Item | Value |
---|---|
geneid | 79707 |
ensemblid | ENSG00000162408.11 |
hgncid | 26265 |
symbol | NOL9 |
name | nucleolar protein 9 |
refseq_nuc | NM_024654.5 |
refseq_prot | NP_078930.4 |
ensembl_nuc | ENST00000377705.6 |
ensembl_prot | ENSP00000366934.5 |
mane_status | MANE Select |
chr | chr1 |
start | 6521347 |
end | 6554513 |
strand | - |
ver | v1.2 |
region | chr1:6521347-6554513 |
region5000 | chr1:6516347-6559513 |
regionname0 | NOL9_chr1_6521347_6554513 |
regionname5000 | NOL9_chr1_6516347_6559513 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 702 | 219 | 40 | 54 | 94 | 8 | 22 | 62 | NOL9_chr1_6516347_6559513 | NOL9 | MADSG others(697): Show |
chr1 | 6516347 | 6559513 |
a0002 | 0/0 | 702 | 93 | 42 | 9 | 34 | 2 | 6 | 25 | NOL9_chr1_6516347_6559513 | NOL9 | MADSG others(697): Show |
chr1 | 6516347 | 6559513 |
a0003 | 1/0 | 702 | 7 | 6 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | MADSG others(697): Show |
chr1 | 6516347 | 6559513 |
a0004 | 0/0 | 702 | 7 | 3 | 0 | 2 | 0 | 2 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | MADSG others(697): Show |
chr1 | 6516347 | 6559513 |
a0005 | 0/0 | 702 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | NOL9_chr1_6516347_6559513 | NOL9 | MADSG others(697): Show |
chr1 | 6516347 | 6559513 |
a0006 | 0/0 | 702 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | MADSG others(697): Show |
chr1 | 6516347 | 6559513 |
a0007 | 0/0 | 702 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | MADSG others(697): Show |
chr1 | 6516347 | 6559513 |
a0008 | 0/0 | 702 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | MADSG others(697): Show |
chr1 | 6516347 | 6559513 |
a0009 | 0/0 | 702 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | MADSG others(697): Show |
chr1 | 6516347 | 6559513 |
a0010 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | MADSG others(693): Show |
chr1 | 6516347 | 6559513 |
a0011 | 0/0 | 702 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | MADSG others(697): Show |
chr1 | 6516347 | 6559513 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2106 | 214 | 40 | 54 | 90 | 8 | 21 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0001c0009 | 0/0 | 2106 | 4 | 0 | 0 | 3 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0001c0015 | 0/0 | 2106 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0002c0002 | 0/0 | 2106 | 60 | 10 | 8 | 34 | 2 | 6 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0002c0003 | 0/0 | 2106 | 14 | 13 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0002c0004 | 0/0 | 2106 | 13 | 13 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0002c0008 | 0/0 | 2106 | 5 | 5 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0002c0012 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0003c0006 | 1/0 | 2106 | 7 | 6 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0004c0005 | 0/0 | 2106 | 7 | 3 | 0 | 2 | 0 | 2 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0005c0007 | 0/0 | 2106 | 6 | 0 | 0 | 6 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0006c0010 | 0/0 | 2106 | 3 | 2 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0007c0017 | 0/0 | 2106 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0008c0016 | 0/0 | 2106 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0009c0011 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 | ||
a0010c0013 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2089): Show |
chr1 | 6516347 | 6559513 | ||
a0011c0014 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | ATGGC others(2101): Show |
chr1 | 6516347 | 6559513 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6630 | 116 | 18 | 31 | 43 | 5 | 19 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0002 | 0/0 | 6632 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0003 | 0/0 | 6630 | 22 | 0 | 0 | 22 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0004 | 0/0 | 6631 | 16 | 1 | 6 | 9 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0005 | 0/0 | 6630 | 9 | 1 | 3 | 1 | 3 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0006 | 0/0 | 6629 | 9 | 7 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6624): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0008 | 0/0 | 6631 | 4 | 4 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0011 | 0/0 | 6630 | 5 | 5 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0014 | 0/0 | 6629 | 3 | 0 | 2 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6624): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0015 | 0/0 | 6630 | 3 | 0 | 3 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0016 | 0/0 | 6631 | 3 | 1 | 1 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0019 | 0/0 | 6630 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0023 | 0/0 | 6630 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0029 | 0/0 | 6631 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0030 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0032 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0034 | 0/0 | 6629 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6624): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0035 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0036 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6623): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0037 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0039 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0040 | 0/0 | 6631 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0041 | 0/0 | 6631 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0042 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0043 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0044 | 0/0 | 6631 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0045 | 0/0 | 6631 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0046 | 0/1 | 6632 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0047 | 0/0 | 6628 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6623): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0048 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0049 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0053 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0001t0057 | 0/0 | 6629 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6624): Show |
chr1 | 6516347 | 6559513 |
a0001c0009t0001 | 0/0 | 6630 | 3 | 0 | 0 | 2 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0009t0050 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0001c0015t0001 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0002 | 0/0 | 6632 | 33 | 3 | 5 | 18 | 2 | 5 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0005 | 0/0 | 6630 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0009 | 0/0 | 6633 | 6 | 2 | 0 | 4 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6628): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0012 | 0/0 | 6633 | 4 | 1 | 1 | 1 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6628): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0018 | 0/0 | 6632 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0023 | 0/0 | 6630 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0024 | 0/0 | 6627 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6622): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0025 | 0/0 | 6634 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6629): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0056 | 0/0 | 6629 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6624): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0060 | 0/0 | 6633 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6628): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0061 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0063 | 0/0 | 6632 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0064 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0065 | 0/0 | 6635 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6630): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0066 | 0/0 | 6633 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6628): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0067 | 0/0 | 6633 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6628): Show |
chr1 | 6516347 | 6559513 |
a0002c0002t0068 | 0/0 | 6631 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0002c0003t0007 | 0/0 | 6632 | 7 | 7 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0002c0003t0026 | 0/0 | 6632 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0002c0003t0027 | 0/0 | 6633 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6628): Show |
chr1 | 6516347 | 6559513 |
a0002c0003t0069 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6628): Show |
chr1 | 6516347 | 6559513 |
a0002c0003t0070 | 0/0 | 6632 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0002c0003t0071 | 0/0 | 6632 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0002c0004t0008 | 0/0 | 6631 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0002c0004t0010 | 0/0 | 6634 | 6 | 6 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6629): Show |
chr1 | 6516347 | 6559513 |
a0002c0004t0028 | 0/0 | 6634 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6629): Show |
chr1 | 6516347 | 6559513 |
a0002c0004t0072 | 0/0 | 6631 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0002c0004t0073 | 0/0 | 6631 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0002c0004t0074 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6623): Show |
chr1 | 6516347 | 6559513 |
a0002c0008t0020 | 0/0 | 6634 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6629): Show |
chr1 | 6516347 | 6559513 |
a0002c0008t0021 | 0/0 | 6634 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6629): Show |
chr1 | 6516347 | 6559513 |
a0002c0008t0051 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6623): Show |
chr1 | 6516347 | 6559513 |
a0002c0012t0002 | 0/0 | 6632 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0003c0006t0013 | 1/0 | 6627 | 4 | 3 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6622): Show |
chr1 | 6516347 | 6559513 |
a0003c0006t0017 | 0/0 | 6628 | 3 | 3 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6623): Show |
chr1 | 6516347 | 6559513 |
a0004c0005t0031 | 0/0 | 6631 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0004c0005t0033 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6624): Show |
chr1 | 6516347 | 6559513 |
a0004c0005t0054 | 0/0 | 6631 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
a0004c0005t0055 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0004c0005t0058 | 0/0 | 6633 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6628): Show |
chr1 | 6516347 | 6559513 |
a0004c0005t0059 | 0/0 | 6633 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6628): Show |
chr1 | 6516347 | 6559513 |
a0004c0005t0062 | 0/0 | 6632 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6627): Show |
chr1 | 6516347 | 6559513 |
a0005c0007t0003 | 0/0 | 6630 | 6 | 0 | 0 | 6 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0006c0010t0022 | 0/0 | 6633 | 2 | 1 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6628): Show |
chr1 | 6516347 | 6559513 |
a0006c0010t0052 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6628): Show |
chr1 | 6516347 | 6559513 |
a0007c0017t0038 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0008c0016t0001 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6625): Show |
chr1 | 6516347 | 6559513 |
a0009c0011t0075 | 0/0 | 6634 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6629): Show |
chr1 | 6516347 | 6559513 |
a0010c0013t0018 | 0/0 | 6620 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6615): Show |
chr1 | 6516347 | 6559513 |
a0011c0014t0004 | 0/0 | 6631 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | GAGGA others(6626): Show |
chr1 | 6516347 | 6559513 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 6 | 2 | 2 | 0 | 2 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0008g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0008g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0008g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0011g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0014g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0014g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0014g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0015g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0015g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0016g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0016g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0016g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0019g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0019g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0023g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0029g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0030g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0032g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0034g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0035g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0036g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0037g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0039g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0040g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0041g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0042g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0043g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0044g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0045g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0046g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0047g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0048g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0049g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0053g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0057g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0009t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0009t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0009t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0009t0050g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0015t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0004 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0012g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0012g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0012g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0012g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0018g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0018g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0023g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0024g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0024g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0025g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0025g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0056g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0060g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0061g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0063g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0064g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0065g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0066g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0067g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0068g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0026g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0026g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0027g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0027g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0069g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0070g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0071g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0010g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0028g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0028g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0072g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0073g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0074g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0008t0020g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0008t0021g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0008t0021g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0008t0051g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0012t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0006t0013g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0006t0013g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0006t0017g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0006t0017g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0006t0017g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0005t0031g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0005t0033g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0005t0054g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0005t0055g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0005t0058g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0005t0059g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0005t0062g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0005c0007t0003g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0005c0007t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0005c0007t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0006c0010t0022g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0006c0010t0022g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0006c0010t0052g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0007c0017t0038g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0008c0016t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0009c0011t0075g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0010c0013t0018g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0011c0014t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0004 | EUR | GBR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0261 | EUR | GBR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00323 | hp2 | a0001 | c0001 | t0005 | g0182 | EUR | FIN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00438 | hp1 | a0002 | c0002 | t0065 | g0072 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00544 | hp1 | a0002 | c0002 | t0064 | g0085 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00544 | hp2 | a0001 | c0001 | t0019 | g0231 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00558 | hp2 | a0002 | c0002 | t0009 | g0075 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00609 | hp1 | a0007 | c0017 | t0038 | g0221 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00609 | hp2 | a0001 | c0001 | t0039 | g0147 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00621 | hp1 | a0008 | c0016 | t0001 | g0237 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00621 | hp2 | a0002 | c0002 | t0066 | g0089 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00642 | hp1 | a0002 | c0002 | t0023 | g0108 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00642 | hp2 | a0001 | c0001 | t0016 | g0191 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00735 | hp1 | a0002 | c0002 | t0012 | g0060 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00735 | hp2 | a0001 | c0001 | t0029 | g0168 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0153 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0194 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01109 | hp1 | a0002 | c0002 | t0005 | g0063 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01167 | hp1 | a0002 | c0003 | t0070 | g0104 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01168 | hp1 | a0001 | c0001 | t0023 | g0123 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01169 | hp1 | a0001 | c0001 | t0057 | g0122 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0033 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01243 | hp1 | a0006 | c0010 | t0022 | g0270 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0084 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01257 | hp1 | a0001 | c0001 | t0014 | g0197 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01257 | hp2 | a0001 | c0001 | t0014 | g0189 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0135 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01433 | hp2 | a0001 | c0001 | t0041 | g0131 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01891 | hp1 | a0003 | c0006 | t0013 | g0010 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01891 | hp2 | a0002 | c0003 | t0026 | g0098 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01928 | hp2 | a0001 | c0001 | t0015 | g0035 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01975 | hp1 | a0001 | c0001 | t0034 | g0215 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01978 | hp1 | a0001 | c0001 | t0040 | g0214 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02027 | hp2 | a0001 | c0015 | t0001 | g0202 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02040 | hp1 | a0001 | c0001 | t0030 | g0160 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0097 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02055 | hp2 | a0002 | c0004 | t0073 | g0038 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02074 | hp2 | a0005 | c0007 | t0003 | g0009 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02083 | hp2 | a0001 | c0001 | t0032 | g0166 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02145 | hp1 | a0001 | c0001 | t0037 | g0248 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02145 | hp2 | a0002 | c0004 | t0028 | g0042 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02148 | hp2 | a0001 | c0001 | t0015 | g0216 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CDX | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02155 | hp2 | a0004 | c0005 | t0054 | g0114 | EAS | CDX | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02165 | hp2 | a0005 | c0007 | t0003 | g0009 | EAS | CDX | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0005 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0005 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02258 | hp2 | a0004 | c0005 | t0062 | g0112 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02273 | hp1 | a0001 | c0001 | t0015 | g0035 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02280 | hp1 | a0002 | c0003 | t0007 | g0055 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02280 | hp2 | a0002 | c0003 | t0007 | g0050 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02451 | hp2 | a0002 | c0004 | t0008 | g0047 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02572 | hp1 | a0003 | c0006 | t0013 | g0010 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02572 | hp2 | a0002 | c0002 | t0012 | g0094 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02615 | hp1 | a0002 | c0003 | t0007 | g0058 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02615 | hp2 | a0001 | c0001 | t0008 | g0254 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02622 | hp1 | a0002 | c0002 | t0009 | g0091 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02622 | hp2 | a0002 | c0003 | t0027 | g0057 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02630 | hp2 | a0002 | c0004 | t0074 | g0043 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02647 | hp1 | a0002 | c0008 | t0051 | g0045 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02647 | hp2 | a0009 | c0011 | t0075 | g0037 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02717 | hp1 | a0002 | c0002 | t0018 | g0103 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0096 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02723 | hp2 | a0002 | c0004 | t0008 | g0048 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02738 | hp2 | a0002 | c0002 | t0012 | g0073 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02809 | hp1 | a0002 | c0008 | t0021 | g0044 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02818 | hp1 | a0003 | c0006 | t0017 | g0116 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02818 | hp2 | a0002 | c0003 | t0027 | g0053 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02886 | hp1 | a0002 | c0002 | t0063 | g0105 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02886 | hp2 | a0003 | c0006 | t0013 | g0010 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02896 | hp1 | a0002 | c0002 | t0068 | g0101 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02896 | hp2 | a0001 | c0001 | t0053 | g0262 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02897 | hp1 | a0002 | c0004 | t0010 | g0003 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02897 | hp2 | a0002 | c0002 | t0018 | g0102 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02922 | hp1 | a0002 | c0003 | t0026 | g0099 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02965 | hp1 | a0002 | c0004 | t0010 | g0040 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02965 | hp2 | a0004 | c0005 | t0033 | g0113 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02970 | hp1 | a0002 | c0004 | t0010 | g0003 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0126 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0128 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03041 | hp2 | a0002 | c0012 | t0002 | g0095 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03098 | hp1 | a0001 | c0001 | t0016 | g0163 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03098 | hp2 | a0002 | c0003 | t0071 | g0054 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03130 | hp1 | a0002 | c0004 | t0010 | g0003 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03139 | hp1 | a0010 | c0013 | t0018 | g0120 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03139 | hp2 | a0002 | c0003 | t0007 | g0049 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03195 | hp2 | a0002 | c0004 | t0010 | g0003 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03209 | hp2 | a0002 | c0003 | t0007 | g0051 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0093 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0067 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03486 | hp1 | a0002 | c0004 | t0010 | g0003 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0129 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0005 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0255 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03579 | hp2 | a0006 | c0010 | t0052 | g0269 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03688 | hp2 | a0004 | c0005 | t0059 | g0109 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03710 | hp2 | a0004 | c0005 | t0058 | g0110 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0175 | SAS | BEB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0070 | SAS | BEB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03834 | hp2 | a0001 | c0009 | t0001 | g0203 | SAS | BEB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18522 | hp1 | a0003 | c0006 | t0017 | g0117 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18522 | hp2 | a0002 | c0008 | t0020 | g0019 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18747 | hp2 | a0001 | c0009 | t0050 | g0204 | EAS | CHB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0124 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18939 | hp1 | a0002 | c0002 | t0024 | g0078 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18939 | hp2 | a0001 | c0001 | t0049 | g0235 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18948 | hp1 | a0001 | c0001 | t0048 | g0179 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18948 | hp2 | a0001 | c0009 | t0001 | g0211 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18949 | hp2 | a0001 | c0001 | t0045 | g0223 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18956 | hp2 | a0001 | c0001 | t0014 | g0209 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18957 | hp1 | a0002 | c0002 | t0012 | g0064 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18959 | hp1 | a0002 | c0002 | t0024 | g0065 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18960 | hp1 | a0002 | c0002 | t0056 | g0107 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18967 | hp1 | a0005 | c0007 | t0003 | g0253 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18967 | hp2 | a0002 | c0002 | t0025 | g0068 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18968 | hp1 | a0002 | c0002 | t0061 | g0106 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18970 | hp1 | a0001 | c0001 | t0035 | g0205 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18973 | hp2 | a0001 | c0001 | t0044 | g0141 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18975 | hp2 | a0001 | c0001 | t0042 | g0146 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18992 | hp2 | a0001 | c0001 | t0043 | g0230 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18994 | hp2 | a0002 | c0002 | t0009 | g0087 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18997 | hp2 | a0002 | c0002 | t0067 | g0090 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18999 | hp2 | a0004 | c0005 | t0055 | g0115 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19000 | hp2 | a0002 | c0002 | t0009 | g0074 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19007 | hp1 | a0001 | c0001 | t0016 | g0183 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19010 | hp2 | a0005 | c0007 | t0003 | g0009 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19012 | hp2 | a0001 | c0009 | t0001 | g0125 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19030 | hp1 | a0002 | c0003 | t0069 | g0100 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19030 | hp2 | a0006 | c0010 | t0022 | g0268 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19043 | hp1 | a0002 | c0004 | t0072 | g0041 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19043 | hp2 | a0002 | c0008 | t0020 | g0019 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19062 | hp1 | a0002 | c0002 | t0060 | g0083 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19066 | hp1 | a0005 | c0007 | t0003 | g0009 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19066 | hp2 | a0002 | c0002 | t0009 | g0071 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19068 | hp2 | a0001 | c0001 | t0019 | g0233 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19079 | hp1 | a0001 | c0001 | t0047 | g0234 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19085 | hp1 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19090 | hp2 | a0002 | c0002 | t0025 | g0077 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19240 | hp2 | a0002 | c0004 | t0028 | g0039 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20129 | hp1 | a0002 | c0003 | t0007 | g0056 | AFR | ASW | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20129 | hp2 | a0011 | c0014 | t0004 | g0121 | AFR | ASW | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0061 | EUR | TSI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0033 | EUR | TSI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | GIH | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | GIH | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02559 | hp1 | a0004 | c0005 | t0031 | g0111 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02559 | hp2 | a0002 | c0003 | t0007 | g0052 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | USA | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG06807 | hp2 | a0001 | c0001 | t0011 | g0005 | AFR | USA | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18955 | hp2 | a0005 | c0007 | t0003 | g0138 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20300 | hp1 | a0002 | c0002 | t0009 | g0092 | AFR | USA | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20300 | hp2 | a0003 | c0006 | t0017 | g0118 | AFR | USA | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA21309 | hp1 | a0001 | c0001 | t0036 | g0154 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA21309 | hp2 | a0002 | c0008 | t0021 | g0046 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
homoSapiens | chm13v2 | a0001 | c0001 | t0046 | g0217 | REF | REF | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
homoSapiens | grch38p0 | a0003 | c0006 | t0013 | g0119 | REF | REF | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:6532574 | G | A | 1 | a0008 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1424C>T | p.Ala475Val | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/12 | 1435/6627 | 1424/2109 | 475/702 | chr1 | 6532574 | |||
chr1:6532740 | T | C | 1 | a0005 | 6 | HG02074.hp2 HG02165.hp2 NA18955.hp2 others(3): Show |
missense_variant | MODERATE | c.1258A>G | p.Ile420Val | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/12 | 1269/6627 | 1258/2109 | 420/702 | chr1 | 6532740 | |||
chr1:6545166 | C | A | 1 | a0007 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.759G>T | p.Gln253His | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 4/12 | 770/6627 | 759/2109 | 253/702 | chr1 | 6545166 | |||
chr1:6550612 | A | G | 1 | a0009 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.400T>C | p.Phe134Leu | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/12 | 411/6627 | 400/2109 | 134/702 | chr1 | 6550612 | |||
chr1:6554264 | G | A | 1 | a0006 | 3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.239C>T | p.Thr80Ile | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 250/6627 | 239/2109 | 80/702 | chr1 | 6554264 | |||
chr1:6554331 | A | C | 9 | a0001 a0002 a0005 others(6): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
missense_variant | MODERATE | c.172T>G | p.Ser58Ala | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 183/6627 | 172/2109 | 58/702 | chr1 | 6554331 | |||
chr1:6554355 | A | G | 10 | a0001 a0002 a0004 others(7): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
missense_variant | MODERATE | c.148T>C | p.Trp50Arg | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 159/6627 | 148/2109 | 50/702 | chr1 | 6554355 | |||
chr1:6554393 | AGCCGGCG others(5): Show |
A | 1 | a0010 | 1 | HG03139.hp1 | disruptive_inframe_deletion | MODERATE | c.98_109delCCCGCCGCC others(3): Show |
p.Pro33_Arg36del | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 120/6627 | 98/2109 | 33/702 | chr1 | 6554393 | |||
chr1:6554466 | A | G | 1 | a0011 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.37T>C | p.Cys13Arg | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 48/6627 | 37/2109 | 13/702 | chr1 | 6554466 | |||
chr1:6554475 | G | A | 6 | a0001 a0005 a0006 others(3): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
missense_variant | MODERATE | c.28C>T | p.Arg10Trp | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 39/6627 | 28/2109 | 10/702 | chr1 | 6554475 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:6526750 | C | T | 1 | a0002c0012 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1905G>A | p.Val635Val | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/12 | 1916/6627 | 1905/2109 | 635/702 | chr1 | 6526750 | |||
chr1:6532570 | A | G | 1 | a0001c0009 | 4 | HG03834.hp2 NA18747.hp2 NA18948.hp2 others(1): Show |
synonymous_variant | LOW | c.1428T>C | p.Asp476Asp | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/12 | 1439/6627 | 1428/2109 | 476/702 | chr1 | 6532570 | |||
chr1:6532651 | A | G | 1 | a0001c0015 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.1347T>C | p.Tyr449Tyr | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/12 | 1358/6627 | 1347/2109 | 449/702 | chr1 | 6532651 | |||
chr1:6533305 | G | A | 1 | a0002c0003 | 14 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(11): Show |
synonymous_variant | LOW | c.1212C>T | p.Ile404Ile | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 7/12 | 1223/6627 | 1212/2109 | 404/702 | chr1 | 6533305 | |||
chr1:6550472 | G | A | 1 | a0002c0008 | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
synonymous_variant | LOW | c.540C>T | p.His180His | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/12 | 551/6627 | 540/2109 | 180/702 | chr1 | 6550472 | |||
chr1:6554170 | G | A | 4 | a0002c0002 a0002c0003 a0002c0012 others(1): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
synonymous_variant | LOW | c.333C>T | p.Leu111Leu | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 344/6627 | 333/2109 | 111/702 | chr1 | 6554170 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:6521490 | T | TGTG | 3 | a0002c0008t0020 a0002c0008t0021 a0002c0008t0051 |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4361_*4363dupCAC | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 4363 | chr1 | 6521490 | ||||||
chr1:6521659 | T | A | 3 | a0002c0003t0026 a0002c0003t0069 a0002c0003t0070 |
4 | HG01167.hp1 HG01891.hp2 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4195A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 4195 | chr1 | 6521659 | ||||||
chr1:6521817 | G | A | 38 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(35): Show |
227 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*4037C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 4037 | chr1 | 6521817 | ||||||
chr1:6521844 | A | G | 1 | a0002c0008t0020 | 2 | NA18522.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4010T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 4010 | chr1 | 6521844 | ||||||
chr1:6521854 | G | C | 1 | a0002c0002t0067 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4000C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 4000 | chr1 | 6521854 | ||||||
chr1:6521870 | C | T | 2 | a0002c0004t0010 a0002c0004t0072 |
7 | HG02897.hp1 HG02965.hp1 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3984G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3984 | chr1 | 6521870 | ||||||
chr1:6522005 | A | C | 3 | a0001c0001t0015 a0001c0001t0034 a0001c0001t0040 |
5 | HG01928.hp2 HG01975.hp1 HG01978.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3849T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3849 | chr1 | 6522005 | ||||||
chr1:6522026 | C | T | 1 | a0001c0001t0041 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3828G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3828 | chr1 | 6522026 | ||||||
chr1:6522045 | C | A | 1 | a0001c0001t0039 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3809G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3809 | chr1 | 6522045 | ||||||
chr1:6522084 | G | A | 1 | a0001c0001t0048 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3770C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3770 | chr1 | 6522084 | ||||||
chr1:6522209 | A | G | 2 | a0001c0001t0011 a0002c0002t0063 |
6 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3645T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3645 | chr1 | 6522209 | ||||||
chr1:6522623 | C | A | 1 | a0002c0003t0071 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3231G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3231 | chr1 | 6522623 | ||||||
chr1:6522712 | T | C | 2 | a0001c0001t0047 a0001c0001t0049 |
2 | NA18939.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3142A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3142 | chr1 | 6522712 | ||||||
chr1:6522736 | T | A | 1 | a0006c0010t0052 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3118A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3118 | chr1 | 6522736 | ||||||
chr1:6522745 | G | A | 36 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(33): Show |
213 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*3109C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3109 | chr1 | 6522745 | ||||||
chr1:6522862 | C | A | 1 | a0001c0001t0043 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2992G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2992 | chr1 | 6522862 | ||||||
chr1:6522883 | C | CAA | 38 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(35): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*2969_*2970dupTT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2970 | chr1 | 6522883 | ||||||
chr1:6522883 | C | CAAA | 6 | a0001c0001t0016 a0001c0001t0040 a0001c0001t0042 others(3): Show |
8 | HG00642.hp2 HG01978.hp1 HG02155.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2968_*2970dupTTT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2970 | chr1 | 6522883 | ||||||
chr1:6522883 | C | CAAAAA | 23 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0009 others(20): Show |
74 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2966_*2970dupTTTT others(1): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2970 | chr1 | 6522883 | ||||||
chr1:6522883 | C | CAAAAAA | 11 | a0002c0002t0012 a0002c0002t0025 a0002c0002t0065 others(8): Show |
19 | HG00438.hp1 HG00621.hp2 HG00735.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2965_*2970dupTTTT others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2970 | chr1 | 6522883 | ||||||
chr1:6522938 | G | A | 1 | a0004c0005t0059 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2916C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2916 | chr1 | 6522938 | ||||||
chr1:6522979 | G | A | 7 | a0002c0008t0020 a0002c0008t0021 a0002c0008t0051 others(4): Show |
9 | HG02258.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2875C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2875 | chr1 | 6522979 | ||||||
chr1:6523123 | C | T | 22 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0009 others(19): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2731G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2731 | chr1 | 6523123 | ||||||
chr1:6523148 | C | T | 2 | a0006c0010t0022 a0006c0010t0052 |
3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2706G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2706 | chr1 | 6523148 | ||||||
chr1:6523168 | AAAG | A | 4 | a0002c0008t0020 a0002c0008t0021 a0002c0008t0051 others(1): Show |
6 | HG02559.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2683_*2685delCTT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2683 | chr1 | 6523168 | ||||||
chr1:6523171 | G | A | 31 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0009 others(28): Show |
88 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2683C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2683 | chr1 | 6523171 | ||||||
chr1:6523171 | G | GA | 3 | a0001c0001t0001 a0001c0001t0006 a0004c0005t0033 |
11 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2682dupT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2682 | chr1 | 6523171 | ||||||
chr1:6523172 | A | G | 31 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0009 others(28): Show |
88 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2682T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2682 | chr1 | 6523172 | ||||||
chr1:6523175 | A | G | 4 | a0002c0008t0020 a0002c0008t0021 a0002c0008t0051 others(1): Show |
6 | HG02559.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2679T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2679 | chr1 | 6523175 | ||||||
chr1:6523210 | C | G | 28 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0009 others(25): Show |
85 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*2644G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2644 | chr1 | 6523210 | ||||||
chr1:6523302 | G | A | 2 | a0006c0010t0022 a0006c0010t0052 |
3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2552C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2552 | chr1 | 6523302 | ||||||
chr1:6523545 | C | G | 1 | a0001c0001t0035 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2309G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2309 | chr1 | 6523545 | ||||||
chr1:6523567 | G | A | 36 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(33): Show |
213 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*2287C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2287 | chr1 | 6523567 | ||||||
chr1:6523579 | C | CA | 42 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(39): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*2274dupT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2274 | chr1 | 6523579 | ||||||
chr1:6523579 | C | CAA | 12 | a0001c0001t0004 a0001c0001t0029 a0001c0001t0041 others(9): Show |
29 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2273_*2274dupTT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2274 | chr1 | 6523579 | ||||||
chr1:6523579 | C | CAAA | 2 | a0002c0004t0010 a0009c0011t0075 |
7 | HG02647.hp2 HG02897.hp1 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2272_*2274dupTTT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2274 | chr1 | 6523579 | ||||||
chr1:6523613 | G | T | 1 | a0001c0001t0032 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2241C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2241 | chr1 | 6523613 | ||||||
chr1:6523615 | C | T | 2 | a0002c0002t0056 a0002c0002t0061 |
2 | NA18960.hp1 NA18968.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2239G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2239 | chr1 | 6523615 | ||||||
chr1:6523641 | T | C | 61 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(58): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*2213A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2213 | chr1 | 6523641 | ||||||
chr1:6523816 | G | A | 3 | a0002c0004t0010 a0002c0004t0028 a0002c0004t0072 |
9 | HG02145.hp2 HG02897.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2038C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2038 | chr1 | 6523816 | ||||||
chr1:6523827 | A | G | 2 | a0002c0003t0026 a0002c0003t0069 |
3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2027T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2027 | chr1 | 6523827 | ||||||
chr1:6523964 | A | G | 83 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(80): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
3_prime_UTR_variant | MODIFIER | c.*1890T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1890 | chr1 | 6523964 | ||||||
chr1:6523985 | C | G | 13 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0009 others(10): Show |
55 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1869G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1869 | chr1 | 6523985 | ||||||
chr1:6524041 | A | G | 41 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(38): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*1813T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1813 | chr1 | 6524041 | ||||||
chr1:6524167 | G | C | 9 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0043 others(6): Show |
36 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1687C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1687 | chr1 | 6524167 | ||||||
chr1:6524237 | G | A | 2 | a0002c0002t0066 a0002c0002t0067 |
2 | HG00621.hp2 NA18997.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1617C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1617 | chr1 | 6524237 | ||||||
chr1:6524251 | G | GTA | 82 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(79): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
3_prime_UTR_variant | MODIFIER | c.*1601_*1602dupTA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1602 | chr1 | 6524251 | ||||||
chr1:6524259 | G | GA | 2 | a0001c0001t0008 a0002c0004t0008 |
6 | HG02451.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1594_*1595insT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1594 | chr1 | 6524259 | ||||||
chr1:6524260 | T | G | 2 | a0001c0001t0008 a0002c0004t0008 |
6 | HG02451.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1594A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1594 | chr1 | 6524260 | ||||||
chr1:6524261 | A | G | 2 | a0001c0001t0008 a0002c0004t0008 |
6 | HG02451.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1593T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1593 | chr1 | 6524261 | ||||||
chr1:6524360 | C | A | 28 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0009 others(25): Show |
85 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1494G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1494 | chr1 | 6524360 | ||||||
chr1:6524410 | C | T | 3 | a0002c0004t0010 a0002c0004t0028 a0002c0004t0072 |
9 | HG02145.hp2 HG02897.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1444G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1444 | chr1 | 6524410 | ||||||
chr1:6524462 | G | A | 1 | a0001c0001t0019 | 2 | HG00544.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1392C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1392 | chr1 | 6524462 | ||||||
chr1:6524483 | G | A | 1 | a0002c0002t0060 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1371C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1371 | chr1 | 6524483 | ||||||
chr1:6524484 | A | G | 1 | a0002c0002t0060 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1370T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1370 | chr1 | 6524484 | ||||||
chr1:6524485 | G | A | 1 | a0002c0002t0060 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1369C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1369 | chr1 | 6524485 | ||||||
chr1:6524597 | T | C | 27 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0009 others(24): Show |
84 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1257A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1257 | chr1 | 6524597 | ||||||
chr1:6524638 | C | T | 1 | a0001c0001t0006 | 9 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1216G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1216 | chr1 | 6524638 | ||||||
chr1:6524741 | A | AT | 3 | a0002c0002t0060 a0004c0005t0058 a0004c0005t0059 |
3 | HG03688.hp2 HG03710.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1112dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1112 | chr1 | 6524741 | ||||||
chr1:6524741 | A | T | 6 | a0002c0004t0010 a0002c0004t0028 a0002c0004t0072 others(3): Show |
12 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1113T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1113 | chr1 | 6524741 | ||||||
chr1:6524743 | TA | T | 3 | a0001c0001t0057 a0002c0002t0056 a0002c0002t0068 |
3 | HG01169.hp1 HG02896.hp1 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1110delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1110 | chr1 | 6524743 | ||||||
chr1:6524744 | A | T | 38 | a0001c0001t0002 a0001c0001t0023 a0002c0002t0002 others(35): Show |
97 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1110T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1110 | chr1 | 6524744 | ||||||
chr1:6524747 | T | A | 2 | a0001c0001t0005 a0002c0002t0005 |
10 | HG00099.hp2 HG00323.hp2 HG00741.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1107A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1107 | chr1 | 6524747 | ||||||
chr1:6524896 | C | T | 3 | a0002c0002t0018 a0002c0002t0068 a0010c0013t0018 |
4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*958G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 958 | chr1 | 6524896 | ||||||
chr1:6524949 | C | T | 1 | a0004c0005t0031 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*905G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 905 | chr1 | 6524949 | ||||||
chr1:6524961 | A | G | 83 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(80): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
3_prime_UTR_variant | MODIFIER | c.*893T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 893 | chr1 | 6524961 | ||||||
chr1:6524981 | C | T | 1 | a0001c0001t0030 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 873 | chr1 | 6524981 | ||||||
chr1:6525024 | C | A | 3 | a0001c0001t0047 a0001c0001t0048 a0001c0001t0049 |
3 | NA18939.hp2 NA18948.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*830G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 830 | chr1 | 6525024 | ||||||
chr1:6525099 | G | A | 1 | a0001c0009t0050 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*755C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 755 | chr1 | 6525099 | ||||||
chr1:6525149 | T | A | 9 | a0002c0002t0018 a0002c0002t0068 a0002c0003t0007 others(6): Show |
18 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*705A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 705 | chr1 | 6525149 | ||||||
chr1:6525267 | A | G | 2 | a0006c0010t0022 a0006c0010t0052 |
3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*587T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 587 | chr1 | 6525267 | ||||||
chr1:6525301 | C | A | 3 | a0002c0008t0020 a0002c0008t0021 a0002c0008t0051 |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*553G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 553 | chr1 | 6525301 | ||||||
chr1:6525343 | A | G | 3 | a0001c0001t0006 a0004c0005t0054 a0004c0005t0055 |
11 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*511T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 511 | chr1 | 6525343 | ||||||
chr1:6525403 | G | T | 6 | a0002c0004t0010 a0002c0004t0028 a0002c0004t0072 others(3): Show |
12 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*451C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 451 | chr1 | 6525403 | ||||||
chr1:6525404 | AC | A | 8 | a0002c0004t0010 a0002c0004t0028 a0002c0004t0072 others(5): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*449delG | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 449 | chr1 | 6525404 | ||||||
chr1:6525479 | C | T | 43 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(40): Show |
234 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*375G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 375 | chr1 | 6525479 | ||||||
chr1:6525591 | G | A | 1 | a0001c0001t0053 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 263 | chr1 | 6525591 | ||||||
chr1:6525744 | C | T | 45 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(42): Show |
237 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*110G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 110 | chr1 | 6525744 | ||||||
chr1:6525848 | C | T | 1 | a0001c0001t0029 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 6 | chr1 | 6525848 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:6526010 | C | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
splice_region_variant&intron_variant | LOW | c.1960-7G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526010 | |||||||
chr1:6526029 | T | C | 1 | a0001c0001t0003g0244 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1960-26A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526029 | |||||||
chr1:6526094 | A | C | 1 | a0001c0001t0001g0016 | 3 | HG01884.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1960-91T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526094 | |||||||
chr1:6526370 | C | T | 5 | a0002c0004t0010g0003 a0002c0004t0010g0040 a0002c0004t0028g0039 others(2): Show |
9 | HG02145.hp2 HG02897.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1959+326G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526370 | |||||||
chr1:6526414 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0016g0163 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1959+282G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526414 | |||||||
chr1:6526461 | G | C | 2 | a0002c0002t0009g0091 a0002c0002t0009g0092 |
2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1959+235C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526461 | |||||||
chr1:6526471 | G | A | 1 | a0001c0001t0037g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1959+225C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526471 | |||||||
chr1:6526493 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1959+203G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526493 | |||||||
chr1:6526842 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1826-13G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6526842 | |||||||
chr1:6526934 | C | T | 7 | a0002c0004t0010g0003 a0002c0004t0010g0040 a0002c0004t0028g0039 others(4): Show |
11 | HG02055.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1826-105G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6526934 | |||||||
chr1:6527012 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1826-183C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527012 | |||||||
chr1:6527120 | G | A | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-291C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527120 | |||||||
chr1:6527171 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1826-342G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527171 | |||||||
chr1:6527244 | CA | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0132 others(31): Show |
40 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1826-416delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527244 | |||||||
chr1:6527260 | AT | A | 2 | a0001c0001t0011g0005 a0001c0001t0011g0124 |
5 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826-432delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527260 | |||||||
chr1:6527263 | C | T | 2 | a0001c0001t0011g0005 a0001c0001t0011g0124 |
5 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826-434G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527263 | |||||||
chr1:6527263 | CAA | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(182): Show |
237 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1826-436_1826-435d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527263 | |||||||
chr1:6527265 | A | C | 2 | a0001c0001t0011g0005 a0001c0001t0011g0124 |
5 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826-436T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527265 | |||||||
chr1:6527409 | G | C | 1 | a0004c0005t0062g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-580C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527409 | |||||||
chr1:6527447 | G | A | 4 | a0001c0009t0001g0125 a0001c0009t0001g0203 a0001c0009t0001g0211 others(1): Show |
4 | HG03834.hp2 NA18747.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.1826-618C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527447 | |||||||
chr1:6527554 | C | T | 45 | a0001c0001t0002g0218 a0002c0002t0002g0004 a0002c0002t0002g0020 others(42): Show |
54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1826-725G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527554 | |||||||
chr1:6527625 | A | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
254 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1826-796T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527625 | |||||||
chr1:6527637 | AAC | A | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
233 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1826-810_1826-809d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527637 | |||||||
chr1:6527638 | AC | A | 8 | a0001c0001t0001g0136 a0001c0001t0001g0149 a0001c0001t0023g0123 others(5): Show |
12 | HG01168.hp1 HG02129.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1826-810delG | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527638 | |||||||
chr1:6527639 | CA | C | 3 | a0001c0001t0011g0005 a0001c0001t0011g0124 a0004c0005t0033g0113 |
6 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-811delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527639 | |||||||
chr1:6527640 | A | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0242 a0002c0004t0073g0038 |
5 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826-811T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527640 | |||||||
chr1:6527702 | G | A | 4 | a0001c0001t0015g0035 a0001c0001t0015g0216 a0001c0001t0034g0215 others(1): Show |
5 | HG01928.hp2 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-873C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527702 | |||||||
chr1:6527800 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
254 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1826-971T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527800 | |||||||
chr1:6527827 | A | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
254 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1826-998T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527827 | |||||||
chr1:6527846 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1826-1017C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527846 | |||||||
chr1:6527942 | C | A | 3 | a0006c0010t0022g0268 a0006c0010t0022g0270 a0006c0010t0052g0269 |
3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+1052G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527942 | |||||||
chr1:6528024 | A | C | 2 | a0002c0004t0073g0038 a0009c0011t0075g0037 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1825+970T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528024 | |||||||
chr1:6528076 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0004g0260 |
2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1825+918C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528076 | |||||||
chr1:6528144 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0181 |
2 | NA18959.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1825+850G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528144 | |||||||
chr1:6528177 | AG | A | 1 | a0001c0001t0011g0005 | 4 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+816delC | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528177 | |||||||
chr1:6528544 | G | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1825+450C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528544 | |||||||
chr1:6528642 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1825+352A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528642 | |||||||
chr1:6528676 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0150 a0001c0001t0001g0195 others(2): Show |
6 | HG02155.hp2 HG03130.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+318T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528676 | |||||||
chr1:6528779 | T | C | 1 | a0002c0004t0074g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1825+215A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528779 | |||||||
chr1:6528811 | C | A | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+183G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528811 | |||||||
chr1:6528850 | C | T | 1 | a0002c0004t0028g0039 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1825+144G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528850 | |||||||
chr1:6528877 | G | A | 1 | a0001c0001t0053g0262 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1825+117C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528877 | |||||||
chr1:6528895 | T | G | 1 | a0002c0008t0021g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1825+99A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528895 | |||||||
chr1:6528900 | T | C | 1 | a0002c0004t0074g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1825+94A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528900 | |||||||
chr1:6529329 | G | A | 4 | a0002c0002t0002g0066 a0002c0002t0002g0076 a0002c0002t0002g0084 others(1): Show |
4 | HG01255.hp2 NA18957.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648-158C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529329 | |||||||
chr1:6529362 | G | A | 1 | a0001c0001t0004g0207 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1648-191C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529362 | |||||||
chr1:6529444 | C | T | 6 | a0002c0004t0010g0003 a0002c0004t0010g0040 a0002c0004t0028g0039 others(3): Show |
10 | HG02145.hp2 HG02630.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1648-273G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529444 | |||||||
chr1:6529481 | G | C | 7 | a0002c0003t0007g0049 a0002c0003t0007g0050 a0002c0003t0007g0051 others(4): Show |
7 | HG02280.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1648-310C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529481 | |||||||
chr1:6529557 | C | T | 1 | a0007c0017t0038g0221 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1648-386G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529557 | |||||||
chr1:6529581 | C | T | 69 | a0001c0001t0002g0218 a0001c0001t0023g0123 a0001c0001t0057g0122 others(66): Show |
78 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1648-410G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529581 | |||||||
chr1:6530053 | A | G | 265 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1648-882T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530053 | |||||||
chr1:6530073 | C | T | 64 | a0001c0001t0002g0218 a0002c0002t0002g0004 a0002c0002t0002g0020 others(61): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1648-902G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530073 | |||||||
chr1:6530093 | T | G | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1648-922A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530093 | |||||||
chr1:6530224 | G | A | 1 | a0004c0005t0062g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1648-1053C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530224 | |||||||
chr1:6530282 | G | A | 4 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648-1111C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530282 | |||||||
chr1:6530323 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1648-1152T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530323 | |||||||
chr1:6530347 | G | A | 64 | a0001c0001t0002g0218 a0002c0002t0002g0004 a0002c0002t0002g0020 others(61): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1648-1176C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530347 | |||||||
chr1:6530369 | G | A | 1 | a0003c0006t0017g0118 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1648-1198C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530369 | |||||||
chr1:6530442 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
237 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1648-1271C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530442 | |||||||
chr1:6530670 | C | G | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1647+1298G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530670 | |||||||
chr1:6530693 | T | G | 1 | a0001c0001t0016g0183 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1647+1275A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530693 | |||||||
chr1:6530809 | C | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0228 |
2 | HG02074.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1647+1159G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530809 | |||||||
chr1:6530896 | C | T | 3 | a0006c0010t0022g0268 a0006c0010t0022g0270 a0006c0010t0052g0269 |
3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1647+1072G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530896 | |||||||
chr1:6530960 | C | A | 4 | a0002c0002t0018g0102 a0002c0002t0018g0103 a0002c0002t0068g0101 others(1): Show |
4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647+1008G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530960 | |||||||
chr1:6531282 | C | T | 2 | a0002c0004t0073g0038 a0009c0011t0075g0037 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1647+686G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531282 | |||||||
chr1:6531310 | T | C | 1 | a0001c0001t0041g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1647+658A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531310 | |||||||
chr1:6531406 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1647+562C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531406 | |||||||
chr1:6531430 | G | T | 1 | a0002c0004t0008g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1647+538C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531430 | |||||||
chr1:6531435 | G | A | 3 | a0001c0001t0001g0195 a0001c0001t0003g0008 a0001c0001t0044g0141 |
6 | HG00408.hp1 HG02080.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647+533C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531435 | |||||||
chr1:6531464 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.1647+504A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531464 | |||||||
chr1:6531523 | A | G | 3 | a0002c0002t0002g0020 a0002c0002t0002g0080 a0002c0002t0060g0083 |
4 | HG00597.hp2 NA18949.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647+445T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531523 | |||||||
chr1:6531560 | G | C | 4 | a0002c0002t0002g0096 a0002c0002t0002g0097 a0002c0002t0012g0094 others(1): Show |
4 | HG02055.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647+408C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531560 | |||||||
chr1:6531565 | C | T | 3 | a0006c0010t0022g0268 a0006c0010t0022g0270 a0006c0010t0052g0269 |
3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1647+403G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531565 | |||||||
chr1:6531581 | G | A | 2 | a0002c0004t0028g0039 a0002c0004t0028g0042 |
2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1647+387C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531581 | |||||||
chr1:6531877 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1647+91A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531877 | |||||||
chr1:6532197 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1536-118G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/11 | chr1 | 6532197 | |||||||
chr1:6532317 | A | G | 64 | a0001c0001t0002g0218 a0002c0002t0002g0004 a0002c0002t0002g0020 others(61): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1535+146T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/11 | chr1 | 6532317 | |||||||
chr1:6532808 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1238-48G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 7/11 | chr1 | 6532808 | |||||||
chr1:6533193 | A | C | 1 | a0001c0001t0042g0146 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1237+87T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 7/11 | chr1 | 6533193 | |||||||
chr1:6533472 | G | A | 48 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(45): Show |
57 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1076-31C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533472 | |||||||
chr1:6533645 | A | G | 1 | a0001c0001t0001g0027 | 2 | NA19064.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1076-204T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533645 | |||||||
chr1:6533681 | C | T | 1 | a0001c0001t0005g0222 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1076-240G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533681 | |||||||
chr1:6533770 | C | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1076-329G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533770 | |||||||
chr1:6533787 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1076-346A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533787 | |||||||
chr1:6533890 | C | CT | 10 | a0002c0004t0010g0003 a0002c0004t0010g0040 a0002c0004t0028g0039 others(7): Show |
14 | HG02145.hp2 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1076-450dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533890 | |||||||
chr1:6533933 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1076-492C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533933 | |||||||
chr1:6533951 | G | A | 1 | a0002c0002t0002g0067 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1076-510C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533951 | |||||||
chr1:6533973 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1076-532G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533973 | |||||||
chr1:6534051 | C | T | 1 | a0003c0006t0017g0118 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1076-610G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534051 | |||||||
chr1:6534138 | C | A | 5 | a0002c0004t0010g0003 a0002c0004t0010g0040 a0002c0004t0028g0039 others(2): Show |
9 | HG02145.hp2 HG02897.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1076-697G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534138 | |||||||
chr1:6534245 | G | A | 2 | a0004c0005t0054g0114 a0004c0005t0055g0115 |
2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1076-804C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534245 | |||||||
chr1:6534324 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1076-883C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534324 | |||||||
chr1:6534501 | G | A | 63 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(60): Show |
72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1076-1060C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534501 | |||||||
chr1:6534713 | A | G | 63 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(60): Show |
72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1076-1272T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534713 | |||||||
chr1:6534728 | G | A | 1 | a0001c0001t0003g0232 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1076-1287C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534728 | |||||||
chr1:6534796 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1076-1355A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534796 | |||||||
chr1:6534870 | C | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1076-1429G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534870 | |||||||
chr1:6534897 | G | A | 5 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(2): Show |
6 | HG02559.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076-1456C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534897 | |||||||
chr1:6534930 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1076-1489T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534930 | |||||||
chr1:6535099 | C | T | 4 | a0004c0005t0033g0113 a0004c0005t0058g0110 a0004c0005t0059g0109 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-1658G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535099 | |||||||
chr1:6535106 | G | T | 1 | a0001c0001t0011g0005 | 4 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-1665C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535106 | |||||||
chr1:6535174 | C | T | 2 | a0004c0005t0054g0114 a0004c0005t0055g0115 |
2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1076-1733G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535174 | |||||||
chr1:6535264 | G | A | 3 | a0006c0010t0022g0268 a0006c0010t0022g0270 a0006c0010t0052g0269 |
3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1076-1823C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535264 | |||||||
chr1:6535429 | A | G | 1 | a0001c0001t0003g0227 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1076-1988T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535429 | |||||||
chr1:6535565 | G | C | 1 | a0001c0001t0001g0242 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1076-2124C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535565 | |||||||
chr1:6535630 | T | C | 2 | a0004c0005t0054g0114 a0004c0005t0055g0115 |
2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1076-2189A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535630 | |||||||
chr1:6535683 | T | C | 1 | a0001c0001t0004g0241 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1076-2242A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535683 | |||||||
chr1:6535729 | C | T | 1 | a0002c0004t0074g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1076-2288G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535729 | |||||||
chr1:6535842 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1076-2401A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535842 | |||||||
chr1:6535877 | G | A | 1 | a0002c0004t0074g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1076-2436C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535877 | |||||||
chr1:6535928 | C | CA | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1076-2488dupT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535928 | |||||||
chr1:6535948 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1076-2507C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535948 | |||||||
chr1:6535975 | G | A | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076-2534C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535975 | |||||||
chr1:6536120 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1076-2679T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536120 | |||||||
chr1:6536139 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1076-2698C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536139 | |||||||
chr1:6536182 | TAA | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1076-2743_1076-274 others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536182 | |||||||
chr1:6536190 | CAA | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1076-2751_1076-275 others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536190 | |||||||
chr1:6536333 | G | A | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076-2892C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536333 | |||||||
chr1:6536345 | CAAATA | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1076-2909_1076-290 others(9): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536345 | |||||||
chr1:6536618 | C | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1076-3177G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536618 | |||||||
chr1:6536634 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1076-3193G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536634 | |||||||
chr1:6536735 | T | C | 2 | a0001c0001t0001g0206 a0001c0001t0004g0207 |
2 | HG00673.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1076-3294A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536735 | |||||||
chr1:6536811 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1076-3370C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536811 | |||||||
chr1:6536874 | G | A | 1 | a0004c0005t0031g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1076-3433C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536874 | |||||||
chr1:6536962 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1076-3521C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536962 | |||||||
chr1:6536986 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0156 a0001c0001t0001g0247 others(1): Show |
7 | HG00438.hp2 NA18952.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076-3545C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536986 | |||||||
chr1:6537027 | C | T | 4 | a0004c0005t0033g0113 a0004c0005t0058g0110 a0004c0005t0059g0109 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-3586G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537027 | |||||||
chr1:6537049 | A | G | 1 | a0002c0004t0074g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1076-3608T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537049 | |||||||
chr1:6537436 | C | T | 18 | a0002c0002t0018g0102 a0002c0002t0018g0103 a0002c0002t0068g0101 others(15): Show |
18 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1076-3995G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537436 | |||||||
chr1:6537801 | T | C | 67 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(64): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1075+4029A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537801 | |||||||
chr1:6537883 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1075+3947T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537883 | |||||||
chr1:6537919 | T | C | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1075+3911A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537919 | |||||||
chr1:6537960 | C | T | 6 | a0001c0001t0006g0012 a0001c0001t0006g0025 a0001c0001t0006g0126 others(3): Show |
9 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1075+3870G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537960 | |||||||
chr1:6537970 | C | T | 1 | a0002c0008t0021g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1075+3860G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537970 | |||||||
chr1:6537978 | C | G | 4 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075+3852G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537978 | |||||||
chr1:6537991 | CA | C | 27 | a0001c0001t0001g0148 a0001c0001t0001g0242 a0001c0001t0001g0266 others(24): Show |
29 | HG00621.hp2 HG01167.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1075+3838delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537991 | |||||||
chr1:6537991 | CAA | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(89): Show |
113 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1075+3837_1075+383 others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537991 | |||||||
chr1:6537991 | CAAA | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(130): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1075+3836_1075+383 others(7): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537991 | |||||||
chr1:6537991 | CAAAA | C | 10 | a0001c0001t0001g0198 a0001c0001t0006g0128 a0001c0001t0014g0189 others(7): Show |
10 | HG00642.hp1 HG01169.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075+3835_1075+383 others(8): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537991 | |||||||
chr1:6538394 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1075+3436G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538394 | |||||||
chr1:6538404 | G | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0029 others(8): Show |
17 | HG00280.hp1 HG00735.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1075+3426C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538404 | |||||||
chr1:6538507 | A | T | 4 | a0001c0001t0015g0035 a0001c0001t0015g0216 a0001c0001t0034g0215 others(1): Show |
5 | HG01928.hp2 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075+3323T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538507 | |||||||
chr1:6538597 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1075+3233T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538597 | |||||||
chr1:6538655 | C | T | 1 | a0001c0001t0001g0027 | 2 | NA19064.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1075+3175G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538655 | |||||||
chr1:6538676 | C | T | 1 | a0002c0002t0002g0069 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1075+3154G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538676 | |||||||
chr1:6538902 | G | A | 2 | a0004c0005t0054g0114 a0004c0005t0055g0115 |
2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1075+2928C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538902 | |||||||
chr1:6538981 | C | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.1075+2849G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538981 | |||||||
chr1:6539062 | A | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0132 others(20): Show |
29 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1075+2768T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539062 | |||||||
chr1:6539172 | C | T | 3 | a0002c0003t0007g0055 a0002c0003t0007g0058 a0002c0003t0071g0054 |
3 | HG02280.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1075+2658G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539172 | |||||||
chr1:6539274 | T | C | 5 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(2): Show |
6 | HG02559.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1075+2556A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539274 | |||||||
chr1:6539302 | T | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.1075+2528A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539302 | |||||||
chr1:6539452 | T | C | 4 | a0001c0001t0001g0149 a0001c0001t0004g0011 a0002c0004t0073g0038 others(1): Show |
6 | HG02055.hp2 HG02129.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075+2378A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539452 | |||||||
chr1:6539463 | C | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.1075+2367G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539463 | |||||||
chr1:6539478 | AATT | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.1075+2349_1075+235 others(7): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539478 | |||||||
chr1:6539497 | T | G | 67 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(64): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1075+2333A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539497 | |||||||
chr1:6539498 | A | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.1075+2332T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539498 | |||||||
chr1:6539517 | G | C | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1075+2313C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539517 | |||||||
chr1:6539563 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0004g0171 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1075+2267G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539563 | |||||||
chr1:6539652 | C | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1075+2178G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539652 | |||||||
chr1:6539659 | AT | A | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1075+2170delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539659 | |||||||
chr1:6539695 | C | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.1075+2135G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539695 | |||||||
chr1:6539708 | T | G | 63 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(60): Show |
72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1075+2122A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539708 | |||||||
chr1:6539872 | G | A | 2 | a0001c0001t0047g0234 a0001c0001t0049g0235 |
2 | NA18939.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1075+1958C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539872 | |||||||
chr1:6539918 | A | C | 1 | a0001c0001t0001g0155 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1075+1912T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539918 | |||||||
chr1:6540014 | T | C | 1 | a0002c0002t0002g0082 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1075+1816A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540014 | |||||||
chr1:6540033 | T | C | 1 | a0002c0002t0002g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1075+1797A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540033 | |||||||
chr1:6540088 | C | T | 1 | a0006c0010t0022g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1075+1742G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540088 | |||||||
chr1:6540124 | C | CTTTT | 17 | a0001c0001t0001g0180 a0001c0001t0001g0198 a0002c0004t0010g0003 others(14): Show |
22 | HG01243.hp1 HG01256.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1075+1702_1075+170 others(8): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | |||||||
chr1:6540124 | C | CTTTTT | 163 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1075+1701_1075+170 others(9): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | |||||||
chr1:6540124 | C | CTTTTTT | 8 | a0001c0001t0001g0188 a0001c0001t0001g0200 a0001c0001t0001g0220 others(5): Show |
8 | HG00323.hp1 HG00323.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1075+1700_1075+170 others(10): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | |||||||
chr1:6540124 | C | CTTTTTTT | 8 | a0002c0002t0002g0082 a0002c0002t0018g0102 a0002c0002t0018g0103 others(5): Show |
8 | HG02280.hp1 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1075+1699_1075+170 others(11): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | |||||||
chr1:6540124 | C | CTTTTTTT others(1): Show |
48 | a0001c0001t0057g0122 a0002c0002t0002g0004 a0002c0002t0002g0020 others(45): Show |
57 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+1698_1075+170 others(12): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | |||||||
chr1:6540124 | C | CTTTTTTT others(2): Show |
10 | a0001c0001t0023g0123 a0002c0002t0002g0059 a0002c0002t0009g0074 others(7): Show |
10 | HG00642.hp1 HG01168.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1075+1697_1075+170 others(13): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | |||||||
chr1:6540124 | C | CTTTTTTT others(3): Show |
1 | a0002c0002t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1075+1696_1075+170 others(14): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | |||||||
chr1:6540124 | C | T | 1 | a0002c0002t0009g0092 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1075+1706G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | |||||||
chr1:6540153 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1075+1677A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540153 | |||||||
chr1:6540188 | G | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1075+1642C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540188 | |||||||
chr1:6540343 | C | T | 8 | a0002c0004t0010g0003 a0002c0004t0010g0040 a0002c0004t0028g0039 others(5): Show |
12 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+1487G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540343 | |||||||
chr1:6540401 | C | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1075+1429G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540401 | |||||||
chr1:6540547 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(182): Show |
243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1075+1283G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540547 | |||||||
chr1:6540744 | C | T | 44 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(41): Show |
53 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.1075+1086G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540744 | |||||||
chr1:6540758 | G | A | 1 | a0002c0002t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1075+1072C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540758 | |||||||
chr1:6540829 | T | TA | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0008g0036 others(3): Show |
7 | HG01109.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075+1000dupT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540829 | |||||||
chr1:6540829 | TA | T | 45 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(42): Show |
54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1075+1000delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540829 | |||||||
chr1:6540863 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1075+967G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540863 | |||||||
chr1:6540928 | G | A | 2 | a0002c0002t0002g0088 a0002c0002t0025g0077 |
2 | NA18992.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1075+902C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540928 | |||||||
chr1:6540947 | T | A | 72 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0002g0004 others(69): Show |
81 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1075+883A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540947 | |||||||
chr1:6541010 | CGT | C | 25 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0144 others(22): Show |
29 | HG00597.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1075+818_1075+819d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541010 | |||||||
chr1:6541010 | CGTT | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1075+817_1075+819d others(5): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541010 | |||||||
chr1:6541010 | CGTTT | C | 3 | a0001c0001t0001g0181 a0001c0001t0001g0210 a0004c0005t0031g0111 |
3 | HG02559.hp1 NA18945.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1075+816_1075+819d others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541010 | |||||||
chr1:6541011 | GT | G | 21 | a0002c0002t0002g0020 a0002c0002t0002g0023 a0002c0002t0002g0024 others(18): Show |
23 | HG00597.hp2 HG00735.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1075+818delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541011 | |||||||
chr1:6541011 | GTT | G | 37 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(34): Show |
43 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.1075+817_1075+818d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541011 | |||||||
chr1:6541014 | T | C | 10 | a0002c0002t0002g0069 a0002c0002t0002g0070 a0002c0002t0002g0079 others(7): Show |
10 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.1075+816A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541014 | |||||||
chr1:6541186 | T | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1075+644A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541186 | |||||||
chr1:6541187 | T | G | 1 | a0001c0009t0001g0211 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1075+643A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541187 | |||||||
chr1:6541224 | G | A | 1 | a0002c0003t0070g0104 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1075+606C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541224 | |||||||
chr1:6541230 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1075+600C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541230 | |||||||
chr1:6541259 | T | C | 74 | a0001c0001t0006g0025 a0001c0001t0023g0123 a0001c0001t0048g0179 others(71): Show |
84 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1075+571A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541259 | |||||||
chr1:6541276 | C | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1075+554G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541276 | |||||||
chr1:6541315 | G | A | 2 | a0001c0001t0011g0005 a0001c0001t0011g0124 |
5 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075+515C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541315 | |||||||
chr1:6541427 | C | T | 1 | a0001c0001t0032g0166 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1075+403G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541427 | |||||||
chr1:6541547 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
255 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1075+283A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541547 | |||||||
chr1:6541639 | A | T | 1 | a0001c0001t0001g0181 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1075+191T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541639 | |||||||
chr1:6541713 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1075+117A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541713 | |||||||
chr1:6542075 | T | A | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG01952.hp2 HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.978-148A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542075 | |||||||
chr1:6542089 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.978-162G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542089 | |||||||
chr1:6542126 | G | A | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.978-199C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542126 | |||||||
chr1:6542146 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.978-219T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542146 | |||||||
chr1:6542163 | AT | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.978-237delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542163 | |||||||
chr1:6542163 | ATT | A | 7 | a0001c0001t0001g0152 a0001c0001t0001g0165 a0001c0001t0034g0215 others(4): Show |
7 | HG01243.hp1 HG01975.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.978-238_978-237del others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542163 | |||||||
chr1:6542181 | C | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.978-254G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542181 | |||||||
chr1:6542184 | T | C | 1 | a0002c0002t0002g0061 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.978-257A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542184 | |||||||
chr1:6542213 | C | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(140): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.978-286G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542213 | |||||||
chr1:6542222 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.978-295T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542222 | |||||||
chr1:6542230 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.978-303C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542230 | |||||||
chr1:6542257 | T | A | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG01952.hp2 HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.978-330A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542257 | |||||||
chr1:6542284 | C | T | 2 | a0001c0001t0016g0183 a0002c0002t0009g0091 |
2 | HG02622.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.978-357G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542284 | |||||||
chr1:6542336 | T | A | 1 | a0004c0005t0058g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.978-409A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542336 | |||||||
chr1:6542343 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.978-416A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542343 | |||||||
chr1:6542410 | A | T | 2 | a0001c0001t0011g0005 a0001c0001t0011g0124 |
5 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.978-483T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542410 | |||||||
chr1:6542465 | A | AT | 191 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.978-539dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542465 | |||||||
chr1:6542526 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.978-599A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542526 | |||||||
chr1:6542604 | T | C | 1 | a0002c0002t0005g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.978-677A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542604 | |||||||
chr1:6542648 | G | A | 1 | a0002c0004t0074g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.978-721C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542648 | |||||||
chr1:6542660 | T | G | 1 | a0002c0002t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.978-733A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542660 | |||||||
chr1:6542676 | C | T | 1 | a0004c0005t0033g0113 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.978-749G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542676 | |||||||
chr1:6542695 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.978-768C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542695 | |||||||
chr1:6542745 | C | A | 1 | a0004c0005t0031g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.978-818G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542745 | |||||||
chr1:6542746 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.978-819G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542746 | |||||||
chr1:6542772 | A | G | 1 | a0002c0002t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.978-845T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542772 | |||||||
chr1:6542844 | G | A | 2 | a0002c0002t0018g0102 a0002c0002t0068g0101 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.978-917C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542844 | |||||||
chr1:6542886 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.978-959T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542886 | |||||||
chr1:6542940 | C | T | 4 | a0001c0001t0004g0153 a0001c0001t0005g0031 a0001c0001t0005g0161 others(1): Show |
5 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.978-1013G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542940 | |||||||
chr1:6542961 | A | T | 1 | a0001c0001t0001g0181 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.978-1034T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542961 | |||||||
chr1:6542983 | T | G | 4 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.978-1056A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542983 | |||||||
chr1:6543091 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.978-1164T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543091 | |||||||
chr1:6543201 | C | CT | 190 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.978-1275dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543201 | |||||||
chr1:6543214 | G | T | 1 | a0006c0010t0022g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.978-1287C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543214 | |||||||
chr1:6543215 | A | T | 1 | a0006c0010t0022g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.978-1288T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543215 | |||||||
chr1:6543218 | C | G | 1 | a0006c0010t0022g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.978-1291G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543218 | |||||||
chr1:6543218 | CAG | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.978-1293_978-1292d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543218 | |||||||
chr1:6543220 | G | C | 1 | a0006c0010t0022g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.978-1293C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543220 | |||||||
chr1:6543261 | T | A | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.978-1334A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543261 | |||||||
chr1:6543294 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.978-1367G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543294 | |||||||
chr1:6543347 | C | T | 2 | a0001c0001t0004g0236 a0008c0016t0001g0237 |
2 | HG00423.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.978-1420G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543347 | |||||||
chr1:6543364 | G | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.978-1437C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543364 | |||||||
chr1:6543386 | G | A | 1 | a0001c0001t0011g0005 | 4 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.977+1440C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543386 | |||||||
chr1:6543462 | TG | T | 7 | a0002c0004t0010g0003 a0002c0004t0010g0040 a0002c0004t0028g0039 others(4): Show |
11 | HG02055.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.977+1363delC | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543462 | |||||||
chr1:6543617 | T | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.977+1209A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543617 | |||||||
chr1:6543712 | A | G | 2 | a0004c0005t0054g0114 a0004c0005t0055g0115 |
2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.977+1114T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543712 | |||||||
chr1:6543848 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.977+978C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543848 | |||||||
chr1:6543912 | G | A | 1 | a0006c0010t0022g0270 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.977+914C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543912 | |||||||
chr1:6544045 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.977+781C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544045 | |||||||
chr1:6544082 | T | C | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.977+744A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544082 | |||||||
chr1:6544100 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.977+726A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544100 | |||||||
chr1:6544156 | T | G | 1 | a0004c0005t0054g0114 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.977+670A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544156 | |||||||
chr1:6544282 | C | CA | 12 | a0002c0002t0012g0073 a0002c0003t0007g0049 a0002c0003t0007g0050 others(9): Show |
13 | HG02280.hp2 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.977+543dupT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544282 | |||||||
chr1:6544282 | CA | C | 9 | a0001c0001t0001g0165 a0001c0001t0023g0123 a0001c0001t0053g0262 others(6): Show |
9 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.977+543delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544282 | |||||||
chr1:6544300 | G | A | 265 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.977+526C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544300 | |||||||
chr1:6544302 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.977+524C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544302 | |||||||
chr1:6544348 | C | A | 1 | a0001c0001t0015g0216 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.977+478G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544348 | |||||||
chr1:6544359 | A | AAAAATAA others(5): Show |
264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.977+466_977+467ins others(12): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544359 | |||||||
chr1:6544521 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.977+305T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544521 | |||||||
chr1:6544525 | A | ACACGCAC others(1): Show |
4 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0005g0161 others(1): Show |
4 | HG00741.hp1 HG00741.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.977+293_977+300dup others(8): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544525 | |||||||
chr1:6544525 | A | G | 59 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(56): Show |
82 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.977+301T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544525 | |||||||
chr1:6544537 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.977+289T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544537 | |||||||
chr1:6544543 | A | AC | 16 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0002g0024 others(13): Show |
17 | HG00621.hp2 HG00642.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.977+282dupG | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544543 | |||||||
chr1:6544543 | A | ACC | 29 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0076 others(26): Show |
31 | HG00558.hp2 HG00673.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.977+281_977+282dup others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544543 | |||||||
chr1:6544543 | A | ACCC | 21 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(18): Show |
27 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.977+280_977+282dup others(3): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544543 | |||||||
chr1:6544544 | C | CGCA | 6 | a0001c0001t0001g0259 a0001c0001t0004g0260 a0001c0001t0015g0035 others(3): Show |
7 | HG01928.hp2 HG01975.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.977+281_977+282ins others(3): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544544 | |||||||
chr1:6544544 | C | CGCACGCA | 150 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.977+281_977+282ins others(7): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544544 | |||||||
chr1:6544544 | C | CGCACGCA others(4): Show |
1 | a0001c0001t0045g0223 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.977+281_977+282ins others(11): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544544 | |||||||
chr1:6544544 | C | CGCACGCA others(4): Show |
2 | a0006c0010t0022g0270 a0006c0010t0052g0269 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.977+281_977+282ins others(11): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544544 | |||||||
chr1:6544545 | C | A | 32 | a0001c0001t0001g0029 a0001c0001t0001g0162 a0001c0001t0001g0164 others(29): Show |
44 | HG00741.hp1 HG00741.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.977+281G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544545 | |||||||
chr1:6544546 | C | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.977+280G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544546 | |||||||
chr1:6544547 | C | A | 32 | a0001c0001t0001g0029 a0001c0001t0001g0162 a0001c0001t0001g0164 others(29): Show |
44 | HG00741.hp1 HG00741.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.977+279G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544547 | |||||||
chr1:6544548 | C | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(155): Show |
205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.977+278G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544548 | |||||||
chr1:6544552 | C | A | 1 | a0001c0001t0045g0223 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.977+274G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544552 | |||||||
chr1:6544553 | CG | C | 26 | a0001c0001t0002g0218 a0001c0001t0003g0243 a0001c0001t0006g0012 others(23): Show |
37 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.977+272delC | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544553 | |||||||
chr1:6544554 | G | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.977+272C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544554 | |||||||
chr1:6544555 | C | A | 1 | a0001c0001t0001g0264 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.977+271G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544555 | |||||||
chr1:6544556 | C | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.977+270G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544556 | |||||||
chr1:6544561 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.977+265T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544561 | |||||||
chr1:6544623 | G | C | 1 | a0001c0001t0001g0159 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.977+203C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544623 | |||||||
chr1:6544629 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.977+197C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544629 | |||||||
chr1:6544644 | G | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0245 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.977+182C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544644 | |||||||
chr1:6544651 | C | T | 1 | a0001c0001t0030g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.977+175G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544651 | |||||||
chr1:6545037 | T | C | 5 | a0002c0004t0010g0003 a0002c0004t0010g0040 a0002c0004t0028g0039 others(2): Show |
9 | HG02145.hp2 HG02897.hp1 HG02965.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.880+8A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 4/11 | chr1 | 6545037 | |||||||
chr1:6545581 | G | A | 1 | a0001c0001t0005g0222 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.745-401C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545581 | |||||||
chr1:6545617 | G | A | 4 | a0004c0005t0033g0113 a0004c0005t0058g0110 a0004c0005t0059g0109 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-437C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545617 | |||||||
chr1:6545710 | G | GCCCATGA others(5): Show |
190 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.745-531_745-530ins others(12): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545710 | |||||||
chr1:6545786 | C | A | 67 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(64): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.745-606G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545786 | |||||||
chr1:6545786 | C | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.745-606G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545786 | |||||||
chr1:6545919 | C | CAA | 15 | a0001c0001t0001g0013 a0001c0001t0001g0132 a0001c0001t0001g0151 others(12): Show |
17 | HG00280.hp1 HG01069.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.745-741_745-740dup others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | |||||||
chr1:6545919 | C | CAAA | 133 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.745-742_745-740dup others(3): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | |||||||
chr1:6545919 | C | CAAAA | 79 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0228 others(76): Show |
97 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.745-743_745-740dup others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | |||||||
chr1:6545919 | C | CAAAAA | 15 | a0001c0001t0003g0018 a0001c0001t0003g0244 a0002c0002t0002g0084 others(12): Show |
17 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.745-744_745-740dup others(5): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | |||||||
chr1:6545919 | CAA | C | 7 | a0002c0003t0007g0049 a0002c0003t0007g0050 a0002c0003t0007g0051 others(4): Show |
7 | HG02280.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-741_745-740del others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | |||||||
chr1:6545919 | CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0001g0150 a0002c0004t0010g0003 a0002c0004t0010g0040 others(6): Show |
13 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.745-748_745-740del others(9): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | |||||||
chr1:6545973 | C | T | 4 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-793G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545973 | |||||||
chr1:6546024 | GA | G | 8 | a0002c0004t0010g0003 a0002c0004t0010g0040 a0002c0004t0028g0039 others(5): Show |
12 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.745-845delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546024 | |||||||
chr1:6546157 | T | C | 2 | a0002c0002t0002g0061 a0002c0002t0012g0060 |
2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.745-977A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546157 | |||||||
chr1:6546548 | C | T | 73 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0002g0004 others(70): Show |
82 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.745-1368G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546548 | |||||||
chr1:6546893 | G | A | 1 | a0004c0005t0055g0115 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.745-1713C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546893 | |||||||
chr1:6546931 | C | T | 10 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0144 others(7): Show |
14 | HG00408.hp2 HG00609.hp2 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.745-1751G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546931 | |||||||
chr1:6546932 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.745-1752C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546932 | |||||||
chr1:6547008 | G | C | 4 | a0002c0002t0018g0102 a0002c0002t0018g0103 a0002c0002t0068g0101 others(1): Show |
4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-1828C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547008 | |||||||
chr1:6547044 | T | G | 1 | a0002c0008t0021g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.745-1864A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547044 | |||||||
chr1:6547082 | C | T | 73 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0002g0004 others(70): Show |
82 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.745-1902G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547082 | |||||||
chr1:6547139 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.745-1959A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547139 | |||||||
chr1:6547319 | T | C | 2 | a0002c0003t0007g0055 a0002c0003t0071g0054 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.745-2139A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547319 | |||||||
chr1:6547370 | T | G | 4 | a0004c0005t0031g0111 a0004c0005t0058g0110 a0004c0005t0059g0109 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-2190A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547370 | |||||||
chr1:6547375 | C | A | 2 | a0002c0002t0002g0061 a0002c0002t0012g0060 |
2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.745-2195G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547375 | |||||||
chr1:6547376 | C | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.744+2195G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547376 | |||||||
chr1:6547518 | GA | G | 78 | a0001c0001t0006g0012 a0001c0001t0006g0025 a0001c0001t0006g0126 others(75): Show |
90 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.744+2052delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547518 | |||||||
chr1:6547687 | T | A | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+1884A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547687 | |||||||
chr1:6547711 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.744+1860G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547711 | |||||||
chr1:6547754 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
239 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.744+1817G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547754 | |||||||
chr1:6547822 | T | C | 2 | a0004c0005t0054g0114 a0004c0005t0055g0115 |
2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.744+1749A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547822 | |||||||
chr1:6547950 | ATCATAGG others(17): Show |
A | 1 | a0001c0001t0001g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.744+1597_744+1620d others(26): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547950 | |||||||
chr1:6547997 | G | C | 261 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(258): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.744+1574C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547997 | |||||||
chr1:6548097 | C | A | 1 | a0001c0001t0001g0246 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.744+1474G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548097 | |||||||
chr1:6548129 | CTTA | C | 16 | a0002c0002t0018g0102 a0002c0002t0068g0101 a0002c0003t0007g0049 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.744+1439_744+1441d others(5): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548129 | |||||||
chr1:6548138 | C | CT | 38 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0130 others(35): Show |
39 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.744+1432dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | |||||||
chr1:6548138 | CT | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0198 others(5): Show |
9 | HG01167.hp1 HG01256.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+1432delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | |||||||
chr1:6548138 | CTT | C | 8 | a0001c0001t0011g0005 a0002c0002t0018g0103 a0002c0004t0010g0003 others(5): Show |
14 | HG02257.hp2 HG02258.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.744+1431_744+1432d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | |||||||
chr1:6548138 | CTTTT | C | 9 | a0001c0001t0006g0012 a0001c0001t0006g0025 a0001c0001t0006g0126 others(6): Show |
12 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.744+1429_744+1432d others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | |||||||
chr1:6548138 | CTTTTTTT others(3): Show |
C | 12 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0002g0062 others(9): Show |
12 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.744+1423_744+1432d others(12): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | |||||||
chr1:6548138 | CTTTTTTT others(4): Show |
C | 59 | a0001c0001t0001g0247 a0002c0002t0002g0004 a0002c0002t0002g0020 others(56): Show |
68 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.744+1422_744+1432d others(13): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | |||||||
chr1:6548138 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0004g0186 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.744+1420_744+1432d others(15): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | |||||||
chr1:6548138 | CTTTTTTT others(7): Show |
C | 2 | a0002c0004t0028g0039 a0002c0004t0028g0042 |
2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.744+1419_744+1432d others(16): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | |||||||
chr1:6548168 | C | A | 3 | a0006c0010t0022g0268 a0006c0010t0022g0270 a0006c0010t0052g0269 |
3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.744+1403G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548168 | |||||||
chr1:6548168 | C | T | 2 | a0001c0001t0011g0005 a0002c0003t0070g0104 |
5 | HG01167.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+1403G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548168 | |||||||
chr1:6548218 | G | C | 4 | a0002c0002t0018g0102 a0002c0002t0018g0103 a0002c0002t0068g0101 others(1): Show |
4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+1353C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548218 | |||||||
chr1:6548233 | CGCCT | C | 47 | a0001c0001t0001g0247 a0002c0002t0002g0004 a0002c0002t0002g0020 others(44): Show |
56 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.744+1334_744+1337d others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548233 | |||||||
chr1:6548259 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
239 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.744+1312G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548259 | |||||||
chr1:6548287 | C | T | 4 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+1284G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548287 | |||||||
chr1:6548337 | G | A | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG01952.hp2 HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.744+1234C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548337 | |||||||
chr1:6548375 | A | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.744+1196T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548375 | |||||||
chr1:6548439 | G | A | 1 | a0002c0008t0051g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.744+1132C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548439 | |||||||
chr1:6548443 | C | T | 66 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0002g0004 others(63): Show |
75 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.744+1128G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548443 | |||||||
chr1:6548462 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.744+1109A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548462 | |||||||
chr1:6548581 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.744+990T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548581 | |||||||
chr1:6548660 | C | T | 4 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+911G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548660 | |||||||
chr1:6548670 | T | A | 6 | a0001c0001t0006g0012 a0001c0001t0006g0025 a0001c0001t0006g0126 others(3): Show |
9 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.744+901A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548670 | |||||||
chr1:6548700 | T | C | 4 | a0002c0002t0018g0102 a0002c0002t0018g0103 a0002c0002t0068g0101 others(1): Show |
4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+871A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548700 | |||||||
chr1:6548889 | C | G | 1 | a0002c0004t0074g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.744+682G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548889 | |||||||
chr1:6548954 | C | T | 74 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0002g0004 others(71): Show |
83 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.744+617G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548954 | |||||||
chr1:6549091 | G | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.744+480C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549091 | |||||||
chr1:6549113 | C | T | 5 | a0004c0005t0031g0111 a0004c0005t0033g0113 a0004c0005t0058g0110 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+458G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549113 | |||||||
chr1:6549150 | G | A | 3 | a0005c0007t0003g0009 a0005c0007t0003g0138 a0005c0007t0003g0253 |
6 | HG02074.hp2 HG02165.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+421C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549150 | |||||||
chr1:6549265 | GAACC | G | 38 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(35): Show |
47 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.744+302_744+305del others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549265 | |||||||
chr1:6549266 | A | C | 1 | a0001c0001t0001g0258 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.744+305T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549266 | |||||||
chr1:6549405 | C | T | 1 | a0001c0001t0044g0141 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.744+166G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549405 | |||||||
chr1:6549499 | C | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
227 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.744+72G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549499 | |||||||
chr1:6549503 | CAT | C | 74 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0002g0004 others(71): Show |
83 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.744+66_744+67delAT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549503 | |||||||
chr1:6549732 | G | GT | 64 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(61): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.617-35dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549732 | |||||||
chr1:6549769 | T | C | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.617-71A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549769 | |||||||
chr1:6549776 | G | A | 1 | a0001c0001t0041g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.617-78C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549776 | |||||||
chr1:6549790 | C | T | 1 | a0001c0001t0041g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.617-92G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549790 | |||||||
chr1:6549791 | A | G | 265 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.617-93T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549791 | |||||||
chr1:6549836 | G | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.617-138C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549836 | |||||||
chr1:6549858 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.617-160G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549858 | |||||||
chr1:6549876 | C | T | 1 | a0001c0009t0001g0125 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.617-178G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549876 | |||||||
chr1:6549898 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.617-200G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549898 | |||||||
chr1:6549989 | C | T | 64 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(61): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.617-291G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549989 | |||||||
chr1:6550037 | AT | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.617-340delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550037 | |||||||
chr1:6550093 | G | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.616+303C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550093 | |||||||
chr1:6550100 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.616+296G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550100 | |||||||
chr1:6550124 | C | T | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.616+272G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550124 | |||||||
chr1:6550134 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.616+262G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550134 | |||||||
chr1:6550135 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.616+261C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550135 | |||||||
chr1:6550157 | G | A | 4 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.616+239C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550157 | |||||||
chr1:6550174 | G | A | 1 | a0002c0003t0070g0104 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.616+222C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550174 | |||||||
chr1:6550177 | G | A | 1 | a0002c0004t0074g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.616+219C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550177 | |||||||
chr1:6550256 | C | T | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.616+140G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550256 | |||||||
chr1:6550277 | C | T | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.616+119G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550277 | |||||||
chr1:6550278 | G | A | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0008g0036 others(4): Show |
8 | HG01109.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.616+118C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550278 | |||||||
chr1:6550306 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.616+90A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550306 | |||||||
chr1:6550322 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.616+74G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550322 | |||||||
chr1:6550683 | C | CT | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
222 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.397-69dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550683 | |||||||
chr1:6550683 | C | CTT | 22 | a0001c0001t0001g0026 a0001c0001t0001g0132 a0001c0001t0001g0133 others(19): Show |
28 | HG01346.hp1 HG01361.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.397-70_397-69dupAA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550683 | |||||||
chr1:6550740 | A | G | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.397-125T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550740 | |||||||
chr1:6550761 | G | A | 1 | a0001c0001t0005g0261 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.397-146C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550761 | |||||||
chr1:6550794 | C | T | 4 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.397-179G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550794 | |||||||
chr1:6550858 | C | T | 2 | a0002c0002t0002g0061 a0002c0002t0012g0060 |
2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.397-243G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550858 | |||||||
chr1:6550950 | T | G | 1 | a0001c0001t0053g0262 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.397-335A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550950 | |||||||
chr1:6550966 | C | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.397-351G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550966 | |||||||
chr1:6550973 | G | A | 1 | a0004c0005t0062g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.397-358C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550973 | |||||||
chr1:6551013 | C | T | 1 | a0002c0004t0074g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.397-398G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551013 | |||||||
chr1:6551021 | G | A | 1 | a0001c0001t0003g0263 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.397-406C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551021 | |||||||
chr1:6551236 | C | T | 1 | a0002c0002t0002g0059 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.397-621G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551236 | |||||||
chr1:6551330 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.397-715T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551330 | |||||||
chr1:6551340 | GAGA | G | 5 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0023g0108 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.397-728_397-726del others(3): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551340 | |||||||
chr1:6551794 | G | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.397-1179C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551794 | |||||||
chr1:6551797 | C | T | 6 | a0001c0001t0006g0012 a0001c0001t0006g0025 a0001c0001t0006g0126 others(3): Show |
9 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.397-1182G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551797 | |||||||
chr1:6551858 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.397-1243G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551858 | |||||||
chr1:6551921 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.397-1306T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551921 | |||||||
chr1:6551967 | G | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.397-1352C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551967 | |||||||
chr1:6552022 | G | A | 18 | a0002c0002t0018g0102 a0002c0002t0018g0103 a0002c0002t0068g0101 others(15): Show |
18 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.397-1407C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552022 | |||||||
chr1:6552048 | G | A | 2 | a0004c0005t0054g0114 a0004c0005t0055g0115 |
2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.397-1433C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552048 | |||||||
chr1:6552209 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.397-1594G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552209 | |||||||
chr1:6552210 | T | C | 1 | a0004c0005t0033g0113 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.397-1595A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552210 | |||||||
chr1:6552212 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.397-1597A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552212 | |||||||
chr1:6552267 | G | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.397-1652C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552267 | |||||||
chr1:6552279 | G | A | 5 | a0004c0005t0031g0111 a0004c0005t0033g0113 a0004c0005t0058g0110 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.397-1664C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552279 | |||||||
chr1:6552292 | C | T | 1 | a0002c0002t0061g0106 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.397-1677G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552292 | |||||||
chr1:6552317 | C | T | 5 | a0002c0003t0007g0049 a0002c0003t0007g0050 a0002c0003t0007g0051 others(2): Show |
5 | HG02280.hp2 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.397-1702G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552317 | |||||||
chr1:6552322 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
233 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.397-1707C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552322 | |||||||
chr1:6552459 | T | TTTTA | 4 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.396+1644_396+1647d others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552459 | |||||||
chr1:6552490 | T | G | 1 | a0010c0013t0018g0120 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.396+1617A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552490 | |||||||
chr1:6552516 | A | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.396+1591T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552516 | |||||||
chr1:6552542 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
227 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.396+1565G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552542 | |||||||
chr1:6552591 | C | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.396+1516G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552591 | |||||||
chr1:6552608 | G | A | 74 | a0001c0001t0023g0123 a0001c0001t0057g0122 a0002c0002t0002g0004 others(71): Show |
83 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.396+1499C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552608 | |||||||
chr1:6552722 | A | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.396+1385T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552722 | |||||||
chr1:6552834 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.396+1273G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552834 | |||||||
chr1:6552845 | T | C | 64 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(61): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.396+1262A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552845 | |||||||
chr1:6552873 | G | T | 64 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(61): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.396+1234C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552873 | |||||||
chr1:6552957 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.396+1150C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552957 | |||||||
chr1:6552969 | G | A | 1 | a0003c0006t0013g0010 | 3 | HG01891.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.396+1138C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552969 | |||||||
chr1:6553130 | A | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.396+977T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553130 | |||||||
chr1:6553147 | T | C | 4 | a0002c0008t0020g0019 a0002c0008t0021g0044 a0002c0008t0021g0046 others(1): Show |
5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.396+960A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553147 | |||||||
chr1:6553314 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.396+793C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553314 | |||||||
chr1:6553322 | G | A | 1 | a0002c0002t0063g0105 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.396+785C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553322 | |||||||
chr1:6553524 | C | CT | 184 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
238 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.396+582dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553524 | |||||||
chr1:6553524 | C | CTT | 4 | a0001c0001t0004g0011 a0001c0001t0011g0005 a0001c0001t0011g0124 others(1): Show |
9 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.396+581_396+582dup others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553524 | |||||||
chr1:6553646 | C | T | 64 | a0002c0002t0002g0004 a0002c0002t0002g0020 a0002c0002t0002g0021 others(61): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.396+461G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553646 | |||||||
chr1:6553790 | C | G | 10 | a0002c0003t0007g0049 a0002c0003t0007g0050 a0002c0003t0007g0051 others(7): Show |
10 | HG02280.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.396+317G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553790 | |||||||
chr1:6553798 | T | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.396+309A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553798 | |||||||
chr1:6553828 | T | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.396+279A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553828 | |||||||
chr1:6553849 | AAAAG | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.396+254_396+257del others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553849 | |||||||
chr1:6553939 | C | T | 7 | a0002c0004t0010g0003 a0002c0004t0010g0040 a0002c0004t0028g0039 others(4): Show |
11 | HG02055.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.396+168G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553939 | |||||||
chr1:6554096 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.396+11G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6554096 |