Item | Value |
---|---|
geneid | 27035 |
ensemblid | ENSG00000007952.18 |
hgncid | 7889 |
symbol | NOX1 |
name | NADPH oxidase 1 |
refseq_nuc | NM_007052.5 |
refseq_prot | NP_008983.2 |
ensembl_nuc | ENST00000372966.8 |
ensembl_prot | ENSP00000362057.3 |
mane_status | MANE Select |
chr | chrX |
start | 100843324 |
end | 100874359 |
strand | - |
ver | v1.2 |
region | chrX:100843324-100874359 |
region5000 | chrX:100838324-100879359 |
regionname0 | NOX1_chrX_100843324_100874359 |
regionname5000 | NOX1_chrX_100838324_100879359 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 564 | 291 | 64 | 51 | 131 | 11 | 32 | 100 | NOX1_chrX_100838324_100879359 | NOX1 | MGNWV others(559): Show |
chrX | 100838324 | 100879359 |
a0002 | 0/0 | 564 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | MGNWV others(559): Show |
chrX | 100838324 | 100879359 |
a0003 | 0/0 | 564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | MGNWV others(559): Show |
chrX | 100838324 | 100879359 |
a0004 | 0/0 | 564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | MGNWV others(559): Show |
chrX | 100838324 | 100879359 |
a0005 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | MGNWV others(559): Show |
chrX | 100838324 | 100879359 |
a0006 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | MGNWV others(559): Show |
chrX | 100838324 | 100879359 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1692 | 288 | 61 | 51 | 131 | 11 | 32 | NOX1_chrX_100838324_100879359 | NOX1 | ATGGG others(1687): Show |
chrX | 100838324 | 100879359 | ||
a0001c0003 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | ATGGG others(1687): Show |
chrX | 100838324 | 100879359 | ||
a0001c0006 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | ATGGG others(1687): Show |
chrX | 100838324 | 100879359 | ||
a0002c0002 | 0/0 | 1692 | 7 | 6 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | ATGGG others(1687): Show |
chrX | 100838324 | 100879359 | ||
a0003c0007 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | ATGGG others(1687): Show |
chrX | 100838324 | 100879359 | ||
a0004c0008 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | ATGGG others(1687): Show |
chrX | 100838324 | 100879359 | ||
a0005c0005 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | ATGGG others(1687): Show |
chrX | 100838324 | 100879359 | ||
a0006c0004 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | ATGGG others(1687): Show |
chrX | 100838324 | 100879359 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2540 | 140 | 31 | 30 | 55 | 6 | 17 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2535): Show |
chrX | 100838324 | 100879359 |
a0001c0001t0002 | 1/0 | 2543 | 133 | 22 | 21 | 69 | 5 | 15 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2538): Show |
chrX | 100838324 | 100879359 |
a0001c0001t0003 | 0/0 | 2543 | 5 | 5 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2538): Show |
chrX | 100838324 | 100879359 |
a0001c0001t0004 | 0/0 | 2543 | 5 | 0 | 0 | 5 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2538): Show |
chrX | 100838324 | 100879359 |
a0001c0001t0005 | 0/0 | 2540 | 2 | 2 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2535): Show |
chrX | 100838324 | 100879359 |
a0001c0001t0006 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2535): Show |
chrX | 100838324 | 100879359 |
a0001c0001t0007 | 0/0 | 2543 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2538): Show |
chrX | 100838324 | 100879359 |
a0001c0001t0008 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2535): Show |
chrX | 100838324 | 100879359 |
a0001c0003t0001 | 0/0 | 2540 | 2 | 2 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2535): Show |
chrX | 100838324 | 100879359 |
a0001c0006t0002 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2538): Show |
chrX | 100838324 | 100879359 |
a0002c0002t0001 | 0/0 | 2540 | 7 | 6 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2535): Show |
chrX | 100838324 | 100879359 |
a0003c0007t0001 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2535): Show |
chrX | 100838324 | 100879359 |
a0004c0008t0002 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2538): Show |
chrX | 100838324 | 100879359 |
a0005c0005t0002 | 0/0 | 2543 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2538): Show |
chrX | 100838324 | 100879359 |
a0006c0004t0001 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | GCTGG others(2535): Show |
chrX | 100838324 | 100879359 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0004g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0001t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0001c0006t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0003c0007t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0004c0008t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0005c0005t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
a0006c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0176 | EUR | FIN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01891 | hp2 | a0003 | c0007 | t0001 | g0271 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CDX | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | CDX | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0164 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0276 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02717 | hp1 | a0001 | c0006 | t0002 | g0257 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02818 | hp2 | a0004 | c0008 | t0002 | g0273 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | MSL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | MSL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0268 | AFR | MSL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | BEB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | STU | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | STU | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0269 | AFR | YRI | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | CHB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | YRI | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | YRI | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18946 | hp1 | a0005 | c0005 | t0002 | g0054 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18984 | hp1 | a0001 | c0001 | t0007 | g0169 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19005 | hp1 | a0006 | c0004 | t0001 | g0183 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19076 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19088 | hp1 | a0001 | c0001 | t0006 | g0203 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | YRI | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | YRI | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0227 | AFR | ASW | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ASW | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0260 | EUR | TSI | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | GIH | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0252 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | USA | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | USA | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | USA | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | USA | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0165 | REF | REF | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0087 | REF | REF | NOX1_chrX_100838324_100879359 | NOX1 | chrX | 100838324 | 100879359 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:100850151 | C | T | 2 | a0002 a0003 |
8 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(5): Show |
missense_variant&splice_region_variant | MODERATE | c.1133G>A | p.Arg378Lys | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 9/13 | 1353/2543 | 1133/1695 | 378/564 | chrX | 100850151 | |||
chrX:100850340 | C | T | 1 | a0005 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.944G>A | p.Arg315His | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 9/13 | 1164/2543 | 944/1695 | 315/564 | chrX | 100850340 | |||
chrX:100862293 | G | A | 1 | a0003 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.682C>T | p.Arg228Trp | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/13 | 902/2543 | 682/1695 | 228/564 | chrX | 100862293 | |||
chrX:100862818 | T | C | 1 | a0004 | 1 | HG02818.hp2 | missense_variant&splice_region_variant | MODERATE | c.340A>G | p.Ile114Val | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 5/13 | 560/2543 | 340/1695 | 114/564 | chrX | 100862818 | |||
chrX:100863233 | C | T | 1 | a0006 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.263G>A | p.Arg88His | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 4/13 | 483/2543 | 263/1695 | 88/564 | chrX | 100863233 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:100848644 | A | G | 1 | a0001c0006 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1554T>C | p.Ala518Ala | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/13 | 1774/2543 | 1554/1695 | 518/564 | chrX | 100848644 | |||
chrX:100862210 | G | A | 1 | a0001c0003 | 2 | HG03579.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.765C>T | p.Ser255Ser | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/13 | 985/2543 | 765/1695 | 255/564 | chrX | 100862210 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:100843366 | TAAG | T | 8 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(5): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*583_*585delCTT | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 13/13 | 583 | chrX | 100843366 | ||||||
chrX:100843570 | C | G | 1 | a0001c0001t0007 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*382G>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 13/13 | 382 | chrX | 100843570 | ||||||
chrX:100843763 | C | T | 1 | a0001c0001t0006 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*189G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 13/13 | 189 | chrX | 100843763 | ||||||
chrX:100843844 | G | A | 1 | a0001c0001t0003 | 5 | HG02559.hp1 HG03130.hp1 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*108C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 13/13 | 108 | chrX | 100843844 | ||||||
chrX:100843880 | C | A | 1 | a0001c0001t0004 | 5 | HG00438.hp2 NA18988.hp1 NA19011.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*72G>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 13/13 | 72 | chrX | 100843880 | ||||||
chrX:100843886 | G | A | 1 | a0001c0001t0005 | 2 | HG01884.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*66C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 13/13 | 66 | chrX | 100843886 | ||||||
chrX:100874344 | G | A | 1 | a0001c0001t0008 | 1 | HG02630.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-205C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/13 | chrX | 100874344 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:100844270 | C | G | 1 | a0001c0001t0001g0016 | 2 | NA18962.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1569-192G>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100844270 | |||||||
chrX:100844351 | AGTCT | A | 16 | a0001c0001t0001g0021 a0001c0001t0001g0103 a0001c0001t0001g0104 others(13): Show |
17 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1569-277_1569-274d others(6): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100844351 | |||||||
chrX:100844621 | T | C | 15 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0002g0196 others(12): Show |
16 | HG02257.hp2 HG02559.hp1 HG02818.hp1 others(13): Show |
intron_variant | MODIFIER | c.1569-543A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100844621 | |||||||
chrX:100844720 | A | C | 5 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0260 others(2): Show |
5 | HG02055.hp1 HG02572.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1569-642T>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100844720 | |||||||
chrX:100844801 | T | C | 168 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(165): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1569-723A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100844801 | |||||||
chrX:100844819 | T | C | 19 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0039 others(16): Show |
21 | HG00423.hp1 HG00642.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1569-741A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100844819 | |||||||
chrX:100844831 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1569-753T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100844831 | |||||||
chrX:100845086 | G | A | 1 | a0001c0001t0002g0052 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1569-1008C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100845086 | |||||||
chrX:100845391 | G | GT | 9 | a0001c0001t0001g0067 a0001c0001t0001g0238 a0001c0001t0001g0253 others(6): Show |
9 | HG02055.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1569-1314dupA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100845391 | |||||||
chrX:100845596 | A | G | 2 | a0001c0001t0002g0263 a0004c0008t0002g0273 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1569-1518T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100845596 | |||||||
chrX:100845611 | G | GT | 27 | a0001c0001t0001g0067 a0001c0001t0002g0005 a0001c0001t0002g0013 others(24): Show |
27 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.1569-1534dupA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100845611 | |||||||
chrX:100845611 | GT | G | 138 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(135): Show |
143 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1569-1534delA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100845611 | |||||||
chrX:100845611 | GTT | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0060 a0001c0001t0001g0144 others(3): Show |
6 | HG00558.hp1 HG02273.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1569-1535_1569-153 others(6): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100845611 | |||||||
chrX:100845659 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0003g0048 |
3 | HG01081.hp2 HG01106.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1569-1581C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100845659 | |||||||
chrX:100845660 | G | T | 1 | a0001c0001t0002g0223 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1569-1582C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100845660 | |||||||
chrX:100845672 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1569-1594T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100845672 | |||||||
chrX:100845723 | C | A | 10 | a0001c0001t0002g0066 a0001c0001t0002g0244 a0001c0001t0002g0254 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1569-1645G>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100845723 | |||||||
chrX:100845793 | CT | C | 152 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(149): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1569-1716delA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100845793 | |||||||
chrX:100846186 | G | T | 5 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0260 others(2): Show |
5 | HG02055.hp1 HG02572.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1569-2108C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846186 | |||||||
chrX:100846719 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1568+1911A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846719 | |||||||
chrX:100846726 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1568+1904G>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846726 | |||||||
chrX:100846765 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1568+1865A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846765 | |||||||
chrX:100846927 | G | GC | 273 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(270): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1568+1702dupG | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846927 | |||||||
chrX:100846953 | T | C | 167 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(164): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1568+1677A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846953 | |||||||
chrX:100846953 | T | G | 14 | a0001c0001t0002g0014 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
15 | HG00438.hp1 HG00597.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.1568+1677A>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846953 | |||||||
chrX:100846968 | A | T | 1 | a0001c0001t0002g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1568+1662T>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846968 | |||||||
chrX:100846970 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1568+1660G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846970 | |||||||
chrX:100846971 | T | A | 1 | a0001c0001t0002g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1568+1659A>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846971 | |||||||
chrX:100846974 | G | C | 1 | a0001c0001t0002g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1568+1656C>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846974 | |||||||
chrX:100846976 | T | C | 1 | a0001c0001t0002g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1568+1654A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846976 | |||||||
chrX:100846977 | C | G | 1 | a0001c0001t0002g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1568+1653G>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846977 | |||||||
chrX:100846978 | A | T | 1 | a0001c0001t0002g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1568+1652T>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846978 | |||||||
chrX:100846980 | G | T | 1 | a0001c0001t0002g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1568+1650C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846980 | |||||||
chrX:100846981 | A | T | 1 | a0001c0001t0002g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1568+1649T>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100846981 | |||||||
chrX:100847003 | T | C | 167 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(164): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1568+1627A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847003 | |||||||
chrX:100847120 | C | T | 153 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(150): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1568+1510G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847120 | |||||||
chrX:100847189 | G | A | 167 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(164): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1568+1441C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847189 | |||||||
chrX:100847287 | C | A | 1 | a0001c0001t0002g0097 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1568+1343G>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847287 | |||||||
chrX:100847323 | C | T | 9 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0002g0196 others(6): Show |
10 | HG02257.hp2 HG02818.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1568+1307G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847323 | |||||||
chrX:100847338 | C | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0272 a0001c0001t0008g0276 |
3 | HG02615.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1568+1292G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847338 | |||||||
chrX:100847345 | C | T | 6 | a0001c0001t0001g0137 a0001c0001t0001g0151 a0001c0001t0001g0193 others(3): Show |
6 | HG01243.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1568+1285G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847345 | |||||||
chrX:100847594 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1568+1036T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847594 | |||||||
chrX:100847691 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1568+939C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847691 | |||||||
chrX:100847717 | G | A | 1 | a0005c0005t0002g0054 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1568+913C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847717 | |||||||
chrX:100847749 | A | G | 5 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0260 others(2): Show |
5 | HG02055.hp1 HG02572.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1568+881T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847749 | |||||||
chrX:100847766 | C | CA | 165 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(162): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1568+863dupT | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847766 | |||||||
chrX:100847766 | C | CAA | 6 | a0001c0001t0001g0037 a0001c0001t0001g0128 a0001c0001t0001g0134 others(3): Show |
6 | HG01978.hp2 HG03471.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1568+862_1568+863d others(4): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100847766 | |||||||
chrX:100848291 | CT | C | 10 | a0001c0001t0001g0047 a0001c0001t0002g0003 a0001c0001t0002g0046 others(7): Show |
11 | HG02257.hp2 HG02818.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1568+338delA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100848291 | |||||||
chrX:100848584 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0274 |
2 | HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1568+46G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 12/12 | chrX | 100848584 | |||||||
chrX:100848805 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1444-51C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 11/12 | chrX | 100848805 | |||||||
chrX:100848892 | A | G | 147 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(144): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1444-138T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 11/12 | chrX | 100848892 | |||||||
chrX:100849090 | A | AAAG | 173 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(170): Show |
180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1443+187_1443+189d others(5): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 11/12 | chrX | 100849090 | |||||||
chrX:100849237 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1443+43C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 11/12 | chrX | 100849237 | |||||||
chrX:100849628 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1296+144C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 10/12 | chrX | 100849628 | |||||||
chrX:100850042 | AT | A | 6 | a0001c0001t0001g0274 a0001c0001t0003g0048 a0001c0001t0003g0171 others(3): Show |
6 | HG02559.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1133+108delA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 9/12 | chrX | 100850042 | |||||||
chrX:100850429 | A | G | 167 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(164): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.898-43T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 8/12 | chrX | 100850429 | |||||||
chrX:100850497 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.898-111G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 8/12 | chrX | 100850497 | |||||||
chrX:100850679 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.898-293G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 8/12 | chrX | 100850679 | |||||||
chrX:100850861 | A | G | 1 | a0001c0001t0005g0252 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.897+372T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 8/12 | chrX | 100850861 | |||||||
chrX:100850894 | C | T | 155 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(152): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.897+339G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 8/12 | chrX | 100850894 | |||||||
chrX:100850951 | C | T | 5 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0260 others(2): Show |
5 | HG02055.hp1 HG02572.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.897+282G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 8/12 | chrX | 100850951 | |||||||
chrX:100850996 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.897+237G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 8/12 | chrX | 100850996 | |||||||
chrX:100851006 | A | AT | 11 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0067 others(8): Show |
11 | HG02559.hp1 HG02615.hp1 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.897+226dupA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 8/12 | chrX | 100851006 | |||||||
chrX:100851049 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.897+184C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 8/12 | chrX | 100851049 | |||||||
chrX:100851656 | C | T | 7 | a0001c0001t0001g0067 a0001c0001t0001g0274 a0001c0001t0003g0048 others(4): Show |
7 | HG02559.hp1 HG03041.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.805-331G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100851656 | |||||||
chrX:100851874 | A | G | 167 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(164): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.805-549T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100851874 | |||||||
chrX:100851920 | A | AAAAAT | 158 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(155): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.805-600_805-596dup others(5): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100851920 | |||||||
chrX:100851925 | T | TAAAAC | 9 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0002g0196 others(6): Show |
10 | HG02257.hp2 HG02818.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.805-601_805-600ins others(5): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100851925 | |||||||
chrX:100852097 | T | A | 10 | a0001c0001t0002g0066 a0001c0001t0002g0244 a0001c0001t0002g0254 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.805-772A>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100852097 | |||||||
chrX:100852326 | G | A | 152 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(149): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.805-1001C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100852326 | |||||||
chrX:100852330 | G | C | 5 | a0001c0001t0003g0048 a0001c0001t0003g0171 a0001c0001t0003g0251 others(2): Show |
5 | HG02559.hp1 HG03130.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-1005C>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100852330 | |||||||
chrX:100852341 | T | C | 163 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(160): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.805-1016A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100852341 | |||||||
chrX:100852361 | C | T | 7 | a0001c0001t0001g0067 a0001c0001t0001g0274 a0001c0001t0003g0048 others(4): Show |
7 | HG02559.hp1 HG03041.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.805-1036G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100852361 | |||||||
chrX:100852362 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.805-1037C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100852362 | |||||||
chrX:100852496 | C | T | 11 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(8): Show |
14 | HG00609.hp1 HG02071.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.805-1171G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100852496 | |||||||
chrX:100852598 | G | T | 5 | a0001c0001t0003g0048 a0001c0001t0003g0171 a0001c0001t0003g0251 others(2): Show |
5 | HG02559.hp1 HG03130.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-1273C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100852598 | |||||||
chrX:100852833 | G | T | 1 | a0001c0003t0001g0268 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.805-1508C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100852833 | |||||||
chrX:100852834 | G | T | 1 | a0001c0003t0001g0268 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.805-1509C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100852834 | |||||||
chrX:100852990 | G | T | 29 | a0001c0001t0001g0067 a0001c0001t0001g0274 a0001c0001t0002g0003 others(26): Show |
30 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.805-1665C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100852990 | |||||||
chrX:100853082 | G | A | 16 | a0001c0001t0002g0066 a0001c0001t0002g0196 a0001c0001t0002g0197 others(13): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.805-1757C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853082 | |||||||
chrX:100853221 | CTCTT | C | 3 | a0001c0001t0002g0196 a0001c0001t0002g0261 a0004c0008t0002g0273 |
3 | HG02809.hp2 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.805-1900_805-1897d others(6): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853221 | |||||||
chrX:100853231 | C | T | 13 | a0001c0001t0002g0066 a0001c0001t0002g0197 a0001c0001t0002g0244 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.805-1906G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853231 | |||||||
chrX:100853233 | T | C | 13 | a0001c0001t0002g0066 a0001c0001t0002g0197 a0001c0001t0002g0244 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.805-1908A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853233 | |||||||
chrX:100853242 | T | C | 13 | a0001c0001t0002g0066 a0001c0001t0002g0197 a0001c0001t0002g0244 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.805-1917A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853242 | |||||||
chrX:100853249 | C | T | 13 | a0001c0001t0002g0066 a0001c0001t0002g0197 a0001c0001t0002g0244 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.805-1924G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853249 | |||||||
chrX:100853250 | C | CTTTCTTT others(33): Show |
1 | a0001c0001t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.805-1926_805-1925i others(42): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853250 | |||||||
chrX:100853253 | C | T | 164 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(161): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.805-1928G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853253 | |||||||
chrX:100853254 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.805-1929G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853254 | |||||||
chrX:100853255 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.805-1930A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853255 | |||||||
chrX:100853256 | T | TTCTTTCT others(57): Show |
1 | a0001c0001t0001g0242 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.805-1932_805-1931i others(66): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853256 | |||||||
chrX:100853257 | C | T | 174 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(171): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.805-1932G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853257 | |||||||
chrX:100853258 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.805-1933G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853258 | |||||||
chrX:100853261 | C | CCTTCCTT others(1): Show |
4 | a0001c0001t0002g0026 a0001c0001t0002g0096 a0001c0001t0002g0122 others(1): Show |
4 | HG00609.hp1 HG01993.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-1937_805-1936i others(10): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | C | CCTTCCTT others(5): Show |
2 | a0001c0001t0002g0028 a0001c0001t0002g0044 |
2 | HG01934.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.805-1937_805-1936i others(14): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | C | CCTTCCTT others(9): Show |
1 | a0001c0001t0002g0043 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.805-1937_805-1936i others(18): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | C | CCTTT | 17 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0024 others(14): Show |
20 | HG00597.hp1 HG01099.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.805-1940_805-1937d others(6): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | C | CCTTTCTT others(1): Show |
8 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0055 others(5): Show |
10 | HG00323.hp2 HG00738.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.805-1944_805-1937d others(10): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | C | CCTTTCTT others(5): Show |
6 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0074 others(3): Show |
8 | HG00621.hp1 HG01975.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.805-1948_805-1937d others(14): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | C | CCTTTCTT others(9): Show |
3 | a0001c0001t0002g0052 a0001c0001t0002g0080 a0001c0001t0002g0120 |
3 | HG01123.hp1 HG02129.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.805-1952_805-1937d others(18): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | C | CCTTTCTT others(13): Show |
1 | a0001c0001t0002g0079 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.805-1956_805-1937d others(22): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | C | T | 182 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(179): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.805-1936G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | CCTTT | C | 8 | a0001c0001t0002g0009 a0001c0001t0002g0088 a0001c0001t0002g0097 others(5): Show |
11 | HG00423.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.805-1940_805-1937d others(6): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | CCTTTCTT others(1): Show |
C | 5 | a0001c0001t0002g0049 a0001c0001t0002g0058 a0001c0001t0002g0077 others(2): Show |
5 | HG02698.hp1 HG03710.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-1944_805-1937d others(10): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | CCTTTCTT others(5): Show |
C | 1 | a0001c0001t0002g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.805-1948_805-1937d others(14): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853261 | CCTTTCTT others(9): Show |
C | 2 | a0001c0001t0002g0059 a0001c0001t0002g0089 |
2 | HG01255.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.805-1952_805-1937d others(18): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853261 | |||||||
chrX:100853264 | T | TTCTTTCT others(49): Show |
1 | a0001c0001t0001g0109 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.805-1940_805-1939i others(58): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853264 | |||||||
chrX:100853265 | T | C | 2 | a0001c0001t0002g0071 a0001c0001t0002g0098 |
2 | HG00558.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.805-1940A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853265 | |||||||
chrX:100853268 | T | TTCTTTCT others(21): Show |
1 | a0001c0003t0001g0227 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.805-1944_805-1943i others(30): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853268 | |||||||
chrX:100853276 | T | TTCTCTCT others(5): Show |
1 | a0001c0001t0002g0265 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.805-1952_805-1951i others(14): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853276 | |||||||
chrX:100853276 | T | TTCTTTCT others(13): Show |
2 | a0001c0001t0002g0254 a0001c0001t0002g0256 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.805-1952_805-1951i others(22): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853276 | |||||||
chrX:100853276 | T | TTCTTTCT others(17): Show |
1 | a0001c0001t0002g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.805-1952_805-1951i others(26): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853276 | |||||||
chrX:100853278 | C | CTTTCTTT others(59): Show |
1 | a0001c0001t0001g0159 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.805-1954_805-1953i others(68): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853278 | |||||||
chrX:100853280 | T | TTCTTTCT others(9): Show |
1 | a0001c0001t0002g0066 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805-1956_805-1955i others(18): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853280 | |||||||
chrX:100853280 | T | TTCTTTCT others(13): Show |
5 | a0001c0001t0002g0255 a0001c0001t0002g0258 a0001c0001t0002g0262 others(2): Show |
5 | HG02055.hp1 HG02717.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-1956_805-1955i others(22): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853280 | |||||||
chrX:100853280 | T | TTCTTTCT others(17): Show |
1 | a0001c0001t0002g0197 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.805-1956_805-1955i others(26): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853280 | |||||||
chrX:100853282 | C | CTTTCTTT others(51): Show |
1 | a0001c0001t0001g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.805-1958_805-1957i others(60): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853282 | |||||||
chrX:100853282 | C | CTTTCTTT others(63): Show |
2 | a0001c0001t0001g0025 a0001c0001t0001g0236 |
2 | HG03669.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.805-1958_805-1957i others(72): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853282 | |||||||
chrX:100853282 | C | CTTTCTTT others(61): Show |
1 | a0001c0001t0001g0210 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.805-1958_805-1957i others(70): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853282 | |||||||
chrX:100853284 | T | TTCTTTCT others(9): Show |
1 | a0001c0001t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.805-1960_805-1959i others(18): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853284 | |||||||
chrX:100853284 | T | TTCTTTCT others(25): Show |
2 | a0001c0001t0001g0104 a0001c0001t0001g0184 |
2 | HG01928.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.805-1960_805-1959i others(34): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853284 | |||||||
chrX:100853284 | T | TTCTTTCT others(54): Show |
1 | a0001c0001t0001g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.805-1960_805-1959i others(63): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853284 | |||||||
chrX:100853284 | T | TTCTTTCT others(21): Show |
1 | a0001c0001t0001g0186 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.805-1960_805-1959i others(30): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853284 | |||||||
chrX:100853284 | T | TTCTTTCT others(29): Show |
1 | a0001c0001t0001g0187 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.805-1960_805-1959i others(38): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853284 | |||||||
chrX:100853286 | C | CTTTCTTT others(39): Show |
1 | a0001c0001t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.805-1962_805-1961i others(48): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853286 | |||||||
chrX:100853286 | C | CTTTCTTT others(51): Show |
2 | a0001c0001t0001g0136 a0001c0001t0001g0166 |
2 | HG01943.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.805-1962_805-1961i others(60): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853286 | |||||||
chrX:100853286 | C | CTTTCTTT others(55): Show |
1 | a0001c0001t0001g0202 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.805-1962_805-1961i others(64): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853286 | |||||||
chrX:100853286 | C | CTTTCTTT others(59): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0158 |
3 | HG00280.hp1 NA18962.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.805-1962_805-1961i others(68): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853286 | |||||||
chrX:100853287 | T | TTTCTTTC others(52): Show |
1 | a0003c0007t0001g0271 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.805-1963_805-1962i others(61): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853287 | |||||||
chrX:100853287 | T | TTTCTTTC others(56): Show |
1 | a0001c0001t0001g0192 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.805-1963_805-1962i others(65): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853287 | |||||||
chrX:100853288 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.805-1963A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853288 | |||||||
chrX:100853288 | T | TCTTTCTT others(28): Show |
1 | a0001c0001t0001g0221 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.805-1964_805-1963i others(37): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853288 | |||||||
chrX:100853288 | T | TTCTCTCT others(5): Show |
1 | a0001c0001t0001g0149 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.805-1964_805-1963i others(14): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853288 | |||||||
chrX:100853288 | T | TTCTCTCT others(35): Show |
1 | a0001c0001t0001g0152 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.805-1964_805-1963i others(44): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853288 | |||||||
chrX:100853288 | T | TTCTTTCT others(13): Show |
1 | a0002c0002t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.805-1964_805-1963i others(22): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853288 | |||||||
chrX:100853288 | T | TTCTTTCT others(21): Show |
3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0239 |
3 | HG00408.hp1 HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.805-1964_805-1963i others(30): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853288 | |||||||
chrX:100853288 | T | TTCTTTCT others(55): Show |
1 | a0001c0001t0001g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.805-1964_805-1963i others(64): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853288 | |||||||
chrX:100853290 | C | CTTTCTCT others(39): Show |
1 | a0002c0002t0001g0211 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.805-1966_805-1965i others(48): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853290 | |||||||
chrX:100853290 | C | CTTTCTTT others(35): Show |
1 | a0001c0001t0001g0134 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.805-1966_805-1965i others(44): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853290 | |||||||
chrX:100853290 | C | CTTTCTTT others(43): Show |
2 | a0001c0001t0001g0220 a0002c0002t0001g0230 |
2 | HG01109.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.805-1966_805-1965i others(52): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853290 | |||||||
chrX:100853290 | C | CTTTCTTT others(47): Show |
2 | a0001c0001t0001g0241 a0001c0001t0001g0248 |
2 | HG03516.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.805-1966_805-1965i others(56): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853290 | |||||||
chrX:100853290 | C | CTTTCTTT others(51): Show |
6 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0154 others(3): Show |
7 | HG00642.hp1 HG01081.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.805-1966_805-1965i others(60): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853290 | |||||||
chrX:100853290 | C | CTTTCTTT others(55): Show |
4 | a0001c0001t0001g0065 a0001c0001t0001g0135 a0001c0001t0001g0204 others(1): Show |
4 | HG04228.hp1 NA18612.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-1966_805-1965i others(64): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853290 | |||||||
chrX:100853291 | T | TTTCTTTC others(46): Show |
1 | a0001c0001t0001g0106 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.805-1967_805-1966i others(55): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853291 | |||||||
chrX:100853292 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0222 a0001c0001t0001g0253 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-1967A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853292 | |||||||
chrX:100853292 | T | TTCTCTCT others(5): Show |
4 | a0001c0001t0001g0020 a0001c0001t0001g0130 a0001c0001t0001g0146 others(1): Show |
5 | HG00323.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-1968_805-1967i others(14): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853292 | |||||||
chrX:100853292 | T | TTCTCTCT others(57): Show |
1 | a0001c0001t0002g0261 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.805-1968_805-1967i others(66): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853292 | |||||||
chrX:100853292 | T | TTCTCTCT others(61): Show |
1 | a0004c0008t0002g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.805-1968_805-1967i others(70): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853292 | |||||||
chrX:100853292 | T | TTCTTTCT others(9): Show |
3 | a0001c0001t0001g0151 a0001c0001t0001g0182 a0001c0001t0001g0249 |
3 | HG03486.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.805-1968_805-1967i others(18): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853292 | |||||||
chrX:100853292 | T | TTCTTTCT others(47): Show |
1 | a0001c0001t0001g0143 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.805-1968_805-1967i others(56): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853292 | |||||||
chrX:100853292 | T | TTCTTTCT others(9): Show |
1 | a0001c0001t0001g0179 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.805-1968_805-1967i others(18): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853292 | |||||||
chrX:100853292 | T | TTCTTTCT others(21): Show |
1 | a0001c0001t0001g0172 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.805-1968_805-1967i others(30): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853292 | |||||||
chrX:100853292 | T | TTCTTTCT others(51): Show |
2 | a0001c0001t0001g0160 a0001c0001t0006g0203 |
2 | NA19088.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.805-1968_805-1967i others(60): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853292 | |||||||
chrX:100853294 | C | CTTTCTCT others(35): Show |
1 | a0002c0002t0001g0164 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.805-1970_805-1969i others(44): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853294 | |||||||
chrX:100853294 | C | CTTTCTCT others(39): Show |
1 | a0001c0001t0001g0232 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.805-1970_805-1969i others(48): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853294 | |||||||
chrX:100853294 | C | CTTTCTTT others(39): Show |
1 | a0001c0001t0001g0126 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.805-1970_805-1969i others(48): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853294 | |||||||
chrX:100853294 | C | CTTTCTTT others(43): Show |
4 | a0001c0001t0001g0111 a0001c0001t0001g0131 a0001c0001t0001g0247 others(1): Show |
4 | HG02257.hp1 HG03195.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-1970_805-1969i others(52): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853294 | |||||||
chrX:100853294 | C | CTTTCTTT others(47): Show |
5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0153 others(2): Show |
5 | HG00099.hp1 HG01106.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-1970_805-1969i others(56): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853294 | |||||||
chrX:100853294 | C | CTTTCTTT others(40): Show |
1 | a0001c0001t0001g0207 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.805-1970_805-1969i others(49): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853294 | |||||||
chrX:100853294 | C | CTTTCTTT others(42): Show |
1 | a0001c0001t0002g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.805-1970_805-1969i others(51): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853294 | |||||||
chrX:100853294 | C | CTTTCTTT others(51): Show |
4 | a0001c0001t0001g0064 a0001c0001t0001g0110 a0001c0001t0001g0125 others(1): Show |
4 | NA18952.hp1 NA19074.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-1970_805-1969i others(60): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853294 | |||||||
chrX:100853296 | T | C | 3 | a0001c0001t0001g0188 a0001c0001t0001g0253 a0001c0001t0005g0266 |
3 | HG01884.hp1 HG02040.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.805-1971A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853296 | |||||||
chrX:100853296 | T | TTCTCTCT others(5): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0147 |
3 | HG01070.hp2 HG01071.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.805-1972_805-1971i others(14): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853296 | |||||||
chrX:100853296 | T | TTCTCTCT others(53): Show |
1 | a0001c0001t0002g0196 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.805-1972_805-1971i others(62): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853296 | |||||||
chrX:100853296 | T | TTCTCTCT others(57): Show |
1 | a0001c0001t0002g0264 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.805-1972_805-1971i others(66): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853296 | |||||||
chrX:100853296 | T | TTCTTTCT others(39): Show |
1 | a0001c0001t0001g0144 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.805-1972_805-1971i others(48): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853296 | |||||||
chrX:100853296 | T | TTCTTTCT others(5): Show |
1 | a0001c0001t0001g0180 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.805-1972_805-1971i others(14): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853296 | |||||||
chrX:100853296 | T | TTCTTTCT others(47): Show |
1 | a0001c0001t0001g0031 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.805-1972_805-1971i others(56): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853296 | |||||||
chrX:100853296 | T | TTCTTTCT others(9): Show |
1 | a0001c0001t0001g0021 | 2 | HG00544.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.805-1972_805-1971i others(18): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853296 | |||||||
chrX:100853296 | T | TTCTTTCT others(51): Show |
1 | a0001c0001t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.805-1972_805-1971i others(60): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853296 | |||||||
chrX:100853298 | C | CTCTCTCT others(31): Show |
1 | a0001c0001t0001g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.805-1974_805-1973i others(40): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853298 | |||||||
chrX:100853298 | C | CTCTCTCT others(35): Show |
1 | a0001c0001t0001g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.805-1974_805-1973i others(44): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853298 | |||||||
chrX:100853298 | C | CTTTCTCT others(39): Show |
2 | a0001c0001t0001g0128 a0001c0001t0001g0216 |
2 | NA19080.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.805-1974_805-1973i others(48): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853298 | |||||||
chrX:100853298 | C | CTTTCTTT others(43): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0215 |
2 | HG03654.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.805-1974_805-1973i others(52): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853298 | |||||||
chrX:100853298 | C | CTTTCTTT others(47): Show |
5 | a0001c0001t0001g0082 a0001c0001t0001g0108 a0001c0001t0001g0139 others(2): Show |
5 | HG01074.hp1 HG02486.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-1974_805-1973i others(56): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853298 | |||||||
chrX:100853298 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0005g0266 |
2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.805-1973G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853298 | |||||||
chrX:100853300 | T | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0253 a0001c0001t0005g0266 |
3 | HG01884.hp1 HG02886.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.805-1975A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853300 | |||||||
chrX:100853300 | T | TTCTCTCT others(5): Show |
3 | a0001c0001t0001g0023 a0001c0001t0001g0145 a0001c0001t0001g0170 |
4 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-1976_805-1975i others(14): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853300 | |||||||
chrX:100853300 | T | TTCTTTCT others(9): Show |
1 | a0001c0001t0001g0103 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.805-1976_805-1975i others(18): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853300 | |||||||
chrX:100853300 | T | TTCTTTCT others(39): Show |
1 | a0001c0001t0001g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.805-1976_805-1975i others(48): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853300 | |||||||
chrX:100853300 | T | TTCTTTCT others(47): Show |
1 | a0001c0001t0001g0162 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.805-1976_805-1975i others(56): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853300 | |||||||
chrX:100853302 | C | CTCTCTCT others(35): Show |
4 | a0001c0001t0001g0214 a0001c0001t0001g0245 a0002c0002t0001g0231 others(1): Show |
4 | HG02622.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-1978_805-1977i others(44): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853302 | |||||||
chrX:100853302 | C | CTTTCTCT others(39): Show |
1 | a0001c0001t0001g0138 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.805-1978_805-1977i others(48): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853302 | |||||||
chrX:100853302 | C | CTTTCTTT others(43): Show |
2 | a0001c0001t0001g0193 a0002c0002t0001g0250 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.805-1978_805-1977i others(52): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853302 | |||||||
chrX:100853302 | CTTTCTTT others(3): Show |
C | 1 | a0001c0001t0002g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.805-1987_805-1978d others(12): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853302 | |||||||
chrX:100853303 | T | TTTCTCTC others(40): Show |
1 | a0001c0001t0001g0060 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.805-1979_805-1978i others(49): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853303 | |||||||
chrX:100853304 | T | C | 4 | a0001c0001t0003g0171 a0001c0001t0003g0251 a0001c0001t0003g0269 others(1): Show |
4 | HG02559.hp1 HG02630.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-1979A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853304 | |||||||
chrX:100853304 | T | TTCTCTCT others(39): Show |
1 | a0001c0001t0001g0037 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.805-1980_805-1979i others(48): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853304 | |||||||
chrX:100853304 | T | TTCTTTCT others(9): Show |
1 | a0001c0001t0001g0173 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.805-1980_805-1979i others(18): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853304 | |||||||
chrX:100853304 | T | TTCTTTCT others(39): Show |
1 | a0001c0001t0001g0038 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.805-1980_805-1979i others(48): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853304 | |||||||
chrX:100853308 | T | C | 5 | a0001c0001t0001g0137 a0001c0001t0002g0046 a0001c0001t0003g0251 others(2): Show |
5 | HG02886.hp2 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-1983A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853308 | |||||||
chrX:100853308 | T | TTCTCTCT others(5): Show |
4 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0199 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-1984_805-1983i others(14): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853308 | |||||||
chrX:100853308 | T | TTCTCTCT others(39): Show |
1 | a0001c0001t0001g0036 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.805-1984_805-1983i others(48): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853308 | |||||||
chrX:100853310 | C | CTCTTTCT others(31): Show |
1 | a0001c0001t0001g0137 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.805-1986_805-1985i others(40): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853310 | |||||||
chrX:100853310 | C | T | 1 | a0001c0001t0003g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.805-1985G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853310 | |||||||
chrX:100853312 | T | C | 2 | a0001c0001t0003g0269 a0001c0001t0003g0270 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.805-1987A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853312 | |||||||
chrX:100853312 | T | TTC | 12 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0142 others(9): Show |
13 | HG00423.hp1 HG01496.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.805-1989_805-1988d others(4): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853312 | |||||||
chrX:100853314 | C | CTCTCTCT others(52): Show |
1 | a0001c0001t0001g0061 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.805-1990_805-1989i others(61): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853314 | |||||||
chrX:100853316 | T | C | 15 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0142 others(12): Show |
16 | HG00423.hp1 HG00544.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.805-1991A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853316 | |||||||
chrX:100853319 | T | C | 1 | a0006c0004t0001g0183 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.805-1994A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853319 | |||||||
chrX:100853319 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0002g0090 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.805-1995_805-1994i others(13): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853319 | |||||||
chrX:100853320 | T | C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
11 | HG01358.hp1 HG01952.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.805-1995A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853320 | |||||||
chrX:100853322 | C | CTT | 14 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0103 others(11): Show |
17 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.805-1998_805-1997i others(4): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853322 | |||||||
chrX:100853322 | C | T | 7 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0212 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.805-1997G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853322 | |||||||
chrX:100853324 | C | CTT | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
7 | HG01358.hp1 HG01952.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.805-2000_805-1999i others(4): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853324 | |||||||
chrX:100853324 | C | T | 114 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0022 others(111): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.805-1999G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853324 | |||||||
chrX:100853326 | C | CTCTCTTT others(21): Show |
1 | a0001c0001t0001g0181 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.805-2002_805-2001i others(30): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853326 | |||||||
chrX:100853326 | C | T | 46 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(43): Show |
52 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.805-2001G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853326 | |||||||
chrX:100853328 | C | T | 106 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0022 others(103): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.805-2003G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853328 | |||||||
chrX:100853330 | T | C | 111 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0025 others(108): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.805-2005A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853330 | |||||||
chrX:100853332 | C | CTCTT | 12 | a0001c0001t0002g0017 a0001c0001t0002g0028 a0001c0001t0002g0052 others(9): Show |
13 | HG01192.hp1 HG03710.hp1 HG03927.hp2 others(10): Show |
intron_variant | MODIFIER | c.805-2011_805-2008d others(6): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTCTTTCT others(1): Show |
3 | a0001c0001t0002g0001 a0001c0001t0002g0040 a0001c0001t0002g0083 |
5 | NA18940.hp1 NA18992.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-2015_805-2008d others(10): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTCTTTCT others(17): Show |
1 | a0001c0001t0002g0197 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.805-2031_805-2008d others(26): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTCTTTCT others(21): Show |
2 | a0001c0001t0001g0274 a0001c0001t0002g0267 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.805-2035_805-2008d others(30): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTCTTTCT others(25): Show |
7 | a0001c0001t0001g0067 a0001c0001t0002g0244 a0001c0001t0002g0256 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.805-2039_805-2008d others(34): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTCTTTCT others(29): Show |
4 | a0001c0001t0002g0066 a0001c0001t0002g0255 a0001c0001t0002g0260 others(1): Show |
4 | HG02965.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-2043_805-2008d others(38): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTCTTTCT others(33): Show |
1 | a0001c0001t0002g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(42): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTT | 15 | a0001c0001t0001g0021 a0001c0001t0001g0103 a0001c0001t0001g0170 others(12): Show |
16 | HG00544.hp1 HG01243.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.805-2008_805-2007i others(4): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTT | 4 | a0001c0001t0001g0212 a0001c0001t0001g0238 a0001c0001t0001g0272 others(1): Show |
4 | HG02615.hp2 HG02818.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-2008_805-2007i others(8): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(3): Show |
3 | a0001c0001t0001g0249 a0001c0001t0002g0190 a0002c0002t0001g0229 |
3 | HG02572.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.805-2008_805-2007i others(12): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(7): Show |
2 | a0001c0001t0001g0151 a0001c0001t0002g0003 |
3 | HG02895.hp1 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.805-2008_805-2007i others(16): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(53): Show |
1 | a0001c0001t0001g0209 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.805-2008_805-2007i others(62): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(41): Show |
1 | a0001c0001t0001g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.805-2008_805-2007i others(50): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(49): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0228 |
2 | HG01358.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.805-2008_805-2007i others(58): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(53): Show |
1 | a0001c0001t0001g0029 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(62): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(61): Show |
1 | a0001c0001t0001g0240 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(70): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(49): Show |
1 | a0001c0001t0001g0034 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(58): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(53): Show |
1 | a0001c0001t0001g0032 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(62): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(57): Show |
1 | a0001c0001t0001g0161 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(66): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(23): Show |
1 | a0001c0001t0001g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(32): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(62): Show |
1 | a0001c0001t0001g0237 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(71): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(49): Show |
1 | a0001c0001t0001g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(58): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(57): Show |
2 | a0001c0001t0001g0219 a0001c0001t0001g0234 |
2 | HG02056.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.805-2008_805-2007i others(66): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(61): Show |
1 | a0001c0001t0002g0233 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.805-2008_805-2007i others(70): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(45): Show |
1 | a0001c0001t0001g0194 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(54): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(53): Show |
1 | a0001c0001t0001g0142 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(62): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | CTTTCTTT others(57): Show |
1 | a0001c0001t0001g0205 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.805-2008_805-2007i others(66): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | C | T | 110 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0023 others(107): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.805-2007G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853332 | CTCTT | C | 4 | a0001c0001t0002g0091 a0001c0001t0002g0114 a0001c0001t0002g0118 others(1): Show |
4 | HG02293.hp1 HG02698.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-2011_805-2008d others(6): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853332 | |||||||
chrX:100853333 | T | TTTCTTTC others(100): Show |
1 | a0001c0001t0001g0222 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.805-2009_805-2008i others(109): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853333 | |||||||
chrX:100853333 | T | TTTCTTTC others(96): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0147 a0001c0001t0001g0148 |
4 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-2009_805-2008i others(105): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853333 | |||||||
chrX:100853333 | T | TTTCTTTC others(92): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0149 |
3 | HG01168.hp1 HG01169.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.805-2009_805-2008i others(101): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853333 | |||||||
chrX:100853333 | T | TTTCTTTC others(88): Show |
1 | a0001c0001t0001g0130 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.805-2009_805-2008i others(97): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853333 | |||||||
chrX:100853333 | T | TTTCTTTC others(88): Show |
2 | a0001c0001t0001g0146 a0001c0001t0001g0150 |
2 | HG02970.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.805-2009_805-2008i others(97): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853333 | |||||||
chrX:100853334 | C | T | 5 | a0001c0001t0002g0069 a0001c0001t0002g0071 a0001c0001t0002g0098 others(2): Show |
5 | HG00558.hp2 HG02074.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-2009G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853334 | |||||||
chrX:100853336 | T | C | 6 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(3): Show |
6 | HG00558.hp2 HG02074.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-2011A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853336 | |||||||
chrX:100853337 | T | C | 9 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0130 others(6): Show |
11 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.805-2012A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853337 | |||||||
chrX:100853337 | T | TCTTTCTT others(98): Show |
1 | a0001c0001t0001g0023 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.805-2013_805-2012i others(107): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853337 | |||||||
chrX:100853337 | T | TCTTTCTT others(94): Show |
1 | a0001c0001t0001g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.805-2013_805-2012i others(103): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853337 | |||||||
chrX:100853365 | T | TTTCTTTC others(68): Show |
1 | a0001c0001t0001g0206 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.805-2041_805-2040i others(77): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853365 | |||||||
chrX:100853367 | T | TTTCTTTC others(40): Show |
1 | a0006c0004t0001g0183 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.805-2043_805-2042i others(49): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853367 | |||||||
chrX:100853423 | CT | C | 6 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0002g0198 others(3): Show |
7 | HG02818.hp1 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.805-2099delA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853423 | |||||||
chrX:100853433 | T | C | 5 | a0001c0001t0001g0170 a0001c0001t0003g0048 a0001c0001t0003g0171 others(2): Show |
5 | HG02559.hp1 HG02630.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-2108A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853433 | |||||||
chrX:100853452 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.805-2127C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853452 | |||||||
chrX:100853528 | G | GTAGCTAA others(128): Show |
2 | a0001c0001t0001g0131 a0001c0001t0002g0260 |
2 | HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.805-2338_805-2204d others(137): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853528 | |||||||
chrX:100853528 | GTAGCTAA others(128): Show |
G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0181 |
2 | HG02738.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.805-2338_805-2204d others(2): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853528 | |||||||
chrX:100853607 | G | C | 1 | a0002c0002t0001g0231 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.805-2282C>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853607 | |||||||
chrX:100853635 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.805-2310C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100853635 | |||||||
chrX:100854016 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.805-2691C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100854016 | |||||||
chrX:100854078 | G | T | 1 | a0001c0001t0001g0173 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.805-2753C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100854078 | |||||||
chrX:100854385 | A | G | 175 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(172): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.805-3060T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100854385 | |||||||
chrX:100854409 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.805-3084C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100854409 | |||||||
chrX:100854469 | C | T | 7 | a0001c0001t0002g0018 a0001c0001t0002g0024 a0001c0001t0002g0120 others(4): Show |
9 | HG00408.hp2 HG01099.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.805-3144G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100854469 | |||||||
chrX:100854627 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.805-3302A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100854627 | |||||||
chrX:100854676 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.805-3351G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100854676 | |||||||
chrX:100854677 | G | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.805-3352C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100854677 | |||||||
chrX:100854929 | T | A | 177 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(174): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.805-3604A>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100854929 | |||||||
chrX:100854954 | T | TA | 176 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(173): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.805-3630dupT | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100854954 | |||||||
chrX:100854978 | T | C | 177 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(174): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.805-3653A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100854978 | |||||||
chrX:100855059 | T | C | 10 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0002c0002t0001g0164 others(7): Show |
10 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.805-3734A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100855059 | |||||||
chrX:100855072 | T | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0272 others(4): Show |
7 | HG02615.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.805-3747A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100855072 | |||||||
chrX:100855191 | C | T | 174 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(171): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.805-3866G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100855191 | |||||||
chrX:100855200 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0191 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.805-3875A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100855200 | |||||||
chrX:100855398 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.805-4073C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100855398 | |||||||
chrX:100855518 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.805-4193C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100855518 | |||||||
chrX:100855742 | A | C | 5 | a0001c0001t0001g0111 a0001c0001t0001g0212 a0001c0001t0001g0246 others(2): Show |
5 | HG02257.hp1 HG02486.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-4417T>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100855742 | |||||||
chrX:100855750 | C | T | 1 | a0001c0001t0002g0009 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.805-4425G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100855750 | |||||||
chrX:100855798 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.805-4473G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100855798 | |||||||
chrX:100855815 | T | A | 1 | a0001c0001t0002g0062 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.805-4490A>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100855815 | |||||||
chrX:100855910 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.805-4585G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100855910 | |||||||
chrX:100856020 | G | A | 3 | a0001c0001t0001g0238 a0001c0001t0001g0272 a0001c0001t0008g0276 |
3 | HG02615.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.805-4695C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100856020 | |||||||
chrX:100856195 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.805-4870C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100856195 | |||||||
chrX:100856299 | C | T | 11 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0133 others(8): Show |
11 | HG00323.hp1 HG01109.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.805-4974G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100856299 | |||||||
chrX:100856499 | G | A | 1 | a0001c0001t0003g0270 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.805-5174C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100856499 | |||||||
chrX:100856627 | C | T | 1 | a0001c0001t0003g0251 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.805-5302G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100856627 | |||||||
chrX:100856730 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA19012.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.805-5405C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100856730 | |||||||
chrX:100856812 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.804+5359T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100856812 | |||||||
chrX:100857711 | C | CT | 11 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(8): Show |
13 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.804+4459dupA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100857711 | |||||||
chrX:100857711 | CT | C | 164 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(161): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.804+4459delA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100857711 | |||||||
chrX:100857711 | CTT | C | 17 | a0001c0001t0001g0047 a0001c0001t0001g0124 a0001c0001t0001g0154 others(14): Show |
18 | HG01884.hp1 HG02109.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.804+4458_804+4459d others(4): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100857711 | |||||||
chrX:100857766 | TTTG | T | 9 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0002c0002t0001g0164 others(6): Show |
9 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.804+4402_804+4404d others(5): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100857766 | |||||||
chrX:100857769 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.804+4402C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100857769 | |||||||
chrX:100857943 | T | C | 181 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(178): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.804+4228A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100857943 | |||||||
chrX:100858021 | G | T | 1 | a0001c0001t0002g0074 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.804+4150C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100858021 | |||||||
chrX:100858090 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.804+4081T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100858090 | |||||||
chrX:100858176 | C | T | 16 | a0001c0001t0001g0238 a0001c0001t0001g0272 a0001c0001t0002g0196 others(13): Show |
16 | HG02055.hp1 HG02257.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.804+3995G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100858176 | |||||||
chrX:100858392 | G | T | 1 | a0001c0001t0001g0246 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.804+3779C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100858392 | |||||||
chrX:100858717 | A | C | 1 | a0001c0001t0001g0022 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.804+3454T>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100858717 | |||||||
chrX:100858818 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.804+3353A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100858818 | |||||||
chrX:100858964 | C | T | 1 | a0001c0001t0002g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.804+3207G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100858964 | |||||||
chrX:100859165 | C | T | 5 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0002g0198 others(2): Show |
6 | HG02818.hp1 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+3006G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100859165 | |||||||
chrX:100859498 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0191 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.804+2673A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100859498 | |||||||
chrX:100859675 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.804+2496A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100859675 | |||||||
chrX:100859708 | G | GT | 7 | a0001c0001t0002g0003 a0001c0001t0002g0026 a0001c0001t0002g0046 others(4): Show |
8 | HG02818.hp1 HG02886.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+2462dupA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100859708 | |||||||
chrX:100859759 | G | GT | 13 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(10): Show |
13 | HG00733.hp1 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.804+2411dupA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100859759 | |||||||
chrX:100859792 | A | G | 180 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(177): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.804+2379T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100859792 | |||||||
chrX:100859821 | G | GT | 21 | a0001c0001t0001g0021 a0001c0001t0001g0103 a0001c0001t0001g0104 others(18): Show |
22 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.804+2349dupA | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100859821 | |||||||
chrX:100859887 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.804+2284G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100859887 | |||||||
chrX:100859977 | G | A | 10 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0260 others(7): Show |
10 | HG02055.hp1 HG02257.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.804+2194C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100859977 | |||||||
chrX:100859996 | G | A | 179 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(176): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.804+2175C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100859996 | |||||||
chrX:100860054 | C | A | 1 | a0001c0001t0002g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.804+2117G>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100860054 | |||||||
chrX:100860120 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.804+2051T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100860120 | |||||||
chrX:100860233 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.804+1938C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100860233 | |||||||
chrX:100860340 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.804+1831G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100860340 | |||||||
chrX:100860436 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0191 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.804+1735G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100860436 | |||||||
chrX:100860448 | C | G | 1 | a0001c0001t0002g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.804+1723G>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100860448 | |||||||
chrX:100860449 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.804+1722G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100860449 | |||||||
chrX:100860889 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0080 |
2 | HG00099.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.804+1282G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100860889 | |||||||
chrX:100861028 | C | T | 4 | a0001c0001t0001g0067 a0001c0001t0001g0274 a0001c0001t0003g0171 others(1): Show |
4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+1143G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100861028 | |||||||
chrX:100861230 | A | T | 1 | a0001c0001t0001g0205 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.804+941T>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100861230 | |||||||
chrX:100861284 | C | A | 2 | a0001c0001t0003g0171 a0001c0001t0003g0251 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.804+887G>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100861284 | |||||||
chrX:100861397 | C | A | 1 | a0001c0001t0002g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.804+774G>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100861397 | |||||||
chrX:100861685 | T | C | 1 | a0001c0001t0002g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.804+486A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100861685 | |||||||
chrX:100861775 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.804+396A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100861775 | |||||||
chrX:100862043 | T | C | 183 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(180): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.804+128A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | 100862043 | |||||||
chrX:100862338 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.672-35C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 6/12 | chrX | 100862338 | |||||||
chrX:100862355 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.671+37C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 6/12 | chrX | 100862355 | |||||||
chrX:100862587 | A | C | 1 | a0001c0001t0001g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.490-14T>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 5/12 | chrX | 100862587 | |||||||
chrX:100862905 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.338-85G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 4/12 | chrX | 100862905 | |||||||
chrX:100862952 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.338-132T>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 4/12 | chrX | 100862952 | |||||||
chrX:100863047 | C | T | 1 | a0002c0002t0001g0164 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.337+112G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 4/12 | chrX | 100863047 | |||||||
chrX:100863786 | T | C | 138 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(135): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.142-191A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100863786 | |||||||
chrX:100863963 | C | CAGATAT | 12 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0182 others(9): Show |
13 | HG00323.hp1 HG02165.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-374_142-369dup others(6): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100863963 | |||||||
chrX:100863963 | C | CAGATATA others(5): Show |
16 | a0001c0001t0001g0045 a0001c0001t0001g0061 a0001c0001t0001g0064 others(13): Show |
16 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.142-380_142-369dup others(12): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100863963 | |||||||
chrX:100863963 | C | CAGATATA others(11): Show |
2 | a0001c0001t0001g0204 a0001c0001t0002g0003 |
3 | HG02895.hp1 HG02897.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.142-386_142-369dup others(18): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100863963 | |||||||
chrX:100864217 | T | A | 1 | a0001c0001t0002g0072 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.142-622A>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100864217 | |||||||
chrX:100864297 | A | T | 9 | a0001c0001t0001g0047 a0001c0001t0002g0003 a0001c0001t0002g0046 others(6): Show |
10 | HG01884.hp1 HG02109.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-702T>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100864297 | |||||||
chrX:100864436 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.142-841A>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100864436 | |||||||
chrX:100864542 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.142-947T>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100864542 | |||||||
chrX:100864625 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.142-1030C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100864625 | |||||||
chrX:100864661 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.142-1066T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100864661 | |||||||
chrX:100864706 | G | T | 9 | a0001c0001t0001g0047 a0001c0001t0002g0003 a0001c0001t0002g0046 others(6): Show |
10 | HG01884.hp1 HG02109.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-1111C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100864706 | |||||||
chrX:100864883 | C | A | 12 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(9): Show |
14 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-1288G>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100864883 | |||||||
chrX:100864891 | T | C | 2 | a0001c0001t0003g0171 a0001c0001t0003g0251 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.142-1296A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100864891 | |||||||
chrX:100865496 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142-1901T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100865496 | |||||||
chrX:100865506 | A | G | 183 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(180): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.142-1911T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100865506 | |||||||
chrX:100866002 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.142-2407G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866002 | |||||||
chrX:100866221 | C | CA | 31 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0030 others(28): Show |
32 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.142-2627dupT | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866221 | |||||||
chrX:100866230 | A | T | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-2635T>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866230 | |||||||
chrX:100866417 | G | A | 3 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0002g0198 |
4 | HG02818.hp1 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-2822C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866417 | |||||||
chrX:100866445 | G | A | 188 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(185): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.142-2850C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866445 | |||||||
chrX:100866486 | C | G | 1 | a0001c0001t0005g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-2891G>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866486 | |||||||
chrX:100866487 | C | T | 1 | a0001c0001t0005g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-2892G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866487 | |||||||
chrX:100866488 | C | CTG | 132 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(129): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.142-2895_142-2894d others(4): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866488 | |||||||
chrX:100866488 | C | CTGTG | 28 | a0001c0001t0001g0021 a0001c0001t0001g0103 a0001c0001t0001g0104 others(25): Show |
30 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-2897_142-2894d others(6): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866488 | |||||||
chrX:100866488 | C | CTGTGTG | 3 | a0001c0001t0001g0124 a0001c0001t0001g0181 a0001c0001t0002g0073 |
3 | HG02738.hp1 HG04204.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.142-2899_142-2894d others(8): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866488 | |||||||
chrX:100866488 | CTG | C | 22 | a0001c0001t0001g0047 a0001c0001t0001g0234 a0001c0001t0001g0235 others(19): Show |
23 | HG00544.hp2 HG02083.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.142-2895_142-2894d others(4): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866488 | |||||||
chrX:100866488 | CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-2905_142-2894d others(14): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866488 | |||||||
chrX:100866489 | T | C | 1 | a0001c0001t0005g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-2894A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866489 | |||||||
chrX:100866490 | G | C | 1 | a0001c0001t0005g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-2895C>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100866490 | |||||||
chrX:100867181 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.141+3538G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100867181 | |||||||
chrX:100867267 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.141+3452C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100867267 | |||||||
chrX:100867271 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | NA18991.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.141+3448G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100867271 | |||||||
chrX:100867310 | G | C | 2 | a0001c0001t0003g0171 a0001c0001t0003g0251 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.141+3409C>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100867310 | |||||||
chrX:100867416 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.141+3303C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100867416 | |||||||
chrX:100867715 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0002g0100 a0001c0001t0002g0101 |
3 | HG01168.hp2 HG01981.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.141+3004C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100867715 | |||||||
chrX:100867794 | AAGAG | A | 177 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(174): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.141+2921_141+2924d others(6): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100867794 | |||||||
chrX:100868498 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.141+2221A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100868498 | |||||||
chrX:100868723 | T | A | 1 | a0001c0001t0001g0241 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.141+1996A>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100868723 | |||||||
chrX:100868724 | A | T | 16 | a0001c0001t0001g0111 a0001c0001t0001g0137 a0001c0001t0001g0151 others(13): Show |
16 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.141+1995T>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100868724 | |||||||
chrX:100868863 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.141+1856C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100868863 | |||||||
chrX:100868979 | G | A | 1 | a0001c0001t0002g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.141+1740C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100868979 | |||||||
chrX:100869014 | A | T | 1 | a0001c0001t0002g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.141+1705T>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869014 | |||||||
chrX:100869016 | A | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0253 |
2 | HG02886.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.141+1703T>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869016 | |||||||
chrX:100869083 | G | A | 9 | a0001c0001t0001g0047 a0001c0001t0002g0003 a0001c0001t0002g0046 others(6): Show |
10 | HG01884.hp1 HG02109.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+1636C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869083 | |||||||
chrX:100869154 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.141+1565C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869154 | |||||||
chrX:100869542 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.141+1177A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869542 | |||||||
chrX:100869561 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.141+1158C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869561 | |||||||
chrX:100869697 | T | C | 9 | a0001c0001t0001g0047 a0001c0001t0002g0003 a0001c0001t0002g0046 others(6): Show |
10 | HG01884.hp1 HG02109.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+1022A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869697 | |||||||
chrX:100869710 | C | T | 1 | a0001c0001t0002g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.141+1009G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869710 | |||||||
chrX:100869740 | A | C | 1 | a0001c0001t0002g0026 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.141+979T>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869740 | |||||||
chrX:100869872 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.141+847T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869872 | |||||||
chrX:100869879 | T | C | 3 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0200 |
3 | HG00733.hp1 HG01934.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.141+840A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869879 | |||||||
chrX:100869975 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.141+744A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100869975 | |||||||
chrX:100870019 | A | G | 3 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | NA18979.hp2 NA19055.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.141+700T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100870019 | |||||||
chrX:100870145 | A | T | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.141+574T>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100870145 | |||||||
chrX:100870253 | TA | T | 7 | a0001c0001t0001g0111 a0001c0001t0001g0172 a0001c0001t0001g0173 others(4): Show |
7 | HG00558.hp2 HG01975.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+465delT | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100870253 | |||||||
chrX:100870393 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.141+326T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100870393 | |||||||
chrX:100870442 | A | G | 1 | a0001c0001t0003g0251 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.141+277T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100870442 | |||||||
chrX:100870633 | A | G | 1 | a0001c0001t0005g0252 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.141+86T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100870633 | |||||||
chrX:100870644 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.141+75A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100870644 | |||||||
chrX:100870679 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
5 | NA18939.hp2 NA18962.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+40T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 2/12 | chrX | 100870679 | |||||||
chrX:100870913 | C | T | 2 | a0001c0001t0003g0171 a0001c0001t0003g0251 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.46-99G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100870913 | |||||||
chrX:100871162 | T | C | 137 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(134): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.46-348A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100871162 | |||||||
chrX:100871318 | C | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG00642.hp1 HG01074.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.46-504G>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100871318 | |||||||
chrX:100871680 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.46-866C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100871680 | |||||||
chrX:100871694 | G | A | 1 | a0001c0001t0007g0169 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.46-880C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100871694 | |||||||
chrX:100871842 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-1028G>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100871842 | |||||||
chrX:100871897 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.46-1083G>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100871897 | |||||||
chrX:100871907 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-1093G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100871907 | |||||||
chrX:100872112 | T | C | 90 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(87): Show |
94 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.46-1298A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100872112 | |||||||
chrX:100872190 | C | G | 1 | a0001c0001t0002g0066 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.46-1376G>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100872190 | |||||||
chrX:100872404 | C | T | 17 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0064 others(14): Show |
17 | HG00558.hp1 HG00597.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-1590G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100872404 | |||||||
chrX:100872526 | G | A | 1 | a0004c0008t0002g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.45+1569C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100872526 | |||||||
chrX:100872739 | C | G | 1 | a0001c0001t0003g0048 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.45+1356G>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100872739 | |||||||
chrX:100872944 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.45+1151G>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100872944 | |||||||
chrX:100872946 | T | C | 8 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0001g0246 others(5): Show |
8 | HG01884.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+1149A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100872946 | |||||||
chrX:100873045 | CGG | C | 26 | a0001c0001t0001g0047 a0001c0001t0001g0253 a0001c0001t0001g0272 others(23): Show |
26 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.45+1048_45+1049del others(2): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100873045 | |||||||
chrX:100873286 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.45+809A>G | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100873286 | |||||||
chrX:100873318 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+777C>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100873318 | |||||||
chrX:100873373 | A | G | 3 | a0001c0001t0001g0047 a0001c0001t0002g0003 a0001c0001t0002g0046 |
4 | HG02886.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+722T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100873373 | |||||||
chrX:100873787 | T | A | 1 | a0001c0001t0002g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+308A>T | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100873787 | |||||||
chrX:100873866 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.45+229T>C | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100873866 | |||||||
chrX:100873926 | G | T | 5 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(2): Show |
5 | HG00733.hp1 HG01934.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+169C>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100873926 | |||||||
chrX:100873950 | C | T | 15 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0030 others(12): Show |
15 | HG00099.hp2 HG00140.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.45+145G>A | NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 1/12 | chrX | 100873950 |