953
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.381-191A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48083953 | ||||||
| chr12:48084124
|
T | C | 8 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(5): Show | 8 | HG01346.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.381-362A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084124 | ||||||
| chr12:48084447
|
G | GT | 146 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 146 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.381-686dupA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084447 | ||||||
| chr12:48084447
|
G | GTT | 15 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0029others(12): Show | 15 | HG01070.hp2 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.381-687_381-686dup others(2): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084447 | ||||||
| chr12:48084447
|
G | GTTTT | 59 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(56): Show | 67 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.381-689_381-686dup others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084447 | ||||||
| chr12:48084447
|
GT | G | 118 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.381-686delA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084447 | ||||||
| chr12:48084447
|
GTTTT | G | 23 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(20): Show | 23 | HG00741.hp2 HG01099.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.381-689_381-686del others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084447 | ||||||
| chr12:48084571
|
C | G | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.381-809G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084571 | ||||||
| chr12:48084693
|
C | T | 2 | a0001c0002t0002g0141a0001c0002t0002g0184 | 2 | NA18946.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.381-931G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084693 | ||||||
| chr12:48084694
|
G | T | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0112others(2): Show | 5 | NA18951.hp1 NA18956.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-932C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084694 | ||||||
| chr12:48084756
|
G | A | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.381-994C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084756 | ||||||
| chr12:48084762
|
T | A | 4 | a0001c0002t0002g0144a0001c0002t0002g0154a0001c0002t0002g0158others(1): Show | 4 | HG00280.hp2 HG01516.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.381-1000A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084762 | ||||||
| chr12:48084881
|
T | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.381-1119A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084881 | ||||||
| chr12:48084917
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.381-1155C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48084917 | ||||||
| chr12:48085219
|
G | A | 10 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(7): Show | 10 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.381-1457C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085219 | ||||||
| chr12:48085220
|
G | A | 1 | a0001c0001t0014g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.381-1458C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085220 | ||||||
| chr12:48085234
|
G | A | 1 | a0001c0001t0006g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.381-1472C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085234 | ||||||
| chr12:48085407
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.381-1645C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085407 | ||||||
| chr12:48085440
|
C | T | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.381-1678G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085440 | ||||||
| chr12:48085539
|
C | A | 2 | a0001c0001t0007g0247a0001c0001t0007g0262 | 2 | NA18952.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.381-1777G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085539 | ||||||
| chr12:48085715
|
C | CA | 78 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(75): Show | 80 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.381-1954dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085715 | ||||||
| chr12:48085715
|
C | CAA | 8 | a0001c0001t0003g0198a0001c0001t0003g0241a0001c0001t0003g0242others(5): Show | 8 | HG01243.hp1 HG01258.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.381-1955_381-1954d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085715 | ||||||
| chr12:48085715
|
CA | C | 7 | a0001c0001t0004g0316a0001c0001t0004g0322a0001c0001t0006g0286others(4): Show | 7 | HG01515.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381-1954delT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085715 | ||||||
| chr12:48085715
|
CAA | C | 11 | a0001c0001t0006g0289a0001c0001t0006g0290a0001c0001t0006g0291others(8): Show | 11 | HG01099.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.381-1955_381-1954d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085715 | ||||||
| chr12:48085715
|
CAAAAAA | C | 115 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(112): Show | 115 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.381-1959_381-1954d others(8): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085715 | ||||||
| chr12:48085715
|
CAAAAAAA | C | 40 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0042others(37): Show | 40 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.381-1960_381-1954d others(9): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085715 | ||||||
| chr12:48085715
|
CAAAAAAA others(2): Show |
C | 65 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(62): Show | 73 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.381-1962_381-1954d others(11): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085715 | ||||||
| chr12:48085715
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0002g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.381-1964_381-1954d others(13): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085715 | ||||||
| chr12:48085715
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.381-1965_381-1954d others(14): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085715 | ||||||
| chr12:48085748
|
G | T | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.381-1986C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085748 | ||||||
| chr12:48085915
|
A | G | 1 | a0001c0001t0004g0315 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.381-2153T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48085915 | ||||||
| chr12:48086049
|
C | G | 342 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(339): Show | 352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.381-2287G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086049 | ||||||
| chr12:48086099
|
T | C | 5 | a0001c0003t0008g0293a0001c0003t0008g0294a0001c0003t0008g0349others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.381-2337A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086099 | ||||||
| chr12:48086224
|
A | G | 1 | a0001c0001t0014g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.381-2462T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086224 | ||||||
| chr12:48086345
|
T | C | 2 | a0001c0001t0001g0058a0001c0001t0020g0038 | 2 | HG00323.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.380+2456A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086345 | ||||||
| chr12:48086357
|
C | T | 1 | a0001c0003t0008g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.380+2444G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086357 | ||||||
| chr12:48086692
|
C | A | 1 | a0001c0001t0003g0223 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.380+2109G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086692 | ||||||
| chr12:48086732
|
T | C | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.380+2069A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086732 | ||||||
| chr12:48086780
|
A | G | 1 | a0001c0001t0004g0327 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.380+2021T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086780 | ||||||
| chr12:48086787
|
C | T | 17 | a0001c0001t0004g0259a0001c0001t0005g0195a0001c0001t0005g0225others(14): Show | 17 | HG02145.hp2 HG02280.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.380+2014G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086787 | ||||||
| chr12:48086813
|
G | A | 1 | a0001c0001t0006g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.380+1988C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086813 | ||||||
| chr12:48086860
|
G | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.380+1941C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086860 | ||||||
| chr12:48086869
|
T | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.380+1932A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48086869 | ||||||
| chr12:48087048
|
A | C | 1 | a0001c0001t0001g0357 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.380+1753T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48087048 | ||||||
| chr12:48087049
|
AAAAAC | A | 12 | a0001c0001t0005g0225a0001c0001t0005g0256a0001c0001t0006g0281others(9): Show | 12 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.380+1747_380+1751d others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48087049 | ||||||
| chr12:48087136
|
T | C | 255 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(252): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.380+1665A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48087136 | ||||||
| chr12:48087223
|
T | C | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.380+1578A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48087223 | ||||||
| chr12:48087388
|
G | A | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.380+1413C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48087388 | ||||||
| chr12:48087650
|
T | C | 11 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(8): Show | 11 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.380+1151A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48087650 | ||||||
| chr12:48087694
|
A | C | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+1107T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48087694 | ||||||
| chr12:48087736
|
T | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.380+1065A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48087736 | ||||||
| chr12:48087804
|
T | C | 352 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(349): Show | 362 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(359): Show |
intron_variant | MODIFIER | c.380+997A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48087804 | ||||||
| chr12:48087829
|
A | G | 1 | a0001c0001t0004g0315 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.380+972T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48087829 | ||||||
| chr12:48087836
|
A | C | 4 | a0001c0003t0008g0294a0001c0003t0008g0349a0001c0003t0008g0350others(1): Show | 4 | HG02723.hp2 HG02886.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+965T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48087836 | ||||||
| chr12:48088056
|
CT | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.380+744delA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48088056 | ||||||
| chr12:48088216
|
C | A | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+585G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48088216 | ||||||
| chr12:48088370
|
T | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.380+431A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48088370 | ||||||
| chr12:48088791
|
A | C | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.380+10T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 5/17 | chr12 | 48088791 | ||||||
| chr12:48089458
|
T | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-498A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48089458 | ||||||
| chr12:48089481
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0078 | 2 | HG03669.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.221-521G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48089481 | ||||||
| chr12:48089501
|
A | G | 5 | a0001c0001t0006g0286a0001c0001t0006g0289a0001c0001t0006g0290others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-541T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48089501 | ||||||
| chr12:48089513
|
T | G | 5 | a0001c0003t0008g0293a0001c0003t0008g0294a0001c0003t0008g0349others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-553A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48089513 | ||||||
| chr12:48089701
|
A | C | 342 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(339): Show | 352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.221-741T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48089701 | ||||||
| chr12:48089709
|
T | G | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-749A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48089709 | ||||||
| chr12:48089712
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.221-752G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48089712 | ||||||
| chr12:48089724
|
T | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-764A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48089724 | ||||||
| chr12:48090190
|
T | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-1230A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48090190 | ||||||
| chr12:48090365
|
A | T | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-1405T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48090365 | ||||||
| chr12:48090424
|
G | A | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-1464C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48090424 | ||||||
| chr12:48090650
|
G | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-1690C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48090650 | ||||||
| chr12:48090760
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.221-1800G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48090760 | ||||||
| chr12:48090833
|
G | C | 24 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(21): Show | 24 | HG00741.hp2 HG01099.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.221-1873C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48090833 | ||||||
| chr12:48090913
|
G | C | 1 | a0001c0001t0001g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.221-1953C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48090913 | ||||||
| chr12:48090928
|
T | C | 2 | a0001c0001t0004g0340a0001c0001t0004g0345 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.221-1968A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48090928 | ||||||
| chr12:48091065
|
T | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-2105A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091065 | ||||||
| chr12:48091088
|
T | G | 3 | a0001c0002t0002g0139a0001c0002t0002g0180a0001c0002t0002g0181 | 3 | HG00323.hp1 HG01433.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.221-2128A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091088 | ||||||
| chr12:48091168
|
G | A | 8 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.221-2208C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091168 | ||||||
| chr12:48091175
|
T | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-2215A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091175 | ||||||
| chr12:48091187
|
C | T | 3 | a0001c0003t0008g0349a0001c0003t0008g0350a0001c0003t0008g0351 | 3 | HG02723.hp2 NA19077.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.221-2227G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091187 | ||||||
| chr12:48091375
|
G | A | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.221-2415C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091375 | ||||||
| chr12:48091592
|
A | C | 1 | a0001c0001t0006g0292 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.221-2632T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091592 | ||||||
| chr12:48091594
|
C | T | 1 | a0001c0001t0006g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.221-2634G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091594 | ||||||
| chr12:48091628
|
C | G | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-2668G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091628 | ||||||
| chr12:48091685
|
A | AT | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-2726dupA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091685 | ||||||
| chr12:48091747
|
T | C | 255 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(252): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.221-2787A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091747 | ||||||
| chr12:48091766
|
C | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(4): Show | 7 | HG02129.hp1 HG02135.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-2806G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091766 | ||||||
| chr12:48091821
|
T | C | 6 | a0001c0002t0002g0135a0001c0002t0002g0136a0001c0002t0002g0140others(3): Show | 6 | HG02258.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-2861A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091821 | ||||||
| chr12:48091836
|
G | A | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.221-2876C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091836 | ||||||
| chr12:48091907
|
T | C | 4 | a0001c0001t0003g0251a0001c0001t0003g0264a0001c0001t0003g0266others(1): Show | 4 | HG01069.hp2 HG01257.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-2947A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091907 | ||||||
| chr12:48091912
|
C | T | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.221-2952G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48091912 | ||||||
| chr12:48092020
|
A | T | 1 | a0001c0001t0004g0327 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.221-3060T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48092020 | ||||||
| chr12:48092157
|
G | C | 342 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(339): Show | 352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.221-3197C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48092157 | ||||||
| chr12:48092342
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.221-3382G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48092342 | ||||||
| chr12:48092466
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.221-3506C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48092466 | ||||||
| chr12:48092469
|
C | G | 3 | a0001c0001t0003g0005a0001c0001t0003g0275a0001c0001t0005g0233 | 4 | HG02622.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-3509G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48092469 | ||||||
| chr12:48092694
|
A | C | 2 | a0001c0001t0001g0058a0001c0001t0020g0038 | 2 | HG00323.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.220+3649T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48092694 | ||||||
| chr12:48092706
|
C | T | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.220+3637G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48092706 | ||||||
| chr12:48092913
|
A | T | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.220+3430T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48092913 | ||||||
| chr12:48092932
|
A | G | 87 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(84): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.220+3411T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48092932 | ||||||
| chr12:48093109
|
C | T | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.220+3234G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093109 | ||||||
| chr12:48093151
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.220+3192A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093151 | ||||||
| chr12:48093247
|
A | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+3096T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093247 | ||||||
| chr12:48093280
|
G | GT | 123 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(120): Show | 123 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.220+3062dupA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093280 | ||||||
| chr12:48093280
|
G | GTT | 26 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(23): Show | 26 | HG00673.hp2 HG01361.hp1 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.220+3061_220+3062d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093280 | ||||||
| chr12:48093280
|
G | T | 1 | a0001c0001t0003g0200 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.220+3063C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093280 | ||||||
| chr12:48093280
|
GT | G | 16 | a0001c0001t0004g0318a0001c0001t0005g0257a0001c0001t0005g0284others(13): Show | 16 | HG00741.hp2 HG01099.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.220+3062delA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093280 | ||||||
| chr12:48093280
|
GTT | G | 9 | a0001c0001t0004g0319a0001c0001t0006g0286a0001c0001t0006g0288others(6): Show | 9 | HG01346.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+3061_220+3062d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093280 | ||||||
| chr12:48093280
|
GTTTTT | G | 51 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(48): Show | 59 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.220+3058_220+3062d others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093280 | ||||||
| chr12:48093280
|
GTTTTTT | G | 14 | a0001c0002t0002g0135a0001c0002t0002g0136a0001c0002t0002g0139others(11): Show | 14 | HG00280.hp2 HG00323.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.220+3057_220+3062d others(8): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093280 | ||||||
| chr12:48093466
|
T | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.220+2877A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093466 | ||||||
| chr12:48093476
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.220+2867C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093476 | ||||||
| chr12:48093531
|
G | A | 1 | a0001c0001t0001g0377 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.220+2812C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093531 | ||||||
| chr12:48093636
|
G | A | 1 | a0001c0002t0002g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.220+2707C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093636 | ||||||
| chr12:48093719
|
T | TA | 211 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(208): Show | 219 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.220+2623dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093719 | ||||||
| chr12:48093719
|
T | TAA | 12 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0076others(9): Show | 12 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.220+2622_220+2623d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093719 | ||||||
| chr12:48093719
|
TA | T | 30 | a0001c0001t0003g0264a0001c0001t0004g0259a0001c0001t0004g0346others(27): Show | 30 | HG01069.hp2 HG01099.hp1 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.220+2623delT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093719 | ||||||
| chr12:48093719
|
TAA | T | 7 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0009g0304others(4): Show | 7 | HG00741.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+2622_220+2623d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093719 | ||||||
| chr12:48093746
|
A | T | 2 | a0001c0003t0008g0350a0001c0003t0008g0351 | 2 | NA19077.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.220+2597T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093746 | ||||||
| chr12:48093781
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.220+2562T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093781 | ||||||
| chr12:48093836
|
T | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.220+2507A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093836 | ||||||
| chr12:48093939
|
G | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.220+2404C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093939 | ||||||
| chr12:48094042
|
CAGAT | C | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+2297_220+2300d others(6): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094042 | ||||||
| chr12:48094051
|
G | A | 5 | a0001c0003t0008g0293a0001c0003t0008g0294a0001c0003t0008g0349others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+2292C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094051 | ||||||
| chr12:48094060
|
C | G | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+2283G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094060 | ||||||
| chr12:48094167
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG01109.hp2 HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.220+2176C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094167 | ||||||
| chr12:48094238
|
G | A | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.220+2105C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094238 | ||||||
| chr12:48094374
|
T | C | 1 | a0001c0001t0003g0203 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.220+1969A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094374 | ||||||
| chr12:48094379
|
C | CA | 7 | a0001c0001t0001g0060a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 7 | NA18943.hp1 NA18953.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+1963dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094379 | ||||||
| chr12:48094445
|
C | T | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.220+1898G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094445 | ||||||
| chr12:48094500
|
C | T | 2 | a0001c0001t0001g0060a0001c0010t0001g0083 | 2 | NA19077.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.220+1843G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094500 | ||||||
| chr12:48094572
|
C | T | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220+1771G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094572 | ||||||
| chr12:48094589
|
T | G | 255 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(252): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.220+1754A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094589 | ||||||
| chr12:48094612
|
G | A | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+1731C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094612 | ||||||
| chr12:48094634
|
C | G | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.220+1709G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094634 | ||||||
| chr12:48094645
|
A | C | 1 | a0001c0001t0001g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.220+1698T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094645 | ||||||
| chr12:48094648
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.220+1695G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094648 | ||||||
| chr12:48094929
|
T | C | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.220+1414A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48094929 | ||||||
| chr12:48095137
|
G | A | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.220+1206C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48095137 | ||||||
| chr12:48095334
|
C | T | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.220+1009G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48095334 | ||||||
| chr12:48095393
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG01167.hp1 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+950C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48095393 | ||||||
| chr12:48095535
|
C | CA | 12 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0103others(9): Show | 12 | HG01099.hp1 HG01123.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.220+807dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48095535 | ||||||
| chr12:48095535
|
C | CAA | 142 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(139): Show | 142 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.220+806_220+807dup others(2): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48095535 | ||||||
| chr12:48095535
|
C | CAAA | 17 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(14): Show | 17 | HG00609.hp1 HG00609.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.220+805_220+807dup others(3): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48095535 | ||||||
| chr12:48095535
|
CA | C | 64 | a0001c0001t0003g0161a0001c0001t0003g0272a0001c0001t0004g0325others(61): Show | 72 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.220+807delT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48095535 | ||||||
| chr12:48095574
|
T | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.220+769A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48095574 | ||||||
| chr12:48095649
|
G | A | 24 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(21): Show | 24 | HG00741.hp2 HG01099.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.220+694C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48095649 | ||||||
| chr12:48095738
|
G | A | 2 | a0001c0002t0002g0144a0001c0002t0002g0154 | 2 | HG00280.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.220+605C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48095738 | ||||||
| chr12:48096149
|
T | C | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.220+194A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48096149 | ||||||
| chr12:48096281
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.220+62G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48096281 | ||||||
| chr12:48096722
|
C | T | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.136-295G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 3/17 | chr12 | 48096722 | ||||||
| chr12:48096813
|
C | A | 1 | a0001c0001t0001g0034 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.136-386G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 3/17 | chr12 | 48096813 | ||||||
| chr12:48096923
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.136-496A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 3/17 | chr12 | 48096923 | ||||||
| chr12:48096935
|
G | A | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136-508C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 3/17 | chr12 | 48096935 | ||||||
| chr12:48097006
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.136-579G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 3/17 | chr12 | 48097006 | ||||||
| chr12:48097051
|
T | A | 67 | a0001c0001t0003g0161a0001c0002t0002g0001a0001c0002t0002g0002others(64): Show | 75 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.136-624A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 3/17 | chr12 | 48097051 | ||||||
| chr12:48097265
|
A | G | 342 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(339): Show | 352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.135+729T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 3/17 | chr12 | 48097265 | ||||||
| chr12:48097503
|
G | A | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.135+491C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 3/17 | chr12 | 48097503 | ||||||
| chr12:48097824
|
C | T | 1 | a0001c0002t0002g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.135+170G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 3/17 | chr12 | 48097824 | ||||||
| chr12:48097844
|
T | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+150A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 3/17 | chr12 | 48097844 | ||||||
| chr12:48098265
|
T | A | 66 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5-141A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098265 | ||||||
| chr12:48098410
|
T | C | 345 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(342): Show | 355 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(352): Show |
intron_variant | MODIFIER | c.5-286A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098410 | ||||||
| chr12:48098415
|
C | T | 1 | a0001c0002t0002g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5-291G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098415 | ||||||
| chr12:48098416
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5-292C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098416 | ||||||
| chr12:48098470
|
C | T | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.5-346G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098470 | ||||||
| chr12:48098557
|
T | G | 10 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(7): Show | 10 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.5-433A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098557 | ||||||
| chr12:48098643
|
C | CA | 31 | a0001c0001t0001g0018a0001c0001t0001g0058a0001c0001t0005g0284others(28): Show | 31 | HG00323.hp2 HG00741.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.5-520dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098643 | ||||||
| chr12:48098643
|
C | CAA | 156 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(153): Show | 156 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.5-521_5-520dupTT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098643 | ||||||
| chr12:48098757
|
A | G | 1 | a0001c0001t0004g0324 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5-633T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098757 | ||||||
| chr12:48098781
|
C | T | 5 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0215others(2): Show | 6 | NA18963.hp1 NA19004.hp2 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.5-657G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098781 | ||||||
| chr12:48098824
|
T | C | 66 | a0001c0001t0003g0161a0001c0002t0002g0001a0001c0002t0002g0002others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5-700A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098824 | ||||||
| chr12:48098997
|
A | G | 31 | a0001c0001t0001g0048a0001c0001t0001g0107a0001c0001t0001g0108others(28): Show | 31 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.5-873T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48098997 | ||||||
| chr12:48099139
|
A | C | 256 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(253): Show | 264 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.5-1015T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48099139 | ||||||
| chr12:48099140
|
G | A | 5 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.5-1016C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48099140 | ||||||
| chr12:48099295
|
T | C | 4 | a0001c0002t0002g0144a0001c0002t0002g0154a0001c0002t0002g0158others(1): Show | 4 | HG00280.hp2 HG01516.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.5-1171A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48099295 | ||||||
| chr12:48099306
|
T | C | 342 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(339): Show | 352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.5-1182A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48099306 | ||||||
| chr12:48099587
|
G | T | 4 | a0001c0002t0002g0144a0001c0002t0002g0154a0001c0002t0002g0158others(1): Show | 4 | HG00280.hp2 HG01516.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.5-1463C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48099587 | ||||||
| chr12:48099591
|
G | A | 153 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(150): Show | 163 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.5-1467C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48099591 | ||||||
| chr12:48099801
|
C | T | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4+1668G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48099801 | ||||||
| chr12:48099884
|
C | T | 3 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0274 | 3 | HG02572.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4+1585G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48099884 | ||||||
| chr12:48099893
|
TATA | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(4): Show | 7 | HG02129.hp1 HG02135.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.4+1573_4+1575delTA others(1): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48099893 | ||||||
| chr12:48099927
|
T | C | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4+1542A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48099927 | ||||||
| chr12:48099948
|
T | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.4+1521A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48099948 | ||||||
| chr12:48100210
|
G | A | 7 | a0001c0002t0002g0003a0001c0002t0002g0147a0001c0002t0002g0148others(4): Show | 8 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.4+1259C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100210 | ||||||
| chr12:48100357
|
G | A | 8 | a0001c0001t0009g0304a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.4+1112C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100357 | ||||||
| chr12:48100413
|
G | A | 1 | a0001c0001t0020g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4+1056C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100413 | ||||||
| chr12:48100492
|
T | G | 256 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(253): Show | 264 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.4+977A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100492 | ||||||
| chr12:48100507
|
T | C | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4+962A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100507 | ||||||
| chr12:48100548
|
T | A | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4+921A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100548 | ||||||
| chr12:48100551
|
C | T | 67 | a0001c0001t0003g0161a0001c0002t0002g0001a0001c0002t0002g0002others(64): Show | 75 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.4+918G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100551 | ||||||
| chr12:48100594
|
C | T | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4+875G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100594 | ||||||
| chr12:48100601
|
C | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0019g0093others(1): Show | 4 | NA18949.hp1 NA18955.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.4+868G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100601 | ||||||
| chr12:48100643
|
A | C | 67 | a0001c0001t0003g0161a0001c0002t0002g0001a0001c0002t0002g0002others(64): Show | 75 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.4+826T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100643 | ||||||
| chr12:48100833
|
T | C | 5 | a0001c0003t0008g0293a0001c0003t0008g0294a0001c0003t0008g0349others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.4+636A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100833 | ||||||
| chr12:48100840
|
TGGTTATA others(40): Show |
T | 1 | a0001c0001t0004g0313 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4+582_4+628delCTGT others(43): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48100840 | ||||||
| chr12:48101061
|
C | T | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4+408G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48101061 | ||||||
| chr12:48101281
|
G | A | 1 | a0001c0001t0001g0363 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4+188C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48101281 | ||||||
| chr12:48101294
|
C | CAAT | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4+172_4+174dupATT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48101294 | ||||||
| chr12:48101440
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0021g0117 | 3 | NA18949.hp1 NA18955.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.4+29T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 2/17 | chr12 | 48101440 | ||||||
| chr12:48101740
|
A | G | 1 | a0001c0002t0002g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-44-224T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48101740 | ||||||
| chr12:48101787
|
C | T | 3 | a0001c0001t0004g0340a0001c0001t0004g0345a0001c0001t0016g0344 | 3 | HG01891.hp2 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-44-271G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48101787 | ||||||
| chr12:48101793
|
C | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0085 | 2 | HG00544.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-44-277G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48101793 | ||||||
| chr12:48101917
|
G | T | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-44-401C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48101917 | ||||||
| chr12:48102113
|
C | CAAAATAA others(15): Show |
1 | a0001c0001t0004g0310 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-44-619_-44-598dup others(22): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102113 | ||||||
| chr12:48102124
|
T | C | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-44-608A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102124 | ||||||
| chr12:48102191
|
G | A | 10 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(7): Show | 10 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44-675C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102191 | ||||||
| chr12:48102381
|
G | A | 3 | a0001c0001t0006g0281a0001c0001t0006g0288a0001c0001t0006g0292 | 3 | HG01346.hp2 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-44-865C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102381 | ||||||
| chr12:48102403
|
GC | G | 127 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-44-888delG | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102403 | ||||||
| chr12:48102410
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-44-894G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102410 | ||||||
| chr12:48102423
|
C | T | 1 | a0001c0001t0004g0323 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-44-907G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102423 | ||||||
| chr12:48102426
|
T | C | 12 | a0001c0001t0003g0005a0001c0001t0003g0204a0001c0001t0003g0234others(9): Show | 13 | HG02055.hp1 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-44-910A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102426 | ||||||
| chr12:48102431
|
C | CA | 53 | a0001c0001t0001g0048a0001c0001t0001g0107a0001c0001t0001g0108others(50): Show | 53 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-44-916dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102431 | ||||||
| chr12:48102431
|
C | CAA | 6 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0378others(3): Show | 6 | HG02630.hp1 HG02896.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-917_-44-916dup others(2): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102431 | ||||||
| chr12:48102431
|
CA | C | 61 | a0001c0001t0003g0005a0001c0001t0003g0198a0001c0001t0003g0203others(58): Show | 62 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.-44-916delT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102431 | ||||||
| chr12:48102454
|
AC | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(105): Show | 108 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-44-939delG | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102454 | ||||||
| chr12:48102455
|
C | A | 47 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(44): Show | 47 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.-44-939G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102455 | ||||||
| chr12:48102478
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-44-962G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102478 | ||||||
| chr12:48102706
|
A | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0052others(2): Show | 5 | HG01070.hp2 HG01243.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-1190T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102706 | ||||||
| chr12:48102748
|
C | T | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-44-1232G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102748 | ||||||
| chr12:48102753
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-44-1237C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102753 | ||||||
| chr12:48102760
|
C | A | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-1244G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102760 | ||||||
| chr12:48102782
|
G | C | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-44-1266C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102782 | ||||||
| chr12:48102789
|
C | T | 11 | a0001c0001t0006g0281a0001c0001t0006g0286a0001c0001t0006g0288others(8): Show | 11 | HG01099.hp1 HG01346.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-44-1273G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102789 | ||||||
| chr12:48102810
|
C | CA | 14 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0356others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-44-1295dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102810 | ||||||
| chr12:48102810
|
CA | C | 74 | a0001c0001t0001g0051a0001c0001t0001g0118a0001c0001t0001g0364others(71): Show | 76 | HG00140.hp1 HG00639.hp2 HG01074.hp2 others(73): Show |
intron_variant | MODIFIER | c.-44-1295delT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102810 | ||||||
| chr12:48102810
|
CAA | C | 19 | a0001c0001t0003g0206a0001c0001t0003g0207a0001c0001t0003g0234others(16): Show | 19 | HG01069.hp2 HG01515.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.-44-1296_-44-1295d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102810 | ||||||
| chr12:48102877
|
C | T | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.-44-1361G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102877 | ||||||
| chr12:48102902
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-44-1386T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102902 | ||||||
| chr12:48102994
|
T | C | 1 | a0001c0001t0003g0274 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-44-1478A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102994 | ||||||
| chr12:48102997
|
C | T | 3 | a0001c0001t0004g0340a0001c0001t0004g0345a0001c0001t0016g0344 | 3 | HG01891.hp2 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-44-1481G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102997 | ||||||
| chr12:48103079
|
C | A | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-44-1563G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103079 | ||||||
| chr12:48103170
|
T | G | 3 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | HG03516.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-44-1654A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103170 | ||||||
| chr12:48103214
|
G | A | 342 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(339): Show | 352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.-44-1698C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103214 | ||||||
| chr12:48103262
|
G | A | 2 | a0001c0001t0005g0284a0001c0001t0005g0285 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-44-1746C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103262 | ||||||
| chr12:48103492
|
C | T | 1 | a0001c0002t0002g0183 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-44-1976G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103492 | ||||||
| chr12:48103636
|
C | T | 2 | a0001c0001t0006g0281a0001c0001t0006g0288 | 2 | HG01346.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-44-2120G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103636 | ||||||
| chr12:48103672
|
TA | T | 224 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(221): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.-44-2157delT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103672 | ||||||
| chr12:48103858
|
C | T | 6 | a0001c0003t0008g0151a0001c0003t0008g0293a0001c0003t0008g0294others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+2170G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103858 | ||||||
| chr12:48103895
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0012g0101a0001c0001t0012g0102 | 3 | HG02080.hp2 NA18966.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-45+2133T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103895 | ||||||
| chr12:48103954
|
T | A | 24 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0295others(21): Show | 24 | HG00741.hp2 HG01099.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.-45+2074A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103954 | ||||||
| chr12:48103959
|
T | C | 1 | a0001c0003t0008g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-45+2069A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103959 | ||||||
| chr12:48103989
|
G | A | 21 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0094others(18): Show | 21 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.-45+2039C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48103989 | ||||||
| chr12:48104047
|
C | G | 1 | a0001c0002t0002g0153 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-45+1981G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104047 | ||||||
| chr12:48104104
|
G | A | 4 | a0001c0003t0008g0294a0001c0003t0008g0349a0001c0003t0008g0350others(1): Show | 4 | HG02723.hp2 HG02886.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+1924C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104104 | ||||||
| chr12:48104135
|
C | T | 2 | a0001c0002t0002g0007a0001c0002t0002g0152 | 2 | NA18967.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-45+1893G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104135 | ||||||
| chr12:48104193
|
A | C | 3 | a0001c0001t0010g0298a0001c0001t0010g0299a0001c0001t0010g0302 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-45+1835T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104193 | ||||||
| chr12:48104221
|
A | AAAAAAAT others(42): Show |
1 | a0001c0001t0004g0313 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-45+1806_-45+1807i others(51): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104221 | ||||||
| chr12:48104226
|
A | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0112a0001c0003t0008g0151 | 3 | HG00597.hp1 HG03516.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.-45+1802T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104226 | ||||||
| chr12:48104227
|
AT | A | 3 | a0001c0003t0008g0349a0001c0003t0008g0350a0001c0003t0008g0351 | 3 | HG02723.hp2 NA19077.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-45+1800delA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104227 | ||||||
| chr12:48104228
|
T | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0100a0001c0001t0001g0128others(16): Show | 19 | HG01074.hp2 HG01099.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.-45+1800A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104228 | ||||||
| chr12:48104230
|
T | A | 5 | a0001c0003t0008g0293a0001c0003t0008g0294a0001c0003t0008g0349others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45+1798A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104230 | ||||||
| chr12:48104234
|
T | G | 1 | a0001c0001t0004g0348 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-45+1794A>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104234 | ||||||
| chr12:48104234
|
TAG | T | 4 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0002t0002g0133others(1): Show | 4 | NA18977.hp1 NA19006.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45+1792_-45+1793d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104234 | ||||||
| chr12:48104236
|
G | T | 297 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(294): Show | 306 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-45+1792C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104236 | ||||||
| chr12:48104238
|
G | T | 204 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 212 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.-45+1790C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104238 | ||||||
| chr12:48104240
|
G | T | 66 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0003g0161others(63): Show | 73 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.-45+1788C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104240 | ||||||
| chr12:48104242
|
G | T | 7 | a0001c0002t0002g0133a0001c0002t0002g0134a0001c0003t0008g0293others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-45+1786C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104242 | ||||||
| chr12:48104244
|
G | T | 1 | a0001c0003t0008g0349 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-45+1784C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104244 | ||||||
| chr12:48104253
|
A | G | 1 | a0001c0001t0004g0313 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-45+1775T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104253 | ||||||
| chr12:48104253
|
AG | A | 5 | a0001c0001t0003g0198a0001c0001t0003g0200a0001c0001t0003g0275others(2): Show | 5 | HG01168.hp2 HG01243.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45+1774delC | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104253 | ||||||
| chr12:48104253
|
AGAC | A | 24 | a0001c0001t0003g0008a0001c0001t0003g0203a0001c0001t0003g0204others(21): Show | 24 | HG00140.hp1 HG01433.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.-45+1772_-45+1774d others(5): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104253 | ||||||
| chr12:48104253
|
AGACG | A | 40 | a0001c0001t0001g0010a0001c0001t0003g0005a0001c0001t0003g0006others(37): Show | 42 | HG00639.hp2 HG01192.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.-45+1771_-45+1774d others(6): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104253 | ||||||
| chr12:48104253
|
AGACGG | A | 32 | a0001c0001t0003g0264a0001c0001t0003g0265a0001c0001t0003g0266others(29): Show | 32 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-45+1770_-45+1774d others(7): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104253 | ||||||
| chr12:48104253
|
AGACGGG | A | 44 | a0001c0001t0003g0161a0001c0001t0003g0271a0001c0001t0003g0272others(41): Show | 48 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-45+1769_-45+1774d others(8): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104253 | ||||||
| chr12:48104253
|
AGACGGGG | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0355others(19): Show | 26 | HG00408.hp1 HG00642.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.-45+1768_-45+1774d others(9): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104253 | ||||||
| chr12:48104253
|
AGACGGGG others(1): Show |
A | 53 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(50): Show | 53 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-45+1767_-45+1774d others(10): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104253 | ||||||
| chr12:48104253
|
AGACGGGG others(2): Show |
A | 82 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(79): Show | 82 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.-45+1766_-45+1774d others(11): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104253 | ||||||
| chr12:48104253
|
AGACGGGG others(3): Show |
A | 26 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(23): Show | 26 | HG00423.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.-45+1765_-45+1774d others(12): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104253 | ||||||
| chr12:48104253
|
AGACGGGG others(4): Show |
A | 3 | a0001c0001t0009g0305a0001c0001t0009g0306a0001c0001t0009g0307 | 3 | HG02809.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-45+1764_-45+1774d others(13): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104253 | ||||||
| chr12:48104254
|
G | C | 3 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0005g0195 | 3 | HG03130.hp2 NA19009.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-45+1774C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104254 | ||||||
| chr12:48104255
|
A | C | 5 | a0001c0001t0003g0198a0001c0001t0003g0200a0001c0001t0003g0275others(2): Show | 5 | HG01168.hp2 HG01243.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45+1773T>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104255 | ||||||
| chr12:48104255
|
A | G | 5 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0003g0196others(2): Show | 5 | HG03130.hp2 NA18968.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45+1773T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104255 | ||||||
| chr12:48104256
|
C | G | 10 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0003g0196others(7): Show | 10 | HG01168.hp2 HG01243.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-45+1772G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104256 | ||||||
| chr12:48104257
|
G | C | 24 | a0001c0001t0003g0008a0001c0001t0003g0203a0001c0001t0003g0204others(21): Show | 24 | HG00140.hp1 HG01433.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.-45+1771C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104257 | ||||||
| chr12:48104258
|
G | C | 40 | a0001c0001t0001g0010a0001c0001t0003g0005a0001c0001t0003g0006others(37): Show | 42 | HG00639.hp2 HG01192.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.-45+1770C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104258 | ||||||
| chr12:48104259
|
G | C | 32 | a0001c0001t0003g0264a0001c0001t0003g0265a0001c0001t0003g0266others(29): Show | 32 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-45+1769C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104259 | ||||||
| chr12:48104260
|
G | C | 44 | a0001c0001t0003g0161a0001c0001t0003g0271a0001c0001t0003g0272others(41): Show | 48 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-45+1768C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104260 | ||||||
| chr12:48104261
|
G | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0355others(19): Show | 26 | HG00408.hp1 HG00642.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.-45+1767C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104261 | ||||||
| chr12:48104262
|
G | C | 53 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(50): Show | 53 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-45+1766C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104262 | ||||||
| chr12:48104263
|
G | C | 82 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(79): Show | 82 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.-45+1765C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104263 | ||||||
| chr12:48104264
|
G | C | 26 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(23): Show | 26 | HG00423.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.-45+1764C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104264 | ||||||
| chr12:48104265
|
G | C | 3 | a0001c0001t0009g0305a0001c0001t0009g0306a0001c0001t0009g0307 | 3 | HG02809.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-45+1763C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104265 | ||||||
| chr12:48104267
|
G | T | 1 | a0001c0001t0014g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-45+1761C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104267 | ||||||
| chr12:48104273
|
G | A | 1 | a0001c0001t0004g0311 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-45+1755C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104273 | ||||||
| chr12:48104274
|
C | G | 2 | a0001c0001t0004g0310a0001c0001t0004g0311 | 2 | HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-45+1754G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104274 | ||||||
| chr12:48104277
|
A | G | 1 | a0001c0001t0004g0310 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-45+1751T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104277 | ||||||
| chr12:48104281
|
A | G | 1 | a0001c0001t0004g0310 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-45+1747T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104281 | ||||||
| chr12:48104283
|
G | GGA | 27 | a0001c0001t0001g0355a0001c0001t0001g0356a0001c0001t0001g0357others(24): Show | 27 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.-45+1743_-45+1744d others(4): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104283 | ||||||
| chr12:48104311
|
TTAGCTTT others(9): Show |
T | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.-45+1701_-45+1716d others(18): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104311 | ||||||
| chr12:48104426
|
T | C | 1 | a0001c0001t0006g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-45+1602A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104426 | ||||||
| chr12:48104448
|
T | C | 1 | a0001c0001t0003g0275 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-45+1580A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104448 | ||||||
| chr12:48104544
|
G | A | 352 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(349): Show | 362 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(359): Show |
intron_variant | MODIFIER | c.-45+1484C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104544 | ||||||
| chr12:48104630
|
C | T | 342 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(339): Show | 352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.-45+1398G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104630 | ||||||
| chr12:48104657
|
G | C | 127 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0008others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-45+1371C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104657 | ||||||
| chr12:48104808
|
C | G | 1 | a0001c0001t0015g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-45+1220G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104808 | ||||||
| chr12:48104966
|
T | C | 3 | a0001c0003t0008g0349a0001c0003t0008g0350a0001c0003t0008g0351 | 3 | HG02723.hp2 NA19077.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-45+1062A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104966 | ||||||
| chr12:48104967
|
A | T | 1 | a0001c0001t0001g0009 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-45+1061T>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104967 | ||||||
| chr12:48105016
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0015g0278 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-45+1012T>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48105016 | ||||||
| chr12:48105318
|
C | T | 2 | a0001c0001t0004g0276a0001c0001t0004g0277 | 2 | HG00140.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-45+710G>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48105318 | ||||||
| chr12:48105348
|
G | T | 308 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(305): Show | 318 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.-45+680C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48105348 | ||||||
| chr12:48105537
|
G | C | 2 | a0001c0001t0001g0352a0001c0001t0001g0353 | 2 | NA18963.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-45+491C>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48105537 | ||||||
| chr12:48105618
|
G | A | 26 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(23): Show | 26 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-45+410C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48105618 | ||||||
| chr12:48105781
|
G | GGA | 4 | a0001c0001t0001g0380a0001c0001t0001g0381a0001c0001t0001g0382others(1): Show | 4 | HG00280.hp1 HG03017.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+245_-45+246dup others(2): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48105781 | ||||||
| chr12:48105922
|
C | A | 1 | a0001c0001t0001g0384 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-45+106G>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48105922 | ||||||
| chr12:48105981
|
G | T | 1 | a0001c0001t0003g0008 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-45+47C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48105981 | ||||||
| chr12:48106000
|
C | G | 1 | a0001c0002t0002g0007 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-45+28G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48106000 |