Item | Value |
---|---|
geneid | 79400 |
ensemblid | ENSG00000255346.11 |
hgncid | 14874 |
symbol | NOX5 |
name | NADPH oxidase 5 |
refseq_nuc | NM_024505.4 |
refseq_prot | NP_078781.3 |
ensembl_nuc | ENST00000388866.8 |
ensembl_prot | ENSP00000373518.3 |
mane_status | MANE Select |
chr | chr15 |
start | 69014695 |
end | 69062762 |
strand | + |
ver | v1.2 |
region | chr15:69014695-69062762 |
region5000 | chr15:69009695-69067762 |
regionname0 | NOX5_chr15_69014695_69062762 |
regionname5000 | NOX5_chr15_69009695_69067762 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 765 | 225 | 51 | 30 | 109 | 6 | 28 | 89 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0002 | 0/1 | 765 | 71 | 11 | 18 | 21 | 8 | 12 | 12 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0003 | 0/0 | 765 | 60 | 9 | 4 | 46 | 0 | 1 | 36 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0004 | 0/0 | 765 | 13 | 0 | 5 | 7 | 0 | 1 | 3 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0005 | 0/0 | 299 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(294): Show |
chr15 | 69009695 | 69067762 |
a0006 | 0/0 | 765 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0007 | 0/0 | 765 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0008 | 0/0 | 765 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0009 | 0/0 | 299 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(294): Show |
chr15 | 69009695 | 69067762 |
a0010 | 0/0 | 765 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0011 | 0/0 | 765 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0012 | 0/0 | 765 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0013 | 0/0 | 765 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0014 | 0/0 | 765 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
a0015 | 0/0 | 765 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | MNTSG others(760): Show |
chr15 | 69009695 | 69067762 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2295 | 158 | 29 | 28 | 70 | 6 | 25 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0001c0003 | 1/0 | 2295 | 66 | 22 | 1 | 39 | 0 | 3 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0001c0016 | 0/0 | 2295 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0002c0002 | 0/1 | 2295 | 70 | 11 | 17 | 21 | 8 | 12 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0002c0018 | 0/0 | 2295 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0003c0004 | 0/0 | 2295 | 56 | 9 | 4 | 42 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0003c0009 | 0/0 | 2295 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0003c0013 | 0/0 | 2295 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0004c0005 | 0/0 | 2295 | 13 | 0 | 5 | 7 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0005c0006 | 0/0 | 2295 | 5 | 5 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0005c0008 | 0/0 | 2295 | 4 | 4 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0006c0007 | 0/0 | 2295 | 5 | 0 | 0 | 5 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0007c0014 | 0/0 | 2295 | 2 | 0 | 2 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0008c0011 | 0/0 | 2295 | 2 | 2 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0009c0010 | 0/0 | 2295 | 2 | 2 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0010c0012 | 0/0 | 2295 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0011c0017 | 0/0 | 2295 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0012c0019 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0013c0015 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0014c0021 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 | ||
a0015c0020 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | ATGAA others(2290): Show |
chr15 | 69009695 | 69067762 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8406 | 52 | 10 | 12 | 18 | 2 | 10 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0002 | 0/0 | 8406 | 84 | 11 | 15 | 45 | 3 | 10 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0009 | 0/0 | 8406 | 4 | 4 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0011 | 0/0 | 8406 | 3 | 0 | 0 | 3 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0012 | 0/0 | 8406 | 2 | 0 | 1 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0013 | 0/0 | 8406 | 2 | 0 | 0 | 0 | 0 | 2 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0022 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0027 | 0/0 | 8406 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0030 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0031 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0032 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0033 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0034 | 0/0 | 8406 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0035 | 0/0 | 8406 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0036 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0037 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0001t0038 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0003t0001 | 0/0 | 8406 | 50 | 12 | 0 | 35 | 0 | 3 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0003t0002 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0003t0005 | 1/0 | 8405 | 10 | 8 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8400): Show |
chr15 | 69009695 | 69067762 |
a0001c0003t0014 | 0/0 | 8406 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0003t0018 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0003t0019 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0003t0024 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0001c0016t0001 | 0/0 | 8406 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0002c0002t0001 | 0/0 | 8406 | 58 | 11 | 16 | 15 | 5 | 11 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0002c0002t0007 | 0/0 | 8406 | 3 | 0 | 1 | 0 | 1 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0002c0002t0010 | 0/0 | 8406 | 3 | 0 | 0 | 3 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0002c0002t0015 | 0/0 | 8406 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0002c0002t0016 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0002c0002t0020 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0002c0002t0021 | 0/1 | 8406 | 1 | 0 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0002c0002t0023 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0002c0002t0029 | 0/0 | 8406 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0002c0018t0007 | 0/0 | 8406 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0003c0004t0003 | 0/0 | 8406 | 45 | 9 | 4 | 31 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0003c0004t0004 | 0/0 | 8406 | 11 | 0 | 0 | 11 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0003c0009t0003 | 0/0 | 8406 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0003c0013t0003 | 0/0 | 8406 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0004c0005t0001 | 0/0 | 8406 | 12 | 0 | 4 | 7 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0004c0005t0025 | 0/0 | 8406 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0005c0006t0006 | 0/0 | 8405 | 4 | 4 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8400): Show |
chr15 | 69009695 | 69067762 |
a0005c0006t0028 | 0/0 | 8405 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8400): Show |
chr15 | 69009695 | 69067762 |
a0005c0008t0006 | 0/0 | 8405 | 3 | 3 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8400): Show |
chr15 | 69009695 | 69067762 |
a0005c0008t0017 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0006c0007t0008 | 0/0 | 8406 | 4 | 0 | 0 | 4 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0006c0007t0026 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0007c0014t0002 | 0/0 | 8406 | 2 | 0 | 2 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0008c0011t0002 | 0/0 | 8406 | 2 | 2 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0009c0010t0006 | 0/0 | 8405 | 2 | 2 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8400): Show |
chr15 | 69009695 | 69067762 |
a0010c0012t0001 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0010c0012t0002 | 0/0 | 8406 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0011c0017t0001 | 0/0 | 8406 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0012c0019t0001 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0013c0015t0039 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCTG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0014c0021t0001 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
a0015c0020t0001 | 0/0 | 8406 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | AGCAG others(8401): Show |
chr15 | 69009695 | 69067762 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0009g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0011g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0011g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0011g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0012g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0012g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0013g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0013g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0022g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0027g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0030g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0031g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0032g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0033g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0034g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0035g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0036g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0037g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0001t0038g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0005g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0005g0228 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0014g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0014g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0018g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0003t0024g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0001c0016t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0004 | 0/0 | 6 | 1 | 2 | 0 | 1 | 2 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0009 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0007g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0007g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0007g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0010g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0015g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0016g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0020g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0021g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0023g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0002t0029g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0002c0018t0007g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0004t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0009t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0009t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0013t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0003c0013t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0004c0005t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0004c0005t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0004c0005t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0004c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0004c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0004c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0004c0005t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0004c0005t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0004c0005t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0004c0005t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0004c0005t0025g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0005c0006t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0005c0006t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0005c0006t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0005c0006t0006g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0005c0006t0028g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0005c0008t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0005c0008t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0005c0008t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0005c0008t0017g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0006c0007t0008g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0006c0007t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0006c0007t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0006c0007t0026g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0007c0014t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0007c0014t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0008c0011t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0008c0011t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0009c0010t0006g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0010c0012t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0010c0012t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0011c0017t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0012c0019t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0013c0015t0039g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0014c0021t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
a0015c0020t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0012 | g0027 | EUR | GBR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0195 | EUR | GBR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | GBR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0152 | EUR | FIN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | FIN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00323 | hp1 | a0002 | c0002 | t0007 | g0215 | EUR | FIN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00323 | hp2 | a0002 | c0002 | t0015 | g0226 | EUR | FIN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00408 | hp1 | a0003 | c0004 | t0003 | g0136 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00423 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00423 | hp2 | a0002 | c0002 | t0020 | g0198 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00438 | hp2 | a0003 | c0004 | t0003 | g0133 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00544 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00597 | hp2 | a0006 | c0007 | t0008 | g0049 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00609 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00621 | hp1 | a0003 | c0004 | t0003 | g0001 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00673 | hp1 | a0004 | c0005 | t0001 | g0038 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | CHS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0206 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0207 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01167 | hp1 | a0003 | c0004 | t0003 | g0135 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01167 | hp2 | a0007 | c0014 | t0002 | g0040 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01169 | hp2 | a0007 | c0014 | t0002 | g0251 | AMR | PUR | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01255 | hp2 | a0001 | c0001 | t0012 | g0222 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01256 | hp1 | a0011 | c0017 | t0001 | g0106 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01346 | hp1 | a0002 | c0018 | t0007 | g0008 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0197 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01361 | hp2 | a0003 | c0004 | t0003 | g0001 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01496 | hp2 | a0001 | c0003 | t0005 | g0014 | AMR | CLM | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01515 | hp2 | a0002 | c0002 | t0029 | g0008 | EUR | IBS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0183 | EUR | IBS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0203 | EUR | IBS | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01884 | hp2 | a0001 | c0003 | t0005 | g0292 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01891 | hp1 | a0008 | c0011 | t0002 | g0302 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01934 | hp1 | a0004 | c0005 | t0001 | g0278 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01934 | hp2 | a0003 | c0004 | t0003 | g0121 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01943 | hp1 | a0004 | c0005 | t0001 | g0044 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01952 | hp1 | a0004 | c0005 | t0001 | g0074 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01978 | hp1 | a0001 | c0016 | t0001 | g0259 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01978 | hp2 | a0002 | c0002 | t0007 | g0196 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01981 | hp1 | a0004 | c0005 | t0025 | g0277 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02015 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02027 | hp1 | a0002 | c0002 | t0010 | g0033 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0067 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02040 | hp1 | a0004 | c0005 | t0001 | g0246 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0214 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02055 | hp2 | a0003 | c0004 | t0003 | g0115 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02071 | hp2 | a0001 | c0001 | t0033 | g0252 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02074 | hp1 | a0003 | c0004 | t0003 | g0125 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02074 | hp2 | a0002 | c0002 | t0010 | g0033 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02080 | hp1 | a0004 | c0005 | t0001 | g0276 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02083 | hp1 | a0003 | c0004 | t0004 | g0112 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02132 | hp1 | a0003 | c0013 | t0003 | g0001 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02132 | hp2 | a0002 | c0002 | t0010 | g0031 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02145 | hp1 | a0001 | c0003 | t0005 | g0014 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02145 | hp2 | a0003 | c0004 | t0003 | g0098 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02148 | hp1 | a0004 | c0005 | t0001 | g0044 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02148 | hp2 | a0003 | c0004 | t0003 | g0005 | AMR | PEL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | CDX | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02155 | hp2 | a0001 | c0001 | t0011 | g0232 | EAS | CDX | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02257 | hp1 | a0005 | c0008 | t0017 | g0085 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02257 | hp2 | a0012 | c0019 | t0001 | g0247 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0188 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02280 | hp1 | a0005 | c0008 | t0006 | g0300 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02280 | hp2 | a0005 | c0006 | t0006 | g0298 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02451 | hp1 | a0003 | c0004 | t0003 | g0054 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02451 | hp2 | a0001 | c0001 | t0009 | g0219 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02523 | hp1 | a0003 | c0004 | t0003 | g0077 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02622 | hp1 | a0005 | c0006 | t0006 | g0299 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02622 | hp2 | a0013 | c0015 | t0039 | g0107 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02647 | hp2 | a0009 | c0010 | t0006 | g0046 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0103 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02698 | hp2 | a0001 | c0001 | t0013 | g0154 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02717 | hp1 | a0001 | c0003 | t0024 | g0301 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02723 | hp1 | a0014 | c0021 | t0001 | g0264 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02723 | hp2 | a0001 | c0003 | t0005 | g0271 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02738 | hp1 | a0001 | c0001 | t0013 | g0184 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0056 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02809 | hp1 | a0003 | c0004 | t0003 | g0099 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02895 | hp1 | a0001 | c0003 | t0005 | g0272 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02896 | hp1 | a0005 | c0006 | t0006 | g0295 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02922 | hp1 | a0001 | c0003 | t0005 | g0273 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02965 | hp1 | a0001 | c0001 | t0036 | g0160 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0036 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0084 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02970 | hp2 | a0005 | c0008 | t0006 | g0294 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0128 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0052 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03139 | hp2 | a0005 | c0008 | t0006 | g0293 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03195 | hp1 | a0015 | c0020 | t0001 | g0053 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0208 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03209 | hp1 | a0005 | c0006 | t0028 | g0297 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03209 | hp2 | a0008 | c0011 | t0002 | g0303 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0216 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0201 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03453 | hp1 | a0003 | c0004 | t0003 | g0124 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03453 | hp2 | a0001 | c0001 | t0022 | g0266 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03486 | hp2 | a0003 | c0004 | t0003 | g0100 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03490 | hp2 | a0001 | c0001 | t0034 | g0040 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03491 | hp2 | a0001 | c0001 | t0027 | g0290 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0034 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | ESN | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | GWD | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03579 | hp1 | a0001 | c0001 | t0032 | g0217 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03669 | hp1 | a0001 | c0001 | t0035 | g0168 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03669 | hp2 | a0004 | c0005 | t0001 | g0038 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | STU | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03704 | hp2 | a0001 | c0003 | t0001 | g0070 | SAS | PJL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | BEB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0205 | SAS | BEB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | BEB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0193 | SAS | STU | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG04115 | hp2 | a0002 | c0002 | t0007 | g0089 | SAS | STU | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | BEB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | STU | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | STU | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | STU | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0066 | SAS | STU | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18522 | hp1 | a0001 | c0003 | t0005 | g0229 | AFR | YRI | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | YRI | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | CHB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18612 | hp2 | a0003 | c0004 | t0003 | g0117 | EAS | CHB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18747 | hp1 | a0004 | c0005 | t0001 | g0245 | EAS | CHB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18747 | hp2 | a0001 | c0003 | t0002 | g0017 | EAS | CHB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18906 | hp1 | a0003 | c0004 | t0003 | g0114 | AFR | YRI | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18906 | hp2 | a0001 | c0001 | t0037 | g0289 | AFR | YRI | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18939 | hp2 | a0004 | c0005 | t0001 | g0274 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0307 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18943 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18944 | hp2 | a0003 | c0004 | t0003 | g0001 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18945 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18945 | hp2 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18951 | hp1 | a0001 | c0003 | t0014 | g0048 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18951 | hp2 | a0001 | c0003 | t0001 | g0058 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18952 | hp1 | a0003 | c0004 | t0003 | g0001 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18952 | hp2 | a0001 | c0003 | t0001 | g0242 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18957 | hp1 | a0001 | c0001 | t0030 | g0029 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18957 | hp2 | a0003 | c0004 | t0003 | g0005 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18959 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18960 | hp2 | a0006 | c0007 | t0026 | g0308 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18963 | hp1 | a0003 | c0004 | t0003 | g0127 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18963 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18968 | hp1 | a0006 | c0007 | t0008 | g0306 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18970 | hp2 | a0003 | c0004 | t0003 | g0005 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18971 | hp1 | a0003 | c0004 | t0003 | g0123 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18972 | hp1 | a0006 | c0007 | t0008 | g0049 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18973 | hp2 | a0002 | c0002 | t0023 | g0031 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18975 | hp1 | a0001 | c0003 | t0001 | g0280 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18975 | hp2 | a0001 | c0001 | t0011 | g0231 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18977 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18978 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18980 | hp1 | a0010 | c0012 | t0002 | g0075 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18980 | hp2 | a0003 | c0004 | t0003 | g0022 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18985 | hp1 | a0003 | c0004 | t0003 | g0076 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18988 | hp1 | a0003 | c0004 | t0003 | g0005 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18989 | hp1 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18989 | hp2 | a0003 | c0004 | t0004 | g0090 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18991 | hp2 | a0003 | c0004 | t0003 | g0001 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18992 | hp1 | a0010 | c0012 | t0001 | g0158 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18992 | hp2 | a0003 | c0009 | t0003 | g0080 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0279 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18994 | hp2 | a0003 | c0004 | t0003 | g0001 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18997 | hp2 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18998 | hp1 | a0003 | c0004 | t0004 | g0132 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA18999 | hp2 | a0001 | c0003 | t0014 | g0057 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19000 | hp1 | a0003 | c0004 | t0004 | g0129 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19001 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19003 | hp1 | a0003 | c0004 | t0003 | g0122 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19004 | hp1 | a0002 | c0002 | t0016 | g0094 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19004 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19005 | hp2 | a0006 | c0007 | t0008 | g0138 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19007 | hp2 | a0001 | c0003 | t0001 | g0305 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19009 | hp2 | a0003 | c0004 | t0003 | g0001 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19010 | hp2 | a0003 | c0004 | t0003 | g0119 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19011 | hp2 | a0003 | c0004 | t0004 | g0130 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0210 | AFR | LWK | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0189 | AFR | LWK | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19043 | hp1 | a0001 | c0003 | t0005 | g0014 | AFR | LWK | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19054 | hp1 | a0001 | c0001 | t0011 | g0233 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19054 | hp2 | a0003 | c0004 | t0004 | g0023 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19055 | hp1 | a0003 | c0004 | t0004 | g0091 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19057 | hp1 | a0003 | c0004 | t0004 | g0092 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19058 | hp2 | a0001 | c0003 | t0018 | g0071 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19060 | hp1 | a0003 | c0004 | t0003 | g0005 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19060 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19063 | hp1 | a0004 | c0005 | t0001 | g0275 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19063 | hp2 | a0003 | c0004 | t0003 | g0108 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19065 | hp1 | a0003 | c0013 | t0003 | g0003 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19065 | hp2 | a0001 | c0001 | t0038 | g0011 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19070 | hp1 | a0003 | c0004 | t0003 | g0116 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19070 | hp2 | a0001 | c0001 | t0031 | g0248 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19074 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19074 | hp2 | a0003 | c0004 | t0004 | g0023 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19075 | hp1 | a0001 | c0003 | t0001 | g0243 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19076 | hp2 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19077 | hp1 | a0001 | c0003 | t0001 | g0281 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19078 | hp1 | a0001 | c0003 | t0001 | g0059 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19078 | hp2 | a0004 | c0005 | t0001 | g0288 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19080 | hp2 | a0003 | c0004 | t0003 | g0118 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19081 | hp1 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19081 | hp2 | a0003 | c0004 | t0003 | g0134 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19082 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19084 | hp1 | a0003 | c0004 | t0004 | g0113 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19086 | hp2 | a0003 | c0009 | t0003 | g0081 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19088 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19088 | hp2 | a0003 | c0004 | t0003 | g0022 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0241 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19091 | hp2 | a0003 | c0004 | t0004 | g0131 | EAS | JPT | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA19240 | hp2 | a0003 | c0004 | t0003 | g0111 | AFR | YRI | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA20129 | hp1 | a0001 | c0003 | t0005 | g0291 | AFR | ASW | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0304 | AFR | ASW | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0181 | EUR | TSI | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | TSI | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA20905 | hp1 | a0003 | c0004 | t0003 | g0120 | SAS | GIH | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0202 | SAS | GIH | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02109 | hp1 | a0001 | c0003 | t0019 | g0051 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0220 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02486 | hp2 | a0003 | c0004 | t0003 | g0055 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0036 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
HG03471 | hp2 | a0005 | c0006 | t0006 | g0296 | AFR | MSL | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | USA | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA20300 | hp2 | a0009 | c0010 | t0006 | g0046 | AFR | USA | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0223 | AFR | LWK | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | LWK | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
homoSapiens | chm13v2 | a0002 | c0002 | t0021 | g0211 | REF | REF | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
homoSapiens | grch38p0 | a0001 | c0003 | t0005 | g0228 | REF | REF | NOX5_chr15_69009695_69067762 | NOX5 | chr15 | 69009695 | 69067762 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:69014764 | C | T | 1 | a0014 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.29C>T | p.Thr10Met | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/16 | 70/8405 | 29/2298 | 10/765 | chr15 | 69014764 | |||
chr15:69028323 | A | G | 1 | a0015 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.283A>G | p.Met95Val | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/16 | 324/8405 | 283/2298 | 95/765 | chr15 | 69028323 | |||
chr15:69028324 | T | A | 1 | a0013 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.284T>A | p.Met95Lys | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/16 | 325/8405 | 284/2298 | 95/765 | chr15 | 69028324 | |||
chr15:69028330 | A | T | 1 | a0012 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.290A>T | p.Lys97Ile | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/16 | 331/8405 | 290/2298 | 97/765 | chr15 | 69028330 | |||
chr15:69031619 | C | G | 1 | a0004 | 13 | HG00673.hp1 HG01934.hp1 HG01943.hp1 others(10): Show |
missense_variant | MODERATE | c.427C>G | p.Pro143Ala | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/16 | 468/8405 | 427/2298 | 143/765 | chr15 | 69031619 | |||
chr15:69033266 | A | C | 1 | a0006 | 5 | HG00597.hp2 NA18960.hp2 NA18968.hp1 others(2): Show |
missense_variant | MODERATE | c.844A>C | p.Ser282Arg | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/16 | 885/8405 | 844/2298 | 282/765 | chr15 | 69033266 | |||
chr15:69035387 | C | T | 1 | a0007 | 2 | HG01167.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.889C>T | p.Arg297Trp | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 6/16 | 930/8405 | 889/2298 | 297/765 | chr15 | 69035387 | |||
chr15:69035394 | C | T | 1 | a0009 | 2 | HG02647.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.896C>T | p.Thr299Met | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 6/16 | 937/8405 | 896/2298 | 299/765 | chr15 | 69035394 | |||
chr15:69035397 | G | A | 2 | a0005 a0009 |
11 | HG02257.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
stop_gained | HIGH | c.899G>A | p.Trp300* | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 6/16 | 940/8405 | 899/2298 | 300/765 | chr15 | 69035397 | |||
chr15:69035886 | C | T | 2 | a0002 a0011 |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
missense_variant | MODERATE | c.1138C>T | p.Leu380Phe | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/16 | 1179/8405 | 1138/2298 | 380/765 | chr15 | 69035886 | |||
chr15:69037148 | G | A | 1 | a0014 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1309G>A | p.Gly437Arg | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/16 | 1350/8405 | 1309/2298 | 437/765 | chr15 | 69037148 | |||
chr15:69042727 | G | T | 1 | a0010 | 2 | NA18980.hp1 NA18992.hp1 |
missense_variant | MODERATE | c.1569G>T | p.Lys523Asn | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/16 | 1610/8405 | 1569/2298 | 523/765 | chr15 | 69042727 | |||
chr15:69042747 | G | A | 1 | a0011 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.1589G>A | p.Arg530His | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/16 | 1630/8405 | 1589/2298 | 530/765 | chr15 | 69042747 | |||
chr15:69047447 | G | A | 2 | a0003 a0013 |
61 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
missense_variant | MODERATE | c.1727G>A | p.Arg576His | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 12/16 | 1768/8405 | 1727/2298 | 576/765 | chr15 | 69047447 | |||
chr15:69047843 | A | G | 1 | a0008 | 2 | HG01891.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.1831A>G | p.Lys611Glu | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/16 | 1872/8405 | 1831/2298 | 611/765 | chr15 | 69047843 | |||
chr15:69056673 | A | G | 1 | a0005 | 5 | HG02280.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.2275A>G | p.Arg759Gly | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 2316/8405 | 2275/2298 | 759/765 | chr15 | 69056673 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:69033241 | C | T | 13 | a0001c0001 a0001c0016 a0002c0002 others(10): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
synonymous_variant | LOW | c.819C>T | p.Cys273Cys | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/16 | 860/8405 | 819/2298 | 273/765 | chr15 | 69033241 | |||
chr15:69035485 | C | T | 14 | a0001c0001 a0001c0016 a0002c0002 others(11): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
synonymous_variant | LOW | c.987C>T | p.Thr329Thr | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 6/16 | 1028/8405 | 987/2298 | 329/765 | chr15 | 69035485 | |||
chr15:69035840 | C | T | 1 | a0003c0013 | 2 | HG02132.hp1 NA19065.hp1 |
synonymous_variant | LOW | c.1092C>T | p.His364His | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/16 | 1133/8405 | 1092/2298 | 364/765 | chr15 | 69035840 | |||
chr15:69048997 | C | T | 1 | a0001c0016 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.1938C>T | p.Phe646Phe | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/16 | 1979/8405 | 1938/2298 | 646/765 | chr15 | 69048997 | |||
chr15:69055335 | C | T | 1 | a0002c0018 | 1 | HG01346.hp1 | splice_region_variant&synonymous_variant | LOW | c.2001C>T | p.Gly667Gly | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 15/16 | 2042/8405 | 2001/2298 | 667/765 | chr15 | 69055335 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:69014698 | A | T | 1 | a0013c0015t0039 | 1 | HG02622.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/16 | chr15 | 69014698 | |||||||
chr15:69014708 | G | A | 1 | a0001c0001t0012 | 2 | HG00099.hp1 HG01255.hp2 |
5_prime_UTR_variant | MODIFIER | c.-28G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/16 | 28 | chr15 | 69014708 | ||||||
chr15:69056747 | T | C | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(52): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
3_prime_UTR_variant | MODIFIER | c.*51T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 51 | chr15 | 69056747 | ||||||
chr15:69056750 | A | G | 1 | a0001c0001t0038 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*54A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 54 | chr15 | 69056750 | ||||||
chr15:69056874 | C | G | 1 | a0001c0001t0011 | 3 | HG02155.hp2 NA18975.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*178C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 178 | chr15 | 69056874 | ||||||
chr15:69057146 | T | A | 3 | a0002c0002t0007 a0002c0002t0015 a0002c0018t0007 |
5 | HG00323.hp1 HG00323.hp2 HG01346.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*450T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 450 | chr15 | 69057146 | ||||||
chr15:69057256 | T | C | 1 | a0001c0001t0013 | 2 | HG02698.hp2 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*560T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 560 | chr15 | 69057256 | ||||||
chr15:69057521 | G | A | 1 | a0002c0002t0010 | 3 | HG02027.hp1 HG02074.hp2 HG02132.hp2 |
3_prime_UTR_variant | MODIFIER | c.*825G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 825 | chr15 | 69057521 | ||||||
chr15:69057536 | C | G | 1 | a0001c0001t0037 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*840C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 840 | chr15 | 69057536 | ||||||
chr15:69057554 | G | A | 1 | a0001c0003t0014 | 2 | NA18951.hp1 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*858G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 858 | chr15 | 69057554 | ||||||
chr15:69057576 | A | G | 1 | a0001c0001t0037 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*880A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 880 | chr15 | 69057576 | ||||||
chr15:69057733 | C | T | 5 | a0003c0004t0003 a0003c0004t0004 a0003c0009t0003 others(2): Show |
61 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1037C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 1037 | chr15 | 69057733 | ||||||
chr15:69057939 | G | T | 1 | a0001c0001t0036 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1243G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 1243 | chr15 | 69057939 | ||||||
chr15:69058135 | A | C | 15 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0013 others(12): Show |
102 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1439A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 1439 | chr15 | 69058135 | ||||||
chr15:69058310 | C | G | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(52): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
3_prime_UTR_variant | MODIFIER | c.*1614C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 1614 | chr15 | 69058310 | ||||||
chr15:69058371 | A | C | 1 | a0002c0002t0015 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1675A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 1675 | chr15 | 69058371 | ||||||
chr15:69058389 | G | A | 1 | a0002c0002t0016 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1693G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 1693 | chr15 | 69058389 | ||||||
chr15:69058449 | G | A | 1 | a0005c0008t0017 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1753G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 1753 | chr15 | 69058449 | ||||||
chr15:69058521 | G | A | 1 | a0001c0001t0030 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1825G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 1825 | chr15 | 69058521 | ||||||
chr15:69058562 | G | A | 1 | a0005c0008t0017 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1866G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 1866 | chr15 | 69058562 | ||||||
chr15:69058581 | C | T | 1 | a0002c0002t0029 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1885C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 1885 | chr15 | 69058581 | ||||||
chr15:69058588 | C | T | 1 | a0001c0001t0035 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1892C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 1892 | chr15 | 69058588 | ||||||
chr15:69058755 | A | G | 4 | a0005c0006t0006 a0005c0006t0028 a0005c0008t0006 others(1): Show |
10 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2059A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 2059 | chr15 | 69058755 | ||||||
chr15:69058918 | C | T | 1 | a0001c0001t0034 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2222C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 2222 | chr15 | 69058918 | ||||||
chr15:69058938 | A | G | 1 | a0001c0001t0027 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2242A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 2242 | chr15 | 69058938 | ||||||
chr15:69059249 | G | A | 1 | a0005c0008t0017 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2553G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 2553 | chr15 | 69059249 | ||||||
chr15:69059489 | G | A | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(52): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
3_prime_UTR_variant | MODIFIER | c.*2793G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 2793 | chr15 | 69059489 | ||||||
chr15:69059696 | A | G | 1 | a0006c0007t0026 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3000A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 3000 | chr15 | 69059696 | ||||||
chr15:69059732 | C | T | 1 | a0001c0001t0009 | 4 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3036C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 3036 | chr15 | 69059732 | ||||||
chr15:69059768 | T | C | 1 | a0001c0003t0018 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3072T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 3072 | chr15 | 69059768 | ||||||
chr15:69059822 | C | T | 1 | a0004c0005t0025 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3126C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 3126 | chr15 | 69059822 | ||||||
chr15:69059864 | C | CA | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(52): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
3_prime_UTR_variant | MODIFIER | c.*3170dupA | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 3171 | INFO_REALIGN_3_PRIME | chr15 | 69059864 | |||||
chr15:69059878 | G | A | 1 | a0005c0006t0028 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 3182 | chr15 | 69059878 | ||||||
chr15:69059911 | A | G | 1 | a0001c0003t0024 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3215A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 3215 | chr15 | 69059911 | ||||||
chr15:69059975 | C | G | 1 | a0002c0002t0023 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3279C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 3279 | chr15 | 69059975 | ||||||
chr15:69060216 | G | A | 2 | a0006c0007t0008 a0006c0007t0026 |
5 | HG00597.hp2 NA18960.hp2 NA18968.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3520G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 3520 | chr15 | 69060216 | ||||||
chr15:69060236 | G | A | 1 | a0005c0008t0017 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3540G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 3540 | chr15 | 69060236 | ||||||
chr15:69060565 | A | T | 1 | a0001c0001t0022 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3869A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 3869 | chr15 | 69060565 | ||||||
chr15:69060750 | C | G | 1 | a0001c0001t0009 | 4 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4054C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 4054 | chr15 | 69060750 | ||||||
chr15:69060990 | C | G | 1 | a0001c0001t0033 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4294C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 4294 | chr15 | 69060990 | ||||||
chr15:69061013 | T | A | 1 | a0001c0003t0019 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4317T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 4317 | chr15 | 69061013 | ||||||
chr15:69061103 | T | G | 1 | a0005c0008t0017 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4407T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 4407 | chr15 | 69061103 | ||||||
chr15:69061124 | G | A | 4 | a0005c0006t0006 a0005c0006t0028 a0005c0008t0006 others(1): Show |
10 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4428G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 4428 | chr15 | 69061124 | ||||||
chr15:69061471 | A | G | 1 | a0003c0004t0004 | 11 | HG02083.hp1 NA18989.hp2 NA18998.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4775A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 4775 | chr15 | 69061471 | ||||||
chr15:69061567 | T | A | 1 | a0002c0002t0020 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4871T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 4871 | chr15 | 69061567 | ||||||
chr15:69061768 | G | A | 1 | a0001c0003t0024 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5072G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 5072 | chr15 | 69061768 | ||||||
chr15:69061815 | C | A | 1 | a0005c0008t0017 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5119C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 5119 | chr15 | 69061815 | ||||||
chr15:69061893 | G | A | 1 | a0001c0001t0031 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5197G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 5197 | chr15 | 69061893 | ||||||
chr15:69062213 | G | C | 1 | a0001c0001t0032 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5517G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 5517 | chr15 | 69062213 | ||||||
chr15:69062452 | CA | C | 4 | a0005c0006t0006 a0005c0006t0028 a0005c0008t0006 others(1): Show |
10 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5758delA | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 5758 | INFO_REALIGN_3_PRIME | chr15 | 69062452 | |||||
chr15:69062453 | A | C | 50 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(47): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
3_prime_UTR_variant | MODIFIER | c.*5757A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 5757 | chr15 | 69062453 | ||||||
chr15:69062453 | A | G | 2 | a0001c0001t0002 a0001c0001t0031 |
4 | NA18941.hp1 NA18970.hp1 NA18994.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5757A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 5757 | chr15 | 69062453 | ||||||
chr15:69062649 | T | C | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(52): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
3_prime_UTR_variant | MODIFIER | c.*5953T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 16/16 | 5953 | chr15 | 69062649 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:69014896 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.50+111G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69014896 | |||||||
chr15:69014952 | G | A | 3 | a0001c0003t0001g0052 a0001c0003t0019g0051 a0015c0020t0001g0053 |
3 | HG02109.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.50+167G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69014952 | |||||||
chr15:69014953 | T | C | 1 | a0003c0004t0003g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50+168T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69014953 | |||||||
chr15:69015105 | A | T | 8 | a0001c0001t0001g0309 a0001c0003t0001g0048 a0001c0003t0001g0305 others(5): Show |
9 | HG00438.hp1 HG00597.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.50+320A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015105 | |||||||
chr15:69015183 | C | A | 1 | a0003c0004t0003g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.50+398C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015183 | |||||||
chr15:69015183 | C | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0003t0001g0304 others(12): Show |
19 | HG01069.hp2 HG01891.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.50+398C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015183 | |||||||
chr15:69015425 | G | A | 34 | a0001c0001t0001g0019 a0001c0001t0002g0082 a0001c0003t0001g0002 others(31): Show |
44 | HG00544.hp1 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.50+640G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015425 | |||||||
chr15:69015699 | AC | A | 3 | a0005c0008t0006g0293 a0005c0008t0006g0294 a0009c0010t0006g0046 |
4 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.50+916delC | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69015699 | ||||||
chr15:69015733 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.50+948G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015733 | |||||||
chr15:69015734 | T | C | 65 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0047 others(62): Show |
82 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.50+949T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015734 | |||||||
chr15:69015739 | G | A | 8 | a0001c0001t0001g0309 a0001c0003t0001g0048 a0001c0003t0001g0305 others(5): Show |
9 | HG00438.hp1 HG00597.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.50+954G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015739 | |||||||
chr15:69015784 | T | C | 240 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0024 others(237): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.50+999T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015784 | |||||||
chr15:69015798 | G | C | 1 | a0002c0002t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.50+1013G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015798 | |||||||
chr15:69015870 | C | T | 1 | a0005c0008t0017g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.50+1085C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015870 | |||||||
chr15:69015883 | C | G | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.50+1098C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015883 | |||||||
chr15:69015942 | G | T | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.50+1157G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015942 | |||||||
chr15:69015953 | A | G | 317 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(314): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.50+1168A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69015953 | |||||||
chr15:69016110 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0008c0011t0002g0302 others(1): Show |
7 | HG01069.hp2 HG01891.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.50+1325A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69016110 | |||||||
chr15:69016426 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.50+1641T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69016426 | |||||||
chr15:69016433 | G | A | 3 | a0001c0001t0011g0231 a0001c0001t0011g0232 a0001c0001t0011g0233 |
3 | HG02155.hp2 NA18975.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.50+1648G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69016433 | |||||||
chr15:69016447 | C | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0008c0011t0002g0302 others(1): Show |
7 | HG01069.hp2 HG01891.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.50+1662C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69016447 | |||||||
chr15:69016502 | C | T | 1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.50+1717C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69016502 | |||||||
chr15:69016545 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.50+1760C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69016545 | |||||||
chr15:69016735 | A | C | 1 | a0002c0002t0015g0226 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.50+1950A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69016735 | |||||||
chr15:69016797 | CATAT | C | 57 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0047 others(54): Show |
73 | HG00544.hp1 HG00609.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.50+2022_50+2025del others(4): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69016797 | ||||||
chr15:69016809 | T | C | 2 | a0002c0002t0001g0087 a0002c0002t0001g0088 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.50+2024T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69016809 | |||||||
chr15:69017059 | G | A | 1 | a0002c0002t0007g0089 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.50+2274G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69017059 | |||||||
chr15:69017137 | G | GTATT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0047 others(3): Show |
11 | HG01069.hp2 HG01261.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.50+2378_50+2381dup others(4): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69017137 | ||||||
chr15:69017137 | G | GTATTTAT others(1): Show |
6 | a0002c0002t0001g0095 a0002c0002t0001g0096 a0002c0002t0001g0097 others(3): Show |
6 | HG00544.hp2 HG01891.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.50+2374_50+2381dup others(8): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69017137 | ||||||
chr15:69017137 | G | GTATTTAT others(5): Show |
2 | a0001c0003t0019g0051 a0002c0002t0001g0093 |
2 | HG02109.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.50+2370_50+2381dup others(12): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69017137 | ||||||
chr15:69017144 | T | C | 3 | a0003c0004t0004g0090 a0003c0004t0004g0091 a0003c0004t0004g0092 |
3 | NA18989.hp2 NA19055.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.50+2359T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69017144 | |||||||
chr15:69017213 | G | A | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.50+2428G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69017213 | |||||||
chr15:69017278 | A | G | 7 | a0001c0003t0024g0301 a0005c0006t0006g0295 a0005c0006t0006g0296 others(4): Show |
7 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.50+2493A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69017278 | |||||||
chr15:69017341 | G | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0008c0011t0002g0302 others(1): Show |
7 | HG01069.hp2 HG01891.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.50+2556G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69017341 | |||||||
chr15:69017344 | G | T | 1 | a0001c0001t0002g0225 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.50+2559G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69017344 | |||||||
chr15:69017447 | C | T | 1 | a0001c0001t0002g0224 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.50+2662C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69017447 | |||||||
chr15:69017775 | T | C | 3 | a0003c0004t0003g0098 a0003c0004t0003g0099 a0003c0004t0003g0100 |
3 | HG02145.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.50+2990T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69017775 | |||||||
chr15:69017775 | T | TAC | 9 | a0001c0001t0001g0037 a0001c0001t0001g0234 a0001c0001t0001g0237 others(6): Show |
10 | HG02135.hp1 HG02738.hp2 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.50+3017_50+3018dup others(2): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69017775 | ||||||
chr15:69017775 | TAC | T | 25 | a0001c0001t0001g0221 a0001c0001t0001g0309 a0001c0001t0002g0218 others(22): Show |
28 | HG00438.hp1 HG00597.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.50+3017_50+3018del others(2): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69017775 | ||||||
chr15:69017775 | TACAC | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0003t0001g0084 others(6): Show |
12 | HG01069.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.50+3015_50+3018del others(4): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69017775 | ||||||
chr15:69017887 | C | T | 2 | a0002c0002t0001g0035 a0002c0002t0001g0216 |
3 | HG03225.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.50+3102C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69017887 | |||||||
chr15:69018186 | A | G | 1 | a0002c0002t0007g0215 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.50+3401A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69018186 | |||||||
chr15:69018241 | G | A | 1 | a0003c0004t0003g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.50+3456G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69018241 | |||||||
chr15:69018306 | T | C | 1 | a0003c0004t0003g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.50+3521T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69018306 | |||||||
chr15:69018399 | T | G | 1 | a0002c0002t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.50+3614T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69018399 | |||||||
chr15:69018624 | C | T | 2 | a0001c0003t0005g0291 a0001c0003t0005g0292 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.50+3839C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69018624 | |||||||
chr15:69018677 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50+3892C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69018677 | |||||||
chr15:69018796 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.50+4011A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69018796 | |||||||
chr15:69018884 | A | T | 51 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0002g0213 others(48): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.50+4099A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69018884 | |||||||
chr15:69019035 | T | A | 5 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.50+4250T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69019035 | |||||||
chr15:69019057 | T | C | 168 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0001g0083 others(165): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.50+4272T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69019057 | |||||||
chr15:69019238 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.50+4453G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69019238 | |||||||
chr15:69019322 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.50+4537G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69019322 | |||||||
chr15:69019554 | C | A | 2 | a0001c0003t0001g0058 a0001c0003t0014g0057 |
2 | NA18951.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.50+4769C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69019554 | |||||||
chr15:69019586 | T | C | 1 | a0001c0003t0001g0241 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.50+4801T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69019586 | |||||||
chr15:69019714 | G | C | 2 | a0001c0001t0002g0104 a0001c0001t0002g0105 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.50+4929G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69019714 | |||||||
chr15:69019728 | T | C | 114 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0002g0213 others(111): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.50+4943T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69019728 | |||||||
chr15:69020120 | A | C | 1 | a0001c0001t0027g0290 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.50+5335A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69020120 | |||||||
chr15:69020213 | T | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0139 others(4): Show |
12 | HG00408.hp2 HG02015.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.50+5428T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69020213 | |||||||
chr15:69020359 | C | T | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.50+5574C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69020359 | |||||||
chr15:69020579 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.50+5794T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69020579 | |||||||
chr15:69020637 | T | G | 1 | a0002c0002t0001g0188 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.50+5852T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69020637 | |||||||
chr15:69020684 | C | A | 2 | a0001c0001t0011g0231 a0001c0001t0011g0232 |
2 | HG02155.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.51-5844C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69020684 | |||||||
chr15:69020873 | G | C | 41 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(38): Show |
52 | HG00544.hp1 HG00609.hp1 HG01952.hp1 others(49): Show |
intron_variant | MODIFIER | c.51-5655G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69020873 | |||||||
chr15:69021123 | A | G | 2 | a0002c0002t0001g0093 a0002c0002t0001g0097 |
2 | HG00544.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.51-5405A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69021123 | |||||||
chr15:69021141 | G | T | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.51-5387G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69021141 | |||||||
chr15:69021224 | C | T | 1 | a0003c0004t0003g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51-5304C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69021224 | |||||||
chr15:69021349 | C | CT | 48 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0002g0142 others(45): Show |
62 | HG00544.hp1 HG00609.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.51-5162dupT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69021349 | ||||||
chr15:69021349 | CT | C | 15 | a0001c0001t0001g0237 a0001c0001t0002g0143 a0001c0001t0002g0244 others(12): Show |
16 | HG00673.hp1 HG01070.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.51-5162delT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69021349 | ||||||
chr15:69021520 | G | A | 1 | a0001c0003t0001g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.51-5008G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69021520 | |||||||
chr15:69021625 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0008c0011t0002g0302 others(1): Show |
7 | HG01069.hp2 HG01891.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.51-4903T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69021625 | |||||||
chr15:69021766 | C | G | 6 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.51-4762C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69021766 | |||||||
chr15:69021787 | T | C | 47 | a0001c0001t0002g0213 a0002c0002t0001g0004 a0002c0002t0001g0008 others(44): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.51-4741T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69021787 | |||||||
chr15:69021888 | G | T | 1 | a0001c0001t0037g0289 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.51-4640G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69021888 | |||||||
chr15:69021896 | C | T | 1 | a0008c0011t0002g0303 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.51-4632C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69021896 | |||||||
chr15:69022019 | T | A | 1 | a0005c0008t0006g0300 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.51-4509T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69022019 | |||||||
chr15:69022145 | A | G | 7 | a0001c0003t0024g0301 a0005c0006t0006g0295 a0005c0006t0006g0296 others(4): Show |
7 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.51-4383A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69022145 | |||||||
chr15:69022263 | A | G | 6 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.51-4265A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69022263 | |||||||
chr15:69022622 | TGA | T | 2 | a0002c0002t0001g0035 a0002c0002t0001g0216 |
3 | HG03225.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.51-3901_51-3900del others(2): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69022622 | ||||||
chr15:69022710 | A | C | 1 | a0004c0005t0001g0288 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.51-3818A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69022710 | |||||||
chr15:69022723 | G | C | 1 | a0005c0006t0006g0296 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.51-3805G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69022723 | |||||||
chr15:69023103 | C | T | 51 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0002g0213 others(48): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.51-3425C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023103 | |||||||
chr15:69023155 | A | G | 7 | a0001c0003t0001g0048 a0001c0003t0001g0307 a0001c0003t0014g0048 others(4): Show |
8 | HG00438.hp1 HG00597.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.51-3373A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023155 | |||||||
chr15:69023163 | G | A | 1 | a0005c0008t0017g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.51-3365G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023163 | |||||||
chr15:69023184 | G | A | 1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.51-3344G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023184 | |||||||
chr15:69023214 | T | C | 7 | a0001c0003t0001g0048 a0001c0003t0001g0307 a0001c0003t0014g0048 others(4): Show |
8 | HG00438.hp1 HG00597.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.51-3314T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023214 | |||||||
chr15:69023498 | G | A | 1 | a0012c0019t0001g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.51-3030G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023498 | |||||||
chr15:69023581 | T | C | 2 | a0001c0003t0001g0016 a0001c0003t0001g0061 |
3 | HG02630.hp1 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.51-2947T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023581 | |||||||
chr15:69023675 | C | A | 47 | a0001c0001t0002g0213 a0002c0002t0001g0004 a0002c0002t0001g0008 others(44): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.51-2853C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023675 | |||||||
chr15:69023686 | C | T | 1 | a0002c0002t0001g0212 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.51-2842C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023686 | |||||||
chr15:69023704 | TGCTGTAT others(1644): Show |
T | 2 | a0008c0011t0002g0302 a0008c0011t0002g0303 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.51-2821_51-1171del | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr15 | 69023704 | ||||||
chr15:69023776 | C | T | 44 | a0001c0001t0002g0104 a0001c0001t0002g0105 a0001c0001t0002g0109 others(41): Show |
60 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.51-2752C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023776 | |||||||
chr15:69023863 | A | G | 106 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0002g0213 others(103): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.51-2665A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023863 | |||||||
chr15:69023899 | C | T | 4 | a0004c0005t0001g0274 a0004c0005t0001g0275 a0004c0005t0001g0276 others(1): Show |
4 | HG02080.hp1 NA18939.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-2629C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023899 | |||||||
chr15:69023983 | C | A | 1 | a0001c0001t0002g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.51-2545C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69023983 | |||||||
chr15:69024005 | G | A | 1 | a0001c0001t0002g0225 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.51-2523G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69024005 | |||||||
chr15:69024286 | A | G | 4 | a0001c0003t0001g0304 a0005c0008t0006g0293 a0005c0008t0006g0294 others(1): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.51-2242A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69024286 | |||||||
chr15:69024291 | T | C | 106 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0002g0213 others(103): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.51-2237T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69024291 | |||||||
chr15:69024384 | G | T | 1 | a0001c0001t0002g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.51-2144G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69024384 | |||||||
chr15:69024446 | A | G | 112 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0002g0213 others(109): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.51-2082A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69024446 | |||||||
chr15:69024747 | T | C | 105 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0002g0213 others(102): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.51-1781T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69024747 | |||||||
chr15:69024887 | C | G | 1 | a0002c0002t0029g0008 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.51-1641C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69024887 | |||||||
chr15:69024929 | T | A | 50 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0024 others(47): Show |
61 | HG00140.hp1 HG00609.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.51-1599T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69024929 | |||||||
chr15:69025067 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0047 |
5 | HG01069.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.51-1461G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69025067 | |||||||
chr15:69025182 | T | G | 1 | a0001c0001t0011g0232 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.51-1346T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69025182 | |||||||
chr15:69025391 | C | T | 2 | a0002c0002t0001g0188 a0002c0002t0001g0210 |
2 | HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.51-1137C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69025391 | |||||||
chr15:69025477 | C | T | 68 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(65): Show |
80 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.51-1051C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69025477 | |||||||
chr15:69025589 | A | G | 6 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.51-939A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69025589 | |||||||
chr15:69025721 | C | T | 1 | a0001c0001t0002g0137 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.51-807C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69025721 | |||||||
chr15:69025748 | T | C | 1 | a0001c0001t0002g0149 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.51-780T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69025748 | |||||||
chr15:69025777 | C | G | 3 | a0005c0008t0006g0293 a0005c0008t0006g0294 a0009c0010t0006g0046 |
4 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.51-751C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69025777 | |||||||
chr15:69025889 | A | T | 49 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0002g0213 others(46): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.51-639A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69025889 | |||||||
chr15:69026041 | A | G | 1 | a0002c0002t0001g0096 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.51-487A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 1/15 | chr15 | 69026041 | |||||||
chr15:69026660 | T | C | 1 | a0001c0001t0002g0225 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.174+9T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69026660 | |||||||
chr15:69026843 | A | G | 1 | a0001c0001t0002g0187 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.174+192A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69026843 | |||||||
chr15:69027088 | C | T | 4 | a0001c0001t0009g0036 a0001c0001t0009g0219 a0001c0001t0009g0220 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+437C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69027088 | |||||||
chr15:69027181 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.174+530G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69027181 | |||||||
chr15:69027254 | C | G | 6 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+603C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69027254 | |||||||
chr15:69027258 | C | T | 12 | a0001c0001t0001g0045 a0001c0001t0001g0234 a0001c0001t0001g0240 others(9): Show |
13 | HG02056.hp1 HG02135.hp1 NA18943.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+607C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69027258 | |||||||
chr15:69027264 | G | A | 7 | a0001c0003t0024g0301 a0005c0006t0006g0295 a0005c0006t0006g0296 others(4): Show |
7 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+613G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69027264 | |||||||
chr15:69027392 | G | A | 7 | a0001c0003t0024g0301 a0005c0006t0006g0295 a0005c0006t0006g0296 others(4): Show |
7 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+741G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69027392 | |||||||
chr15:69027499 | A | T | 3 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0299 |
3 | HG02622.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.175-716A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69027499 | |||||||
chr15:69027814 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.175-401G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69027814 | |||||||
chr15:69027944 | T | G | 1 | a0001c0001t0009g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.175-271T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69027944 | |||||||
chr15:69027961 | A | G | 1 | a0013c0015t0039g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.175-254A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69027961 | |||||||
chr15:69028032 | C | G | 3 | a0001c0003t0001g0304 a0005c0008t0006g0300 a0005c0008t0017g0085 |
3 | HG02257.hp1 HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.175-183C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69028032 | |||||||
chr15:69028066 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0047 |
5 | HG01069.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-149G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | chr15 | 69028066 | |||||||
chr15:69028114 | A | AC | 18 | a0003c0004t0003g0133 a0003c0004t0003g0134 a0003c0004t0003g0135 others(15): Show |
21 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.175-94dupC | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr15 | 69028114 | ||||||
chr15:69028378 | C | T | 1 | a0015c0020t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.325+13C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69028378 | |||||||
chr15:69028388 | G | T | 2 | a0001c0001t0002g0104 a0001c0001t0002g0105 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.325+23G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69028388 | |||||||
chr15:69028511 | C | T | 4 | a0002c0002t0001g0086 a0002c0002t0001g0128 a0002c0002t0001g0208 others(1): Show |
4 | HG02886.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+146C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69028511 | |||||||
chr15:69028566 | C | T | 4 | a0006c0007t0008g0049 a0006c0007t0008g0138 a0006c0007t0008g0306 others(1): Show |
5 | HG00597.hp2 NA18960.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.325+201C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69028566 | |||||||
chr15:69028766 | T | C | 311 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(308): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.325+401T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69028766 | |||||||
chr15:69028834 | C | CT | 115 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0024 others(112): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.325+480dupT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr15 | 69028834 | ||||||
chr15:69028835 | T | C | 1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.325+470T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69028835 | |||||||
chr15:69029418 | T | C | 1 | a0001c0001t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.325+1053T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69029418 | |||||||
chr15:69029527 | G | A | 1 | a0002c0002t0007g0089 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.325+1162G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69029527 | |||||||
chr15:69029608 | A | G | 9 | a0001c0001t0009g0036 a0001c0001t0009g0219 a0001c0001t0009g0220 others(6): Show |
11 | HG00597.hp2 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.325+1243A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69029608 | |||||||
chr15:69029618 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.325+1253C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69029618 | |||||||
chr15:69029641 | C | T | 3 | a0002c0002t0001g0186 a0002c0002t0001g0206 a0002c0002t0001g0207 |
3 | HG00735.hp1 HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.325+1276C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69029641 | |||||||
chr15:69029681 | C | CT | 14 | a0001c0001t0001g0287 a0001c0001t0009g0036 a0001c0001t0009g0219 others(11): Show |
16 | HG00597.hp2 HG02074.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.325+1330dupT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr15 | 69029681 | ||||||
chr15:69029765 | C | T | 1 | a0003c0004t0003g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.325+1400C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69029765 | |||||||
chr15:69029958 | C | T | 1 | a0002c0002t0010g0033 | 2 | HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.326-1560C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69029958 | |||||||
chr15:69029988 | G | A | 45 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(42): Show |
56 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.326-1530G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69029988 | |||||||
chr15:69030042 | T | C | 1 | a0001c0001t0009g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.326-1476T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030042 | |||||||
chr15:69030080 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.326-1438T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030080 | |||||||
chr15:69030096 | G | A | 45 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(42): Show |
56 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.326-1422G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030096 | |||||||
chr15:69030169 | A | G | 245 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(242): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.326-1349A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030169 | |||||||
chr15:69030278 | C | T | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.326-1240C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030278 | |||||||
chr15:69030279 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.326-1239G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030279 | |||||||
chr15:69030280 | C | T | 1 | a0002c0002t0001g0205 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.326-1238C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030280 | |||||||
chr15:69030327 | T | C | 4 | a0001c0001t0002g0153 a0001c0001t0002g0185 a0001c0001t0013g0154 others(1): Show |
4 | HG02698.hp2 HG02738.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-1191T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030327 | |||||||
chr15:69030348 | T | G | 1 | a0002c0002t0001g0212 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.326-1170T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030348 | |||||||
chr15:69030351 | T | C | 1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.326-1167T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030351 | |||||||
chr15:69030603 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.326-915C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030603 | |||||||
chr15:69030693 | A | G | 4 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(1): Show |
4 | HG00738.hp2 HG01106.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-825A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030693 | |||||||
chr15:69030739 | C | T | 1 | a0003c0004t0003g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.326-779C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030739 | |||||||
chr15:69030850 | A | C | 1 | a0001c0001t0001g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.326-668A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030850 | |||||||
chr15:69030889 | A | G | 1 | a0001c0003t0001g0241 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.326-629A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69030889 | |||||||
chr15:69031047 | C | T | 1 | a0005c0008t0017g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.326-471C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69031047 | |||||||
chr15:69031471 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.326-47A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 3/15 | chr15 | 69031471 | |||||||
chr15:69031840 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.620+28T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | chr15 | 69031840 | |||||||
chr15:69031861 | C | T | 3 | a0001c0001t0009g0036 a0001c0001t0009g0219 a0001c0001t0009g0220 |
4 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+49C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | chr15 | 69031861 | |||||||
chr15:69031991 | G | T | 39 | a0003c0004t0003g0001 a0003c0004t0003g0003 a0003c0004t0003g0005 others(36): Show |
55 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.620+179G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | chr15 | 69031991 | |||||||
chr15:69032300 | AT | A | 6 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.620+490delT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr15 | 69032300 | ||||||
chr15:69032409 | CT | C | 10 | a0001c0001t0001g0146 a0001c0001t0002g0153 a0001c0001t0002g0185 others(7): Show |
11 | HG00140.hp1 HG00597.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.620+614delT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr15 | 69032409 | ||||||
chr15:69032516 | T | G | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.621-527T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | chr15 | 69032516 | |||||||
chr15:69032657 | C | T | 43 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(40): Show |
54 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.621-386C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | chr15 | 69032657 | |||||||
chr15:69032777 | T | C | 1 | a0001c0003t0001g0062 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.621-266T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | chr15 | 69032777 | |||||||
chr15:69032906 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.621-137C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | chr15 | 69032906 | |||||||
chr15:69032968 | G | A | 2 | a0002c0002t0001g0035 a0002c0002t0001g0216 |
3 | HG03225.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.621-75G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | chr15 | 69032968 | |||||||
chr15:69032995 | G | C | 1 | a0013c0015t0039g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.621-48G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | chr15 | 69032995 | |||||||
chr15:69033010 | C | G | 1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.621-33C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | chr15 | 69033010 | |||||||
chr15:69033036 | C | T | 1 | a0005c0008t0017g0085 | 1 | HG02257.hp1 | splice_region_variant&intron_variant | LOW | c.621-7C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 4/15 | chr15 | 69033036 | |||||||
chr15:69033457 | C | T | 1 | a0005c0008t0017g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.855+180C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69033457 | |||||||
chr15:69033476 | A | G | 1 | a0001c0001t0002g0180 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.855+199A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69033476 | |||||||
chr15:69033499 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.855+222T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69033499 | |||||||
chr15:69033540 | T | A | 9 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(6): Show |
10 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.855+263T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69033540 | |||||||
chr15:69033676 | G | GT | 41 | a0003c0004t0003g0001 a0003c0004t0003g0003 a0003c0004t0003g0005 others(38): Show |
57 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.855+410dupT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr15 | 69033676 | ||||||
chr15:69033696 | T | C | 2 | a0001c0001t0002g0101 a0001c0001t0002g0224 |
2 | NA19055.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.855+419T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69033696 | |||||||
chr15:69033701 | C | CT | 89 | a0001c0001t0001g0270 a0001c0003t0001g0002 a0001c0003t0001g0010 others(86): Show |
117 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.855+440dupT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr15 | 69033701 | ||||||
chr15:69033798 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.855+521G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69033798 | |||||||
chr15:69033885 | G | C | 1 | a0001c0001t0002g0156 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.855+608G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69033885 | |||||||
chr15:69034062 | C | T | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.855+785C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69034062 | |||||||
chr15:69034077 | A | G | 1 | a0001c0003t0005g0273 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.855+800A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69034077 | |||||||
chr15:69034391 | C | T | 206 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(203): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.856-963C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69034391 | |||||||
chr15:69034459 | T | C | 302 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(299): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.856-895T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69034459 | |||||||
chr15:69034589 | T | C | 1 | a0001c0001t0002g0139 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.856-765T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69034589 | |||||||
chr15:69034691 | G | T | 1 | a0003c0009t0003g0081 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.856-663G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69034691 | |||||||
chr15:69034838 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.856-516G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69034838 | |||||||
chr15:69034880 | C | A | 2 | a0004c0005t0001g0274 a0004c0005t0001g0275 |
2 | NA18939.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.856-474C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69034880 | |||||||
chr15:69034904 | G | A | 1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.856-450G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69034904 | |||||||
chr15:69035012 | T | C | 1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.856-342T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69035012 | |||||||
chr15:69035128 | A | T | 1 | a0001c0003t0001g0073 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.856-226A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69035128 | |||||||
chr15:69035153 | C | A | 1 | a0001c0001t0001g0238 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.856-201C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69035153 | |||||||
chr15:69035219 | T | C | 1 | a0003c0004t0003g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.856-135T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69035219 | |||||||
chr15:69035302 | G | C | 1 | a0001c0003t0001g0020 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.856-52G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 5/15 | chr15 | 69035302 | |||||||
chr15:69035635 | C | T | 2 | a0002c0002t0001g0012 a0002c0002t0001g0032 |
5 | NA18947.hp1 NA18950.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1010-123C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 6/15 | chr15 | 69035635 | |||||||
chr15:69035658 | C | T | 199 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0024 others(196): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1010-100C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 6/15 | chr15 | 69035658 | |||||||
chr15:69036266 | G | A | 43 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(40): Show |
54 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1188+330G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/15 | chr15 | 69036266 | |||||||
chr15:69036316 | TTCTC | T | 3 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0299 |
3 | HG02622.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1188+382_1188+385d others(6): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr15 | 69036316 | ||||||
chr15:69036344 | C | T | 1 | a0003c0004t0003g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1188+408C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/15 | chr15 | 69036344 | |||||||
chr15:69036493 | G | A | 2 | a0001c0003t0005g0014 a0001c0003t0005g0273 |
4 | HG01496.hp2 HG02145.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-535G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/15 | chr15 | 69036493 | |||||||
chr15:69036495 | C | G | 44 | a0003c0004t0003g0001 a0003c0004t0003g0003 a0003c0004t0003g0005 others(41): Show |
60 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1189-533C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/15 | chr15 | 69036495 | |||||||
chr15:69036764 | G | A | 1 | a0010c0012t0001g0158 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1189-264G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/15 | chr15 | 69036764 | |||||||
chr15:69036876 | T | C | 250 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(247): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1189-152T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/15 | chr15 | 69036876 | |||||||
chr15:69036907 | C | A | 44 | a0003c0004t0003g0001 a0003c0004t0003g0003 a0003c0004t0003g0005 others(41): Show |
60 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1189-121C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/15 | chr15 | 69036907 | |||||||
chr15:69036979 | C | A | 44 | a0003c0004t0003g0001 a0003c0004t0003g0003 a0003c0004t0003g0005 others(41): Show |
60 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1189-49C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/15 | chr15 | 69036979 | |||||||
chr15:69036981 | C | A | 2 | a0001c0003t0001g0058 a0001c0003t0014g0057 |
2 | NA18951.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1189-47C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/15 | chr15 | 69036981 | |||||||
chr15:69037003 | T | A | 2 | a0001c0003t0001g0063 a0001c0003t0001g0064 |
2 | NA18974.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1189-25T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 7/15 | chr15 | 69037003 | |||||||
chr15:69037251 | C | T | 6 | a0001c0003t0001g0223 a0006c0007t0008g0049 a0006c0007t0008g0138 others(3): Show |
7 | HG00597.hp2 HG02622.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.1371+41C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69037251 | |||||||
chr15:69037283 | G | A | 55 | a0001c0001t0001g0230 a0002c0002t0001g0004 a0002c0002t0001g0008 others(52): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1371+73G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69037283 | |||||||
chr15:69037284 | A | G | 310 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(307): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1371+74A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69037284 | |||||||
chr15:69037398 | G | A | 2 | a0003c0004t0003g0076 a0003c0004t0003g0077 |
2 | HG02523.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1371+188G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69037398 | |||||||
chr15:69037475 | G | A | 304 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(301): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1371+265G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69037475 | |||||||
chr15:69037584 | G | A | 1 | a0001c0001t0002g0159 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1371+374G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69037584 | |||||||
chr15:69037930 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0009g0219 |
6 | HG01069.hp2 HG02451.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1371+720T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69037930 | |||||||
chr15:69038003 | G | C | 1 | a0005c0008t0006g0300 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1371+793G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69038003 | |||||||
chr15:69038072 | A | G | 1 | a0002c0002t0001g0204 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1372-785A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69038072 | |||||||
chr15:69038144 | G | T | 2 | a0002c0002t0001g0035 a0002c0002t0001g0216 |
3 | HG03225.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1372-713G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69038144 | |||||||
chr15:69038168 | G | C | 10 | a0003c0004t0004g0023 a0003c0004t0004g0090 a0003c0004t0004g0091 others(7): Show |
11 | HG02083.hp1 NA18989.hp2 NA18998.hp1 others(8): Show |
intron_variant | MODIFIER | c.1372-689G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69038168 | |||||||
chr15:69038564 | A | G | 1 | a0003c0004t0003g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1372-293A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69038564 | |||||||
chr15:69038608 | G | A | 311 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(308): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1372-249G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69038608 | |||||||
chr15:69038632 | A | G | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1372-225A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69038632 | |||||||
chr15:69038743 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1372-114G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 8/15 | chr15 | 69038743 | |||||||
chr15:69039020 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0047 |
5 | HG01069.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504+31C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69039020 | |||||||
chr15:69039041 | G | A | 44 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(41): Show |
55 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1504+52G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69039041 | |||||||
chr15:69039111 | A | G | 9 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(6): Show |
10 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1504+122A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69039111 | |||||||
chr15:69039378 | G | T | 89 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(86): Show |
102 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1504+389G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69039378 | |||||||
chr15:69039380 | G | A | 6 | a0001c0003t0001g0223 a0006c0007t0008g0049 a0006c0007t0008g0138 others(3): Show |
7 | HG00597.hp2 HG02622.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.1504+391G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69039380 | |||||||
chr15:69039385 | G | A | 42 | a0003c0004t0003g0001 a0003c0004t0003g0003 a0003c0004t0003g0005 others(39): Show |
58 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1504+396G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69039385 | |||||||
chr15:69039418 | G | A | 201 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0024 others(198): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1504+429G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69039418 | |||||||
chr15:69039799 | C | T | 1 | a0005c0008t0017g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1504+810C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69039799 | |||||||
chr15:69039800 | G | A | 4 | a0001c0001t0036g0160 a0005c0008t0006g0293 a0005c0008t0006g0294 others(1): Show |
5 | HG02647.hp2 HG02965.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1504+811G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69039800 | |||||||
chr15:69039966 | A | C | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1504+977A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69039966 | |||||||
chr15:69040006 | A | C | 1 | a0001c0003t0001g0281 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1504+1017A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69040006 | |||||||
chr15:69040143 | C | T | 51 | a0001c0001t0002g0007 a0001c0001t0002g0026 a0001c0001t0002g0027 others(48): Show |
57 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.1504+1154C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69040143 | |||||||
chr15:69040165 | C | G | 1 | a0013c0015t0039g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1504+1176C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69040165 | |||||||
chr15:69040403 | C | T | 1 | a0001c0001t0009g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1504+1414C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69040403 | |||||||
chr15:69040411 | C | A | 311 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(308): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1504+1422C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69040411 | |||||||
chr15:69040601 | A | G | 1 | a0001c0001t0036g0160 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1504+1612A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69040601 | |||||||
chr15:69040634 | G | A | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1504+1645G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69040634 | |||||||
chr15:69040824 | C | T | 1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1504+1835C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69040824 | |||||||
chr15:69040874 | G | A | 1 | a0001c0001t0031g0248 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1505-1789G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69040874 | |||||||
chr15:69041109 | G | A | 1 | a0002c0002t0015g0226 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1505-1554G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69041109 | |||||||
chr15:69041166 | G | A | 3 | a0003c0004t0004g0129 a0003c0004t0004g0130 a0003c0004t0004g0131 |
3 | NA19000.hp1 NA19011.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1505-1497G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69041166 | |||||||
chr15:69041616 | C | T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0238 others(2): Show |
6 | NA18946.hp1 NA18953.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.1505-1047C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69041616 | |||||||
chr15:69041787 | A | G | 1 | a0002c0002t0001g0030 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1505-876A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69041787 | |||||||
chr15:69041826 | T | C | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1505-837T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69041826 | |||||||
chr15:69041871 | A | AT | 11 | a0002c0002t0001g0209 a0003c0004t0003g0124 a0005c0006t0006g0295 others(8): Show |
12 | HG02257.hp1 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1505-782dupT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr15 | 69041871 | ||||||
chr15:69041892 | C | G | 1 | a0001c0001t0002g0149 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1505-771C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69041892 | |||||||
chr15:69041947 | A | G | 1 | a0005c0008t0017g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1505-716A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69041947 | |||||||
chr15:69042068 | T | TA | 101 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0024 others(98): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1505-580dupA | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr15 | 69042068 | ||||||
chr15:69042177 | C | T | 4 | a0001c0001t0002g0244 a0001c0001t0002g0255 a0001c0001t0002g0256 others(1): Show |
4 | NA18941.hp1 NA18970.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1505-486C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69042177 | |||||||
chr15:69042557 | C | T | 1 | a0005c0008t0017g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1505-106C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69042557 | |||||||
chr15:69042617 | C | T | 10 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(7): Show |
11 | HG02257.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1505-46C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 9/15 | chr15 | 69042617 | |||||||
chr15:69042853 | A | G | 14 | a0001c0001t0002g0007 a0001c0001t0002g0029 a0001c0001t0002g0082 others(11): Show |
18 | HG00597.hp1 HG00609.hp2 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.1647+48A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69042853 | |||||||
chr15:69042972 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1647+167G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69042972 | |||||||
chr15:69043339 | A | G | 1 | a0001c0003t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1647+534A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043339 | |||||||
chr15:69043398 | G | A | 3 | a0001c0001t0009g0036 a0001c0001t0009g0219 a0001c0001t0009g0220 |
4 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647+593G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043398 | |||||||
chr15:69043407 | G | A | 6 | a0001c0003t0001g0223 a0006c0007t0008g0049 a0006c0007t0008g0138 others(3): Show |
7 | HG00597.hp2 HG02622.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.1647+602G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043407 | |||||||
chr15:69043522 | T | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
7 | HG01070.hp2 HG01071.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1647+717T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043522 | |||||||
chr15:69043676 | C | T | 1 | a0001c0003t0001g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1647+871C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043676 | |||||||
chr15:69043790 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0008c0011t0002g0302 others(1): Show |
7 | HG01069.hp2 HG01891.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1647+985A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043790 | |||||||
chr15:69043796 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1647+991C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043796 | |||||||
chr15:69043797 | G | A | 7 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0052 others(4): Show |
9 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1647+992G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043797 | |||||||
chr15:69043845 | T | C | 1 | a0008c0011t0002g0302 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1647+1040T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043845 | |||||||
chr15:69043854 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1647+1049A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043854 | |||||||
chr15:69043942 | T | G | 250 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(247): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1647+1137T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043942 | |||||||
chr15:69043978 | G | C | 1 | a0001c0001t0002g0165 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1647+1173G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69043978 | |||||||
chr15:69044105 | A | G | 1 | a0002c0002t0001g0096 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1647+1300A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69044105 | |||||||
chr15:69044182 | TA | T | 7 | a0001c0001t0001g0083 a0001c0003t0001g0223 a0006c0007t0008g0049 others(4): Show |
8 | HG00597.hp2 HG02622.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.1647+1391delA | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69044182 | ||||||
chr15:69044391 | C | G | 311 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(308): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1647+1586C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69044391 | |||||||
chr15:69044694 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1647+1889T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69044694 | |||||||
chr15:69044840 | A | C | 197 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0024 others(194): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1648-1982A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69044840 | |||||||
chr15:69044949 | A | G | 7 | a0002c0002t0001g0035 a0002c0002t0001g0086 a0002c0002t0001g0128 others(4): Show |
8 | HG02055.hp1 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1648-1873A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69044949 | |||||||
chr15:69044995 | C | T | 5 | a0001c0001t0002g0152 a0001c0001t0002g0156 a0001c0001t0002g0164 others(2): Show |
5 | HG00280.hp1 HG01081.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648-1827C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69044995 | |||||||
chr15:69045450 | T | G | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1648-1372T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045450 | |||||||
chr15:69045453 | A | C | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1369A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045453 | |||||||
chr15:69045455 | A | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1367A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045455 | |||||||
chr15:69045457 | T | C | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1365T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045457 | |||||||
chr15:69045461 | A | C | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1361A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045461 | |||||||
chr15:69045466 | T | C | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1356T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045466 | |||||||
chr15:69045470 | T | C | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1352T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045470 | |||||||
chr15:69045472 | CCCTCCCT others(1): Show |
C | 40 | a0003c0004t0003g0001 a0003c0004t0003g0003 a0003c0004t0003g0005 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1648-1334_1648-132 others(12): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045472 | ||||||
chr15:69045478 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1344C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045478 | |||||||
chr15:69045482 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1340C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045482 | |||||||
chr15:69045484 | C | T | 2 | a0002c0002t0001g0210 a0003c0009t0003g0080 |
2 | NA18992.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1648-1338C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045484 | |||||||
chr15:69045486 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1336C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045486 | |||||||
chr15:69045490 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1332C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045490 | |||||||
chr15:69045492 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1330C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045492 | |||||||
chr15:69045494 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1328C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045494 | |||||||
chr15:69045496 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1326C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045496 | |||||||
chr15:69045498 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1324C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045498 | |||||||
chr15:69045500 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1322C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045500 | |||||||
chr15:69045502 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1320C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045502 | |||||||
chr15:69045504 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1318C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045504 | |||||||
chr15:69045506 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1316C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045506 | |||||||
chr15:69045508 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1648-1314C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045508 | |||||||
chr15:69045528 | C | T | 2 | a0002c0002t0001g0210 a0003c0009t0003g0080 |
2 | NA18992.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1648-1294C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045528 | |||||||
chr15:69045536 | T | TCTTTCTT others(10): Show |
1 | a0001c0001t0001g0147 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1648-1286_1648-128 others(21): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045536 | |||||||
chr15:69045536 | T | TCTTTCTT others(22): Show |
1 | a0001c0001t0002g0166 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1648-1286_1648-128 others(33): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045536 | |||||||
chr15:69045536 | T | TCTTTCTT others(34): Show |
1 | a0003c0004t0004g0129 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1648-1286_1648-128 others(45): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045536 | |||||||
chr15:69045536 | T | TCTTTCTT others(38): Show |
1 | a0003c0004t0004g0090 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1648-1286_1648-128 others(49): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045536 | |||||||
chr15:69045536 | T | TTCTTTCT others(23): Show |
1 | a0001c0001t0002g0224 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1648-1285_1648-128 others(34): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTCTTTCT others(27): Show |
1 | a0003c0009t0003g0080 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1648-1285_1648-128 others(38): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTTTCTTT others(1): Show |
6 | a0001c0001t0002g0109 a0001c0001t0002g0150 a0001c0001t0002g0165 others(3): Show |
9 | HG00280.hp2 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1648-1259_1648-125 others(12): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTTTCTTT others(5): Show |
16 | a0001c0001t0001g0024 a0001c0001t0001g0146 a0001c0001t0002g0006 others(13): Show |
28 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1648-1263_1648-125 others(16): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTTTCTTT others(9): Show |
37 | a0001c0001t0001g0083 a0001c0001t0001g0261 a0001c0001t0001g0309 others(34): Show |
45 | HG00408.hp2 HG00423.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1648-1267_1648-125 others(20): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTTTCTTT others(13): Show |
34 | a0001c0001t0001g0037 a0001c0001t0001g0260 a0001c0001t0002g0050 others(31): Show |
38 | HG00323.hp1 HG00673.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1648-1271_1648-125 others(24): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTTTCTTT others(17): Show |
39 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0045 others(36): Show |
45 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1648-1275_1648-125 others(28): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTTTCTTT others(21): Show |
26 | a0001c0001t0001g0042 a0001c0001t0001g0238 a0001c0001t0001g0263 others(23): Show |
28 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.1648-1279_1648-125 others(32): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTTTCTTT others(25): Show |
39 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0144 others(36): Show |
53 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1648-1283_1648-125 others(36): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTTTCTTT others(29): Show |
27 | a0001c0001t0001g0043 a0001c0001t0001g0145 a0001c0001t0001g0234 others(24): Show |
34 | HG00609.hp2 HG00621.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(40): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTTTCTTT others(33): Show |
12 | a0001c0001t0001g0265 a0001c0001t0002g0187 a0001c0001t0002g0254 others(9): Show |
17 | HG01167.hp1 HG01978.hp1 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(44): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTTTCTTT others(37): Show |
5 | a0001c0001t0031g0248 a0003c0004t0003g0100 a0003c0004t0003g0136 others(2): Show |
5 | HG00408.hp1 HG01934.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(48): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045536 | T | TTTTCTTT others(18): Show |
1 | a0001c0001t0001g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1648-1279_1648-127 others(29): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045536 | ||||||
chr15:69045541 | T | TTTCTTTC others(6): Show |
1 | a0001c0001t0001g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1648-1269_1648-126 others(17): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045541 | ||||||
chr15:69045546 | T | TTCTTTCT others(11): Show |
1 | a0002c0002t0001g0195 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1648-1274_1648-125 others(22): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045546 | ||||||
chr15:69045548 | C | CTTTCTTT others(43): Show |
1 | a0005c0006t0006g0295 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(54): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045548 | ||||||
chr15:69045548 | C | CTTTCTTT others(47): Show |
1 | a0005c0006t0028g0297 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(58): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045548 | ||||||
chr15:69045548 | C | CTTTCTTT others(47): Show |
2 | a0005c0006t0006g0296 a0005c0006t0006g0299 |
2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(58): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045548 | ||||||
chr15:69045548 | C | CTTTCTTT others(55): Show |
1 | a0005c0008t0006g0300 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(66): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045548 | ||||||
chr15:69045548 | C | CTTTCTTT others(59): Show |
4 | a0005c0006t0006g0298 a0005c0008t0006g0293 a0005c0008t0006g0294 others(1): Show |
5 | HG02280.hp2 HG02647.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(70): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045548 | ||||||
chr15:69045552 | C | CTTTCTTT others(39): Show |
1 | a0001c0003t0001g0073 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(50): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045552 | ||||||
chr15:69045552 | C | CTTTCTTT others(43): Show |
1 | a0001c0003t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(54): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045552 | ||||||
chr15:69045552 | C | CTTTCTTT others(47): Show |
7 | a0001c0003t0001g0059 a0001c0003t0001g0061 a0001c0003t0001g0065 others(4): Show |
7 | HG03540.hp2 NA18945.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(58): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045552 | ||||||
chr15:69045552 | C | CTTTCTTT others(38): Show |
1 | a0001c0003t0001g0072 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(49): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045552 | ||||||
chr15:69045552 | C | CTTTCTTT others(51): Show |
11 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(8): Show |
19 | HG00609.hp1 HG02027.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(62): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045552 | ||||||
chr15:69045552 | C | CTTTCTTT others(55): Show |
12 | a0001c0003t0001g0017 a0001c0003t0001g0048 a0001c0003t0001g0058 others(9): Show |
12 | HG00438.hp1 HG00544.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(66): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045552 | ||||||
chr15:69045552 | C | CTTTCTTT others(59): Show |
3 | a0001c0003t0001g0018 a0001c0003t0001g0079 a0001c0003t0018g0071 |
4 | NA18959.hp1 NA19001.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(70): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045552 | ||||||
chr15:69045552 | C | CTTTCTTT others(58): Show |
1 | a0001c0003t0001g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(69): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045552 | ||||||
chr15:69045552 | C | CTTTCTTT others(63): Show |
1 | a0001c0003t0001g0064 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(74): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045552 | ||||||
chr15:69045556 | C | CTTTCTTT others(39): Show |
1 | a0001c0003t0001g0021 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(50): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045556 | ||||||
chr15:69045556 | C | CTTTCTTT others(43): Show |
2 | a0001c0003t0001g0189 a0001c0003t0019g0051 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(54): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045556 | ||||||
chr15:69045556 | C | CTTTCTTT others(47): Show |
2 | a0001c0003t0001g0052 a0015c0020t0001g0053 |
2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(58): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045556 | ||||||
chr15:69045556 | C | CTTTCTTT others(55): Show |
1 | a0001c0003t0001g0020 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1648-1252_1648-125 others(66): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045556 | ||||||
chr15:69045560 | C | CTTTCTTT others(23): Show |
1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(34): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045560 | ||||||
chr15:69045565 | T | TTTCTTTC others(32): Show |
1 | a0003c0004t0003g0121 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(43): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045565 | ||||||
chr15:69045569 | T | TTTCTTCT others(23): Show |
1 | a0001c0001t0002g0255 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(34): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045569 | ||||||
chr15:69045570 | T | TTCTTTCT others(22): Show |
1 | a0001c0001t0002g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1648-1252_1648-125 others(33): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045570 | |||||||
chr15:69045571 | C | T | 7 | a0001c0001t0001g0047 a0001c0001t0002g0159 a0001c0001t0002g0164 others(4): Show |
8 | HG01069.hp2 HG01169.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1648-1251C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045571 | |||||||
chr15:69045572 | C | CTTT | 3 | a0001c0001t0001g0047 a0001c0001t0002g0175 a0001c0001t0002g0179 |
4 | HG01069.hp2 HG02647.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648-1250_1648-124 others(7): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045572 | |||||||
chr15:69045572 | C | CTTTCTTT others(19): Show |
1 | a0007c0014t0002g0251 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1648-1250_1648-124 others(30): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045572 | |||||||
chr15:69045582 | T | G | 1 | a0003c0009t0003g0080 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1648-1240T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045582 | |||||||
chr15:69045582 | T | TTTCTTTC others(17): Show |
1 | a0001c0001t0002g0179 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1648-1238_1648-123 others(28): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045582 | ||||||
chr15:69045584 | TTC | T | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp2 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1648-1236_1648-123 others(6): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045584 | ||||||
chr15:69045585 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1648-1237T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045585 | |||||||
chr15:69045586 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1648-1236C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045586 | |||||||
chr15:69045598 | CT | C | 9 | a0001c0001t0001g0015 a0001c0003t0001g0084 a0001c0003t0024g0301 others(6): Show |
11 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1648-1214delT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045598 | ||||||
chr15:69045599 | T | TTCCCTTT others(20): Show |
1 | a0001c0001t0001g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1648-1222_1648-122 others(31): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045599 | ||||||
chr15:69045599 | T | TTTCTTCC others(24): Show |
1 | a0001c0001t0001g0047 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1648-1221_1648-122 others(35): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr15 | 69045599 | ||||||
chr15:69045609 | C | T | 1 | a0003c0004t0003g0121 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1648-1213C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045609 | |||||||
chr15:69045723 | A | G | 1 | a0001c0003t0001g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1648-1099A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045723 | |||||||
chr15:69045762 | A | T | 1 | a0003c0009t0003g0080 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1648-1060A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045762 | |||||||
chr15:69045774 | A | C | 1 | a0001c0001t0037g0289 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1648-1048A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045774 | |||||||
chr15:69045788 | G | C | 2 | a0001c0001t0001g0269 a0012c0019t0001g0247 |
2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1648-1034G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045788 | |||||||
chr15:69045795 | C | T | 1 | a0001c0003t0001g0067 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1648-1027C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045795 | |||||||
chr15:69045914 | G | C | 310 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(307): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1648-908G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045914 | |||||||
chr15:69045914 | G | T | 1 | a0001c0001t0035g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1648-908G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045914 | |||||||
chr15:69045943 | A | G | 2 | a0001c0001t0002g0253 a0001c0001t0002g0257 |
2 | HG01346.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1648-879A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69045943 | |||||||
chr15:69046002 | C | T | 1 | a0005c0008t0017g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1648-820C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69046002 | |||||||
chr15:69046198 | G | A | 1 | a0002c0002t0020g0198 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1648-624G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69046198 | |||||||
chr15:69046263 | G | A | 34 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0017 others(31): Show |
42 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1648-559G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69046263 | |||||||
chr15:69046269 | C | G | 1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1648-553C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69046269 | |||||||
chr15:69046305 | A | T | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1648-517A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69046305 | |||||||
chr15:69046643 | T | G | 4 | a0006c0007t0008g0049 a0006c0007t0008g0138 a0006c0007t0008g0306 others(1): Show |
5 | HG00597.hp2 NA18960.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.1648-179T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69046643 | |||||||
chr15:69046696 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1648-126G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 10/15 | chr15 | 69046696 | |||||||
chr15:69046950 | T | A | 1 | a0005c0008t0006g0300 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1692+84T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 11/15 | chr15 | 69046950 | |||||||
chr15:69046971 | C | G | 1 | a0001c0003t0001g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1692+105C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 11/15 | chr15 | 69046971 | |||||||
chr15:69047003 | A | G | 1 | a0010c0012t0002g0075 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1692+137A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 11/15 | chr15 | 69047003 | |||||||
chr15:69047054 | C | G | 1 | a0001c0001t0001g0041 | 2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1692+188C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 11/15 | chr15 | 69047054 | |||||||
chr15:69047218 | C | T | 1 | a0003c0004t0003g0108 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1693-195C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 11/15 | chr15 | 69047218 | |||||||
chr15:69047346 | TCC | T | 3 | a0004c0005t0001g0038 a0004c0005t0001g0245 a0004c0005t0001g0246 |
4 | HG00673.hp1 HG02040.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1693-64_1693-63del others(2): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr15 | 69047346 | ||||||
chr15:69047356 | G | A | 1 | a0001c0003t0001g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1693-57G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 11/15 | chr15 | 69047356 | |||||||
chr15:69047828 | A | T | 1 | a0001c0003t0001g0021 | 2 | HG02895.hp2 HG02897.hp1 |
splice_acceptor_variant&intron_variant | HIGH | c.1818-2A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 12/15 | chr15 | 69047828 | |||||||
chr15:69047958 | A | G | 3 | a0001c0003t0005g0014 a0001c0003t0005g0272 a0001c0003t0005g0273 |
5 | HG01496.hp2 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1899+47A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69047958 | |||||||
chr15:69048003 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1899+92C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048003 | |||||||
chr15:69048027 | C | A | 1 | a0001c0001t0001g0261 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1899+116C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048027 | |||||||
chr15:69048073 | G | A | 1 | a0003c0004t0003g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1899+162G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048073 | |||||||
chr15:69048112 | A | C | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1899+201A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048112 | |||||||
chr15:69048158 | G | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0047 |
5 | HG01069.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1899+247G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048158 | |||||||
chr15:69048220 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1899+309C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048220 | |||||||
chr15:69048306 | G | A | 1 | a0015c0020t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1899+395G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048306 | |||||||
chr15:69048354 | G | A | 255 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(252): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1899+443G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048354 | |||||||
chr15:69048397 | G | A | 1 | a0015c0020t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1899+486G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048397 | |||||||
chr15:69048513 | A | C | 17 | a0002c0002t0001g0012 a0002c0002t0001g0032 a0002c0002t0001g0093 others(14): Show |
21 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.1900-446A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048513 | |||||||
chr15:69048539 | G | T | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1900-420G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048539 | |||||||
chr15:69048549 | AAAT | A | 43 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(40): Show |
54 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1900-397_1900-395d others(5): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr15 | 69048549 | ||||||
chr15:69048724 | A | C | 44 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(41): Show |
55 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1900-235A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048724 | |||||||
chr15:69048727 | T | C | 2 | a0001c0001t0002g0218 a0001c0001t0032g0217 |
2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1900-232T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048727 | |||||||
chr15:69048823 | T | C | 1 | a0003c0004t0004g0091 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1900-136T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048823 | |||||||
chr15:69048953 | C | T | 1 | a0006c0007t0008g0306 | 1 | NA18968.hp1 | splice_region_variant&intron_variant | LOW | c.1900-6C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 13/15 | chr15 | 69048953 | |||||||
chr15:69049114 | C | G | 1 | a0001c0003t0001g0021 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1999+56C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69049114 | |||||||
chr15:69049192 | C | CT | 18 | a0001c0001t0001g0013 a0001c0001t0001g0235 a0001c0001t0001g0236 others(15): Show |
23 | HG00597.hp2 HG01261.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1999+151dupT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr15 | 69049192 | ||||||
chr15:69049192 | CT | C | 39 | a0001c0001t0001g0262 a0001c0001t0002g0140 a0001c0001t0002g0176 others(36): Show |
57 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1999+151delT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr15 | 69049192 | ||||||
chr15:69049255 | G | A | 2 | a0002c0002t0007g0196 a0002c0002t0007g0215 |
2 | HG00323.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1999+197G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69049255 | |||||||
chr15:69049265 | C | T | 44 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(41): Show |
55 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1999+207C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69049265 | |||||||
chr15:69049280 | C | T | 44 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(41): Show |
55 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1999+222C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69049280 | |||||||
chr15:69049296 | A | G | 1 | a0001c0001t0001g0013 | 3 | HG01261.hp1 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1999+238A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69049296 | |||||||
chr15:69049351 | C | T | 3 | a0001c0001t0009g0036 a0001c0001t0009g0219 a0001c0001t0009g0220 |
4 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1999+293C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69049351 | |||||||
chr15:69049465 | T | A | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1999+407T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69049465 | |||||||
chr15:69049538 | G | A | 1 | a0003c0004t0003g0098 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1999+480G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69049538 | |||||||
chr15:69049748 | G | C | 2 | a0003c0004t0003g0116 a0003c0004t0003g0119 |
2 | NA19010.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1999+690G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69049748 | |||||||
chr15:69049886 | G | C | 1 | a0001c0001t0027g0290 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1999+828G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69049886 | |||||||
chr15:69050006 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1999+948C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69050006 | |||||||
chr15:69050103 | C | T | 1 | a0001c0003t0001g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1999+1045C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69050103 | |||||||
chr15:69050139 | C | T | 6 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1999+1081C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69050139 | |||||||
chr15:69050385 | T | A | 1 | a0001c0001t0037g0289 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1999+1327T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69050385 | |||||||
chr15:69050429 | C | A | 1 | a0003c0004t0003g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1999+1371C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69050429 | |||||||
chr15:69051093 | T | C | 311 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(308): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1999+2035T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051093 | |||||||
chr15:69051183 | GTCTCC | G | 9 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(6): Show |
10 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1999+2138_1999+214 others(9): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr15 | 69051183 | ||||||
chr15:69051187 | CCT | C | 44 | a0003c0004t0003g0001 a0003c0004t0003g0003 a0003c0004t0003g0005 others(41): Show |
60 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1999+2133_1999+213 others(6): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr15 | 69051187 | ||||||
chr15:69051248 | G | A | 311 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(308): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1999+2190G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051248 | |||||||
chr15:69051280 | C | T | 1 | a0003c0004t0003g0117 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1999+2222C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051280 | |||||||
chr15:69051337 | T | G | 1 | a0002c0002t0001g0195 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1999+2279T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051337 | |||||||
chr15:69051359 | G | A | 2 | a0001c0003t0001g0018 a0001c0003t0001g0068 |
3 | HG00544.hp1 NA19001.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1999+2301G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051359 | |||||||
chr15:69051420 | T | G | 311 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(308): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1999+2362T>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051420 | |||||||
chr15:69051517 | G | C | 54 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(51): Show |
66 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1999+2459G>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051517 | |||||||
chr15:69051548 | C | T | 1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1999+2490C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051548 | |||||||
chr15:69051585 | G | A | 1 | a0003c0004t0003g0117 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1999+2527G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051585 | |||||||
chr15:69051603 | G | A | 1 | a0001c0001t0002g0224 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1999+2545G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051603 | |||||||
chr15:69051772 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1999+2714T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051772 | |||||||
chr15:69051842 | G | GT | 11 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
16 | HG01070.hp2 HG01071.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1999+2794dupT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr15 | 69051842 | ||||||
chr15:69051852 | T | A | 4 | a0001c0001t0002g0102 a0001c0001t0009g0036 a0001c0001t0009g0219 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999+2794T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051852 | |||||||
chr15:69051952 | G | A | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1999+2894G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051952 | |||||||
chr15:69051985 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1999+2927A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69051985 | |||||||
chr15:69052037 | T | C | 4 | a0006c0007t0008g0049 a0006c0007t0008g0138 a0006c0007t0008g0306 others(1): Show |
5 | HG00597.hp2 NA18960.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999+2979T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69052037 | |||||||
chr15:69052059 | T | C | 46 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0024 others(43): Show |
57 | HG00140.hp1 HG00673.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.1999+3001T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69052059 | |||||||
chr15:69052076 | G | A | 1 | a0002c0002t0001g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1999+3018G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69052076 | |||||||
chr15:69052191 | T | C | 2 | a0001c0003t0001g0016 a0001c0003t0001g0061 |
3 | HG02630.hp1 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1999+3133T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69052191 | |||||||
chr15:69052207 | GACCCTGT others(11): Show |
G | 1 | a0001c0001t0022g0266 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2000-3125_2000-310 others(22): Show |
NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr15 | 69052207 | ||||||
chr15:69052217 | C | CA | 53 | a0001c0001t0001g0260 a0001c0001t0001g0269 a0001c0001t0001g0282 others(50): Show |
69 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.2000-3102dupA | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr15 | 69052217 | ||||||
chr15:69052283 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2000-3051C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69052283 | |||||||
chr15:69052472 | A | G | 203 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(200): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2000-2862A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69052472 | |||||||
chr15:69052519 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2000-2815G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69052519 | |||||||
chr15:69052764 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2000-2570C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69052764 | |||||||
chr15:69052980 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2000-2354G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69052980 | |||||||
chr15:69053110 | A | G | 3 | a0001c0001t0009g0036 a0001c0001t0009g0219 a0001c0001t0009g0220 |
4 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2000-2224A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053110 | |||||||
chr15:69053186 | C | CT | 2 | a0001c0001t0001g0013 a0001c0001t0001g0236 |
4 | HG01261.hp1 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2000-2147dupT | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr15 | 69053186 | ||||||
chr15:69053218 | G | T | 1 | a0002c0002t0001g0204 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2000-2116G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053218 | |||||||
chr15:69053359 | C | T | 1 | a0004c0005t0001g0276 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2000-1975C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053359 | |||||||
chr15:69053368 | A | C | 1 | a0001c0003t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2000-1966A>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053368 | |||||||
chr15:69053423 | T | C | 1 | a0014c0021t0001g0264 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2000-1911T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053423 | |||||||
chr15:69053448 | A | G | 2 | a0001c0003t0001g0066 a0001c0003t0001g0070 |
2 | HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2000-1886A>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053448 | |||||||
chr15:69053521 | A | T | 1 | a0002c0002t0001g0188 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2000-1813A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053521 | |||||||
chr15:69053549 | A | T | 3 | a0001c0001t0002g0166 a0001c0001t0002g0171 a0001c0001t0002g0172 |
3 | HG00735.hp2 HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2000-1785A>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053549 | |||||||
chr15:69053611 | T | A | 1 | a0001c0001t0002g0050 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2000-1723T>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053611 | |||||||
chr15:69053834 | G | A | 43 | a0001c0003t0001g0002 a0001c0003t0001g0010 a0001c0003t0001g0016 others(40): Show |
54 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.2000-1500G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053834 | |||||||
chr15:69053873 | C | T | 1 | a0011c0017t0001g0106 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2000-1461C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053873 | |||||||
chr15:69053975 | C | G | 1 | a0001c0003t0001g0021 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2000-1359C>G | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69053975 | |||||||
chr15:69054359 | G | A | 1 | a0001c0001t0033g0252 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2000-975G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69054359 | |||||||
chr15:69054537 | G | A | 6 | a0005c0006t0006g0295 a0005c0006t0006g0296 a0005c0006t0006g0298 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2000-797G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69054537 | |||||||
chr15:69054606 | T | C | 212 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(209): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2000-728T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69054606 | |||||||
chr15:69054948 | G | A | 1 | a0001c0003t0024g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2000-386G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69054948 | |||||||
chr15:69054994 | C | T | 1 | a0002c0002t0001g0212 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2000-340C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69054994 | |||||||
chr15:69055060 | C | T | 1 | a0001c0003t0005g0229 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2000-274C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69055060 | |||||||
chr15:69055253 | G | A | 251 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(248): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.2000-81G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69055253 | |||||||
chr15:69055312 | G | A | 3 | a0005c0008t0006g0293 a0005c0008t0006g0294 a0009c0010t0006g0046 |
4 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2000-22G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 14/15 | chr15 | 69055312 | |||||||
chr15:69055682 | TG | T | 3 | a0005c0008t0006g0293 a0005c0008t0006g0294 a0009c0010t0006g0046 |
4 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2166+183delG | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 15/15 | chr15 | 69055682 | |||||||
chr15:69055864 | G | T | 2 | a0001c0003t0001g0304 a0001c0003t0024g0301 |
2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2166+364G>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 15/15 | chr15 | 69055864 | |||||||
chr15:69055884 | C | T | 1 | a0001c0003t0001g0021 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2166+384C>T | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 15/15 | chr15 | 69055884 | |||||||
chr15:69055925 | T | C | 57 | a0001c0001t0009g0036 a0001c0001t0009g0219 a0001c0001t0009g0220 others(54): Show |
70 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.2166+425T>C | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 15/15 | chr15 | 69055925 | |||||||
chr15:69056249 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2167-316G>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 15/15 | chr15 | 69056249 | |||||||
chr15:69056318 | C | A | 1 | a0004c0005t0001g0074 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2167-247C>A | NOX5 | ENSG00000255346.11 | transcript | ENST00000388866.8 | protein_coding | 15/15 | chr15 | 69056318 |