Item | Value |
---|---|
geneid | 9099 |
ensemblid | ENSG00000036672.16 |
hgncid | 12618 |
symbol | USP2 |
name | ubiquitin specific peptidase 2 |
refseq_nuc | NM_004205.5 |
refseq_prot | NP_004196.4 |
ensembl_nuc | ENST00000260187.7 |
ensembl_prot | ENSP00000260187.2 |
mane_status | MANE Select |
chr | chr11 |
start | 119355215 |
end | 119381690 |
strand | - |
ver | v1.2 |
region | chr11:119355215-119381690 |
region5000 | chr11:119350215-119386690 |
regionname0 | USP2_chr11_119355215_119381690 |
regionname5000 | USP2_chr11_119350215_119386690 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 605 | 195 | 65 | 36 | 52 | 14 | 26 | 27 | USP2_chr11_119350215_119386690 | USP2 | MSQLS others(600): Show |
chr11 | 119350215 | 119386690 |
a0002 | 0/0 | 605 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | USP2_chr11_119350215_119386690 | USP2 | MSQLS others(600): Show |
chr11 | 119350215 | 119386690 |
a0003 | 0/0 | 605 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | MSQLS others(600): Show |
chr11 | 119350215 | 119386690 |
a0004 | 0/0 | 605 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | MSQLS others(600): Show |
chr11 | 119350215 | 119386690 |
a0005 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | MSQLS others(600): Show |
chr11 | 119350215 | 119386690 |
a0006 | 0/0 | 605 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | MSQLS others(600): Show |
chr11 | 119350215 | 119386690 |
a0007 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | MSQLS others(600): Show |
chr11 | 119350215 | 119386690 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1815 | 101 | 19 | 14 | 38 | 10 | 19 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0001c0002 | 1/0 | 1815 | 27 | 11 | 7 | 2 | 2 | 4 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0001c0003 | 0/0 | 1815 | 27 | 12 | 9 | 4 | 1 | 1 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0001c0004 | 0/0 | 1815 | 25 | 14 | 4 | 4 | 1 | 2 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0001c0005 | 0/0 | 1815 | 12 | 7 | 1 | 4 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0001c0007 | 0/0 | 1815 | 2 | 1 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0001c0012 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0002c0006 | 0/0 | 1815 | 2 | 0 | 0 | 2 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0003c0010 | 0/0 | 1815 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0004c0011 | 0/0 | 1815 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0005c0008 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0006c0013 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 | ||
a0007c0009 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | ATGTC others(1810): Show |
chr11 | 119350215 | 119386690 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3698 | 40 | 12 | 4 | 12 | 2 | 9 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0001t0002 | 0/0 | 3699 | 48 | 3 | 7 | 22 | 7 | 9 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3694): Show |
chr11 | 119350215 | 119386690 |
a0001c0001t0003 | 0/0 | 3697 | 3 | 1 | 0 | 1 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0001t0006 | 0/0 | 3700 | 4 | 0 | 3 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3695): Show |
chr11 | 119350215 | 119386690 |
a0001c0001t0014 | 0/0 | 3699 | 2 | 0 | 0 | 2 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3694): Show |
chr11 | 119350215 | 119386690 |
a0001c0001t0027 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0001t0028 | 0/0 | 3699 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3694): Show |
chr11 | 119350215 | 119386690 |
a0001c0001t0034 | 0/0 | 3699 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3694): Show |
chr11 | 119350215 | 119386690 |
a0001c0001t0035 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0001 | 0/0 | 3698 | 2 | 1 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0002 | 0/0 | 3699 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3694): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0003 | 0/0 | 3697 | 10 | 1 | 5 | 1 | 1 | 2 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0005 | 0/0 | 3696 | 3 | 1 | 1 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3691): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0007 | 0/0 | 3696 | 3 | 3 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3691): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0009 | 0/0 | 3694 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3689): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0012 | 1/0 | 3697 | 2 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0017 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0018 | 0/0 | 3699 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3694): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0022 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0031 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0002t0033 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0003t0001 | 0/0 | 3698 | 11 | 7 | 3 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0003t0002 | 0/0 | 3699 | 5 | 1 | 3 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3694): Show |
chr11 | 119350215 | 119386690 |
a0001c0003t0003 | 0/0 | 3697 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0003t0010 | 0/0 | 3698 | 3 | 2 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0003t0013 | 0/0 | 3700 | 2 | 0 | 0 | 2 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3695): Show |
chr11 | 119350215 | 119386690 |
a0001c0003t0019 | 0/0 | 3699 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3694): Show |
chr11 | 119350215 | 119386690 |
a0001c0003t0024 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0003t0025 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3695): Show |
chr11 | 119350215 | 119386690 |
a0001c0003t0026 | 0/0 | 3697 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0003t0036 | 0/0 | 3698 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0004t0001 | 0/0 | 3698 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0004t0003 | 0/0 | 3697 | 7 | 0 | 2 | 3 | 1 | 1 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0004t0004 | 0/0 | 3698 | 7 | 7 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0004t0005 | 0/0 | 3696 | 2 | 1 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3691): Show |
chr11 | 119350215 | 119386690 |
a0001c0004t0007 | 0/0 | 3696 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3691): Show |
chr11 | 119350215 | 119386690 |
a0001c0004t0008 | 0/0 | 3696 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3691): Show |
chr11 | 119350215 | 119386690 |
a0001c0004t0011 | 0/0 | 3697 | 3 | 3 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0004t0020 | 0/0 | 3694 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3689): Show |
chr11 | 119350215 | 119386690 |
a0001c0004t0021 | 0/0 | 3699 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3694): Show |
chr11 | 119350215 | 119386690 |
a0001c0004t0029 | 0/0 | 3697 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0005t0001 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0005t0003 | 0/0 | 3697 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0005t0008 | 0/0 | 3696 | 3 | 3 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3691): Show |
chr11 | 119350215 | 119386690 |
a0001c0005t0009 | 0/0 | 3694 | 3 | 0 | 1 | 2 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3689): Show |
chr11 | 119350215 | 119386690 |
a0001c0005t0015 | 0/0 | 3697 | 2 | 2 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0005t0030 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0005t0032 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0001c0007t0001 | 0/0 | 3698 | 2 | 1 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0001c0012t0023 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0002c0006t0002 | 0/0 | 3699 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3694): Show |
chr11 | 119350215 | 119386690 |
a0002c0006t0006 | 0/0 | 3700 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3695): Show |
chr11 | 119350215 | 119386690 |
a0003c0010t0001 | 0/0 | 3698 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0004c0011t0001 | 0/0 | 3698 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0005c0008t0003 | 0/0 | 3697 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3692): Show |
chr11 | 119350215 | 119386690 |
a0006c0013t0016 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
a0007c0009t0001 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | AGGCG others(3693): Show |
chr11 | 119350215 | 119386690 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0083 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0001 | 0/0 | 13 | 0 | 2 | 8 | 1 | 2 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0012 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0014g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0027g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0028g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0034g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0001t0035g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0003g0004 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0005g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0009g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0012g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0012g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0022g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0031g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0002t0033g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0010g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0013g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0013g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0019g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0024g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0025g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0026g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0003t0036g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0004g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0011g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0020g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0021g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0004t0029g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0005t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0005t0008g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0005t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0005t0009g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0005t0015g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0005t0015g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0005t0030g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0005t0032g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0007t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0007t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0001c0012t0023g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0002c0006t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0002c0006t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0003c0010t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0004c0011t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0005c0008t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0006c0013t0016g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
a0007c0009t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | GBR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0052 | EUR | GBR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0103 | EUR | GBR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | GBR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | FIN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00323 | hp2 | a0001 | c0003 | t0002 | g0148 | EUR | FIN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00673 | hp2 | a0001 | c0001 | t0006 | g0116 | EAS | CHS | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0130 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00735 | hp2 | a0001 | c0003 | t0002 | g0009 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00741 | hp1 | a0001 | c0003 | t0026 | g0132 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0108 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01071 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0088 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01106 | hp1 | a0001 | c0002 | t0012 | g0025 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01167 | hp2 | a0001 | c0002 | t0005 | g0045 | AMR | PUR | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01258 | hp1 | a0001 | c0002 | t0003 | g0058 | AMR | CLM | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0049 | AMR | CLM | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01261 | hp1 | a0001 | c0003 | t0002 | g0009 | AMR | CLM | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0146 | AMR | CLM | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01346 | hp2 | a0001 | c0004 | t0003 | g0109 | AMR | CLM | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01433 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | CLM | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01433 | hp2 | a0003 | c0010 | t0001 | g0139 | AMR | CLM | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01496 | hp2 | a0004 | c0011 | t0001 | g0138 | AMR | CLM | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01515 | hp1 | a0001 | c0002 | t0005 | g0059 | EUR | IBS | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01515 | hp2 | a0001 | c0001 | t0028 | g0106 | EUR | IBS | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01884 | hp1 | a0001 | c0002 | t0033 | g0066 | AFR | ACB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01891 | hp2 | a0001 | c0004 | t0004 | g0134 | AFR | ACB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01943 | hp1 | a0001 | c0004 | t0003 | g0142 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01943 | hp2 | a0001 | c0007 | t0001 | g0159 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01975 | hp1 | a0001 | c0004 | t0005 | g0141 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01975 | hp2 | a0001 | c0003 | t0003 | g0055 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01981 | hp2 | a0001 | c0004 | t0001 | g0143 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG01993 | hp2 | a0001 | c0002 | t0003 | g0061 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02027 | hp1 | a0005 | c0008 | t0003 | g0079 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02071 | hp1 | a0001 | c0003 | t0013 | g0030 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02074 | hp1 | a0001 | c0005 | t0001 | g0160 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02155 | hp1 | a0001 | c0004 | t0003 | g0112 | EAS | CDX | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | CDX | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02165 | hp1 | a0001 | c0003 | t0019 | g0027 | EAS | CDX | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02257 | hp1 | a0001 | c0004 | t0004 | g0075 | AFR | ACB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02258 | hp1 | a0001 | c0004 | t0011 | g0072 | AFR | ACB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02273 | hp1 | a0001 | c0002 | t0003 | g0063 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02273 | hp2 | a0001 | c0005 | t0009 | g0007 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02300 | hp1 | a0001 | c0003 | t0036 | g0050 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02451 | hp1 | a0001 | c0002 | t0007 | g0035 | AFR | ACB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02451 | hp2 | a0001 | c0003 | t0010 | g0029 | AFR | ACB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02602 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02630 | hp2 | a0001 | c0007 | t0001 | g0155 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02647 | hp1 | a0001 | c0005 | t0008 | g0020 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02647 | hp2 | a0001 | c0002 | t0031 | g0065 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0051 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02717 | hp2 | a0001 | c0001 | t0035 | g0102 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02886 | hp1 | a0001 | c0002 | t0007 | g0034 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0068 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02895 | hp2 | a0001 | c0004 | t0008 | g0150 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02896 | hp1 | a0001 | c0004 | t0021 | g0135 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0046 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02922 | hp2 | a0001 | c0004 | t0004 | g0003 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02965 | hp2 | a0001 | c0002 | t0017 | g0023 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02970 | hp1 | a0001 | c0005 | t0015 | g0156 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02970 | hp2 | a0001 | c0004 | t0007 | g0126 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0147 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG02976 | hp2 | a0001 | c0005 | t0008 | g0152 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03098 | hp1 | a0001 | c0001 | t0034 | g0123 | AFR | MSL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03098 | hp2 | a0001 | c0003 | t0002 | g0047 | AFR | MSL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03139 | hp1 | a0001 | c0004 | t0011 | g0011 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03139 | hp2 | a0001 | c0005 | t0032 | g0157 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03195 | hp2 | a0006 | c0013 | t0016 | g0021 | AFR | ESN | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03453 | hp1 | a0001 | c0003 | t0024 | g0043 | AFR | MSL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03486 | hp1 | a0001 | c0002 | t0005 | g0036 | AFR | MSL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03486 | hp2 | a0001 | c0004 | t0011 | g0011 | AFR | MSL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03540 | hp1 | a0001 | c0005 | t0030 | g0153 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03540 | hp2 | a0001 | c0003 | t0025 | g0044 | AFR | GWD | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03579 | hp1 | a0001 | c0004 | t0004 | g0003 | AFR | MSL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03654 | hp2 | a0001 | c0003 | t0010 | g0026 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0057 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03704 | hp2 | a0001 | c0004 | t0029 | g0119 | SAS | PJL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | BEB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03942 | hp2 | a0001 | c0004 | t0003 | g0110 | SAS | BEB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | STU | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | STU | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18522 | hp1 | a0001 | c0002 | t0007 | g0033 | AFR | YRI | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18522 | hp2 | a0001 | c0002 | t0022 | g0053 | AFR | YRI | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18747 | hp1 | a0001 | c0004 | t0003 | g0091 | EAS | CHB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18906 | hp1 | a0001 | c0004 | t0004 | g0003 | AFR | YRI | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18906 | hp2 | a0001 | c0003 | t0010 | g0028 | AFR | YRI | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18940 | hp1 | a0001 | c0002 | t0003 | g0060 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18940 | hp2 | a0007 | c0009 | t0001 | g0080 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18949 | hp1 | a0001 | c0003 | t0013 | g0024 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18949 | hp2 | a0002 | c0006 | t0006 | g0149 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19010 | hp1 | a0001 | c0005 | t0003 | g0158 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19011 | hp1 | a0001 | c0005 | t0009 | g0007 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19011 | hp2 | a0002 | c0006 | t0002 | g0107 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | LWK | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19030 | hp2 | a0001 | c0002 | t0018 | g0022 | AFR | LWK | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19043 | hp2 | a0001 | c0012 | t0023 | g0151 | AFR | LWK | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19056 | hp1 | a0001 | c0004 | t0020 | g0032 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19060 | hp1 | a0001 | c0001 | t0014 | g0115 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19065 | hp2 | a0001 | c0001 | t0014 | g0105 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19067 | hp2 | a0001 | c0002 | t0009 | g0054 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19070 | hp1 | a0001 | c0004 | t0003 | g0090 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19090 | hp2 | a0001 | c0005 | t0009 | g0007 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19240 | hp1 | a0001 | c0004 | t0005 | g0097 | AFR | YRI | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA19240 | hp2 | a0001 | c0005 | t0008 | g0020 | AFR | YRI | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ASW | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA20129 | hp2 | a0001 | c0005 | t0015 | g0154 | AFR | ASW | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA20752 | hp2 | a0001 | c0004 | t0003 | g0085 | EUR | TSI | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0099 | EUR | TSI | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0129 | EUR | TSI | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | GIH | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | GIH | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0048 | AFR | MSL | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG06807 | hp1 | a0001 | c0001 | t0027 | g0092 | AFR | USA | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
HG06807 | hp2 | a0001 | c0004 | t0004 | g0003 | AFR | USA | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
NA20300 | hp2 | a0001 | c0004 | t0004 | g0003 | AFR | USA | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0083 | REF | REF | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
homoSapiens | grch38p0 | a0001 | c0002 | t0012 | g0031 | REF | REF | USP2_chr11_119350215_119386690 | USP2 | chr11 | 119350215 | 119386690 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:119359048 | T | C | 1 | a0004 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1148A>G | p.Asn383Ser | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 6/13 | 1407/3697 | 1148/1818 | 383/605 | chr11 | 119359048 | |||
chr11:119359312 | G | T | 1 | a0002 | 2 | NA18949.hp2 NA19011.hp2 |
missense_variant | MODERATE | c.980C>A | p.Thr327Asn | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 5/13 | 1239/3697 | 980/1818 | 327/605 | chr11 | 119359312 | |||
chr11:119372960 | C | T | 2 | a0003 a0004 |
2 | HG01433.hp2 HG01496.hp2 |
missense_variant | MODERATE | c.521G>A | p.Arg174Gln | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/13 | 780/3697 | 521/1818 | 174/605 | chr11 | 119372960 | |||
chr11:119373147 | C | T | 1 | a0007 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.334G>A | p.Gly112Arg | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/13 | 593/3697 | 334/1818 | 112/605 | chr11 | 119373147 | |||
chr11:119373156 | C | T | 1 | a0005 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.325G>A | p.Gly109Arg | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/13 | 584/3697 | 325/1818 | 109/605 | chr11 | 119373156 | |||
chr11:119373323 | G | A | 1 | a0006 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.158C>T | p.Pro53Leu | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/13 | 417/3697 | 158/1818 | 53/605 | chr11 | 119373323 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:119359254 | G | A | 8 | a0001c0001 a0001c0003 a0001c0007 others(5): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
synonymous_variant | LOW | c.1038C>T | p.Tyr346Tyr | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 5/13 | 1297/3697 | 1038/1818 | 346/605 | chr11 | 119359254 | |||
chr11:119372902 | T | C | 4 | a0001c0005 a0001c0007 a0001c0012 others(1): Show |
16 | HG01943.hp2 HG02074.hp1 HG02273.hp2 others(13): Show |
synonymous_variant | LOW | c.579A>G | p.Glu193Glu | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/13 | 838/3697 | 579/1818 | 193/605 | chr11 | 119372902 | |||
chr11:119373202 | C | T | 1 | a0001c0012 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.279G>A | p.Glu93Glu | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/13 | 538/3697 | 279/1818 | 93/605 | chr11 | 119373202 | |||
chr11:119373385 | C | T | 7 | a0001c0001 a0001c0004 a0002c0006 others(4): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
synonymous_variant | LOW | c.96G>A | p.Pro32Pro | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/13 | 355/3697 | 96/1818 | 32/605 | chr11 | 119373385 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:119355222 | T | G | 1 | a0001c0004t0011 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1613A>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 1613 | chr11 | 119355222 | ||||||
chr11:119355497 | T | G | 1 | a0001c0005t0030 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1338A>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 1338 | chr11 | 119355497 | ||||||
chr11:119355682 | C | G | 1 | a0001c0003t0026 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1153G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 1153 | chr11 | 119355682 | ||||||
chr11:119355683 | G | C | 1 | a0001c0003t0026 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1152C>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 1152 | chr11 | 119355683 | ||||||
chr11:119355722 | TA | T | 2 | a0001c0001t0028 a0001c0003t0026 |
2 | HG00741.hp1 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1112delT | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 1112 | chr11 | 119355722 | ||||||
chr11:119355973 | G | A | 1 | a0001c0001t0014 | 2 | NA19060.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*862C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 862 | chr11 | 119355973 | ||||||
chr11:119355975 | G | A | 1 | a0001c0001t0027 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*860C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 860 | chr11 | 119355975 | ||||||
chr11:119356047 | T | TA | 18 | a0001c0001t0001 a0001c0001t0027 a0001c0001t0035 others(15): Show |
76 | HG00323.hp1 HG00544.hp2 HG00642.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*787dupT | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 787 | chr11 | 119356047 | ||||||
chr11:119356047 | T | TAA | 9 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0034 others(6): Show |
61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*786_*787dupTT | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 787 | chr11 | 119356047 | ||||||
chr11:119356047 | T | TAAA | 5 | a0001c0001t0006 a0001c0001t0028 a0001c0003t0013 others(2): Show |
9 | HG00673.hp2 HG00735.hp1 HG00741.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*785_*787dupTTT | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 787 | chr11 | 119356047 | ||||||
chr11:119356047 | TA | T | 4 | a0001c0002t0005 a0001c0002t0007 a0001c0004t0005 others(1): Show |
9 | HG01167.hp2 HG01515.hp1 HG01975.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*787delT | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 787 | chr11 | 119356047 | ||||||
chr11:119356049 | A | T | 2 | a0001c0002t0007 a0001c0004t0007 |
4 | HG02451.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*786T>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 786 | chr11 | 119356049 | ||||||
chr11:119356061 | A | AC | 2 | a0001c0004t0008 a0001c0005t0008 |
4 | HG02647.hp1 HG02895.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*773_*774insG | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 773 | chr11 | 119356061 | ||||||
chr11:119356248 | C | A | 2 | a0001c0005t0015 a0001c0005t0030 |
3 | HG02970.hp1 HG03540.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*587G>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 587 | chr11 | 119356248 | ||||||
chr11:119356258 | T | A | 2 | a0001c0002t0031 a0001c0002t0033 |
2 | HG01884.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*577A>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 577 | chr11 | 119356258 | ||||||
chr11:119356431 | G | A | 14 | a0001c0002t0009 a0001c0002t0018 a0001c0002t0022 others(11): Show |
23 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*404C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 404 | chr11 | 119356431 | ||||||
chr11:119356443 | G | A | 1 | a0001c0005t0032 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*392C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 392 | chr11 | 119356443 | ||||||
chr11:119356459 | C | A | 1 | a0001c0002t0033 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*376G>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 376 | chr11 | 119356459 | ||||||
chr11:119356490 | C | G | 2 | a0001c0003t0024 a0001c0003t0025 |
2 | HG03453.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*345G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 345 | chr11 | 119356490 | ||||||
chr11:119356512 | G | A | 1 | a0001c0001t0034 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*323C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 323 | chr11 | 119356512 | ||||||
chr11:119356534 | C | G | 2 | a0001c0002t0022 a0001c0012t0023 |
2 | NA18522.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*301G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 301 | chr11 | 119356534 | ||||||
chr11:119356534 | C | T | 7 | a0001c0002t0007 a0001c0002t0009 a0001c0004t0004 others(4): Show |
17 | HG01891.hp2 HG02257.hp1 HG02273.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*301G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 301 | chr11 | 119356534 | ||||||
chr11:119356561 | G | A | 1 | a0001c0001t0035 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*274C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 274 | chr11 | 119356561 | ||||||
chr11:119356730 | CTT | C | 2 | a0001c0004t0008 a0001c0005t0008 |
4 | HG02647.hp1 HG02895.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*103_*104delAA | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 103 | chr11 | 119356730 | ||||||
chr11:119356744 | GTGT | G | 3 | a0001c0002t0009 a0001c0004t0020 a0001c0005t0009 |
5 | HG02273.hp2 NA19011.hp1 NA19056.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*88_*90delACA | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 88 | chr11 | 119356744 | ||||||
chr11:119356763 | G | A | 1 | a0001c0003t0036 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*72C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 13/13 | 72 | chr11 | 119356763 | ||||||
chr11:119381479 | C | G | 1 | a0001c0004t0020 | 1 | NA19056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-48G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/13 | 7999 | chr11 | 119381479 | ||||||
chr11:119381489 | T | G | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(50): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
5_prime_UTR_variant | MODIFIER | c.-58A>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/13 | 8009 | chr11 | 119381489 | ||||||
chr11:119381623 | C | T | 2 | a0001c0002t0017 a0001c0002t0018 |
2 | HG02965.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-192G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/13 | 8143 | chr11 | 119381623 | ||||||
chr11:119381675 | C | T | 1 | a0006c0013t0016 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-244G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/13 | 8195 | chr11 | 119381675 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:119356964 | G | C | 2 | a0001c0002t0031g0065 a0001c0002t0033g0066 |
2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1731-42C>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 12/12 | chr11 | 119356964 | |||||||
chr11:119357077 | G | A | 2 | a0001c0002t0031g0065 a0001c0002t0033g0066 |
2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1730+110C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 12/12 | chr11 | 119357077 | |||||||
chr11:119357100 | A | AG | 6 | a0001c0001t0002g0103 a0001c0001t0002g0114 a0001c0002t0018g0022 others(3): Show |
6 | HG00140.hp1 HG00544.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1730+86dupC | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 12/12 | chr11 | 119357100 | |||||||
chr11:119357133 | G | C | 2 | a0001c0002t0018g0022 a0001c0004t0029g0119 |
2 | HG03704.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1730+54C>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 12/12 | chr11 | 119357133 | |||||||
chr11:119357134 | G | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(103): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1730+53C>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 12/12 | chr11 | 119357134 | |||||||
chr11:119357469 | T | G | 1 | a0001c0004t0029g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1609+14A>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 11/12 | chr11 | 119357469 | |||||||
chr11:119357837 | TGA | T | 9 | a0001c0001t0002g0078 a0001c0001t0002g0086 a0001c0001t0002g0087 others(6): Show |
9 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1423-4_1423-3delTC | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 9/12 | chr11 | 119357837 | |||||||
chr11:119357916 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1422+65C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 9/12 | chr11 | 119357916 | |||||||
chr11:119357952 | G | C | 1 | a0001c0001t0002g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1422+29C>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 9/12 | chr11 | 119357952 | |||||||
chr11:119358124 | C | T | 1 | a0001c0005t0032g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1341+25G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 8/12 | chr11 | 119358124 | |||||||
chr11:119358129 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1341+20G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 8/12 | chr11 | 119358129 | |||||||
chr11:119358298 | C | T | 6 | a0001c0002t0007g0033 a0001c0002t0007g0034 a0001c0002t0007g0035 others(3): Show |
6 | HG02451.hp1 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1238-46G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 7/12 | chr11 | 119358298 | |||||||
chr11:119358323 | AT | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(124): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1238-72delA | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 7/12 | chr11 | 119358323 | |||||||
chr11:119358461 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1238-209C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 7/12 | chr11 | 119358461 | |||||||
chr11:119358648 | T | C | 1 | a0001c0003t0013g0024 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1237+125A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 7/12 | chr11 | 119358648 | |||||||
chr11:119358651 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1237+122G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 7/12 | chr11 | 119358651 | |||||||
chr11:119358664 | T | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(127): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1237+109A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 7/12 | chr11 | 119358664 | |||||||
chr11:119358863 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1173-26A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 6/12 | chr11 | 119358863 | |||||||
chr11:119358886 | T | A | 1 | a0001c0004t0003g0109 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1173-49A>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 6/12 | chr11 | 119358886 | |||||||
chr11:119359694 | C | T | 1 | a0001c0001t0003g0084 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.826-34G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 3/12 | chr11 | 119359694 | |||||||
chr11:119359784 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.826-124T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 3/12 | chr11 | 119359784 | |||||||
chr11:119359847 | T | C | 4 | a0001c0004t0004g0003 a0001c0004t0004g0075 a0001c0004t0004g0134 others(1): Show |
8 | HG01891.hp2 HG02257.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.826-187A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 3/12 | chr11 | 119359847 | |||||||
chr11:119359928 | G | A | 4 | a0001c0004t0004g0003 a0001c0004t0004g0075 a0001c0004t0004g0134 others(1): Show |
8 | HG01891.hp2 HG02257.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.825+256C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 3/12 | chr11 | 119359928 | |||||||
chr11:119359936 | T | C | 1 | a0001c0001t0002g0144 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.825+248A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 3/12 | chr11 | 119359936 | |||||||
chr11:119360156 | G | A | 1 | a0001c0003t0001g0062 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.825+28C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 3/12 | chr11 | 119360156 | |||||||
chr11:119360248 | A | G | 1 | a0001c0005t0032g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.775-14T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119360248 | |||||||
chr11:119360412 | ATTTTC | A | 4 | a0001c0002t0009g0054 a0001c0004t0020g0032 a0001c0005t0003g0158 others(1): Show |
6 | HG02273.hp2 NA19010.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-183_775-179del others(5): Show |
USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119360412 | |||||||
chr11:119360427 | CT | C | 10 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0006g0108 others(7): Show |
10 | HG00323.hp1 HG00741.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.775-194delA | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119360427 | |||||||
chr11:119360624 | C | A | 1 | a0005c0008t0003g0079 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.775-390G>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119360624 | |||||||
chr11:119360875 | T | C | 2 | a0001c0002t0031g0065 a0001c0002t0033g0066 |
2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.775-641A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119360875 | |||||||
chr11:119360886 | C | G | 2 | a0001c0001t0003g0073 a0001c0003t0010g0028 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.775-652G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119360886 | |||||||
chr11:119360957 | A | G | 47 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.775-723T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119360957 | |||||||
chr11:119361154 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0035g0102 |
2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.775-920G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119361154 | |||||||
chr11:119361271 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0002g0099 |
2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.775-1037G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119361271 | |||||||
chr11:119361313 | C | G | 1 | a0001c0002t0007g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.775-1079G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119361313 | |||||||
chr11:119361589 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.775-1355T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119361589 | |||||||
chr11:119361611 | G | C | 3 | a0001c0002t0022g0053 a0001c0003t0024g0043 a0001c0003t0025g0044 |
3 | HG03453.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.775-1377C>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119361611 | |||||||
chr11:119361973 | A | G | 1 | a0001c0005t0015g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.775-1739T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119361973 | |||||||
chr11:119361988 | C | T | 4 | a0001c0002t0007g0033 a0001c0002t0007g0034 a0001c0002t0007g0035 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-1754G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119361988 | |||||||
chr11:119361989 | G | A | 4 | a0001c0004t0004g0003 a0001c0004t0004g0075 a0001c0004t0004g0134 others(1): Show |
8 | HG01891.hp2 HG02257.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-1755C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119361989 | |||||||
chr11:119362021 | A | C | 2 | a0001c0002t0001g0064 a0001c0002t0017g0023 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.775-1787T>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119362021 | |||||||
chr11:119362151 | C | T | 1 | a0001c0004t0020g0032 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.775-1917G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119362151 | |||||||
chr11:119362203 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(132): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.775-1969T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119362203 | |||||||
chr11:119362400 | G | A | 37 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0001t0002g0001 others(34): Show |
53 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.775-2166C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119362400 | |||||||
chr11:119362668 | C | G | 3 | a0001c0002t0022g0053 a0001c0003t0024g0043 a0001c0003t0025g0044 |
3 | HG03453.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.775-2434G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119362668 | |||||||
chr11:119362669 | A | G | 3 | a0001c0002t0022g0053 a0001c0003t0024g0043 a0001c0003t0025g0044 |
3 | HG03453.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.775-2435T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119362669 | |||||||
chr11:119362843 | CA | C | 4 | a0001c0002t0007g0033 a0001c0002t0007g0034 a0001c0002t0007g0035 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-2610delT | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119362843 | |||||||
chr11:119363046 | G | A | 3 | a0001c0001t0003g0073 a0001c0003t0010g0028 a0001c0003t0010g0029 |
3 | HG02258.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.775-2812C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119363046 | |||||||
chr11:119363509 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.775-3275G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119363509 | |||||||
chr11:119363625 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.775-3391C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119363625 | |||||||
chr11:119363633 | G | A | 1 | a0001c0004t0005g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.775-3399C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119363633 | |||||||
chr11:119363954 | G | C | 1 | a0001c0001t0002g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.775-3720C>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119363954 | |||||||
chr11:119363960 | G | A | 1 | a0001c0005t0032g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.775-3726C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119363960 | |||||||
chr11:119364122 | G | A | 3 | a0001c0002t0022g0053 a0001c0003t0024g0043 a0001c0003t0025g0044 |
3 | HG03453.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.775-3888C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119364122 | |||||||
chr11:119364204 | C | T | 1 | a0001c0001t0002g0099 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.775-3970G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119364204 | |||||||
chr11:119364234 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.775-4000G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119364234 | |||||||
chr11:119364283 | T | C | 1 | a0001c0002t0003g0058 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.775-4049A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119364283 | |||||||
chr11:119364338 | C | G | 1 | a0001c0001t0002g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.775-4104G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119364338 | |||||||
chr11:119364486 | T | C | 2 | a0001c0005t0001g0160 a0001c0005t0003g0158 |
2 | HG02074.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.775-4252A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119364486 | |||||||
chr11:119364686 | G | A | 1 | a0001c0004t0011g0072 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.775-4452C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119364686 | |||||||
chr11:119364694 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(99): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.775-4460G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119364694 | |||||||
chr11:119365250 | G | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0076 others(26): Show |
35 | HG00642.hp1 HG00642.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.775-5016C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365250 | |||||||
chr11:119365443 | TG | T | 3 | a0001c0004t0008g0150 a0001c0005t0008g0020 a0001c0005t0008g0152 |
4 | HG02647.hp1 HG02895.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-5210delC | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365443 | |||||||
chr11:119365482 | C | T | 45 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0117 others(42): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.775-5248G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365482 | |||||||
chr11:119365700 | T | A | 7 | a0001c0001t0001g0125 a0001c0001t0003g0073 a0001c0001t0027g0092 others(4): Show |
7 | HG01433.hp2 HG01496.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-5466A>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365700 | |||||||
chr11:119365786 | A | G | 3 | a0001c0005t0015g0154 a0001c0005t0015g0156 a0001c0005t0030g0153 |
3 | HG02970.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.775-5552T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365786 | |||||||
chr11:119365880 | C | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0076 others(26): Show |
35 | HG00642.hp1 HG00642.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.775-5646G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365880 | |||||||
chr11:119365893 | G | T | 4 | a0001c0002t0005g0036 a0001c0002t0031g0065 a0001c0002t0033g0066 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-5659C>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365893 | |||||||
chr11:119365894 | T | A | 4 | a0001c0002t0005g0036 a0001c0002t0031g0065 a0001c0002t0033g0066 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-5660A>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365894 | |||||||
chr11:119365897 | TG | T | 2 | a0001c0001t0001g0133 a0001c0003t0001g0046 |
2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.775-5664delC | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365897 | |||||||
chr11:119365898 | G | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0076 others(11): Show |
19 | HG00642.hp1 HG00642.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.775-5664C>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365898 | |||||||
chr11:119365898 | GT | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(95): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.775-5665delA | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365898 | |||||||
chr11:119365934 | G | A | 1 | a0001c0004t0020g0032 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.775-5700C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365934 | |||||||
chr11:119365957 | C | T | 4 | a0001c0002t0007g0033 a0001c0002t0007g0034 a0001c0002t0007g0035 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-5723G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365957 | |||||||
chr11:119365982 | C | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0076 others(26): Show |
35 | HG00642.hp1 HG00642.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.775-5748G>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365982 | |||||||
chr11:119365988 | G | A | 1 | a0001c0002t0003g0051 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.775-5754C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119365988 | |||||||
chr11:119366014 | C | T | 4 | a0001c0004t0004g0003 a0001c0004t0004g0075 a0001c0004t0004g0134 others(1): Show |
8 | HG01891.hp2 HG02257.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-5780G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119366014 | |||||||
chr11:119366041 | C | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0019 others(43): Show |
55 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.775-5807G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119366041 | |||||||
chr11:119366042 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0003t0001g0010 others(1): Show |
6 | HG00642.hp2 HG01891.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-5808C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119366042 | |||||||
chr11:119366084 | G | A | 43 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0117 others(40): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.775-5850C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119366084 | |||||||
chr11:119366143 | C | T | 4 | a0001c0002t0007g0033 a0001c0002t0007g0034 a0001c0002t0007g0035 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-5909G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119366143 | |||||||
chr11:119366507 | C | T | 132 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(129): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.774+6200G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119366507 | |||||||
chr11:119366647 | TAA | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0019 others(55): Show |
74 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.774+6058_774+6059d others(4): Show |
USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119366647 | |||||||
chr11:119366953 | G | C | 7 | a0001c0001t0002g0015 a0001c0004t0020g0032 a0001c0005t0001g0160 others(4): Show |
10 | HG02074.hp1 HG02273.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.774+5754C>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119366953 | |||||||
chr11:119367036 | C | T | 1 | a0001c0002t0003g0058 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.774+5671G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119367036 | |||||||
chr11:119367281 | A | C | 1 | a0001c0005t0032g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.774+5426T>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119367281 | |||||||
chr11:119367406 | C | T | 1 | a0001c0004t0003g0090 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.774+5301G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119367406 | |||||||
chr11:119367604 | C | T | 1 | a0001c0005t0032g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.774+5103G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119367604 | |||||||
chr11:119367671 | T | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(129): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.774+5036A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119367671 | |||||||
chr11:119367745 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(123): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.774+4962C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119367745 | |||||||
chr11:119367761 | C | T | 4 | a0001c0004t0004g0003 a0001c0004t0004g0075 a0001c0004t0004g0134 others(1): Show |
8 | HG01891.hp2 HG02257.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+4946G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119367761 | |||||||
chr11:119367941 | C | T | 4 | a0001c0002t0007g0033 a0001c0002t0007g0034 a0001c0002t0007g0035 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+4766G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119367941 | |||||||
chr11:119368048 | C | G | 1 | a0001c0004t0003g0112 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.774+4659G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119368048 | |||||||
chr11:119368181 | C | G | 2 | a0001c0005t0015g0154 a0001c0005t0030g0153 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.774+4526G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119368181 | |||||||
chr11:119368294 | C | A | 1 | a0001c0003t0013g0030 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.774+4413G>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119368294 | |||||||
chr11:119368361 | G | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0076 others(10): Show |
18 | HG00642.hp2 HG01167.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.774+4346C>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119368361 | |||||||
chr11:119368396 | G | A | 1 | a0001c0002t0003g0060 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+4311C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119368396 | |||||||
chr11:119368665 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(103): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.774+4042C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119368665 | |||||||
chr11:119368728 | A | G | 5 | a0001c0003t0001g0008 a0001c0003t0001g0046 a0001c0003t0001g0067 others(2): Show |
6 | HG00642.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+3979T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119368728 | |||||||
chr11:119368796 | AC | A | 3 | a0001c0004t0004g0003 a0001c0004t0004g0075 a0001c0004t0021g0135 |
7 | HG02257.hp1 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.774+3910delG | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119368796 | |||||||
chr11:119368967 | A | G | 4 | a0001c0002t0007g0033 a0001c0002t0017g0023 a0001c0002t0018g0022 others(1): Show |
4 | HG02965.hp2 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+3740T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119368967 | |||||||
chr11:119368979 | C | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(134): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.774+3728G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119368979 | |||||||
chr11:119369169 | T | G | 11 | a0001c0001t0001g0019 a0001c0001t0002g0137 a0001c0001t0002g0144 others(8): Show |
13 | HG00735.hp2 HG01258.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.774+3538A>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119369169 | |||||||
chr11:119369207 | G | C | 3 | a0001c0004t0004g0003 a0001c0004t0004g0134 a0001c0004t0021g0135 |
7 | HG01891.hp2 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.774+3500C>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119369207 | |||||||
chr11:119369212 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0037 others(47): Show |
57 | HG00544.hp2 HG00609.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.774+3495G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119369212 | |||||||
chr11:119369214 | T | G | 1 | a0001c0001t0006g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.774+3493A>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119369214 | |||||||
chr11:119369361 | A | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(138): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.774+3346T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119369361 | |||||||
chr11:119369503 | T | TA | 5 | a0001c0001t0002g0111 a0001c0002t0005g0036 a0001c0002t0031g0065 others(2): Show |
5 | HG00639.hp2 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+3203dupT | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119369503 | |||||||
chr11:119369698 | G | A | 1 | a0001c0012t0023g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.774+3009C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119369698 | |||||||
chr11:119369746 | A | G | 13 | a0001c0001t0002g0012 a0001c0001t0002g0078 a0001c0001t0002g0086 others(10): Show |
14 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(11): Show |
intron_variant | MODIFIER | c.774+2961T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119369746 | |||||||
chr11:119369894 | C | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0117 others(11): Show |
28 | HG00280.hp2 HG00544.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.774+2813G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119369894 | |||||||
chr11:119369914 | C | T | 31 | a0001c0002t0001g0056 a0001c0002t0001g0064 a0001c0002t0002g0057 others(28): Show |
36 | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.774+2793G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119369914 | |||||||
chr11:119369962 | T | C | 2 | a0001c0002t0007g0034 a0001c0002t0007g0035 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.774+2745A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119369962 | |||||||
chr11:119370047 | C | T | 36 | a0001c0002t0001g0056 a0001c0002t0001g0064 a0001c0002t0002g0057 others(33): Show |
42 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.774+2660G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119370047 | |||||||
chr11:119370099 | T | C | 75 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(72): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.774+2608A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119370099 | |||||||
chr11:119370115 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(144): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.774+2592A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119370115 | |||||||
chr11:119370129 | C | T | 1 | a0001c0002t0003g0051 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.774+2578G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119370129 | |||||||
chr11:119370449 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.774+2258T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119370449 | |||||||
chr11:119370539 | T | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.774+2168A>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119370539 | |||||||
chr11:119370582 | C | T | 1 | a0001c0003t0026g0132 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.774+2125G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119370582 | |||||||
chr11:119370608 | A | AAG | 146 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(143): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.774+2097_774+2098d others(4): Show |
USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119370608 | |||||||
chr11:119370658 | C | A | 1 | a0001c0001t0002g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.774+2049G>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119370658 | |||||||
chr11:119370742 | G | A | 5 | a0001c0003t0001g0008 a0001c0003t0001g0046 a0001c0003t0001g0048 others(2): Show |
6 | HG00642.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+1965C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119370742 | |||||||
chr11:119371033 | T | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.774+1674A>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119371033 | |||||||
chr11:119371090 | G | C | 1 | a0001c0001t0002g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.774+1617C>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119371090 | |||||||
chr11:119371464 | G | A | 3 | a0001c0004t0004g0003 a0001c0004t0004g0134 a0001c0004t0021g0135 |
7 | HG01891.hp2 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.774+1243C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119371464 | |||||||
chr11:119371567 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.774+1140A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119371567 | |||||||
chr11:119371699 | C | G | 1 | a0001c0001t0002g0081 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.774+1008G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119371699 | |||||||
chr11:119371846 | C | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(144): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.774+861G>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119371846 | |||||||
chr11:119372005 | C | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(144): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.774+702G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119372005 | |||||||
chr11:119372154 | A | G | 1 | a0001c0003t0013g0024 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.774+553T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119372154 | |||||||
chr11:119372439 | G | C | 2 | a0001c0001t0002g0129 a0001c0001t0006g0130 |
2 | HG00735.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.774+268C>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119372439 | |||||||
chr11:119372481 | C | T | 4 | a0001c0003t0001g0049 a0001c0003t0002g0009 a0001c0003t0002g0146 others(1): Show |
5 | HG00735.hp2 HG01258.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+226G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119372481 | |||||||
chr11:119372487 | C | T | 6 | a0001c0002t0001g0064 a0001c0002t0005g0036 a0001c0002t0031g0065 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.774+220G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 2/12 | chr11 | 119372487 | |||||||
chr11:119373566 | C | T | 1 | a0001c0005t0032g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-41-45G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119373566 | |||||||
chr11:119373670 | C | T | 5 | a0001c0003t0001g0008 a0001c0003t0001g0046 a0001c0003t0001g0048 others(2): Show |
6 | HG00642.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41-149G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119373670 | |||||||
chr11:119373810 | A | C | 1 | a0001c0005t0032g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-41-289T>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119373810 | |||||||
chr11:119373852 | C | T | 1 | a0001c0002t0005g0045 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-41-331G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119373852 | |||||||
chr11:119374058 | G | T | 1 | a0001c0003t0026g0132 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-41-537C>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119374058 | |||||||
chr11:119374249 | T | G | 1 | a0001c0001t0002g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-41-728A>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119374249 | |||||||
chr11:119374300 | T | A | 8 | a0001c0002t0001g0064 a0001c0002t0005g0036 a0001c0002t0017g0023 others(5): Show |
8 | HG01884.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-41-779A>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119374300 | |||||||
chr11:119374475 | A | G | 5 | a0001c0001t0002g0071 a0001c0001t0003g0073 a0001c0004t0008g0150 others(2): Show |
6 | HG02258.hp1 HG02258.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-954T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119374475 | |||||||
chr11:119374639 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-41-1118C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119374639 | |||||||
chr11:119374732 | C | G | 1 | a0004c0011t0001g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-41-1211G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119374732 | |||||||
chr11:119375256 | C | G | 1 | a0001c0001t0002g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-41-1735G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119375256 | |||||||
chr11:119375369 | G | A | 2 | a0001c0002t0017g0023 a0001c0002t0018g0022 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-41-1848C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119375369 | |||||||
chr11:119375476 | C | T | 2 | a0001c0003t0024g0043 a0001c0003t0025g0044 |
2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-41-1955G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119375476 | |||||||
chr11:119375498 | T | A | 1 | a0001c0002t0003g0063 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-41-1977A>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119375498 | |||||||
chr11:119375516 | G | T | 1 | a0001c0001t0002g0077 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-41-1995C>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119375516 | |||||||
chr11:119375572 | C | A | 4 | a0001c0005t0015g0154 a0001c0005t0015g0156 a0001c0005t0030g0153 others(1): Show |
4 | HG02630.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-2051G>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119375572 | |||||||
chr11:119375791 | C | T | 8 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0002g0071 others(5): Show |
9 | HG02257.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-41-2270G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119375791 | |||||||
chr11:119375857 | C | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-41-2336G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119375857 | |||||||
chr11:119375998 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(91): Show |
123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.-41-2477G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119375998 | |||||||
chr11:119376156 | TTCAC | T | 2 | a0001c0001t0002g0137 a0001c0004t0020g0032 |
2 | HG02523.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-41-2639_-41-2636d others(6): Show |
USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119376156 | |||||||
chr11:119376186 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-41-2665C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119376186 | |||||||
chr11:119376223 | C | A | 1 | a0001c0002t0007g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-41-2702G>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119376223 | |||||||
chr11:119376268 | A | G | 1 | a0001c0012t0023g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-41-2747T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119376268 | |||||||
chr11:119376272 | C | T | 2 | a0001c0005t0008g0020 a0001c0005t0008g0152 |
3 | HG02647.hp1 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-41-2751G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119376272 | |||||||
chr11:119376693 | C | T | 4 | a0001c0005t0001g0160 a0001c0005t0003g0158 a0001c0005t0009g0007 others(1): Show |
6 | HG01943.hp2 HG02074.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-3172G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119376693 | |||||||
chr11:119376861 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-41-3340C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119376861 | |||||||
chr11:119377182 | G | A | 1 | a0001c0004t0008g0150 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-41-3661C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119377182 | |||||||
chr11:119377289 | T | A | 1 | a0001c0005t0015g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-41-3768A>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119377289 | |||||||
chr11:119377610 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(127): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.-42+3863G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119377610 | |||||||
chr11:119377725 | C | T | 2 | a0001c0002t0007g0034 a0001c0002t0007g0035 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-42+3748G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119377725 | |||||||
chr11:119377906 | C | T | 4 | a0001c0005t0008g0020 a0001c0005t0008g0152 a0001c0012t0023g0151 others(1): Show |
5 | HG02647.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42+3567G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119377906 | |||||||
chr11:119377999 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-42+3474C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119377999 | |||||||
chr11:119378075 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0002g0070 |
2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-42+3398G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119378075 | |||||||
chr11:119378145 | T | C | 11 | a0001c0001t0001g0019 a0001c0001t0001g0140 a0001c0001t0002g0137 others(8): Show |
12 | HG01433.hp2 HG01496.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.-42+3328A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119378145 | |||||||
chr11:119378175 | G | A | 2 | a0001c0002t0017g0023 a0001c0002t0018g0022 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-42+3298C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119378175 | |||||||
chr11:119378177 | G | A | 2 | a0001c0002t0017g0023 a0001c0002t0018g0022 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-42+3296C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119378177 | |||||||
chr11:119378202 | A | C | 1 | a0001c0004t0020g0032 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-42+3271T>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119378202 | |||||||
chr11:119378235 | C | T | 1 | a0006c0013t0016g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-42+3238G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119378235 | |||||||
chr11:119378645 | A | G | 8 | a0001c0002t0001g0064 a0001c0002t0005g0036 a0001c0002t0017g0023 others(5): Show |
8 | HG01884.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-42+2828T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119378645 | |||||||
chr11:119378778 | A | G | 28 | a0001c0002t0001g0056 a0001c0002t0002g0057 a0001c0002t0003g0004 others(25): Show |
34 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-42+2695T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119378778 | |||||||
chr11:119378837 | A | G | 4 | a0001c0005t0008g0020 a0001c0005t0008g0152 a0001c0012t0023g0151 others(1): Show |
5 | HG02647.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42+2636T>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119378837 | |||||||
chr11:119379280 | G | A | 1 | a0001c0003t0002g0146 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-42+2193C>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119379280 | |||||||
chr11:119379350 | C | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-42+2123G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119379350 | |||||||
chr11:119379728 | T | A | 4 | a0001c0005t0001g0160 a0001c0005t0003g0158 a0001c0005t0009g0007 others(1): Show |
6 | HG01943.hp2 HG02074.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+1745A>T | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119379728 | |||||||
chr11:119379917 | C | CT | 7 | a0001c0005t0001g0160 a0001c0005t0009g0007 a0001c0005t0015g0154 others(4): Show |
9 | HG01943.hp2 HG02074.hp1 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.-42+1555dupA | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119379917 | |||||||
chr11:119379917 | C | CTT | 6 | a0001c0003t0001g0147 a0001c0003t0002g0148 a0001c0004t0020g0032 others(3): Show |
6 | HG00323.hp2 HG02976.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+1554_-42+1555d others(4): Show |
USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119379917 | |||||||
chr11:119379917 | C | CTTT | 129 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(126): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.-42+1553_-42+1555d others(5): Show |
USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119379917 | |||||||
chr11:119379917 | C | CTTTT | 7 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0002g0038 others(4): Show |
7 | HG00673.hp1 HG01106.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42+1552_-42+1555d others(6): Show |
USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119379917 | |||||||
chr11:119379917 | CTTTTTTT others(3): Show |
C | 1 | a0001c0004t0008g0150 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-42+1546_-42+1555d others(12): Show |
USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119379917 | |||||||
chr11:119379917 | CTTTTTTT others(4): Show |
C | 1 | a0001c0005t0032g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-42+1545_-42+1555d others(13): Show |
USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119379917 | |||||||
chr11:119380055 | C | T | 4 | a0001c0005t0008g0020 a0001c0005t0008g0152 a0001c0012t0023g0151 others(1): Show |
5 | HG02647.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42+1418G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119380055 | |||||||
chr11:119380142 | C | T | 2 | a0001c0002t0007g0034 a0001c0002t0007g0035 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-42+1331G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119380142 | |||||||
chr11:119380164 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-42+1309G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119380164 | |||||||
chr11:119380380 | A | T | 1 | a0001c0012t0023g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-42+1093T>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119380380 | |||||||
chr11:119380798 | C | G | 1 | a0001c0002t0007g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-42+675G>C | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119380798 | |||||||
chr11:119380868 | T | C | 4 | a0001c0005t0001g0160 a0001c0005t0003g0158 a0001c0005t0009g0007 others(1): Show |
6 | HG01943.hp2 HG02074.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+605A>G | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119380868 | |||||||
chr11:119381441 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-42+32G>A | USP2 | ENSG00000036672.16 | transcript | ENST00000260187.7 | protein_coding | 1/12 | chr11 | 119381441 |