Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MDDIA others(639): Show |
chr12 | 48037897 | 48111079 |
| a0002 | 0/0 | 644 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | MDDIA others(639): Show |
chr12 | 48037897 | 48111079 |
| a0003 | 0/0 | 644 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | MDDIA others(639): Show |
chr12 | 48037897 | 48111079 |
| a0004 | 0/0 | 644 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | MDDIA others(639): Show |
chr12 | 48037897 | 48111079 |
| a0005 | 0/0 | 644 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | MDDIA others(639): Show |
chr12 | 48037897 | 48111079 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1932 | 306 | 82 | 50 | 130 | 10 | 32 | SENP1_chr12_48037897_48111079 | SENP1 | ATGGA others(1927): Show |
chr12 | 48037897 | 48111079 | ||
| a0001c0002 | 0/0 | 1932 | 74 | 9 | 18 | 37 | 4 | 6 | SENP1_chr12_48037897_48111079 | SENP1 | ATGGA others(1927): Show |
chr12 | 48037897 | 48111079 | ||
| a0001c0003 | 0/0 | 1932 | 6 | 4 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | ATGGA others(1927): Show |
chr12 | 48037897 | 48111079 | ||
| a0001c0005 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | ATGGA others(1927): Show |
chr12 | 48037897 | 48111079 | ||
| a0001c0009 | 0/0 | 1932 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | ATGGA others(1927): Show |
chr12 | 48037897 | 48111079 | ||
| a0001c0010 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | ATGGA others(1927): Show |
chr12 | 48037897 | 48111079 | ||
| a0002c0004 | 0/0 | 1932 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | ATGGA others(1927): Show |
chr12 | 48037897 | 48111079 | ||
| a0003c0008 | 0/0 | 1932 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | ATGGA others(1927): Show |
chr12 | 48037897 | 48111079 | ||
| a0004c0007 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | ATGGA others(1927): Show |
chr12 | 48037897 | 48111079 | ||
| a0005c0006 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | ATGGA others(1927): Show |
chr12 | 48037897 | 48111079 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4454 | 145 | 16 | 27 | 88 | 3 | 11 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0002 | 1/0 | 4456 | 97 | 27 | 18 | 27 | 7 | 17 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0004 | 0/0 | 4458 | 20 | 17 | 1 | 0 | 0 | 2 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4453): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0005 | 0/0 | 4456 | 10 | 8 | 2 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0006 | 0/0 | 4456 | 9 | 0 | 0 | 9 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0008 | 0/0 | 4456 | 4 | 4 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0009 | 0/0 | 4462 | 3 | 3 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4457): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0010 | 0/0 | 4458 | 2 | 2 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4453): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0011 | 0/0 | 4454 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0012 | 0/0 | 4454 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0013 | 0/1 | 4454 | 1 | 0 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0014 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0015 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0016 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0017 | 0/0 | 4456 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0018 | 0/0 | 4454 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0019 | 0/0 | 4454 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0020 | 0/0 | 4456 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0021 | 0/0 | 4454 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0022 | 0/0 | 4436 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4431): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0023 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0001t0024 | 0/0 | 4456 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0002t0003 | 0/0 | 4454 | 74 | 9 | 18 | 37 | 4 | 6 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0001c0003t0007 | 0/0 | 4454 | 6 | 4 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0001c0005t0001 | 0/0 | 4454 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0001c0009t0002 | 0/0 | 4456 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0001c0010t0001 | 0/0 | 4454 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0002c0004t0001 | 0/0 | 4454 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4449): Show |
chr12 | 48037897 | 48111079 |
| a0003c0008t0004 | 0/0 | 4458 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4453): Show |
chr12 | 48037897 | 48111079 |
| a0004c0007t0006 | 0/0 | 4456 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4451): Show |
chr12 | 48037897 | 48111079 |
| a0005c0006t0004 | 0/0 | 4458 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | GCGTT others(4453): Show |
chr12 | 48037897 | 48111079 |
| actghapid | grch38/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 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0093 | 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 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0117 | 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 |
| a0001c0001t0001g0369 | 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 |
| a0001c0001t0001g0373 | 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 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0309 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0258 | 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 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0009g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0009g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0009g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0010g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0010g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0011g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0011g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0012g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0012g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0013g0380 | 0/1 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0016g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0017g0324 | 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 |
| a0001c0001t0019g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0020g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0021g0118 | 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 |
| a0001c0001t0023g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0001t0024g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0002 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0002t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0007g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0007g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0003t0007g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0009t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0001c0010t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0002c0004t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0002c0004t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0003c0008t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0004c0007t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| a0005c0006t0004g0226 | 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 | t0002 | g0210 | EUR | GBR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0277 | EUR | GBR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0382 | EUR | FIN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0144 | EUR | FIN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0181 | EUR | FIN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0377 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0041 | 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 | t0003 | g0145 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0147 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00673 | hp1 | a0002 | c0004 | t0001 | g0374 | EAS | CHS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00673 | hp2 | a0001 | c0001 | t0012 | g0023 | 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 | t0003 | g0191 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0148 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0073 | 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 | t0002 | g0331 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0283 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | 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 | t0002 | g0264 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | 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 | t0003 | 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 | t0002 | g0318 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0177 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0295 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01106 | hp1 | a0003 | c0008 | t0004 | g0333 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0166 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0330 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0076 | 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 | t0003 | g0003 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | 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 | t0003 | g0287 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01192 | hp1 | a0001 | c0001 | t0024 | g0245 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0175 | AMR | PUR | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0194 | 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 | t0003 | g0137 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0282 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0242 | 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 | t0002 | g0320 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0336 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0288 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01361 | hp2 | a0001 | c0001 | t0017 | g0324 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0139 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0212 | 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 | t0002 | g0209 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0204 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0315 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0154 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0267 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0271 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0325 | EUR | IBS | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | 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 | t0003 | g0178 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0342 | 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 | g0033 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0316 | 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 | t0003 | g0173 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0029 | 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 | g0021 | 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 | t0003 | g0179 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0157 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0190 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0096 | 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 | g0020 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0165 | 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 | t0002 | g0219 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0189 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0375 | 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 | t0005 | g0286 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0259 | 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 | g0067 | 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 | t0005 | g0291 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02258 | hp2 | a0001 | c0002 | t0003 | g0171 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | 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 | g0058 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0066 | 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 | t0003 | g0001 | AMR | PEL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02523 | hp1 | a0001 | c0001 | t0012 | g0025 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02523 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | KHV | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0230 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02622 | hp2 | a0001 | c0003 | t0007 | g0293 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0292 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0345 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0304 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0160 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0332 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0346 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02723 | hp2 | a0001 | c0003 | t0007 | g0349 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0159 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0314 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0343 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0305 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0347 | 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 | t0007 | g0294 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0296 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0290 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0225 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0251 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0170 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0383 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0136 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0348 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03130 | hp1 | a0001 | c0002 | t0003 | g0140 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0344 | 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 | t0004 | g0227 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0176 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03225 | hp1 | a0001 | c0001 | t0016 | g0340 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0323 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0299 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03486 | hp1 | a0001 | c0001 | t0023 | g0303 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | 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 | t0002 | g0335 | 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 | t0003 | g0002 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0334 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03516 | hp1 | a0001 | c0003 | t0007 | g0151 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0301 | AFR | ESN | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0297 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | GWD | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0300 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0289 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0285 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03654 | hp2 | a0001 | c0001 | t0020 | g0040 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0084 | 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 | g0071 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | BEB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0001 | SAS | BEB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0321 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0381 | SAS | BEB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0338 | SAS | BEB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0313 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0158 | SAS | STU | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | 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 | t0008 | g0307 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0138 | EAS | CHB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CHB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18940 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0378 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0263 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18948 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18949 | hp1 | a0001 | c0001 | t0021 | g0118 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18949 | hp2 | a0001 | c0002 | t0003 | 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 | g0097 | 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 | t0006 | g0262 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0123 | 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 | t0003 | 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 | t0003 | 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 | t0003 | g0168 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | 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 | t0006 | g0261 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18965 | hp1 | a0001 | c0002 | t0003 | g0155 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18966 | hp2 | a0001 | c0001 | t0011 | g0101 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | 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 | g0046 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18971 | hp1 | a0002 | c0004 | t0001 | g0370 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18972 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18974 | hp1 | a0001 | c0005 | t0001 | g0085 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0060 | 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 | t0003 | g0146 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18984 | hp2 | a0001 | c0001 | t0006 | g0260 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18985 | hp1 | a0004 | c0007 | t0006 | g0235 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0061 | 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 | g0121 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | 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 | t0003 | g0149 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0216 | 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 | g0077 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0203 | 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 | t0002 | g0214 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0153 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19006 | hp1 | a0001 | c0002 | t0003 | g0134 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19006 | hp2 | a0001 | c0001 | t0019 | g0094 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19007 | hp2 | a0001 | c0001 | t0011 | g0102 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0163 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | 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 | t0002 | g0217 | 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 | g0088 | AFR | LWK | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19030 | hp2 | a0005 | c0006 | t0004 | g0226 | AFR | LWK | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | LWK | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0269 | 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 | t0003 | g0004 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19057 | hp1 | a0001 | c0001 | t0006 | g0236 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0122 | 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 | t0002 | g0195 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0200 | 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 | g0371 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0174 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19066 | hp1 | a0001 | c0002 | t0003 | g0141 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19067 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19072 | hp1 | a0001 | c0001 | t0006 | g0268 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19077 | hp1 | a0001 | c0003 | t0007 | g0351 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19077 | hp2 | a0001 | c0010 | t0001 | g0091 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0080 | 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 | t0003 | g0164 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0215 | 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 | t0006 | g0233 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0133 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19091 | hp1 | a0001 | c0003 | t0007 | g0350 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0306 | AFR | YRI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0258 | AFR | ASW | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0180 | EUR | TSI | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01123 | hp1 | a0001 | c0009 | t0002 | g0337 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | 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 | g0081 | AFR | ACB | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0135 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | MSL | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0302 | AFR | USA | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | USA | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | USA | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | USA | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | 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 | a0001 | c0001 | t0013 | g0380 | REF | REF | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0309 | REF | REF | SENP1_chr12_48037897_48111079 | SENP1 | chr12 | 48037897 | 48111079 |
| view | 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 | a0004 | 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 | a0004 | 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 | a0003 | 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 |
| view | 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 |
| view | 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 | a0001c0001t0005 | 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 | a0001c0003t0007 | 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 | a0001c0001t0011 | 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 | a0001c0001t0010 a0001c0002t0003 |
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 | a0001c0003t0007 | 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 | a0001c0001t0008 a0001c0001t0023 |
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 | a0001c0001t0005 a0001c0001t0015 |
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 | a0001c0001t0023 | 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 | a0001c0001t0004 a0001c0001t0010 a0003c0008t0004 others(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 | a0001c0001t0009 | 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 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(8): Show |
236 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(233): 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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(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 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(7): Show |
157 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*815A>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 18/18 | 815 | chr12 | 48044507 | ||||||
| chr12:48044683 | G | A | 2 | a0001c0001t0008 a0001c0001t0023 |
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 | a0001c0001t0012 | 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 | a0001c0001t0024 | 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 | a0001c0001t0006 a0004c0007t0006 |
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 |
| view | 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0005g0295 | 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0001t0002g0222 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0026 others(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 | a0001c0001t0002g0222 | 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 | a0001c0002t0003g0142 | 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 | a0001c0001t0001g0372 | 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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0003c0008t0004g0333 | 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 | a0001c0001t0002g0341 a0001c0001t0002g0342 |
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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0004c0007t0006g0235 | 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 | a0004c0007t0006g0235 | 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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | a0001c0001t0001g0022 | 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 | a0001c0001t0005g0308 | 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | a0001c0003t0007g0151 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0016g0340 | 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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0002g0341 a0001c0001t0002g0342 a0001c0001t0016g0340 others(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 | a0004c0007t0006g0235 | 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 | a0004c0007t0006g0235 | 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 | a0001c0001t0002g0204 a0001c0001t0002g0209 a0001c0001t0002g0210 others(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 | 351 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(348): Show |
361 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(358): 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 | a0001c0002t0003g0165 | 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 | a0001c0001t0002g0329 | 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 | a0004c0007t0006g0235 | 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 | a0004c0007t0006g0235 | 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 | a0001c0001t0005g0295 | 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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(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 | a0001c0002t0003g0179 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0002g0311 | 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 | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0248 a0001c0001t0002g0250 others(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 | a0001c0002t0003g0166 | 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 | 153 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(150): Show |
153 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1408-1951dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48051082 | |||||||
| chr12:48051449 | T | G | 8 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0002t0003g0282 | 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 | a0001c0001t0002g0241 | 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 | a0001c0001t0002g0273 | 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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0005g0295 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0215 a0001c0001t0002g0269 |
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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0092 | 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 | a0001c0003t0007g0293 a0001c0003t0007g0294 a0001c0003t0007g0349 others(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 | 341 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(338): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0074 a0001c0001t0001g0088 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0004g0270 | 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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0080 a0001c0001t0001g0107 others(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 | a0001c0002t0003g0149 a0001c0002t0003g0150 a0001c0002t0003g0164 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0002g0341 a0001c0001t0002g0342 a0001c0001t0016g0340 |
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 | a0001c0001t0002g0341 a0001c0001t0002g0342 |
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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | 159 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(156): Show |
159 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(156): 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 | a0001c0001t0001g0068 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0002g0213 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0238 others(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 | a0001c0003t0007g0293 a0001c0003t0007g0294 a0001c0003t0007g0349 others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0002t0003g0152 | 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 | a0001c0001t0002g0316 | 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 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0238 others(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 | a0001c0001t0017g0324 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0014 a0001c0001t0006g0233 a0001c0001t0006g0261 |
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 | a0001c0001t0002g0314 a0001c0009t0002g0337 |
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 | 253 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): 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 | a0001c0003t0007g0151 | 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0002t0003g0179 | 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 | a0001c0002t0003g0152 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | 188 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0069 others(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 | a0001c0001t0014g0339 a0001c0005t0001g0085 |
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 | a0001c0001t0014g0339 a0001c0005t0001g0085 |
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 | a0001c0001t0014g0339 a0001c0005t0001g0085 |
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 | a0001c0001t0014g0339 a0001c0005t0001g0085 |
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 | a0001c0001t0014g0339 a0001c0005t0001g0085 |
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 | a0001c0001t0014g0339 a0001c0005t0001g0085 |
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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | 338 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(335): Show |
348 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(345): 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0002g0318 a0001c0001t0002g0328 a0001c0001t0002g0334 others(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 | a0001c0002t0003g0189 | 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 | 81 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
81 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(78): 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 | a0001c0001t0002g0341 a0001c0001t0002g0342 a0001c0001t0002g0344 others(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 | a0001c0001t0002g0334 a0001c0001t0002g0335 |
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 | a0003c0008t0004g0333 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0043 others(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 | a0001c0005t0001g0085 | 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 | a0001c0001t0004g0285 a0001c0001t0004g0297 a0001c0001t0004g0300 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0001t0004g0284 a0001c0001t0005g0281 a0001c0001t0005g0286 others(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 | a0001c0001t0004g0285 a0001c0001t0004g0297 a0001c0001t0004g0300 others(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 | a0001c0001t0004g0225 a0001c0001t0004g0257 a0001c0001t0006g0193 others(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 | a0001c0001t0004g0225 a0001c0001t0004g0257 a0001c0001t0004g0285 others(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 | a0001c0001t0004g0225 a0001c0001t0004g0257 a0001c0001t0004g0285 others(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 | a0001c0001t0004g0225 a0001c0001t0004g0257 a0001c0001t0004g0285 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0200 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0161 a0001c0001t0002g0194 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0045 others(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 | 123 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(120): Show |
123 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(120): 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 | a0001c0001t0002g0208 a0001c0001t0004g0230 |
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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0002g0208 a0001c0001t0004g0230 |
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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0003t0007g0350 a0001c0003t0007g0351 |
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 | a0001c0001t0009g0302 | 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 | a0001c0001t0016g0340 | 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 | a0001c0001t0002g0208 a0001c0001t0004g0230 |
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 | a0001c0001t0002g0208 a0001c0001t0004g0230 |
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 | a0001c0001t0004g0285 a0001c0002t0003g0283 |
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 | a0001c0003t0007g0293 | 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 | a0001c0001t0002g0341 a0001c0001t0002g0342 |
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 | a0001c0001t0002g0206 | 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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0002t0003g0001 others(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 | a0001c0001t0004g0225 a0001c0001t0004g0257 a0001c0001t0006g0193 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0045 others(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 | a0001c0001t0002g0347 | 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 | a0001c0001t0002g0343 | 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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0023g0303 | 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 | 121 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(118): Show |
121 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(118): 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 | a0001c0001t0002g0266 | 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 | 133 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(130): Show |
133 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(130): 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 | a0001c0001t0001g0032 a0001c0001t0001g0054 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0043 others(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 | a0001c0002t0003g0145 a0001c0002t0003g0156 a0001c0002t0003g0165 others(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 | a0001c0002t0003g0145 a0001c0002t0003g0154 a0001c0002t0003g0156 others(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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0003t0007g0349 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0003t0007g0349 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0043 others(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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0002g0344 others(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 | a0001c0002t0003g0190 | 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 | a0001c0002t0003g0003 a0001c0002t0003g0147 a0001c0002t0003g0148 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0004 others(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 | a0001c0002t0003g0133 a0001c0002t0003g0168 |
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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0002g0344 others(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 | a0001c0003t0007g0151 | 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 | a0001c0003t0007g0293 a0001c0003t0007g0294 a0001c0003t0007g0350 others(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 | a0001c0001t0002g0264 a0001c0001t0002g0267 a0001c0001t0002g0271 |
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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0002g0344 others(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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0002g0344 others(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 | a0001c0001t0001g0028 a0001c0001t0002g0315 a0001c0001t0002g0325 others(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 | a0001c0001t0002g0249 | 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 | 130 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(127): Show |
130 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0002g0344 others(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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0002g0344 others(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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0002g0344 others(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 | a0003c0008t0004g0333 | 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 | a0001c0001t0002g0331 | 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 | a0001c0001t0002g0347 | 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 | a0001c0001t0002g0161 a0001c0001t0002g0194 a0001c0001t0002g0195 others(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 | a0001c0001t0002g0006 | 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 | a0001c0001t0002g0008 a0001c0001t0002g0219 a0001c0001t0002g0266 |
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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0002g0344 others(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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0002g0344 others(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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0002g0344 others(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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0002g0344 others(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 | a0001c0001t0002g0214 a0001c0001t0002g0220 a0001c0001t0002g0274 others(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 | a0001c0001t0023g0303 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0161 a0001c0001t0002g0194 others(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 | a0001c0001t0005g0289 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0368 a0001c0001t0005g0281 others(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 | a0001c0001t0002g0208 a0001c0001t0002g0269 a0001c0001t0004g0230 others(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 | a0001c0001t0002g0265 | 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 | a0001c0001t0002g0215 | 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 | a0001c0001t0023g0303 | 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 | a0001c0001t0002g0269 | 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 | a0001c0001t0002g0273 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0032 others(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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0002g0269 a0001c0001t0002g0343 a0001c0002t0003g0190 |
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 | a0001c0002t0003g0145 a0001c0002t0003g0154 a0001c0002t0003g0156 others(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 | a0001c0001t0002g0215 a0001c0001t0002g0269 a0001c0002t0003g0190 |
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 | a0001c0001t0002g0008 a0001c0001t0002g0219 a0001c0001t0002g0266 others(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 | a0001c0001t0002g0338 | 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 | a0001c0001t0002g0006 a0001c0002t0003g0003 a0001c0002t0003g0147 others(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 | 2 | a0001c0001t0002g0310 a0001c0001t0002g0322 |
2 | HG00438.hp2 HG03834.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(29): Show |
T | 1 | a0001c0001t0002g0215 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1407+6665_1407+670 others(40): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057010 | |||||||
| chr12:48057010 | CATATTAC others(65): Show |
T | 1 | a0001c0001t0002g0269 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1407+6629_1407+670 others(76): Show |
SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057010 | |||||||
| chr12:48057010 | CATATTAC others(101): Show |
C | 1 | a0001c0001t0023g0303 | 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 | a0001c0001t0002g0264 a0001c0001t0002g0267 a0001c0001t0002g0271 others(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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0002t0003g0152 | 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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0002g0249 a0001c0001t0002g0264 a0001c0001t0002g0267 others(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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | 139 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(136): Show |
139 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(136): 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0003t0007g0151 | 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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.1407+6539delA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 13/17 | chr12 | 48057170 | |||||||
| chr12:48057205 | T | C | 6 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0001g0373 | 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 | a0001c0001t0002g0347 | 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 | a0002c0004t0001g0370 | 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0080 a0001c0001t0001g0107 others(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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0003t0007g0151 | 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 | a0001c0001t0001g0092 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): 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 | 341 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(338): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): 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 | a0001c0001t0002g0341 a0001c0001t0002g0342 a0001c0001t0006g0193 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0107 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | 92 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(89): 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 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0073 others(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 | a0001c0001t0002g0343 a0001c0001t0002g0344 a0001c0001t0002g0345 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0002g0208 a0001c0001t0002g0244 |
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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0002t0003g0148 a0001c0002t0003g0191 |
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 | a0001c0001t0001g0049 a0001c0001t0001g0123 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0062 a0001c0001t0001g0086 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0001t0002g0241 | 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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0003t0007g0294 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0269 |
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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | a0001c0001t0002g0327 | 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | a0001c0001t0002g0265 | 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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0001g0037 | 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 | a0001c0002t0003g0139 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0002g0219 a0001c0001t0002g0220 |
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 | a0001c0002t0003g0137 | 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 | a0001c0003t0007g0151 | 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 | a0001c0001t0024g0245 | 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 | a0001c0001t0001g0379 | 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | 243 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(248): 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 | a0001c0001t0002g0341 a0001c0001t0002g0342 a0001c0001t0016g0340 |
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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0122 |
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 | a0001c0001t0002g0348 | 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 | a0001c0001t0002g0348 | 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 | a0001c0001t0002g0320 | 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 | a0001c0001t0002g0266 | 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0003t0007g0293 a0001c0003t0007g0294 a0001c0003t0007g0349 others(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 | a0001c0002t0003g0138 a0001c0002t0003g0145 a0001c0002t0003g0167 others(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 | a0001c0001t0001g0100 | 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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0009g0299 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0001t0002g0341 a0001c0001t0002g0342 a0001c0001t0016g0340 |
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 | a0001c0001t0005g0281 a0001c0001t0005g0288 |
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 | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0006g0262 | 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 | a0001c0001t0005g0286 | 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 | 157 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(154): Show |
157 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(154): 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(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 | a0001c0001t0002g0205 a0001c0002t0003g0001 a0001c0002t0003g0002 others(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 | a0001c0001t0002g0343 | 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 | a0001c0002t0003g0175 | 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0004g0227 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0088 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0110 others(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 | a0001c0001t0002g0210 | 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 | a0001c0001t0002g0344 | 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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0003t0007g0151 | 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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0001g0048 a0001c0001t0001g0080 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0080 | 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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0003t0007g0151 | 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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0080 a0001c0001t0001g0107 others(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 | 230 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(227): Show |
238 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.996-833A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48067798 | |||||||
| chr12:48067852 | G | T | 341 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(338): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): 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 | a0001c0001t0001g0373 | 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0033 others(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 | a0001c0001t0006g0236 a0001c0001t0006g0262 |
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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0002t0003g0153 a0001c0002t0003g0163 a0001c0002t0003g0192 |
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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0002g0219 a0001c0001t0002g0220 |
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 | a0001c0001t0002g0205 | 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0002t0003g0185 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0080 a0001c0001t0001g0107 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0360 a0001c0001t0001g0365 a0001c0001t0001g0367 others(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 | a0001c0001t0004g0301 a0001c0001t0005g0288 a0001c0001t0005g0289 others(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 | 208 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(205): Show |
216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.996-2188delT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 9/17 | chr12 | 48069152 | |||||||
| chr12:48069152 | CAA | C | 77 | a0001c0001t0001g0125 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0002g0243 a0001c0001t0002g0264 a0001c0001t0002g0267 others(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 | a0001c0003t0007g0294 | 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 | a0001c0001t0001g0384 a0001c0002t0003g0138 |
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 | a0001c0002t0003g0182 | 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 | a0001c0002t0003g0135 | 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 | a0001c0002t0003g0282 | 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 | a0001c0001t0016g0340 | 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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0002t0003g0134 | 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 | a0001c0003t0007g0151 | 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 | a0001c0001t0001g0021 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0002g0310 | 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 | a0001c0003t0007g0294 | 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 | a0001c0001t0005g0295 | 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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0004g0297 | 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 | a0001c0001t0001g0089 | 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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0003t0007g0294 | 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 | a0001c0002t0003g0146 | 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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0002g0246 a0001c0001t0002g0247 |
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 | a0001c0001t0008g0306 | 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 | a0001c0002t0003g0141 a0001c0002t0003g0162 a0001c0002t0003g0184 |
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 | a0001c0002t0003g0181 | 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 | a0001c0001t0002g0314 a0001c0009t0002g0337 |
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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0103 others(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 | a0001c0001t0005g0289 | 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0002t0003g0141 a0001c0002t0003g0184 |
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 | a0001c0001t0005g0289 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0016g0340 | 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 | a0001c0001t0004g0196 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0002t0003g0174 | 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 | a0001c0001t0002g0204 | 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0002t0003g0182 | 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 | 230 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(227): Show |
238 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(235): 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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0003t0007g0294 a0001c0003t0007g0349 a0001c0003t0007g0350 others(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 | a0001c0003t0007g0294 a0001c0003t0007g0349 a0001c0003t0007g0350 others(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 | a0001c0001t0002g0239 | 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): 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 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0238 others(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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | 160 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(157): Show |
160 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(157): 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 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(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 | a0001c0001t0002g0338 | 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 | a0001c0003t0007g0151 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0003t0007g0351 | 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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0248 a0001c0001t0002g0250 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0002t0003g0180 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0096 |
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 | a0001c0001t0005g0281 | 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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0117 others(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 | a0001c0001t0004g0230 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0371 a0001c0001t0012g0023 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0065 |
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 | 155 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(152): Show |
155 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(152): 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | 188 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0012g0025 | 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 | a0001c0001t0001g0076 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0375 |
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 | a0001c0001t0001g0046 | 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 | a0001c0003t0007g0349 a0001c0003t0007g0350 a0001c0003t0007g0351 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0002g0249 a0001c0001t0005g0281 a0001c0001t0005g0286 others(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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0103 others(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 | a0001c0001t0002g0266 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0002g0161 a0001c0001t0005g0281 a0001c0001t0005g0286 others(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 | a0001c0001t0002g0265 a0001c0001t0002g0336 a0001c0003t0007g0349 others(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 | a0001c0001t0002g0276 a0001c0001t0002g0323 a0001c0001t0017g0324 |
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 | a0001c0001t0002g0277 a0001c0001t0002g0318 a0001c0001t0002g0319 others(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 | a0001c0001t0002g0310 a0001c0001t0002g0316 a0001c0001t0002g0317 others(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 | a0001c0001t0002g0214 a0001c0001t0002g0216 a0001c0001t0002g0218 others(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 | a0001c0001t0001g0093 a0001c0001t0002g0006 a0001c0001t0002g0197 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0195 a0001c0001t0002g0198 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0338 a0001c0001t0004g0301 others(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 | a0001c0001t0002g0200 a0001c0001t0002g0331 a0001c0010t0001g0091 |
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 | a0001c0001t0002g0219 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0002g0239 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0238 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0354 a0001c0001t0002g0005 others(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 | a0001c0001t0002g0341 a0001c0001t0002g0342 a0001c0001t0016g0340 |
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 | a0001c0001t0001g0032 a0001c0001t0005g0291 a0001c0001t0005g0292 |
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 | a0001c0001t0004g0231 | 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 | a0001c0001t0002g0241 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0066 a0001c0001t0002g0272 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0074 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0092 a0001c0001t0002g0244 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0081 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0362 a0001c0001t0001g0378 |
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 | a0001c0001t0001g0365 a0001c0001t0001g0375 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0002g0204 others(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 | a0001c0001t0001g0369 a0001c0001t0001g0371 a0001c0001t0001g0372 others(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 |
20 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0019 others(17): Show |
20 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(17): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0355 others(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 | a0001c0001t0001g0363 a0001c0001t0001g0366 a0001c0001t0006g0262 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0041 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0279 a0001c0001t0001g0356 others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0360 a0001c0001t0001g0368 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0109 a0001c0003t0007g0293 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0065 others(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 | a0001c0001t0006g0193 a0001c0001t0006g0233 a0001c0001t0006g0261 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0112 |
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 | a0001c0001t0006g0234 a0001c0001t0006g0236 |
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 | a0001c0001t0001g0027 | 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 | a0001c0001t0006g0260 | 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 | a0001c0001t0006g0263 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0002t0003g0186 |
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 | 174 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(171): Show |
174 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(171): 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 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0004g0297 others(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 | a0001c0001t0002g0266 a0001c0001t0004g0297 a0001c0001t0004g0300 others(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 | a0001c0001t0001g0093 a0001c0003t0007g0349 a0001c0003t0007g0350 others(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 | a0001c0002t0003g0186 | 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 | 251 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(248): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): 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 | a0001c0002t0003g0186 | 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 | a0001c0002t0003g0186 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0002t0003g0186 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0002t0003g0186 | 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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | 3 | a0001c0001t0001g0381 a0001c0001t0001g0382 a0001c0001t0001g0383 |
3 | HG00280.hp1 HG03017.hp1 HG04184.hp1 |
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 | a0001c0002t0003g0146 a0001c0002t0003g0174 a0001c0002t0003g0179 others(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 | a0001c0001t0006g0193 a0004c0007t0006g0235 |
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 | a0001c0001t0001g0047 | 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 | a0001c0003t0007g0294 | 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
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 | a0001c0001t0002g0341 a0001c0001t0002g0342 |
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 | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): 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 | a0001c0001t0001g0010 a0001c0001t0001g0068 |
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 | a0001c0003t0007g0293 a0001c0003t0007g0294 a0001c0003t0007g0349 others(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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0003t0007g0151 | 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 | a0001c0003t0007g0293 a0001c0003t0007g0294 a0001c0003t0007g0349 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0002g0273 | 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0062 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0128 | 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 | a0002c0004t0001g0370 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0043 others(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 | a0001c0003t0007g0294 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0001g0032 | 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 | a0001c0003t0007g0350 a0001c0003t0007g0351 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0069 |
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 | 282 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(279): Show |
292 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.552+2020dupA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 6/17 | chr12 | 48081570 | |||||||
| chr12:48081570 | G | GTT | 40 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0002g0344 | 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 | a0001c0001t0002g0241 | 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 | a0001c0001t0001g0031 | 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 | a0001c0002t0003g0185 | 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 | 230 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(227): Show |
238 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(235): 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 | a0001c0003t0007g0293 | 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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0004g0231 | 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 | a0001c0001t0002g0315 a0001c0001t0002g0325 a0001c0001t0004g0332 |
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 | a0001c0001t0002g0275 | 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0093 |
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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0001g0080 a0001c0001t0004g0297 a0001c0001t0004g0300 others(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 | 83 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(80): Show |
83 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(80): 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 | a0001c0001t0001g0365 a0001c0001t0001g0367 a0001c0001t0001g0369 |
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 | a0001c0001t0012g0023 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0123 |
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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
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 | 230 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(227): Show |
238 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(235): 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0051 others(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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | 14 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0030 others(11): Show |
14 | HG01070.hp2 HG01099.hp2 HG01243.hp2 others(11): 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0002t0003g0141 a0001c0002t0003g0184 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0112 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0002t0003g0144 a0001c0002t0003g0154 a0001c0002t0003g0158 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0005g0308 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0006g0236 a0001c0001t0006g0262 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0001t0002g0194 a0001c0001t0002g0239 a0001c0001t0002g0242 others(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 | a0001c0001t0002g0315 a0001c0001t0002g0323 a0001c0001t0005g0286 others(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 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(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 | 114 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(111): Show |
114 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(111): 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0043 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0002t0003g0177 | 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0003t0007g0151 | 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 | a0001c0001t0002g0321 | 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 | 341 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(338): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): 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 | a0001c0003t0007g0293 a0001c0003t0007g0294 a0001c0003t0007g0349 others(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 | a0001c0001t0001g0057 a0001c0001t0020g0040 |
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 | a0001c0003t0007g0294 | 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 | a0001c0001t0002g0223 | 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 | a0001c0001t0002g0322 | 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 | a0001c0001t0002g0256 a0001c0001t0004g0196 a0001c0001t0004g0225 others(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 | a0001c0001t0005g0308 | 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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0004g0225 a0001c0001t0004g0257 a0001c0001t0005g0281 others(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 | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): 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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | 351 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(348): Show |
361 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(358): 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 | a0001c0001t0002g0321 | 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 | a0001c0003t0007g0294 a0001c0003t0007g0349 a0001c0003t0007g0350 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0084 |
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 | a0001c0001t0005g0286 a0001c0001t0005g0290 a0001c0001t0005g0291 others(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 | a0001c0003t0007g0293 a0001c0003t0007g0294 a0001c0003t0007g0349 others(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 | 341 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(338): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | a0001c0001t0002g0341 a0001c0001t0002g0342 |
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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0002t0003g0139 a0001c0002t0003g0180 a0001c0002t0003g0181 |
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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0003t0007g0349 a0001c0003t0007g0350 a0001c0003t0007g0351 |
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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0005g0289 | 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 | a0001c0001t0005g0308 | 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): 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 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0002t0003g0135 a0001c0002t0003g0136 a0001c0002t0003g0140 others(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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0002g0243 a0001c0001t0002g0264 a0001c0001t0002g0267 others(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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0002g0322 | 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 | 341 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(338): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): 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 | a0001c0001t0002g0205 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0275 a0001c0001t0004g0237 |
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 | a0001c0001t0001g0057 a0001c0001t0020g0040 |
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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0001g0071 | 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | 122 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(119): Show |
122 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.220+3062dupA | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093280 | |||||||
| chr12:48093280 | G | GTT | 26 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0002g0195 | 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 | a0001c0001t0002g0334 a0001c0001t0004g0258 a0001c0001t0004g0284 others(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 | a0001c0001t0002g0335 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0002t0003g0135 a0001c0002t0003g0136 a0001c0002t0003g0139 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0378 | 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 | a0001c0002t0003g0182 | 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 | 210 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(207): Show |
218 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.220+2623dupT | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093719 | |||||||
| chr12:48093719 | T | TAA | 12 | a0001c0001t0001g0073 a0001c0001t0001g0081 a0001c0001t0001g0082 others(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 | a0001c0001t0002g0256 a0001c0001t0002g0264 a0001c0001t0002g0343 others(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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0008g0304 others(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 | a0001c0003t0007g0350 a0001c0003t0007g0351 |
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 | a0001c0001t0001g0022 | 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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.220+2507A>G | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 4/17 | chr12 | 48093836 | |||||||
| chr12:48093939 | G | A | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0003t0007g0293 a0001c0003t0007g0294 a0001c0003t0007g0349 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0001t0002g0211 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0077 a0001c0001t0001g0078 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0001g0059 a0001c0010t0001g0091 |
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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0003t0007g0151 | 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 16 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0017 others(13): Show |
16 | HG00609.hp1 HG00609.hp2 HG02129.hp1 others(13): 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 | a0001c0001t0002g0161 a0001c0001t0002g0271 a0001c0001t0002g0318 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | a0001c0002t0003g0144 a0001c0002t0003g0154 |
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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0002g0161 a0001c0002t0003g0001 a0001c0002t0003g0002 others(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 | 341 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(338): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): 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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0002t0003g0175 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0002t0003g0001 a0001c0002t0003g0002 a0001c0002t0003g0003 others(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 | 344 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(341): Show |
354 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(351): 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 | a0001c0002t0003g0160 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0057 a0001c0001t0004g0284 others(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 | 155 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(152): Show |
155 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(152): 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 | a0001c0001t0002g0317 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0214 others(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 | a0001c0001t0002g0161 a0001c0002t0003g0001 a0001c0002t0003g0002 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | 255 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(252): Show |
263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): 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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0002t0003g0144 a0001c0002t0003g0154 a0001c0002t0003g0158 others(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 | 341 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(338): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): 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 | a0001c0002t0003g0144 a0001c0002t0003g0154 a0001c0002t0003g0158 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0274 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0002t0003g0003 a0001c0002t0003g0147 a0001c0002t0003g0148 others(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 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0008g0306 others(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 | a0001c0001t0020g0040 | 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 | 255 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(252): Show |
263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0002g0161 a0001c0002t0003g0001 a0001c0002t0003g0002 others(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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0019g0094 others(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 | a0001c0001t0002g0161 a0001c0002t0003g0001 a0001c0002t0003g0002 others(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 | a0001c0003t0007g0293 a0001c0003t0007g0294 a0001c0003t0007g0349 others(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 | a0001c0001t0002g0313 | 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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0021g0118 |
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 | a0001c0002t0003g0157 | 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 | a0001c0001t0002g0341 a0001c0001t0002g0342 a0001c0001t0016g0340 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0093 |
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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0002g0310 | 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0005g0281 a0001c0001t0005g0288 a0001c0001t0005g0289 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0001t0002g0316 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0238 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0379 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0194 a0001c0001t0002g0205 others(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 | 107 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(104): Show |
107 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-44-939delG | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48102454 | |||||||
| chr12:48102455 | C | A | 47 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0001t0005g0281 a0001c0001t0005g0286 a0001c0001t0005g0288 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0356 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0119 a0001c0001t0001g0364 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0238 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0002g0274 | 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 | a0001c0001t0002g0341 a0001c0001t0002g0342 a0001c0001t0016g0340 |
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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0004g0297 a0001c0001t0004g0300 a0001c0001t0004g0301 |
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 | 341 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(338): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): 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 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
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 | a0001c0002t0003g0183 | 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 | a0001c0001t0005g0281 a0001c0001t0005g0288 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0003t0007g0151 a0001c0003t0007g0293 a0001c0003t0007g0294 others(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 | a0001c0001t0001g0044 a0001c0001t0011g0101 a0001c0001t0011g0102 |
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 | a0001c0001t0004g0284 a0001c0001t0004g0285 a0001c0001t0004g0297 others(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 | a0001c0003t0007g0151 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0095 others(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 | a0001c0002t0003g0153 | 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 | a0001c0003t0007g0294 a0001c0003t0007g0349 a0001c0003t0007g0350 others(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 | a0001c0002t0003g0007 a0001c0002t0003g0152 |
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 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0009g0302 |
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 | a0001c0001t0002g0313 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0112 a0001c0003t0007g0151 |
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 | a0001c0003t0007g0349 a0001c0003t0007g0350 a0001c0003t0007g0351 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0067 a0001c0001t0001g0117 others(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 | a0001c0003t0007g0293 a0001c0003t0007g0294 a0001c0003t0007g0349 others(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 | a0001c0001t0002g0348 | 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 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0002t0003g0133 others(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 | 296 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(293): Show |
305 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.-45+1792C>A | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104236 | |||||||
| chr12:48104238 | G | T | 203 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(200): Show |
211 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(208): 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 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0002g0161 others(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 | a0001c0002t0003g0133 a0001c0002t0003g0134 a0001c0003t0007g0293 others(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 | a0001c0003t0007g0349 | 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 | a0001c0001t0002g0313 | 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 | a0001c0001t0002g0194 a0001c0001t0002g0195 a0001c0001t0002g0275 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0203 a0001c0001t0002g0204 others(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 | a0001c0001t0001g0010 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0002g0256 a0001c0001t0002g0264 a0001c0001t0002g0265 others(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 | a0001c0001t0002g0161 a0001c0001t0002g0271 a0001c0001t0002g0272 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0355 others(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 | 52 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(49): Show |
52 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(49): 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0008g0305 a0001c0001t0008g0306 a0001c0001t0008g0307 |
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 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0004g0196 |
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 | a0001c0001t0002g0194 a0001c0001t0002g0195 a0001c0001t0002g0275 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(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 | a0001c0001t0002g0194 a0001c0001t0002g0195 a0001c0001t0002g0199 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0203 a0001c0001t0002g0204 others(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 | a0001c0001t0001g0010 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0002g0256 a0001c0001t0002g0264 a0001c0001t0002g0265 others(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 | a0001c0001t0002g0161 a0001c0001t0002g0271 a0001c0001t0002g0272 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0355 others(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 | 52 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(49): Show |
52 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(49): 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0008g0305 a0001c0001t0008g0306 a0001c0001t0008g0307 |
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 | a0001c0001t0002g0311 | 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 | a0001c0001t0002g0310 a0001c0001t0002g0311 |
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 | a0001c0001t0002g0310 | 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 | a0001c0001t0002g0310 | 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 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(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 | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): 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 | a0001c0001t0005g0308 | 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 | a0001c0001t0002g0275 | 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 | 351 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(348): Show |
361 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(358): Show |
intron_variant | MODIFIER | c.-45+1484C>T | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48104544 | |||||||
| chr12:48104630 | C | T | 341 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(338): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(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 | a0001c0003t0007g0349 a0001c0003t0007g0350 a0001c0003t0007g0351 |
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 | a0001c0001t0001g0279 a0001c0001t0015g0278 |
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 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
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 | 307 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(304): Show |
317 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(314): 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 | a0001c0001t0001g0352 a0001c0001t0001g0353 |
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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(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 | 3 | a0001c0001t0001g0381 a0001c0001t0001g0382 a0001c0001t0001g0383 |
3 | HG00280.hp1 HG03017.hp1 HG04184.hp1 |
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 | a0001c0001t0002g0008 | 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 | a0001c0002t0003g0007 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-45+28G>C | SENP1 | ENSG00000079387.15 | transcript | ENST00000549518.6 | protein_coding | 1/17 | chr12 | 48106000 |