Item | Value |
---|---|
geneid | 4688 |
ensemblid | ENSG00000116701.16 |
hgncid | 7661 |
symbol | NCF2 |
name | neutrophil cytosolic factor 2 |
refseq_nuc | NM_000433.4 |
refseq_prot | NP_000424.2 |
ensembl_nuc | ENST00000367535.8 |
ensembl_prot | ENSP00000356505.4 |
mane_status | MANE Select |
chr | chr1 |
start | 183555562 |
end | 183590459 |
strand | - |
ver | v1.2 |
region | chr1:183555562-183590459 |
region5000 | chr1:183550562-183595459 |
regionname0 | NCF2_chr1_183555562_183590459 |
regionname5000 | NCF2_chr1_183550562_183595459 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 526 | 187 | 64 | 26 | 63 | 11 | 21 | 45 | NCF2_chr1_183550562_183595459 | NCF2 | MSLVE others(521): Show |
chr1 | 183550562 | 183595459 |
a0002 | 0/0 | 526 | 184 | 24 | 46 | 91 | 4 | 19 | 74 | NCF2_chr1_183550562_183595459 | NCF2 | MSLVE others(521): Show |
chr1 | 183550562 | 183595459 |
a0003 | 0/0 | 526 | 10 | 1 | 2 | 7 | 0 | 0 | 4 | NCF2_chr1_183550562_183595459 | NCF2 | MSLVE others(521): Show |
chr1 | 183550562 | 183595459 |
a0004 | 0/0 | 526 | 9 | 0 | 0 | 9 | 0 | 0 | 5 | NCF2_chr1_183550562_183595459 | NCF2 | MSLVE others(521): Show |
chr1 | 183550562 | 183595459 |
a0005 | 0/0 | 526 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | MSLVE others(521): Show |
chr1 | 183550562 | 183595459 |
a0006 | 0/0 | 526 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | MSLVE others(521): Show |
chr1 | 183550562 | 183595459 |
a0007 | 0/0 | 526 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | MSLVE others(521): Show |
chr1 | 183550562 | 183595459 |
a0008 | 0/0 | 526 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | MSLVE others(521): Show |
chr1 | 183550562 | 183595459 |
a0009 | 0/0 | 526 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | MSLVE others(521): Show |
chr1 | 183550562 | 183595459 |
a0010 | 0/0 | 526 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | MSLVE others(521): Show |
chr1 | 183550562 | 183595459 |
a0011 | 0/0 | 526 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | MSLVE others(521): Show |
chr1 | 183550562 | 183595459 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1578 | 186 | 63 | 26 | 63 | 11 | 21 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0001c0010 | 0/0 | 1578 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0002c0002 | 0/0 | 1578 | 181 | 24 | 46 | 91 | 4 | 16 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0002c0007 | 0/0 | 1578 | 3 | 0 | 0 | 0 | 0 | 3 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0003c0003 | 0/0 | 1578 | 10 | 1 | 2 | 7 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0004c0004 | 0/0 | 1578 | 9 | 0 | 0 | 9 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0005c0005 | 0/0 | 1578 | 7 | 7 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0006c0006 | 0/0 | 1578 | 3 | 0 | 1 | 0 | 2 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0007c0008 | 0/0 | 1578 | 2 | 0 | 1 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0008c0013 | 0/0 | 1578 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0009c0009 | 0/0 | 1578 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0010c0011 | 0/0 | 1578 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 | ||
a0011c0012 | 0/0 | 1578 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | ATGTC others(1573): Show |
chr1 | 183550562 | 183595459 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2267 | 109 | 58 | 10 | 35 | 0 | 5 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0001c0001t0002 | 0/0 | 2270 | 55 | 2 | 10 | 23 | 7 | 13 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2265): Show |
chr1 | 183550562 | 183595459 |
a0001c0001t0003 | 1/0 | 2267 | 17 | 3 | 6 | 0 | 4 | 3 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0001c0001t0005 | 0/0 | 2264 | 4 | 0 | 0 | 4 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2259): Show |
chr1 | 183550562 | 183595459 |
a0001c0001t0006 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0001c0010t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0002c0002t0001 | 0/0 | 2267 | 177 | 23 | 46 | 88 | 4 | 16 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0002c0002t0002 | 0/0 | 2270 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2265): Show |
chr1 | 183550562 | 183595459 |
a0002c0002t0003 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0002c0007t0002 | 0/0 | 2270 | 3 | 0 | 0 | 0 | 0 | 3 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2265): Show |
chr1 | 183550562 | 183595459 |
a0003c0003t0001 | 0/0 | 2267 | 10 | 1 | 2 | 7 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0004c0004t0001 | 0/0 | 2267 | 9 | 0 | 0 | 9 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0005c0005t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0005c0005t0004 | 0/0 | 2267 | 6 | 6 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ACTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0006c0006t0001 | 0/0 | 2267 | 3 | 0 | 1 | 0 | 2 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0007c0008t0002 | 0/0 | 2270 | 2 | 0 | 1 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2265): Show |
chr1 | 183550562 | 183595459 |
a0008c0013t0001 | 0/0 | 2267 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0009c0009t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0010c0011t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
a0011c0012t0001 | 0/0 | 2267 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | ATTCT others(2262): Show |
chr1 | 183550562 | 183595459 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0001c0010t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0001 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0002t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0007t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0007t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0002c0007t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0003c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0004c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0005c0005t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0006c0006t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0006c0006t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0006c0006t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0007c0008t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0007c0008t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0008c0013t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0009c0009t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0010c0011t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
a0011c0012t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0022 | EUR | GBR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0134 | EUR | GBR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00140 | hp1 | a0006 | c0006 | t0001 | g0108 | EUR | GBR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0197 | EUR | GBR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0233 | EUR | FIN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0073 | EUR | FIN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0334 | EUR | FIN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0254 | EUR | FIN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00597 | hp2 | a0004 | c0004 | t0001 | g0230 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0342 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00621 | hp1 | a0003 | c0003 | t0001 | g0147 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | CHS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0215 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0152 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0302 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01074 | hp2 | a0006 | c0006 | t0001 | g0285 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0313 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0348 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0266 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0096 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0283 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0329 | AMR | PUR | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0161 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0115 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0344 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0343 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0260 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0200 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0338 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0022 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0259 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0339 | EUR | IBS | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0286 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0297 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0335 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0320 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0331 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0337 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0347 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0174 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02083 | hp1 | a0003 | c0003 | t0001 | g0094 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02132 | hp2 | a0004 | c0004 | t0001 | g0157 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02135 | hp2 | a0004 | c0004 | t0001 | g0224 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0116 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CDX | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CDX | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | CDX | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0332 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0321 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0275 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0336 | AMR | PEL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0294 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0105 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0257 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0059 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02735 | hp2 | a0008 | c0013 | t0001 | g0056 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02809 | hp1 | a0005 | c0005 | t0004 | g0033 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02896 | hp2 | a0005 | c0005 | t0004 | g0031 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02897 | hp2 | a0005 | c0005 | t0004 | g0032 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03130 | hp2 | a0005 | c0005 | t0004 | g0034 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0304 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03209 | hp2 | a0009 | c0009 | t0001 | g0120 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0309 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0239 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03486 | hp2 | a0005 | c0005 | t0004 | g0036 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0270 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ESN | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03540 | hp1 | a0002 | c0002 | t0003 | g0295 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03540 | hp2 | a0010 | c0011 | t0001 | g0326 | AFR | GWD | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0299 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0163 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0277 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03710 | hp1 | a0011 | c0012 | t0001 | g0341 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0242 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0138 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0228 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0227 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0132 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04184 | hp2 | a0002 | c0007 | t0002 | g0237 | SAS | BEB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG04228 | hp2 | a0002 | c0007 | t0002 | g0063 | SAS | STU | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0328 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18612 | hp2 | a0004 | c0004 | t0001 | g0149 | EAS | CHB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18943 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18952 | hp1 | a0004 | c0004 | t0001 | g0156 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18959 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18966 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18969 | hp1 | a0004 | c0004 | t0001 | g0060 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18971 | hp2 | a0003 | c0003 | t0001 | g0222 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18990 | hp2 | a0004 | c0004 | t0001 | g0150 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19006 | hp2 | a0001 | c0001 | t0005 | g0289 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19030 | hp2 | a0005 | c0005 | t0004 | g0035 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0251 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19063 | hp1 | a0004 | c0004 | t0001 | g0153 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19085 | hp1 | a0004 | c0004 | t0001 | g0104 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0303 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0274 | AFR | ASW | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ASW | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0282 | EUR | TSI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20752 | hp2 | a0007 | c0008 | t0002 | g0141 | EUR | TSI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0181 | EUR | TSI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20805 | hp2 | a0006 | c0006 | t0001 | g0211 | EUR | TSI | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20905 | hp1 | a0002 | c0007 | t0002 | g0154 | SAS | GIH | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0271 | SAS | GIH | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01123 | hp1 | a0007 | c0008 | t0002 | g0071 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03471 | hp1 | a0001 | c0010 | t0001 | g0052 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | MSL | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | USA | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
HG06807 | hp2 | a0005 | c0005 | t0001 | g0345 | AFR | USA | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | USA | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA20300 | hp2 | a0003 | c0003 | t0001 | g0076 | AFR | USA | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0333 | AFR | LWK | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0208 | REF | REF | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0198 | REF | REF | NCF2_chr1_183550562_183595459 | NCF2 | chr1 | 183550562 | 183595459 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183556147 | C | G | 1 | a0010 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1552G>C | p.Asp518His | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 1682/2267 | 1552/1581 | 518/526 | chr1 | 183556147 | |||
chr1:183560222 | T | C | 1 | a0011 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1342A>G | p.Asn448Asp | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/15 | 1472/2267 | 1342/1581 | 448/526 | chr1 | 183560222 | |||
chr1:183563229 | T | A | 1 | a0008 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1256A>T | p.Asn419Ile | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/15 | 1386/2267 | 1256/1581 | 419/526 | chr1 | 183563229 | |||
chr1:183563301 | C | T | 1 | a0007 | 2 | HG01123.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.1184G>A | p.Arg395Gln | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/15 | 1314/2267 | 1184/1581 | 395/526 | chr1 | 183563301 | |||
chr1:183563302 | G | A | 1 | a0003 | 10 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(7): Show |
missense_variant | MODERATE | c.1183C>T | p.Arg395Trp | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/15 | 1313/2267 | 1183/1581 | 395/526 | chr1 | 183563302 | |||
chr1:183563445 | G | T | 1 | a0006 | 3 | HG00140.hp1 HG01074.hp2 NA20805.hp2 |
missense_variant | MODERATE | c.1167C>A | p.His389Gln | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 12/15 | 1297/2267 | 1167/1581 | 389/526 | chr1 | 183563445 | |||
chr1:183566954 | A | G | 1 | a0005 | 7 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
missense_variant | MODERATE | c.890T>C | p.Val297Ala | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/15 | 1020/2267 | 890/1581 | 297/526 | chr1 | 183566954 | |||
chr1:183567223 | G | A | 1 | a0004 | 9 | HG00597.hp2 HG02132.hp2 HG02135.hp2 others(6): Show |
missense_variant | MODERATE | c.836C>T | p.Thr279Met | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 8/15 | 966/2267 | 836/1581 | 279/526 | chr1 | 183567223 | |||
chr1:183573231 | C | T | 1 | a0009 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.563G>A | p.Arg188Lys | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/15 | 693/2267 | 563/1581 | 188/526 | chr1 | 183573231 | |||
chr1:183573252 | T | C | 8 | a0002 a0003 a0004 others(5): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
missense_variant | MODERATE | c.542A>G | p.Lys181Arg | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/15 | 672/2267 | 542/1581 | 181/526 | chr1 | 183573252 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183556196 | C | T | 1 | a0001c0010 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1503G>A | p.Gly501Gly | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 1633/2267 | 1503/1581 | 501/526 | chr1 | 183556196 | |||
chr1:183566926 | C | T | 1 | a0002c0007 | 3 | HG04184.hp2 HG04228.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.918G>A | p.Gln306Gln | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/15 | 1048/2267 | 918/1581 | 306/526 | chr1 | 183566926 | |||
chr1:183573188 | C | T | 1 | a0006c0006 | 3 | HG00140.hp1 HG01074.hp2 NA20805.hp2 |
synonymous_variant | LOW | c.606G>A | p.Ala202Ala | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/15 | 736/2267 | 606/1581 | 202/526 | chr1 | 183573188 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183555571 | AAAAC | A | 1 | a0001c0001t0005 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*543_*546delGTTT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 543 | chr1 | 183555571 | ||||||
chr1:183555600 | T | TA | 1 | a0001c0001t0005 | 4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*517dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 517 | chr1 | 183555600 | ||||||
chr1:183555715 | A | AGAT | 4 | a0001c0001t0002 a0002c0002t0002 a0002c0007t0002 others(1): Show |
63 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*400_*402dupATC | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 402 | chr1 | 183555715 | ||||||
chr1:183555720 | C | A | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(15): Show |
387 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(384): Show |
3_prime_UTR_variant | MODIFIER | c.*398G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 398 | chr1 | 183555720 | ||||||
chr1:183555733 | T | A | 1 | a0001c0001t0006 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*385A>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 15/15 | 385 | chr1 | 183555733 | ||||||
chr1:183590458 | A | G | 1 | a0005c0005t0004 | 6 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-129T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/15 | 129 | chr1 | 183590458 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183556317 | T | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0319 |
3 | HG02717.hp1 HG02896.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1469-87A>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556317 | |||||||
chr1:183556317 | T | G | 335 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(332): Show |
385 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(382): Show |
intron_variant | MODIFIER | c.1469-87A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556317 | |||||||
chr1:183556485 | A | T | 75 | a0001c0001t0001g0011 a0001c0001t0001g0315 a0001c0001t0001g0316 others(72): Show |
85 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.1469-255T>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556485 | |||||||
chr1:183556669 | C | G | 1 | a0004c0004t0001g0153 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1469-439G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556669 | |||||||
chr1:183556726 | G | A | 1 | a0001c0001t0001g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1469-496C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556726 | |||||||
chr1:183556921 | T | C | 1 | a0001c0001t0001g0354 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1469-691A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183556921 | |||||||
chr1:183557136 | G | A | 1 | a0002c0002t0001g0179 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1469-906C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557136 | |||||||
chr1:183557191 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1469-961G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557191 | |||||||
chr1:183557203 | G | A | 336 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(333): Show |
387 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(384): Show |
intron_variant | MODIFIER | c.1469-973C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557203 | |||||||
chr1:183557264 | A | G | 2 | a0002c0002t0001g0160 a0002c0002t0001g0201 |
2 | HG01361.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1469-1034T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557264 | |||||||
chr1:183557365 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1469-1135A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557365 | |||||||
chr1:183557586 | G | A | 1 | a0006c0006t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1469-1356C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557586 | |||||||
chr1:183557671 | A | G | 2 | a0001c0001t0003g0245 a0001c0001t0003g0266 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1469-1441T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557671 | |||||||
chr1:183557812 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1469-1582G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557812 | |||||||
chr1:183557881 | A | AT | 9 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1469-1652dupA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557881 | |||||||
chr1:183557968 | T | C | 78 | a0001c0001t0001g0011 a0001c0001t0001g0315 a0001c0001t0001g0316 others(75): Show |
89 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1469-1738A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183557968 | |||||||
chr1:183558068 | T | C | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1469-1838A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558068 | |||||||
chr1:183558123 | C | T | 78 | a0001c0001t0001g0011 a0001c0001t0001g0315 a0001c0001t0001g0316 others(75): Show |
89 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1469-1893G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558123 | |||||||
chr1:183558221 | C | T | 1 | a0002c0002t0001g0145 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1468+1875G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558221 | |||||||
chr1:183558222 | T | G | 2 | a0002c0002t0001g0095 a0002c0002t0001g0096 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1468+1874A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558222 | |||||||
chr1:183558248 | A | T | 2 | a0002c0002t0001g0018 a0002c0002t0001g0128 |
3 | HG01261.hp1 HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1468+1848T>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558248 | |||||||
chr1:183558330 | C | G | 1 | a0001c0001t0001g0354 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1468+1766G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558330 | |||||||
chr1:183558355 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1468+1741G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558355 | |||||||
chr1:183558597 | G | A | 2 | a0002c0002t0001g0102 a0002c0002t0001g0235 |
2 | NA18967.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1468+1499C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558597 | |||||||
chr1:183558602 | G | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0049 others(2): Show |
7 | HG02145.hp1 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+1494C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558602 | |||||||
chr1:183558614 | G | A | 1 | a0002c0002t0001g0192 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1468+1482C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558614 | |||||||
chr1:183558695 | G | T | 1 | a0001c0001t0001g0065 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1468+1401C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558695 | |||||||
chr1:183558855 | G | C | 78 | a0001c0001t0001g0011 a0001c0001t0001g0315 a0001c0001t0001g0316 others(75): Show |
89 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1468+1241C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183558855 | |||||||
chr1:183559035 | C | T | 4 | a0002c0002t0001g0067 a0002c0002t0001g0225 a0002c0002t0001g0291 others(1): Show |
4 | HG01952.hp2 NA18944.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+1061G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559035 | |||||||
chr1:183559092 | T | C | 2 | a0001c0001t0001g0118 a0001c0010t0001g0052 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1468+1004A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559092 | |||||||
chr1:183559118 | C | G | 1 | a0001c0001t0003g0296 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1468+978G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559118 | |||||||
chr1:183559152 | G | A | 4 | a0004c0004t0001g0149 a0004c0004t0001g0150 a0004c0004t0001g0153 others(1): Show |
4 | HG02132.hp2 NA18612.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+944C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559152 | |||||||
chr1:183559308 | A | C | 2 | a0002c0002t0001g0338 a0002c0002t0001g0339 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1468+788T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559308 | |||||||
chr1:183559732 | G | A | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+364C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559732 | |||||||
chr1:183559737 | T | G | 1 | a0001c0001t0001g0354 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1468+359A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559737 | |||||||
chr1:183559920 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1468+176A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559920 | |||||||
chr1:183559977 | G | A | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+119C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 14/14 | chr1 | 183559977 | |||||||
chr1:183560379 | C | T | 1 | a0002c0002t0001g0344 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1291-106G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560379 | |||||||
chr1:183560519 | G | A | 53 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0009 others(50): Show |
60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1291-246C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560519 | |||||||
chr1:183560569 | G | A | 1 | a0004c0004t0001g0153 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1291-296C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560569 | |||||||
chr1:183560592 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1291-319C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560592 | |||||||
chr1:183560675 | A | T | 1 | a0001c0001t0001g0354 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1291-402T>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560675 | |||||||
chr1:183560831 | A | G | 1 | a0001c0001t0002g0262 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1291-558T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560831 | |||||||
chr1:183560927 | G | T | 2 | a0002c0002t0001g0102 a0002c0002t0001g0235 |
2 | NA18967.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1291-654C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183560927 | |||||||
chr1:183561015 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1291-742T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561015 | |||||||
chr1:183561141 | C | A | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0142 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1291-868G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561141 | |||||||
chr1:183561366 | A | G | 7 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0292 others(4): Show |
8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291-1093T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561366 | |||||||
chr1:183561484 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1291-1211T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561484 | |||||||
chr1:183561569 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1291-1296T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561569 | |||||||
chr1:183561576 | G | C | 1 | a0003c0003t0001g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1291-1303C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561576 | |||||||
chr1:183561641 | C | CT | 74 | a0001c0001t0001g0011 a0001c0001t0001g0315 a0001c0001t0001g0316 others(71): Show |
84 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.1291-1369dupA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561641 | |||||||
chr1:183561695 | GT | G | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291-1423delA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561695 | |||||||
chr1:183561779 | C | CT | 11 | a0001c0001t0001g0047 a0001c0001t0001g0068 a0001c0001t0001g0078 others(8): Show |
11 | HG01109.hp2 HG01175.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1290+1415dupA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | |||||||
chr1:183561779 | CT | C | 40 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(37): Show |
45 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1290+1415delA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | |||||||
chr1:183561779 | CTT | C | 27 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0064 others(24): Show |
29 | HG00140.hp2 HG00609.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.1290+1414_1290+141 others(6): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | |||||||
chr1:183561779 | CTTT | C | 26 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0044 others(23): Show |
27 | HG00597.hp1 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1290+1413_1290+141 others(7): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | |||||||
chr1:183561779 | CTTTT | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0121 a0001c0001t0001g0122 others(11): Show |
15 | HG00408.hp2 HG01069.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1290+1412_1290+141 others(8): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | |||||||
chr1:183561779 | CTTTTTTT others(7): Show |
C | 15 | a0001c0001t0001g0186 a0001c0001t0001g0325 a0001c0001t0002g0040 others(12): Show |
15 | HG00438.hp2 HG02293.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.1290+1402_1290+141 others(18): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | |||||||
chr1:183561779 | CTTTTTTT others(8): Show |
C | 73 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0118 others(70): Show |
87 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1290+1401_1290+141 others(19): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | |||||||
chr1:183561779 | CTTTTTTT others(9): Show |
C | 54 | a0001c0001t0001g0180 a0001c0001t0002g0058 a0001c0001t0002g0135 others(51): Show |
70 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1290+1400_1290+141 others(20): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | |||||||
chr1:183561779 | CTTTTTTT others(10): Show |
C | 31 | a0002c0002t0001g0020 a0002c0002t0001g0070 a0002c0002t0001g0075 others(28): Show |
35 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1290+1399_1290+141 others(21): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | |||||||
chr1:183561779 | CTTTTTTT others(11): Show |
C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0028 others(5): Show |
11 | HG01168.hp1 HG02145.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1290+1398_1290+141 others(22): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | |||||||
chr1:183561779 | CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0001g0272 a0002c0002t0001g0243 |
2 | HG03831.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1290+1397_1290+141 others(23): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183561779 | |||||||
chr1:183562207 | T | C | 2 | a0001c0001t0002g0218 a0001c0001t0002g0269 |
2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1290+988A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562207 | |||||||
chr1:183562385 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1290+810T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562385 | |||||||
chr1:183562481 | G | C | 1 | a0002c0002t0001g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1290+714C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562481 | |||||||
chr1:183562523 | A | G | 1 | a0002c0002t0001g0189 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1290+672T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562523 | |||||||
chr1:183562528 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1290+667G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562528 | |||||||
chr1:183562662 | G | A | 1 | a0001c0001t0001g0353 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1290+533C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562662 | |||||||
chr1:183562803 | G | A | 72 | a0002c0002t0001g0008 a0002c0002t0001g0012 a0002c0002t0001g0015 others(69): Show |
80 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1290+392C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562803 | |||||||
chr1:183562823 | C | CA | 7 | a0001c0001t0001g0111 a0001c0001t0001g0241 a0001c0001t0002g0218 others(4): Show |
7 | HG01175.hp2 HG01515.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1290+371dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562823 | |||||||
chr1:183562823 | C | CAA | 73 | a0001c0001t0001g0011 a0001c0001t0001g0315 a0001c0001t0001g0316 others(70): Show |
83 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1290+370_1290+371d others(4): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562823 | |||||||
chr1:183562823 | CA | C | 6 | a0001c0001t0001g0194 a0001c0001t0001g0248 a0001c0001t0005g0027 others(3): Show |
7 | HG01975.hp1 HG02015.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1290+371delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562823 | |||||||
chr1:183562978 | C | T | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1290+217G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562978 | |||||||
chr1:183562994 | G | A | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1290+201C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183562994 | |||||||
chr1:183563065 | G | A | 39 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(36): Show |
42 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1290+130C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 13/14 | chr1 | 183563065 | |||||||
chr1:183563310 | G | C | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1179-4C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 12/14 | chr1 | 183563310 | |||||||
chr1:183563337 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1179-31G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 12/14 | chr1 | 183563337 | |||||||
chr1:183563376 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1178+58G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 12/14 | chr1 | 183563376 | |||||||
chr1:183563871 | G | A | 1 | a0002c0002t0001g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1026+134C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 11/14 | chr1 | 183563871 | |||||||
chr1:183563896 | G | C | 1 | a0002c0002t0001g0277 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1026+109C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 11/14 | chr1 | 183563896 | |||||||
chr1:183563925 | C | A | 1 | a0001c0001t0001g0354 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1026+80G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 11/14 | chr1 | 183563925 | |||||||
chr1:183564082 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0330 |
2 | HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1001-52G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564082 | |||||||
chr1:183564194 | C | T | 2 | a0001c0001t0001g0312 a0001c0001t0001g0354 |
2 | HG01069.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1001-164G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564194 | |||||||
chr1:183564449 | G | T | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-419C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564449 | |||||||
chr1:183564450 | T | C | 1 | a0002c0002t0001g0277 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1001-420A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564450 | |||||||
chr1:183564650 | T | A | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-620A>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564650 | |||||||
chr1:183564775 | C | T | 180 | a0001c0001t0001g0180 a0001c0001t0002g0175 a0002c0002t0001g0001 others(177): Show |
214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1001-745G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564775 | |||||||
chr1:183564801 | C | T | 1 | a0002c0002t0001g0129 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1001-771G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564801 | |||||||
chr1:183564942 | A | G | 1 | a0002c0002t0001g0116 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1000+762T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564942 | |||||||
chr1:183564969 | G | T | 1 | a0002c0002t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1000+735C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183564969 | |||||||
chr1:183565007 | T | C | 2 | a0001c0001t0002g0254 a0001c0001t0002g0282 |
2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1000+697A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565007 | |||||||
chr1:183565104 | G | C | 1 | a0002c0002t0001g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1000+600C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565104 | |||||||
chr1:183565409 | C | G | 324 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(321): Show |
372 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.1000+295G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565409 | |||||||
chr1:183565530 | G | A | 4 | a0002c0002t0001g0067 a0002c0002t0001g0225 a0002c0002t0001g0291 others(1): Show |
4 | HG01952.hp2 NA18944.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+174C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565530 | |||||||
chr1:183565546 | G | T | 2 | a0002c0002t0001g0023 a0002c0002t0001g0234 |
3 | HG00642.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1000+158C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565546 | |||||||
chr1:183565559 | A | G | 1 | a0002c0002t0001g0332 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1000+145T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 10/14 | chr1 | 183565559 | |||||||
chr1:183565800 | C | T | 179 | a0001c0001t0001g0180 a0001c0001t0002g0175 a0002c0002t0001g0001 others(176): Show |
213 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.925-21G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183565800 | |||||||
chr1:183565810 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0247 a0001c0001t0001g0264 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.925-31G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183565810 | |||||||
chr1:183565833 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.925-54C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183565833 | |||||||
chr1:183566012 | C | T | 1 | a0002c0002t0001g0201 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.925-233G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566012 | |||||||
chr1:183566021 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.925-242C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566021 | |||||||
chr1:183566177 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.925-398C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566177 | |||||||
chr1:183566251 | T | C | 1 | a0001c0001t0001g0351 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.925-472A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566251 | |||||||
chr1:183566417 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.924+503A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566417 | |||||||
chr1:183566668 | A | AC | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0028 others(4): Show |
10 | HG02145.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.924+251dupG | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566668 | |||||||
chr1:183566860 | C | A | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.924+60G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 9/14 | chr1 | 183566860 | |||||||
chr1:183567126 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0140 a0001c0001t0001g0185 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.855+78C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 8/14 | chr1 | 183567126 | |||||||
chr1:183567790 | C | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0247 a0001c0001t0001g0264 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.714-445G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183567790 | |||||||
chr1:183567905 | G | A | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.714-560C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183567905 | |||||||
chr1:183568020 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714-675G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568020 | |||||||
chr1:183568133 | C | T | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0191 |
3 | NA18948.hp2 NA18963.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.714-788G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568133 | |||||||
chr1:183568138 | A | G | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.714-793T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568138 | |||||||
chr1:183568159 | C | G | 2 | a0002c0002t0001g0095 a0002c0002t0001g0096 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.714-814G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568159 | |||||||
chr1:183568339 | T | G | 205 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0028 others(202): Show |
243 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.713+803A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568339 | |||||||
chr1:183568343 | G | T | 181 | a0001c0001t0001g0180 a0001c0001t0002g0175 a0002c0002t0001g0001 others(178): Show |
215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.713+799C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568343 | |||||||
chr1:183568467 | A | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0185 a0001c0001t0001g0307 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.713+675T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568467 | |||||||
chr1:183568691 | C | T | 15 | a0002c0002t0001g0008 a0002c0002t0001g0012 a0002c0002t0001g0017 others(12): Show |
21 | HG00735.hp2 HG00738.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.713+451G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568691 | |||||||
chr1:183568724 | G | C | 181 | a0001c0001t0001g0180 a0001c0001t0002g0175 a0002c0002t0001g0001 others(178): Show |
215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.713+418C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568724 | |||||||
chr1:183568777 | C | A | 1 | a0002c0002t0001g0090 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.713+365G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568777 | |||||||
chr1:183568799 | A | G | 339 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(336): Show |
390 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(387): Show |
intron_variant | MODIFIER | c.713+343T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568799 | |||||||
chr1:183568890 | A | G | 205 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0028 others(202): Show |
243 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.713+252T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568890 | |||||||
chr1:183568948 | T | C | 2 | a0002c0002t0001g0238 a0002c0002t0001g0239 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.713+194A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568948 | |||||||
chr1:183568955 | T | G | 1 | a0002c0002t0001g0258 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.713+187A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 7/14 | chr1 | 183568955 | |||||||
chr1:183569299 | A | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0049 others(2): Show |
7 | HG02145.hp1 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-114T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183569299 | |||||||
chr1:183569590 | T | A | 181 | a0001c0001t0001g0180 a0001c0001t0002g0175 a0002c0002t0001g0001 others(178): Show |
215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.670-405A>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183569590 | |||||||
chr1:183569652 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.670-467C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183569652 | |||||||
chr1:183569793 | T | C | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-608A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183569793 | |||||||
chr1:183569990 | A | G | 184 | a0001c0001t0001g0180 a0001c0001t0002g0175 a0001c0001t0005g0027 others(181): Show |
219 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.669+790T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183569990 | |||||||
chr1:183570313 | C | T | 2 | a0001c0001t0002g0246 a0001c0001t0002g0267 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.669+467G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570313 | |||||||
chr1:183570314 | G | T | 180 | a0001c0001t0001g0180 a0002c0002t0001g0001 a0002c0002t0001g0002 others(177): Show |
214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.669+466C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570314 | |||||||
chr1:183570393 | C | T | 1 | a0002c0002t0001g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.669+387G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570393 | |||||||
chr1:183570428 | A | G | 1 | a0002c0002t0001g0089 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.669+352T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570428 | |||||||
chr1:183570533 | C | T | 1 | a0001c0001t0002g0276 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.669+247G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570533 | |||||||
chr1:183570715 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.669+65C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 6/14 | chr1 | 183570715 | |||||||
chr1:183570916 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.610-77G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183570916 | |||||||
chr1:183571067 | A | C | 2 | a0002c0002t0002g0099 a0002c0002t0002g0100 |
2 | HG00408.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.610-228T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571067 | |||||||
chr1:183571080 | TA | T | 183 | a0001c0001t0001g0180 a0001c0001t0005g0027 a0001c0001t0005g0174 others(180): Show |
218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.610-242delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571080 | |||||||
chr1:183571110 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.610-271A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571110 | |||||||
chr1:183571114 | C | CT | 170 | a0001c0001t0001g0180 a0001c0001t0001g0183 a0001c0001t0001g0193 others(167): Show |
204 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.610-276dupA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571114 | |||||||
chr1:183571114 | CT | C | 14 | a0001c0001t0001g0044 a0001c0001t0001g0121 a0001c0001t0001g0122 others(11): Show |
14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.610-276delA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571114 | |||||||
chr1:183571114 | CTTTTTTT others(4): Show |
C | 1 | a0007c0008t0002g0141 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.610-286_610-276del others(11): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571114 | |||||||
chr1:183571279 | G | A | 1 | a0002c0002t0001g0020 | 2 | HG00642.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.610-440C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571279 | |||||||
chr1:183571280 | G | A | 2 | a0002c0002t0001g0328 a0002c0002t0001g0329 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.610-441C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571280 | |||||||
chr1:183571376 | C | T | 2 | a0001c0001t0003g0245 a0001c0001t0003g0266 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.610-537G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571376 | |||||||
chr1:183571641 | G | T | 180 | a0001c0001t0001g0180 a0002c0002t0001g0001 a0002c0002t0001g0002 others(177): Show |
214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.610-802C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571641 | |||||||
chr1:183571963 | C | T | 182 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0003 others(179): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.610-1124G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571963 | |||||||
chr1:183571964 | A | ATGGATAT others(10): Show |
1 | a0001c0001t0005g0289 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.610-1142_610-1126d others(19): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571964 | |||||||
chr1:183571991 | T | C | 182 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0003 others(179): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.610-1152A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183571991 | |||||||
chr1:183572337 | G | A | 3 | a0001c0001t0001g0261 a0001c0001t0001g0349 a0001c0001t0001g0350 |
3 | HG01168.hp2 HG01243.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.609+848C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183572337 | |||||||
chr1:183572707 | A | C | 182 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0003 others(179): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.609+478T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183572707 | |||||||
chr1:183572731 | C | T | 182 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0003 others(179): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.609+454G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183572731 | |||||||
chr1:183573012 | T | C | 1 | a0001c0001t0002g0081 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.609+173A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183573012 | |||||||
chr1:183573143 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.609+42C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | 183573143 | |||||||
chr1:183573343 | T | C | 1 | a0002c0002t0001g0119 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.502-51A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183573343 | |||||||
chr1:183573612 | G | T | 181 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0003 others(178): Show |
215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.502-320C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183573612 | |||||||
chr1:183573659 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.502-367C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183573659 | |||||||
chr1:183573732 | A | G | 10 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0118 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.502-440T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183573732 | |||||||
chr1:183573918 | C | T | 182 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0003 others(179): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.501+569G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183573918 | |||||||
chr1:183574076 | C | T | 1 | a0002c0002t0001g0098 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.501+411G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183574076 | |||||||
chr1:183574445 | C | A | 1 | a0002c0002t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.501+42G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 4/14 | chr1 | 183574445 | |||||||
chr1:183574637 | C | T | 2 | a0002c0002t0001g0095 a0002c0002t0001g0096 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.367-16G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183574637 | |||||||
chr1:183574639 | G | A | 1 | a0001c0001t0001g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.367-18C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183574639 | |||||||
chr1:183575123 | C | T | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0142 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.367-502G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575123 | |||||||
chr1:183575207 | T | C | 1 | a0004c0004t0001g0156 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.367-586A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575207 | |||||||
chr1:183575208 | G | A | 1 | a0004c0004t0001g0156 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.367-587C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575208 | |||||||
chr1:183575252 | T | C | 1 | a0001c0001t0003g0296 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.367-631A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575252 | |||||||
chr1:183575339 | A | G | 1 | a0002c0002t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.367-718T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575339 | |||||||
chr1:183575353 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.367-732A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575353 | |||||||
chr1:183575357 | C | A | 1 | a0001c0001t0002g0137 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.367-736G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575357 | |||||||
chr1:183575443 | G | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0043 |
2 | NA18993.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.367-822C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575443 | |||||||
chr1:183575508 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.367-887C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575508 | |||||||
chr1:183575542 | C | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0028 others(8): Show |
15 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.367-921G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575542 | |||||||
chr1:183575559 | G | A | 55 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(52): Show |
58 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.367-938C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575559 | |||||||
chr1:183575593 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0028 others(4): Show |
10 | HG02145.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-972G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575593 | |||||||
chr1:183575815 | A | C | 1 | a0001c0001t0001g0354 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.367-1194T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183575815 | |||||||
chr1:183576103 | C | T | 6 | a0005c0005t0004g0031 a0005c0005t0004g0032 a0005c0005t0004g0033 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.367-1482G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576103 | |||||||
chr1:183576131 | G | A | 2 | a0001c0001t0001g0177 a0002c0002t0001g0176 |
2 | HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.366+1468C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576131 | |||||||
chr1:183576143 | A | G | 1 | a0002c0002t0001g0089 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.366+1456T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576143 | |||||||
chr1:183576190 | G | A | 1 | a0004c0004t0001g0157 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.366+1409C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576190 | |||||||
chr1:183576297 | A | G | 1 | a0001c0001t0003g0313 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.366+1302T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576297 | |||||||
chr1:183576462 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.366+1137C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576462 | |||||||
chr1:183576468 | G | A | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0177 others(9): Show |
12 | HG01123.hp2 HG01192.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.366+1131C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576468 | |||||||
chr1:183576504 | C | T | 2 | a0001c0001t0001g0312 a0001c0001t0001g0354 |
2 | HG01069.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.366+1095G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576504 | |||||||
chr1:183576505 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.366+1094C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576505 | |||||||
chr1:183576522 | G | C | 1 | a0001c0001t0001g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.366+1077C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576522 | |||||||
chr1:183576530 | C | T | 141 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0142 others(138): Show |
166 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.366+1069G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576530 | |||||||
chr1:183576533 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.366+1066T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576533 | |||||||
chr1:183576535 | C | A | 2 | a0002c0002t0001g0105 a0002c0002t0001g0274 |
2 | HG02698.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.366+1064G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576535 | |||||||
chr1:183576549 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.366+1050G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576549 | |||||||
chr1:183576550 | G | A | 9 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(6): Show |
9 | HG00423.hp1 HG01168.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.366+1049C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576550 | |||||||
chr1:183576681 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.366+918C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576681 | |||||||
chr1:183576926 | G | A | 139 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0142 others(136): Show |
165 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.366+673C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576926 | |||||||
chr1:183576990 | T | C | 1 | a0001c0001t0003g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.366+609A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183576990 | |||||||
chr1:183577062 | G | T | 6 | a0002c0002t0001g0015 a0002c0002t0001g0051 a0002c0002t0001g0061 others(3): Show |
7 | NA18960.hp1 NA18969.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.366+537C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577062 | |||||||
chr1:183577181 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.366+418G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577181 | |||||||
chr1:183577192 | C | T | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.366+407G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577192 | |||||||
chr1:183577338 | G | A | 267 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(264): Show |
315 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.366+261C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577338 | |||||||
chr1:183577367 | G | A | 17 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0037 others(14): Show |
20 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.366+232C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577367 | |||||||
chr1:183577385 | G | T | 3 | a0002c0002t0001g0095 a0002c0002t0001g0096 a0002c0002t0001g0219 |
3 | HG01168.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.366+214C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 3/14 | chr1 | 183577385 | |||||||
chr1:183577779 | G | T | 1 | a0001c0001t0003g0313 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.258-72C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577779 | |||||||
chr1:183577787 | C | T | 1 | a0002c0002t0001g0127 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.258-80G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577787 | |||||||
chr1:183577795 | T | C | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.258-88A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577795 | |||||||
chr1:183577838 | G | C | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-131C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577838 | |||||||
chr1:183577862 | T | C | 7 | a0002c0002t0001g0007 a0002c0002t0001g0093 a0002c0002t0001g0123 others(4): Show |
9 | HG00673.hp2 NA18959.hp1 NA19001.hp1 others(6): Show |
intron_variant | MODIFIER | c.258-155A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577862 | |||||||
chr1:183577877 | C | T | 1 | a0002c0002t0001g0160 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.258-170G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577877 | |||||||
chr1:183577897 | T | C | 45 | a0001c0001t0001g0133 a0001c0001t0001g0207 a0002c0002t0001g0008 others(42): Show |
53 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.258-190A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577897 | |||||||
chr1:183577905 | G | A | 1 | a0002c0002t0001g0160 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.258-198C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183577905 | |||||||
chr1:183578038 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-331G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578038 | |||||||
chr1:183578120 | A | G | 1 | a0001c0001t0003g0313 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.258-413T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578120 | |||||||
chr1:183578216 | G | C | 1 | a0002c0002t0001g0227 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.258-509C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578216 | |||||||
chr1:183578220 | A | C | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.258-513T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578220 | |||||||
chr1:183578355 | C | CT | 70 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(67): Show |
74 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.258-649dupA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578355 | |||||||
chr1:183578355 | C | CTT | 6 | a0001c0001t0001g0046 a0001c0001t0001g0185 a0001c0001t0001g0307 others(3): Show |
6 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-650_258-649dup others(2): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578355 | |||||||
chr1:183578507 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.258-800C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578507 | |||||||
chr1:183578547 | G | A | 1 | a0002c0002t0001g0161 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.258-840C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578547 | |||||||
chr1:183578554 | C | T | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-847G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578554 | |||||||
chr1:183578576 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-869C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578576 | |||||||
chr1:183578693 | C | T | 1 | a0002c0002t0001g0242 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.258-986G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578693 | |||||||
chr1:183578737 | T | G | 75 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(72): Show |
79 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.258-1030A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578737 | |||||||
chr1:183578972 | G | A | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-1265C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578972 | |||||||
chr1:183578981 | A | C | 1 | a0002c0002t0001g0243 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.258-1274T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183578981 | |||||||
chr1:183579123 | C | T | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.258-1416G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579123 | |||||||
chr1:183579361 | C | T | 75 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(72): Show |
79 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.258-1654G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579361 | |||||||
chr1:183579464 | C | T | 1 | a0002c0002t0001g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.258-1757G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579464 | |||||||
chr1:183579492 | C | T | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.258-1785G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579492 | |||||||
chr1:183579497 | C | T | 1 | a0003c0003t0001g0094 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.258-1790G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579497 | |||||||
chr1:183579508 | C | T | 48 | a0001c0001t0001g0047 a0001c0001t0001g0133 a0001c0001t0001g0207 others(45): Show |
56 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.258-1801G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579508 | |||||||
chr1:183579520 | A | G | 2 | a0002c0002t0001g0304 a0002c0002t0001g0309 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.258-1813T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579520 | |||||||
chr1:183579688 | G | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0028 others(4): Show |
10 | HG02145.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-1981C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579688 | |||||||
chr1:183579738 | C | CA | 128 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0121 others(125): Show |
156 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.258-2032dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579738 | |||||||
chr1:183579738 | C | CAA | 33 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0122 others(30): Show |
33 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.258-2033_258-2032d others(4): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579738 | |||||||
chr1:183579738 | CA | C | 9 | a0001c0001t0001g0118 a0001c0001t0001g0191 a0001c0001t0002g0126 others(6): Show |
9 | HG00323.hp2 HG01070.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-2032delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579738 | |||||||
chr1:183579738 | CAAAAAAA others(3): Show |
C | 24 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0083 others(21): Show |
24 | HG01123.hp2 HG01192.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.258-2041_258-2032d others(12): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579738 | |||||||
chr1:183579766 | A | G | 2 | a0002c0002t0001g0089 a0002c0002t0001g0125 |
2 | HG00639.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.258-2059T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579766 | |||||||
chr1:183579781 | T | C | 1 | a0002c0002t0001g0201 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.258-2074A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579781 | |||||||
chr1:183579857 | A | G | 75 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(72): Show |
79 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.258-2150T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579857 | |||||||
chr1:183579970 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.258-2263T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579970 | |||||||
chr1:183579991 | A | G | 1 | a0002c0002t0001g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.258-2284T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183579991 | |||||||
chr1:183580086 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.258-2379C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580086 | |||||||
chr1:183580348 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.258-2641C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580348 | |||||||
chr1:183580423 | G | A | 1 | a0005c0005t0004g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.258-2716C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580423 | |||||||
chr1:183580468 | C | G | 1 | a0002c0002t0001g0255 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.258-2761G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580468 | |||||||
chr1:183580469 | AATTTCCA others(1721): Show |
A | 1 | a0002c0002t0001g0255 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.258-4490_258-2763d others(2): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580469 | |||||||
chr1:183580498 | G | A | 1 | a0001c0001t0003g0313 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.258-2791C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580498 | |||||||
chr1:183580622 | G | T | 130 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0140 others(127): Show |
156 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.258-2915C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580622 | |||||||
chr1:183580672 | T | C | 1 | a0002c0002t0001g0328 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.258-2965A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580672 | |||||||
chr1:183580699 | C | T | 2 | a0002c0002t0001g0302 a0002c0002t0001g0303 |
2 | HG01074.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.258-2992G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580699 | |||||||
chr1:183580717 | C | G | 52 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(49): Show |
56 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.258-3010G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580717 | |||||||
chr1:183580775 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258-3068C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580775 | |||||||
chr1:183580839 | C | T | 1 | a0001c0001t0003g0313 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.258-3132G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580839 | |||||||
chr1:183580978 | C | CA | 134 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(131): Show |
145 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.258-3272dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580978 | |||||||
chr1:183580978 | CA | C | 50 | a0001c0001t0001g0047 a0001c0001t0001g0133 a0001c0001t0001g0207 others(47): Show |
58 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.258-3272delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183580978 | |||||||
chr1:183581174 | C | T | 3 | a0001c0001t0005g0027 a0001c0001t0005g0174 a0001c0001t0005g0289 |
4 | HG02015.hp1 HG02027.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-3467G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581174 | |||||||
chr1:183581231 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-3524T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581231 | |||||||
chr1:183581281 | C | CA | 113 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0049 others(110): Show |
135 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.258-3575dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581281 | |||||||
chr1:183581281 | C | CAA | 22 | a0001c0001t0001g0310 a0001c0001t0001g0327 a0002c0002t0001g0053 others(19): Show |
22 | HG01361.hp2 HG01891.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.258-3576_258-3575d others(4): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581281 | |||||||
chr1:183581281 | C | CAAAAA | 13 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0184 others(10): Show |
14 | HG01884.hp1 HG02015.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.258-3579_258-3575d others(7): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581281 | |||||||
chr1:183581281 | C | CAAAAAA | 57 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(54): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.258-3580_258-3575d others(8): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581281 | |||||||
chr1:183581281 | C | CAAAAAAA | 8 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0182 others(5): Show |
8 | HG01243.hp2 HG01884.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-3581_258-3575d others(9): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581281 | |||||||
chr1:183581297 | AG | A | 54 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0043 others(51): Show |
61 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.258-3591delC | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581297 | |||||||
chr1:183581298 | G | A | 196 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(193): Show |
235 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.258-3591C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581298 | |||||||
chr1:183581308 | A | C | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0140 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-3601T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581308 | |||||||
chr1:183581314 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-3607C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581314 | |||||||
chr1:183581315 | A | AAAAG | 81 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(78): Show |
85 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.258-3612_258-3609d others(6): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581315 | |||||||
chr1:183581315 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-3608T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581315 | |||||||
chr1:183581340 | A | C | 129 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0140 others(126): Show |
151 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.258-3633T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581340 | |||||||
chr1:183581347 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.258-3640C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581347 | |||||||
chr1:183581489 | T | C | 1 | a0001c0001t0003g0080 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.258-3782A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581489 | |||||||
chr1:183581516 | C | T | 1 | a0001c0001t0001g0351 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.258-3809G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581516 | |||||||
chr1:183581595 | C | G | 1 | a0001c0001t0001g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.258-3888G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581595 | |||||||
chr1:183581674 | GT | G | 127 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0140 others(124): Show |
148 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.258-3968delA | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581674 | |||||||
chr1:183581678 | T | G | 1 | a0001c0001t0001g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.258-3971A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581678 | |||||||
chr1:183581707 | T | C | 1 | a0002c0002t0001g0161 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.258-4000A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581707 | |||||||
chr1:183581708 | G | A | 1 | a0002c0002t0001g0161 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.258-4001C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581708 | |||||||
chr1:183581747 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.258-4040C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581747 | |||||||
chr1:183581754 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.258-4047G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581754 | |||||||
chr1:183581869 | G | A | 1 | a0002c0002t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.258-4162C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581869 | |||||||
chr1:183581910 | G | A | 81 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(78): Show |
85 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.258-4203C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581910 | |||||||
chr1:183581911 | C | A | 1 | a0001c0001t0003g0296 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.258-4204G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581911 | |||||||
chr1:183581957 | T | G | 3 | a0001c0001t0002g0058 a0001c0001t0002g0134 a0001c0001t0002g0196 |
3 | HG00099.hp2 HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.258-4250A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183581957 | |||||||
chr1:183582027 | T | C | 78 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(75): Show |
82 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.258-4320A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183582027 | |||||||
chr1:183582198 | C | T | 1 | a0002c0002t0001g0255 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.258-4491G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183582198 | |||||||
chr1:183582625 | G | A | 85 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(82): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.257+4270C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183582625 | |||||||
chr1:183582904 | C | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0312 a0001c0001t0001g0354 |
3 | HG01069.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.257+3991G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183582904 | |||||||
chr1:183582958 | T | TA | 81 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(78): Show |
85 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.257+3936dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183582958 | |||||||
chr1:183583012 | C | T | 1 | a0002c0002t0001g0335 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.257+3883G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583012 | |||||||
chr1:183583371 | G | A | 1 | a0001c0001t0003g0313 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.257+3524C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583371 | |||||||
chr1:183583391 | A | G | 26 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0083 others(23): Show |
26 | HG01123.hp2 HG01192.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.257+3504T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583391 | |||||||
chr1:183583520 | A | G | 1 | a0002c0002t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.257+3375T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583520 | |||||||
chr1:183583621 | C | T | 2 | a0002c0002t0001g0087 a0002c0002t0001g0209 |
2 | NA18961.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.257+3274G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583621 | |||||||
chr1:183583763 | G | A | 1 | a0005c0005t0001g0345 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.257+3132C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583763 | |||||||
chr1:183583909 | A | G | 1 | a0002c0002t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.257+2986T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583909 | |||||||
chr1:183583989 | C | T | 2 | a0001c0001t0002g0306 a0001c0001t0002g0334 |
2 | HG00323.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.257+2906G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183583989 | |||||||
chr1:183584191 | A | G | 8 | a0001c0001t0001g0025 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
9 | HG00597.hp1 HG02155.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.257+2704T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584191 | |||||||
chr1:183584348 | C | T | 1 | a0002c0002t0001g0123 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.257+2547G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584348 | |||||||
chr1:183584349 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.257+2546C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584349 | |||||||
chr1:183584425 | C | T | 283 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0021 others(280): Show |
330 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.257+2470G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584425 | |||||||
chr1:183584433 | T | C | 7 | a0001c0001t0001g0314 a0005c0005t0004g0031 a0005c0005t0004g0032 others(4): Show |
7 | HG02809.hp1 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+2462A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584433 | |||||||
chr1:183584502 | A | C | 12 | a0001c0001t0001g0185 a0001c0001t0001g0244 a0001c0001t0001g0248 others(9): Show |
12 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.257+2393T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584502 | |||||||
chr1:183584533 | C | T | 4 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0351 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+2362G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584533 | |||||||
chr1:183584559 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.257+2336G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584559 | |||||||
chr1:183584735 | C | T | 95 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0037 others(92): Show |
114 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.257+2160G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584735 | |||||||
chr1:183584915 | A | C | 14 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0086 others(11): Show |
15 | HG01081.hp1 HG01978.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.257+1980T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584915 | |||||||
chr1:183584916 | TA | T | 14 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0086 others(11): Show |
15 | HG01081.hp1 HG01978.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.257+1978delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183584916 | |||||||
chr1:183585038 | T | G | 1 | a0001c0001t0001g0316 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.257+1857A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585038 | |||||||
chr1:183585146 | A | G | 113 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0025 others(110): Show |
123 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.257+1749T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585146 | |||||||
chr1:183585314 | T | C | 122 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0028 others(119): Show |
134 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.257+1581A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585314 | |||||||
chr1:183585398 | G | A | 32 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0292 others(29): Show |
35 | HG01069.hp1 HG01074.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.257+1497C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585398 | |||||||
chr1:183585410 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.257+1485C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585410 | |||||||
chr1:183585574 | G | A | 2 | a0002c0002t0001g0200 a0002c0002t0001g0235 |
2 | HG01515.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.257+1321C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585574 | |||||||
chr1:183585579 | C | T | 37 | a0001c0001t0001g0030 a0001c0001t0001g0183 a0001c0001t0001g0184 others(34): Show |
40 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.257+1316G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585579 | |||||||
chr1:183585612 | G | A | 5 | a0001c0001t0001g0305 a0001c0001t0001g0307 a0001c0001t0001g0308 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+1283C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585612 | |||||||
chr1:183585624 | C | CAAAAAAA others(3): Show |
47 | a0001c0001t0001g0030 a0001c0001t0001g0183 a0001c0001t0001g0184 others(44): Show |
51 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.257+1261_257+1270d others(12): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(4): Show |
50 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 others(47): Show |
55 | HG00558.hp2 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.257+1260_257+1270d others(13): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0191 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.257+1259_257+1270d others(14): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0292 a0001c0001t0001g0319 |
2 | HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.257+1270_257+1271i others(18): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(10): Show |
14 | a0001c0001t0001g0298 a0001c0001t0001g0300 a0001c0001t0001g0301 others(11): Show |
14 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.257+1270_257+1271i others(19): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(11): Show |
9 | a0001c0001t0001g0028 a0001c0001t0001g0247 a0001c0001t0001g0248 others(6): Show |
10 | HG01433.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.257+1270_257+1271i others(20): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.257+1270_257+1271i others(21): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(14): Show |
5 | a0001c0001t0001g0011 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
7 | HG02647.hp2 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+1270_257+1271i others(23): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0318 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.257+1270_257+1271i others(24): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(17): Show |
2 | a0001c0010t0001g0052 a0002c0002t0001g0054 |
2 | HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.257+1270_257+1271i others(26): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(18): Show |
2 | a0001c0001t0001g0241 a0001c0001t0003g0240 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.257+1270_257+1271i others(27): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(21): Show |
5 | a0005c0005t0004g0031 a0005c0005t0004g0032 a0005c0005t0004g0033 others(2): Show |
5 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+1270_257+1271i others(30): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585624 | C | CAAAAAAA others(22): Show |
1 | a0005c0005t0004g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.257+1270_257+1271i others(31): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585624 | |||||||
chr1:183585642 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.257+1253A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585642 | |||||||
chr1:183585699 | T | C | 1 | a0002c0002t0001g0192 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.257+1196A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183585699 | |||||||
chr1:183586032 | C | G | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.257+863G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586032 | |||||||
chr1:183586035 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.257+860A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586035 | |||||||
chr1:183586035 | T | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0312 others(7): Show |
13 | HG01099.hp2 HG02109.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+860A>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586035 | |||||||
chr1:183586060 | C | A | 1 | a0002c0007t0002g0237 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.257+835G>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586060 | |||||||
chr1:183586063 | G | A | 1 | a0002c0002t0001g0348 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.257+832C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586063 | |||||||
chr1:183586094 | G | T | 31 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0292 others(28): Show |
34 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.257+801C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586094 | |||||||
chr1:183586211 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.257+684C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586211 | |||||||
chr1:183586226 | C | T | 1 | a0002c0007t0002g0063 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.257+669G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586226 | |||||||
chr1:183586227 | G | A | 4 | a0001c0001t0001g0244 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+668C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586227 | |||||||
chr1:183586235 | A | G | 94 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0043 others(91): Show |
104 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.257+660T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586235 | |||||||
chr1:183586238 | C | G | 94 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0043 others(91): Show |
104 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.257+657G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586238 | |||||||
chr1:183586271 | C | T | 345 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(342): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.257+624G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586271 | |||||||
chr1:183586319 | A | C | 44 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 others(41): Show |
49 | HG00323.hp2 HG00558.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.257+576T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586319 | |||||||
chr1:183586379 | T | C | 6 | a0005c0005t0004g0031 a0005c0005t0004g0032 a0005c0005t0004g0033 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+516A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586379 | |||||||
chr1:183586411 | A | G | 1 | a0002c0002t0001g0242 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.257+484T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586411 | |||||||
chr1:183586504 | A | G | 3 | a0001c0001t0002g0259 a0001c0001t0002g0260 a0001c0001t0002g0278 |
3 | HG01515.hp1 HG01517.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.257+391T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586504 | |||||||
chr1:183586575 | C | T | 1 | a0002c0002t0001g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.257+320G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586575 | |||||||
chr1:183586622 | T | C | 345 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(342): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.257+273A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586622 | |||||||
chr1:183586644 | C | T | 94 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0043 others(91): Show |
104 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.257+251G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586644 | |||||||
chr1:183586744 | G | A | 31 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0292 others(28): Show |
34 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.257+151C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586744 | |||||||
chr1:183586828 | C | T | 6 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0005g0027 others(3): Show |
7 | HG02015.hp1 HG02056.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+67G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | 183586828 | |||||||
chr1:183586990 | G | A | 1 | a0002c0002t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.175-13C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183586990 | |||||||
chr1:183587075 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.175-98T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587075 | |||||||
chr1:183587126 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.175-149G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587126 | |||||||
chr1:183587156 | A | G | 137 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0030 others(134): Show |
150 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.175-179T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587156 | |||||||
chr1:183587186 | C | T | 2 | a0001c0001t0001g0298 a0002c0002t0001g0299 |
2 | HG01192.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.175-209G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587186 | |||||||
chr1:183587260 | T | C | 44 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 others(41): Show |
49 | HG00323.hp2 HG00558.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.175-283A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587260 | |||||||
chr1:183587261 | G | A | 2 | a0001c0001t0002g0276 a0002c0002t0001g0277 |
2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.175-284C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587261 | |||||||
chr1:183587295 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.175-318G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587295 | |||||||
chr1:183587485 | T | C | 94 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0043 others(91): Show |
104 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.175-508A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587485 | |||||||
chr1:183587509 | G | C | 2 | a0001c0001t0001g0349 a0001c0001t0001g0350 |
2 | HG01168.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.175-532C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587509 | |||||||
chr1:183587524 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.175-547C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587524 | |||||||
chr1:183587536 | G | A | 6 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0005g0027 others(3): Show |
7 | HG02015.hp1 HG02056.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-559C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587536 | |||||||
chr1:183587595 | C | CAAA | 24 | a0001c0001t0001g0047 a0001c0001t0001g0261 a0001c0001t0001g0264 others(21): Show |
25 | HG00558.hp2 HG00738.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-621_175-619dup others(3): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | |||||||
chr1:183587595 | C | CAAAA | 14 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 others(11): Show |
16 | HG01175.hp1 HG01175.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.175-622_175-619dup others(4): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | |||||||
chr1:183587595 | C | CAAAAAAA others(4): Show |
1 | a0006c0006t0001g0285 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.175-629_175-619dup others(11): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | |||||||
chr1:183587595 | CA | C | 155 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0037 others(152): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.175-619delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | |||||||
chr1:183587595 | CAA | C | 36 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(33): Show |
41 | HG01256.hp1 HG01891.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.175-620_175-619del others(2): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | |||||||
chr1:183587595 | CAAA | C | 18 | a0001c0001t0001g0292 a0001c0001t0001g0298 a0001c0001t0001g0300 others(15): Show |
18 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.175-621_175-619del others(3): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | |||||||
chr1:183587595 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0351 a0001c0001t0001g0352 |
2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.175-628_175-619del others(10): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | |||||||
chr1:183587595 | CAAAAAAA others(4): Show |
C | 38 | a0001c0001t0001g0030 a0001c0001t0001g0324 a0001c0001t0001g0325 others(35): Show |
42 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.175-629_175-619del others(11): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | |||||||
chr1:183587595 | CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0001g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.175-632_175-619del others(14): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587595 | |||||||
chr1:183587635 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.175-658T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587635 | |||||||
chr1:183587661 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0319 |
3 | HG02717.hp1 HG02896.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.175-684C>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587661 | |||||||
chr1:183587772 | C | T | 1 | a0001c0010t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.175-795G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587772 | |||||||
chr1:183587773 | G | A | 1 | a0001c0001t0001g0353 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.175-796C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587773 | |||||||
chr1:183587821 | T | C | 2 | a0002c0002t0001g0238 a0002c0002t0001g0239 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.175-844A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183587821 | |||||||
chr1:183588184 | A | G | 4 | a0001c0001t0001g0244 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-1207T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588184 | |||||||
chr1:183588206 | A | T | 6 | a0001c0001t0001g0310 a0001c0001t0003g0296 a0002c0002t0001g0293 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-1229T>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588206 | |||||||
chr1:183588224 | C | G | 1 | a0002c0002t0001g0051 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.175-1247G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588224 | |||||||
chr1:183588420 | A | C | 1 | a0002c0002t0001g0050 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.175-1443T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588420 | |||||||
chr1:183588427 | A | C | 1 | a0001c0001t0001g0292 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.175-1450T>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588427 | |||||||
chr1:183588458 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.175-1481C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588458 | |||||||
chr1:183588474 | C | CA | 88 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0043 others(85): Show |
97 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.175-1498dupT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588474 | |||||||
chr1:183588611 | TA | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0049 |
5 | HG02145.hp1 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+1544delT | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588611 | |||||||
chr1:183588650 | T | C | 1 | a0001c0001t0001g0354 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.174+1506A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588650 | |||||||
chr1:183588664 | T | C | 6 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0005g0027 others(3): Show |
7 | HG02015.hp1 HG02056.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+1492A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588664 | |||||||
chr1:183588808 | C | T | 1 | a0003c0003t0001g0048 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.174+1348G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183588808 | |||||||
chr1:183589032 | A | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.174+1124T>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589032 | |||||||
chr1:183589039 | T | C | 76 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0030 others(73): Show |
84 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.174+1117A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589039 | |||||||
chr1:183589141 | G | A | 1 | a0002c0002t0001g0242 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.174+1015C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589141 | |||||||
chr1:183589143 | C | T | 30 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0292 others(27): Show |
33 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.174+1013G>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589143 | |||||||
chr1:183589212 | T | C | 1 | a0002c0002t0001g0243 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.174+944A>G | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589212 | |||||||
chr1:183589222 | A | G | 76 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0030 others(73): Show |
84 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.174+934T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589222 | |||||||
chr1:183589288 | G | A | 76 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0030 others(73): Show |
84 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.174+868C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589288 | |||||||
chr1:183589302 | G | A | 127 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0030 others(124): Show |
140 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.174+854C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589302 | |||||||
chr1:183589303 | A | G | 76 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0030 others(73): Show |
84 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.174+853T>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589303 | |||||||
chr1:183589646 | TAA | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
12 | HG02523.hp2 NA18945.hp2 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.174+508_174+509del others(2): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589646 | |||||||
chr1:183589668 | G | T | 30 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0292 others(27): Show |
33 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.174+488C>A | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589668 | |||||||
chr1:183589748 | CATGAAAG others(13): Show |
C | 20 | a0001c0001t0001g0292 a0001c0001t0001g0298 a0001c0001t0001g0300 others(17): Show |
20 | HG01074.hp1 HG01192.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.174+388_174+407del others(20): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589748 | |||||||
chr1:183589806 | G | A | 30 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0292 others(27): Show |
33 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.174+350C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589806 | |||||||
chr1:183589861 | G | A | 38 | a0001c0001t0001g0030 a0001c0001t0001g0324 a0001c0001t0001g0325 others(35): Show |
42 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.174+295C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589861 | |||||||
chr1:183589970 | G | A | 75 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0030 others(72): Show |
83 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.174+186C>T | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183589970 | |||||||
chr1:183590148 | C | G | 2 | a0001c0001t0001g0037 a0002c0002t0001g0038 |
2 | HG02976.hp1 NA18906.hp1 |
splice_region_variant&intron_variant | LOW | c.174+8G>C | NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 1/14 | chr1 | 183590148 |