Item | Value |
---|---|
geneid | 25957 |
ensemblid | ENSG00000132424.17 |
hgncid | 21222 |
symbol | PNISR |
name | PNN interacting serine and arginine rich protein |
refseq_nuc | NM_032870.4 |
refseq_prot | NP_116259.2 |
ensembl_nuc | ENST00000369239.10 |
ensembl_prot | ENSP00000358242.5 |
mane_status | MANE Select |
chr | chr6 |
start | 99398050 |
end | 99425308 |
strand | - |
ver | v1.2 |
region | chr6:99398050-99425308 |
region5000 | chr6:99393050-99430308 |
regionname0 | PNISR_chr6_99398050_99425308 |
regionname5000 | PNISR_chr6_99393050_99430308 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 805 | 396 | 85 | 82 | 169 | 14 | 44 | 136 | PNISR_chr6_99393050_99430308 | PNISR | MWDQG others(800): Show |
chr6 | 99393050 | 99430308 |
a0002 | 0/0 | 805 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PNISR_chr6_99393050_99430308 | PNISR | MWDQG others(800): Show |
chr6 | 99393050 | 99430308 |
a0003 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | MWDQG others(800): Show |
chr6 | 99393050 | 99430308 |
a0004 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | MWDQG others(800): Show |
chr6 | 99393050 | 99430308 |
a0005 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | MWDQG others(800): Show |
chr6 | 99393050 | 99430308 |
a0006 | 0/0 | 805 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | MWDQG others(800): Show |
chr6 | 99393050 | 99430308 |
a0007 | 0/0 | 805 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | MWDQG others(800): Show |
chr6 | 99393050 | 99430308 |
a0008 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | MWDQG others(800): Show |
chr6 | 99393050 | 99430308 |
a0009 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | MWDQG others(800): Show |
chr6 | 99393050 | 99430308 |
a0010 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | MWDQG others(800): Show |
chr6 | 99393050 | 99430308 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2415 | 391 | 85 | 82 | 166 | 13 | 43 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0001c0003 | 0/0 | 2415 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0001c0004 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0001c0013 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0001c0014 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0002c0002 | 0/0 | 2415 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0003c0006 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0004c0012 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0005c0010 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0006c0011 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0007c0009 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0008c0007 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0009c0005 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 | ||
a0010c0008 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATGTG others(2410): Show |
chr6 | 99393050 | 99430308 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5113 | 186 | 34 | 31 | 99 | 4 | 17 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0002 | 1/0 | 5113 | 164 | 42 | 33 | 61 | 7 | 20 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0003 | 0/0 | 5113 | 21 | 0 | 16 | 0 | 2 | 3 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0004 | 0/0 | 5113 | 4 | 3 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0005 | 0/0 | 5113 | 2 | 0 | 1 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0006 | 0/0 | 5113 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0007 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0008 | 0/0 | 5113 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0009 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0010 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0011 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0012 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0013 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0014 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0015 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0016 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0017 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0001t0018 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0003t0001 | 0/0 | 5113 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0004t0002 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0013t0001 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0001c0014t0001 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0002c0002t0001 | 0/0 | 5113 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0003c0006t0001 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0004c0012t0002 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0005c0010t0001 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0006c0011t0002 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0007c0009t0002 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0008c0007t0001 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0009c0005t0001 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
a0010c0008t0004 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | ATCTT others(5108): Show |
chr6 | 99393050 | 99430308 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 45 | 3 | 18 | 21 | 0 | 3 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0002 | 0/0 | 28 | 0 | 2 | 23 | 0 | 3 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 0 | 0 | 4 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0009 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0010 | 0/0 | 4 | 1 | 0 | 0 | 2 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0003 | 0/0 | 20 | 0 | 3 | 16 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0005 | 0/0 | 8 | 0 | 2 | 3 | 0 | 3 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0011 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0020 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0003g0004 | 0/0 | 10 | 0 | 8 | 0 | 1 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0003g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0008g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0010g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0012g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0013g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0014g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0015g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0016g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0017g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0001t0018g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0013t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0001c0014t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0003c0006t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0004c0012t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0005c0010t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0006c0011t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0007c0009t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0008c0007t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0009c0005t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
a0010c0008t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0040 | EUR | GBR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0234 | EUR | GBR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0023 | EUR | FIN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0206 | EUR | FIN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00323 | hp2 | a0001 | c0014 | t0001 | g0068 | EUR | FIN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00642 | hp1 | a0001 | c0001 | t0008 | g0051 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0190 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02015 | hp1 | a0003 | c0006 | t0001 | g0107 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02055 | hp2 | a0001 | c0001 | t0017 | g0137 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0108 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02135 | hp2 | a0004 | c0012 | t0002 | g0210 | EAS | KHV | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02165 | hp1 | a0005 | c0010 | t0001 | g0102 | EAS | CDX | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02602 | hp1 | a0006 | c0011 | t0002 | g0179 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02647 | hp1 | a0001 | c0001 | t0018 | g0187 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02735 | hp2 | a0001 | c0004 | t0002 | g0188 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03041 | hp2 | a0001 | c0001 | t0015 | g0045 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03225 | hp1 | a0001 | c0001 | t0016 | g0174 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ESN | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03579 | hp2 | a0001 | c0001 | t0013 | g0060 | AFR | MSL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03654 | hp1 | a0007 | c0009 | t0002 | g0212 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | STU | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03831 | hp1 | a0001 | c0001 | t0012 | g0103 | SAS | BEB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | BEB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | STU | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0191 | SAS | BEB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | STU | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | STU | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | STU | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0048 | SAS | STU | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | STU | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | YRI | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | CHB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18944 | hp2 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18969 | hp1 | a0001 | c0001 | t0014 | g0109 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18970 | hp1 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18989 | hp1 | a0008 | c0007 | t0001 | g0100 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18989 | hp2 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18995 | hp2 | a0009 | c0005 | t0001 | g0112 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19000 | hp1 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | LWK | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19043 | hp1 | a0010 | c0008 | t0004 | g0055 | AFR | LWK | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19064 | hp2 | a0001 | c0001 | t0011 | g0092 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19085 | hp1 | a0001 | c0013 | t0001 | g0113 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19087 | hp1 | a0001 | c0001 | t0010 | g0067 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | YRI | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | YRI | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ASW | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ASW | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0162 | EUR | TSI | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0160 | EUR | TSI | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0157 | EUR | TSI | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | GIH | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | GIH | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0052 | AFR | USA | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | USA | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0065 | REF | REF | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0135 | REF | REF | PNISR_chr6_99393050_99430308 | PNISR | chr6 | 99393050 | 99430308 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:99400825 | T | A | 1 | a0010 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.2133A>T | p.Leu711Phe | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 2338/5113 | 2133/2418 | 711/805 | chr6 | 99400825 | |||
chr6:99400901 | C | G | 1 | a0008 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.2057G>C | p.Arg686Pro | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 2262/5113 | 2057/2418 | 686/805 | chr6 | 99400901 | |||
chr6:99400941 | T | C | 1 | a0007 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.2017A>G | p.Ile673Val | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 2222/5113 | 2017/2418 | 673/805 | chr6 | 99400941 | |||
chr6:99401040 | G | A | 1 | a0005 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1918C>T | p.Arg640Cys | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 2123/5113 | 1918/2418 | 640/805 | chr6 | 99401040 | |||
chr6:99401048 | C | T | 1 | a0003 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1910G>A | p.Arg637Gln | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 2115/5113 | 1910/2418 | 637/805 | chr6 | 99401048 | |||
chr6:99401262 | T | C | 1 | a0006 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.1696A>G | p.Ile566Val | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1901/5113 | 1696/2418 | 566/805 | chr6 | 99401262 | |||
chr6:99401315 | C | T | 1 | a0009 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.1643G>A | p.Arg548Gln | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1848/5113 | 1643/2418 | 548/805 | chr6 | 99401315 | |||
chr6:99401349 | T | C | 1 | a0004 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.1609A>G | p.Ser537Gly | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1814/5113 | 1609/2418 | 537/805 | chr6 | 99401349 | |||
chr6:99410819 | T | C | 1 | a0002 | 2 | NA18962.hp2 NA19055.hp2 |
missense_variant | MODERATE | c.423A>G | p.Ile141Met | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/12 | 628/5113 | 423/2418 | 141/805 | chr6 | 99410819 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:99402703 | C | T | 1 | a0001c0004 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.1164G>A | p.Leu388Leu | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 11/12 | 1369/5113 | 1164/2418 | 388/805 | chr6 | 99402703 | |||
chr6:99404637 | G | A | 1 | a0001c0013 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.1068C>T | p.Tyr356Tyr | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 9/12 | 1273/5113 | 1068/2418 | 356/805 | chr6 | 99404637 | |||
chr6:99410783 | G | A | 1 | a0001c0014 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.459C>T | p.Pro153Pro | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/12 | 664/5113 | 459/2418 | 153/805 | chr6 | 99410783 | |||
chr6:99410927 | T | C | 1 | a0001c0003 | 2 | NA18944.hp2 NA19000.hp1 |
synonymous_variant | LOW | c.315A>G | p.Pro105Pro | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/12 | 520/5113 | 315/2418 | 105/805 | chr6 | 99410927 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:99398352 | C | T | 1 | a0001c0001t0013 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2188G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 2188 | chr6 | 99398352 | ||||||
chr6:99398433 | T | C | 1 | a0001c0001t0017 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2107A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 2107 | chr6 | 99398433 | ||||||
chr6:99398474 | C | T | 1 | a0001c0001t0006 | 2 | HG02056.hp2 NA18989.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2066G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 2066 | chr6 | 99398474 | ||||||
chr6:99398528 | G | A | 2 | a0001c0001t0004 a0010c0008t0004 |
5 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2012C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 2012 | chr6 | 99398528 | ||||||
chr6:99398535 | A | T | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*2005T>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 2005 | chr6 | 99398535 | ||||||
chr6:99398704 | T | C | 1 | a0001c0001t0009 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1836A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1836 | chr6 | 99398704 | ||||||
chr6:99399072 | G | A | 1 | a0001c0001t0014 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1468C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1468 | chr6 | 99399072 | ||||||
chr6:99399104 | T | G | 1 | a0001c0001t0015 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1436A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1436 | chr6 | 99399104 | ||||||
chr6:99399342 | A | C | 1 | a0001c0001t0016 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1198T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1198 | chr6 | 99399342 | ||||||
chr6:99399342 | A | G | 1 | a0001c0001t0012 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1198T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1198 | chr6 | 99399342 | ||||||
chr6:99399384 | G | T | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*1156C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1156 | chr6 | 99399384 | ||||||
chr6:99399430 | G | T | 1 | a0001c0001t0008 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1110C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1110 | chr6 | 99399430 | ||||||
chr6:99399431 | A | G | 1 | a0001c0001t0011 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1109T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1109 | chr6 | 99399431 | ||||||
chr6:99399488 | T | C | 1 | a0001c0001t0018 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1052A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1052 | chr6 | 99399488 | ||||||
chr6:99399502 | G | T | 1 | a0001c0001t0005 | 2 | HG01175.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1038C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 1038 | chr6 | 99399502 | ||||||
chr6:99399710 | A | T | 3 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0009 |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*830T>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 830 | chr6 | 99399710 | ||||||
chr6:99399717 | A | G | 1 | a0001c0001t0010 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*823T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 823 | chr6 | 99399717 | ||||||
chr6:99400380 | A | T | 3 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0009 |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*160T>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 160 | chr6 | 99400380 | ||||||
chr6:99400519 | C | T | 1 | a0001c0001t0007 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 12/12 | 21 | chr6 | 99400519 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:99401710 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1328-80C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 11/11 | chr6 | 99401710 | |||||||
chr6:99401800 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1328-170T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 11/11 | chr6 | 99401800 | |||||||
chr6:99401934 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0057 |
5 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1328-304A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 11/11 | chr6 | 99401934 | |||||||
chr6:99401982 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1328-352G>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 11/11 | chr6 | 99401982 | |||||||
chr6:99401984 | T | C | 2 | a0001c0001t0002g0213 a0001c0001t0002g0215 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1328-354A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 11/11 | chr6 | 99401984 | |||||||
chr6:99402071 | A | G | 1 | a0001c0001t0001g0025 | 2 | NA18987.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1328-441T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 11/11 | chr6 | 99402071 | |||||||
chr6:99402329 | G | T | 1 | a0001c0001t0002g0166 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1327+211C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 11/11 | chr6 | 99402329 | |||||||
chr6:99402389 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1327+151T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 11/11 | chr6 | 99402389 | |||||||
chr6:99402474 | GGTTA | G | 9 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(6): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1327+62_1327+65del others(4): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 11/11 | chr6 | 99402474 | |||||||
chr6:99402500 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(3): Show |
11 | HG01099.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1327+40G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 11/11 | chr6 | 99402500 | |||||||
chr6:99402828 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1157-118C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99402828 | |||||||
chr6:99402851 | A | ATT | 111 | a0001c0001t0001g0086 a0001c0001t0002g0003 a0001c0001t0002g0005 others(108): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1157-142_1157-141i others(4): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99402851 | |||||||
chr6:99402854 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(108): Show |
231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1157-144G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99402854 | |||||||
chr6:99402953 | G | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(219): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1157-243C>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99402953 | |||||||
chr6:99403020 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1157-310G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99403020 | |||||||
chr6:99403063 | C | A | 1 | a0001c0001t0004g0048 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1157-353G>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99403063 | |||||||
chr6:99403153 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1157-443A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99403153 | |||||||
chr6:99403260 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1157-550A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99403260 | |||||||
chr6:99403326 | G | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(3): Show |
11 | HG01099.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1156+503C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99403326 | |||||||
chr6:99403401 | C | T | 2 | a0001c0001t0002g0171 a0001c0001t0002g0173 |
2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1156+428G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99403401 | |||||||
chr6:99403414 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1156+415T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99403414 | |||||||
chr6:99403561 | A | T | 1 | a0001c0001t0002g0222 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1156+268T>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99403561 | |||||||
chr6:99403644 | T | C | 5 | a0001c0001t0004g0048 a0001c0001t0004g0058 a0001c0001t0004g0059 others(2): Show |
5 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1156+185A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 10/11 | chr6 | 99403644 | |||||||
chr6:99403991 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1103-109C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 9/11 | chr6 | 99403991 | |||||||
chr6:99404101 | T | C | 110 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(107): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1103-219A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 9/11 | chr6 | 99404101 | |||||||
chr6:99404223 | A | AT | 9 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(6): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1103-342dupA | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 9/11 | chr6 | 99404223 | |||||||
chr6:99404343 | T | C | 1 | a0009c0005t0001g0112 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1102+260A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 9/11 | chr6 | 99404343 | |||||||
chr6:99404391 | T | C | 9 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(6): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1102+212A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 9/11 | chr6 | 99404391 | |||||||
chr6:99404404 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(3): Show |
11 | HG01099.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1102+199G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 9/11 | chr6 | 99404404 | |||||||
chr6:99404459 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1102+144C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 9/11 | chr6 | 99404459 | |||||||
chr6:99405014 | A | C | 1 | a0001c0001t0002g0195 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1003-312T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405014 | |||||||
chr6:99405283 | G | T | 2 | a0001c0001t0001g0022 a0001c0001t0015g0045 |
3 | HG01099.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1003-581C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405283 | |||||||
chr6:99405285 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(4): Show |
12 | HG01099.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1003-583G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405285 | |||||||
chr6:99405329 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1003-627A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405329 | |||||||
chr6:99405411 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1002+620C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405411 | |||||||
chr6:99405527 | G | A | 1 | a0010c0008t0004g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1002+504C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405527 | |||||||
chr6:99405556 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1002+475T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405556 | |||||||
chr6:99405671 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1002+360G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405671 | |||||||
chr6:99405851 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(94): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1002+180G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405851 | |||||||
chr6:99405921 | A | C | 2 | a0001c0001t0002g0199 a0001c0001t0002g0200 |
2 | NA18945.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1002+110T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405921 | |||||||
chr6:99405973 | CA | C | 108 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(105): Show |
154 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1002+57delT | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405973 | |||||||
chr6:99405990 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(221): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.1002+41C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 8/11 | chr6 | 99405990 | |||||||
chr6:99406358 | A | G | 1 | a0001c0001t0017g0137 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.865-190T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99406358 | |||||||
chr6:99406518 | T | C | 1 | a0001c0001t0002g0214 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.865-350A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99406518 | |||||||
chr6:99406822 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.865-654A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99406822 | |||||||
chr6:99406843 | T | C | 1 | a0001c0004t0002g0188 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.865-675A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99406843 | |||||||
chr6:99406993 | A | T | 110 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(107): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.865-825T>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99406993 | |||||||
chr6:99407021 | AT | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(227): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.865-854delA | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407021 | |||||||
chr6:99407130 | G | A | 2 | a0001c0001t0002g0171 a0001c0001t0002g0173 |
2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.864+951C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407130 | |||||||
chr6:99407157 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(219): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.864+924C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407157 | |||||||
chr6:99407193 | G | A | 1 | a0001c0001t0004g0048 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.864+888C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407193 | |||||||
chr6:99407261 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0089 |
2 | NA18942.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.864+820C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407261 | |||||||
chr6:99407338 | C | CA | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(120): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.864+742dupT | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407338 | |||||||
chr6:99407338 | C | CAA | 6 | a0001c0001t0001g0028 a0001c0001t0001g0114 a0001c0001t0002g0171 others(3): Show |
7 | HG02451.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+741_864+742dup others(2): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407338 | |||||||
chr6:99407403 | A | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(3): Show |
11 | HG01099.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.864+678T>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407403 | |||||||
chr6:99407479 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.864+602G>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407479 | |||||||
chr6:99407692 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.864+389C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407692 | |||||||
chr6:99407754 | T | C | 2 | a0001c0001t0002g0167 a0001c0001t0002g0232 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.864+327A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407754 | |||||||
chr6:99407831 | T | G | 1 | a0001c0001t0002g0232 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.864+250A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 7/11 | chr6 | 99407831 | |||||||
chr6:99408285 | G | A | 1 | a0010c0008t0004g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.674-14C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 6/11 | chr6 | 99408285 | |||||||
chr6:99408353 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.674-82G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 6/11 | chr6 | 99408353 | |||||||
chr6:99408465 | A | G | 110 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(107): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.674-194T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 6/11 | chr6 | 99408465 | |||||||
chr6:99408720 | TATA | T | 4 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0064 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+450_674-450del others(3): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 6/11 | chr6 | 99408720 | |||||||
chr6:99408741 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.673+432C>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 6/11 | chr6 | 99408741 | |||||||
chr6:99408872 | T | C | 1 | a0010c0008t0004g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.673+301A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 6/11 | chr6 | 99408872 | |||||||
chr6:99408969 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(219): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.673+204T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 6/11 | chr6 | 99408969 | |||||||
chr6:99409406 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.502-62G>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/11 | chr6 | 99409406 | |||||||
chr6:99409548 | G | A | 1 | a0001c0001t0001g0025 | 2 | NA18987.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.502-204C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/11 | chr6 | 99409548 | |||||||
chr6:99409657 | C | A | 1 | a0001c0001t0002g0204 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.502-313G>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/11 | chr6 | 99409657 | |||||||
chr6:99409897 | T | G | 114 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0062 others(111): Show |
163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.502-553A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/11 | chr6 | 99409897 | |||||||
chr6:99409957 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.502-613G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/11 | chr6 | 99409957 | |||||||
chr6:99410099 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.501+642T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/11 | chr6 | 99410099 | |||||||
chr6:99410137 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.501+604G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/11 | chr6 | 99410137 | |||||||
chr6:99410146 | A | G | 1 | a0001c0001t0003g0053 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.501+595T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/11 | chr6 | 99410146 | |||||||
chr6:99410210 | C | T | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | NA18977.hp2 NA18989.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+531G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/11 | chr6 | 99410210 | |||||||
chr6:99410525 | G | T | 1 | a0001c0001t0002g0232 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.501+216C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/11 | chr6 | 99410525 | |||||||
chr6:99410534 | T | C | 1 | a0001c0001t0002g0166 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.501+207A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 5/11 | chr6 | 99410534 | |||||||
chr6:99411398 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.278-434C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99411398 | |||||||
chr6:99411468 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
7 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-504G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99411468 | |||||||
chr6:99411566 | T | C | 5 | a0001c0001t0002g0036 a0001c0001t0002g0192 a0001c0001t0002g0193 others(2): Show |
6 | HG01433.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-602A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99411566 | |||||||
chr6:99411582 | TTA | T | 5 | a0001c0001t0004g0048 a0001c0001t0004g0058 a0001c0001t0004g0059 others(2): Show |
5 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-620_278-619del others(2): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99411582 | |||||||
chr6:99411616 | T | TTTTG | 122 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(119): Show |
171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.278-656_278-653dup others(4): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99411616 | |||||||
chr6:99411676 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.278-712C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99411676 | |||||||
chr6:99411790 | G | GT | 20 | a0001c0001t0002g0036 a0001c0001t0002g0043 a0001c0001t0002g0138 others(17): Show |
22 | HG00735.hp2 HG01258.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.277+760dupA | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99411790 | |||||||
chr6:99411798 | T | TG | 9 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0056 others(6): Show |
14 | HG00642.hp2 HG01069.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.277+752_277+753ins others(1): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99411798 | |||||||
chr6:99411799 | T | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(98): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.277+752A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99411799 | |||||||
chr6:99411930 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.277+621G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99411930 | |||||||
chr6:99412376 | A | G | 2 | a0001c0001t0002g0199 a0001c0001t0002g0200 |
2 | NA18945.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.277+175T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99412376 | |||||||
chr6:99412441 | A | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(3): Show |
11 | HG01099.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+110T>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99412441 | |||||||
chr6:99412471 | T | A | 2 | a0001c0001t0001g0022 a0001c0001t0015g0045 |
3 | HG01099.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.277+80A>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99412471 | |||||||
chr6:99412510 | T | G | 5 | a0001c0001t0004g0048 a0001c0001t0004g0058 a0001c0001t0004g0059 others(2): Show |
5 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.277+41A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 4/11 | chr6 | 99412510 | |||||||
chr6:99412855 | A | G | 77 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0021 others(74): Show |
99 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.89-116T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99412855 | |||||||
chr6:99412871 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(109): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.89-132A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99412871 | |||||||
chr6:99412977 | TA | T | 9 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(6): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.89-239delT | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99412977 | |||||||
chr6:99413094 | CA | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(220): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.89-356delT | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413094 | |||||||
chr6:99413256 | T | G | 1 | a0001c0001t0001g0094 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.89-517A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413256 | |||||||
chr6:99413275 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.89-536G>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413275 | |||||||
chr6:99413337 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.89-598A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413337 | |||||||
chr6:99413391 | T | TATCC | 30 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0026 others(27): Show |
40 | HG00323.hp2 HG01106.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.89-656_89-653dupGG others(2): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413391 | |||||||
chr6:99413391 | T | TATCCATC others(1): Show |
5 | a0001c0001t0001g0069 a0001c0001t0001g0118 a0001c0001t0001g0125 others(2): Show |
5 | HG00733.hp2 HG01168.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-660_89-653dupGG others(6): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413391 | |||||||
chr6:99413391 | TATCC | T | 57 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0061 others(54): Show |
101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.89-656_89-653delGG others(2): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413391 | |||||||
chr6:99413391 | TATCCATC others(1): Show |
T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(9): Show |
19 | HG01099.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.89-660_89-653delGG others(6): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413391 | |||||||
chr6:99413391 | TATCCATC others(5): Show |
T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0184 a0001c0001t0002g0197 |
3 | HG03453.hp2 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.89-664_89-653delGG others(10): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413391 | |||||||
chr6:99413426 | CCATCCAT others(5): Show |
C | 1 | a0001c0001t0004g0048 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.89-699_89-688delAA others(10): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413426 | |||||||
chr6:99413446 | G | GATCC | 1 | a0001c0001t0001g0018 | 3 | HG00621.hp1 NA18950.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.89-711_89-708dupGG others(2): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413446 | |||||||
chr6:99413448 | T | A | 2 | a0001c0001t0002g0167 a0001c0001t0002g0232 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.89-709A>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413448 | |||||||
chr6:99413463 | A | C | 1 | a0001c0001t0001g0094 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.89-724T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413463 | |||||||
chr6:99413479 | A | C | 1 | a0001c0001t0001g0094 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.89-740T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413479 | |||||||
chr6:99413636 | A | C | 1 | a0001c0001t0001g0094 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.89-897T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413636 | |||||||
chr6:99413790 | T | TCATA | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(219): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.88+781_88+782insTA others(2): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413790 | |||||||
chr6:99413834 | A | G | 1 | a0001c0001t0013g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.88+738T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413834 | |||||||
chr6:99413835 | A | G | 1 | a0001c0001t0013g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.88+737T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413835 | |||||||
chr6:99413904 | A | G | 1 | a0001c0001t0001g0017 | 3 | HG02056.hp1 HG02165.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.88+668T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413904 | |||||||
chr6:99413927 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.88+645A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99413927 | |||||||
chr6:99414011 | A | C | 1 | a0001c0001t0001g0094 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.88+561T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99414011 | |||||||
chr6:99414074 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0066 others(4): Show |
12 | HG00323.hp2 HG00733.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.88+498G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99414074 | |||||||
chr6:99414075 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(93): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.88+497C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99414075 | |||||||
chr6:99414158 | C | G | 1 | a0001c0001t0002g0196 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.88+414G>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99414158 | |||||||
chr6:99414235 | C | T | 1 | a0005c0010t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.88+337G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99414235 | |||||||
chr6:99414254 | A | G | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | NA18977.hp2 NA18989.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+318T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99414254 | |||||||
chr6:99414302 | C | T | 1 | a0001c0001t0013g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.88+270G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99414302 | |||||||
chr6:99414326 | A | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0047 |
4 | HG02055.hp1 HG02109.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+246T>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99414326 | |||||||
chr6:99414338 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0066 others(4): Show |
12 | HG00323.hp2 HG00733.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.88+234C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99414338 | |||||||
chr6:99414420 | T | C | 13 | a0001c0001t0002g0032 a0001c0001t0002g0146 a0001c0001t0002g0147 others(10): Show |
14 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.88+152A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99414420 | |||||||
chr6:99414509 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0119 |
3 | HG02451.hp1 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.88+63A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 3/11 | chr6 | 99414509 | |||||||
chr6:99414708 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-31-18A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99414708 | |||||||
chr6:99414849 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0046 a0001c0001t0001g0047 |
5 | HG02055.hp1 HG02109.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-159G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99414849 | |||||||
chr6:99414932 | A | T | 1 | a0001c0001t0002g0003 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-31-242T>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99414932 | |||||||
chr6:99414985 | G | T | 1 | a0001c0001t0002g0031 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-31-295C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99414985 | |||||||
chr6:99415369 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(48): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-31-679C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99415369 | |||||||
chr6:99415388 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-31-698T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99415388 | |||||||
chr6:99415893 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-32+456G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99415893 | |||||||
chr6:99415911 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-32+438G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99415911 | |||||||
chr6:99415971 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(109): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-32+378C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99415971 | |||||||
chr6:99415992 | T | C | 2 | a0001c0001t0002g0167 a0001c0001t0002g0232 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-32+357A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99415992 | |||||||
chr6:99416102 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(3): Show |
11 | HG01099.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32+247T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99416102 | |||||||
chr6:99416186 | C | A | 1 | a0001c0001t0013g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-32+163G>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99416186 | |||||||
chr6:99416268 | A | C | 4 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0064 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32+81T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99416268 | |||||||
chr6:99416305 | A | G | 7 | a0001c0001t0002g0031 a0001c0001t0002g0139 a0001c0001t0002g0140 others(4): Show |
8 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32+44T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99416305 | |||||||
chr6:99416321 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-32+28T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 2/11 | chr6 | 99416321 | |||||||
chr6:99416709 | A | AG | 13 | a0001c0001t0002g0032 a0001c0001t0002g0146 a0001c0001t0002g0147 others(10): Show |
14 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-111-282dupC | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99416709 | |||||||
chr6:99416816 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-111-388G>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99416816 | |||||||
chr6:99416908 | T | A | 1 | a0001c0001t0002g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-111-480A>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99416908 | |||||||
chr6:99417016 | G | T | 2 | a0001c0001t0002g0167 a0001c0001t0002g0232 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-111-588C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417016 | |||||||
chr6:99417088 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(109): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-111-660G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417088 | |||||||
chr6:99417347 | T | G | 1 | a0001c0001t0001g0028 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-111-919A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417347 | |||||||
chr6:99417448 | T | C | 1 | a0001c0001t0001g0010 | 4 | HG00099.hp1 HG00140.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-1020A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417448 | |||||||
chr6:99417497 | AACAGAAG others(27): Show |
A | 1 | a0001c0001t0003g0054 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-111-1103_-111-107 others(38): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417497 | |||||||
chr6:99417586 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-111-1158G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417586 | |||||||
chr6:99417776 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(109): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-111-1348T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417776 | |||||||
chr6:99417825 | G | T | 7 | a0001c0001t0002g0031 a0001c0001t0002g0139 a0001c0001t0002g0140 others(4): Show |
8 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-111-1397C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417825 | |||||||
chr6:99417833 | C | T | 1 | a0001c0001t0002g0153 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-111-1405G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417833 | |||||||
chr6:99417968 | C | CA | 22 | a0001c0001t0002g0003 a0001c0001t0002g0020 a0001c0001t0002g0033 others(19): Show |
45 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.-111-1541dupT | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417968 | |||||||
chr6:99417968 | CA | C | 13 | a0001c0001t0001g0063 a0001c0001t0001g0070 a0001c0001t0001g0074 others(10): Show |
14 | HG01975.hp2 HG02145.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.-111-1541delT | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417968 | |||||||
chr6:99417968 | CAA | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(96): Show |
219 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-111-1542_-111-154 others(6): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417968 | |||||||
chr6:99417968 | CAAA | C | 6 | a0001c0001t0001g0061 a0001c0001t0001g0079 a0001c0001t0001g0080 others(3): Show |
6 | HG01069.hp2 HG02083.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-111-1543_-111-154 others(7): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417968 | |||||||
chr6:99417977 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-111-1549T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99417977 | |||||||
chr6:99418065 | T | C | 77 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0021 others(74): Show |
99 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.-111-1637A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418065 | |||||||
chr6:99418118 | G | C | 9 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(6): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-111-1690C>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418118 | |||||||
chr6:99418281 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-111-1853G>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418281 | |||||||
chr6:99418413 | G | C | 1 | a0001c0001t0013g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-111-1985C>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418413 | |||||||
chr6:99418447 | TA | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-111-2020delT | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418447 | |||||||
chr6:99418447 | TAA | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0097 others(2): Show |
8 | HG00673.hp1 HG01074.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-2021_-111-202 others(6): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418447 | |||||||
chr6:99418462 | A | C | 11 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0002g0169 others(8): Show |
13 | HG00323.hp1 HG00639.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.-111-2034T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418462 | |||||||
chr6:99418539 | T | A | 9 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(6): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-111-2111A>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418539 | |||||||
chr6:99418557 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0057 |
5 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-2129A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418557 | |||||||
chr6:99418719 | T | C | 1 | a0001c0001t0013g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-111-2291A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418719 | |||||||
chr6:99418787 | A | G | 1 | a0001c0001t0003g0023 | 2 | HG00280.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-111-2359T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418787 | |||||||
chr6:99418794 | T | G | 1 | a0001c0001t0002g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-111-2366A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418794 | |||||||
chr6:99418991 | T | C | 1 | a0001c0001t0013g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-111-2563A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99418991 | |||||||
chr6:99419043 | C | T | 47 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(44): Show |
63 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-111-2615G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419043 | |||||||
chr6:99419058 | G | A | 5 | a0001c0001t0002g0036 a0001c0001t0002g0192 a0001c0001t0002g0193 others(2): Show |
6 | HG01433.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-2630C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419058 | |||||||
chr6:99419088 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | NA19002.hp1 NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-111-2660G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419088 | |||||||
chr6:99419151 | T | A | 1 | a0001c0001t0002g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-111-2723A>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419151 | |||||||
chr6:99419152 | C | A | 1 | a0001c0001t0002g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-111-2724G>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CA | 13 | a0001c0001t0002g0019 a0001c0001t0002g0036 a0001c0001t0002g0136 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-111-2725dupT | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAA | 6 | a0001c0001t0002g0021 a0001c0001t0002g0037 a0001c0001t0002g0043 others(3): Show |
10 | HG01255.hp1 HG01884.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.-111-2730_-111-272 others(10): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA | 7 | a0001c0001t0002g0038 a0001c0001t0002g0139 a0001c0001t0002g0199 others(4): Show |
8 | HG01261.hp1 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-2731_-111-272 others(11): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0169 others(5): Show |
10 | HG00099.hp2 HG01109.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-111-2732_-111-272 others(12): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0204 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-111-2734_-111-272 others(14): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0205 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-111-2735_-111-272 others(15): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(5): Show |
6 | a0001c0001t0002g0041 a0001c0001t0002g0140 a0001c0001t0002g0206 others(3): Show |
7 | HG00323.hp1 HG02965.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.-111-2736_-111-272 others(16): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(6): Show |
6 | a0001c0001t0002g0031 a0001c0001t0002g0141 a0001c0001t0002g0142 others(3): Show |
7 | HG01123.hp1 HG01261.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-111-2737_-111-272 others(17): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0002g0042 a0001c0001t0002g0177 a0004c0012t0002g0210 |
4 | HG02135.hp2 NA19064.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-2738_-111-272 others(18): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0002g0228 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-111-2739_-111-272 others(19): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0002g0211 a0007c0009t0002g0212 |
2 | HG01175.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-111-2740_-111-272 others(20): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | HG01257.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-111-2741_-111-272 others(21): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0002g0143 a0001c0001t0002g0215 a0001c0001t0002g0216 |
3 | HG01258.hp2 HG02647.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-111-2742_-111-272 others(22): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0002g0144 a0001c0001t0002g0217 |
2 | HG03041.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-111-2743_-111-272 others(23): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0002g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-111-2749_-111-272 others(29): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | C | CAAAAAAA others(26): Show |
1 | a0001c0001t0002g0230 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-111-2757_-111-272 others(37): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419152 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0002g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-111-2737_-111-272 others(17): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419152 | |||||||
chr6:99419168 | AAAAAAAA others(16): Show |
A | 1 | a0001c0003t0001g0029 | 2 | NA18944.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-111-2763_-111-274 others(27): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419168 | |||||||
chr6:99419169 | AAAAAAAA others(15): Show |
A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | NA19002.hp1 NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-111-2763_-111-274 others(26): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419169 | |||||||
chr6:99419171 | AAAAAAAA others(13): Show |
A | 2 | a0001c0001t0002g0167 a0001c0001t0002g0232 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-111-2763_-111-274 others(24): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419171 | |||||||
chr6:99419174 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0002g0186 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-111-2763_-111-274 others(21): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419174 | |||||||
chr6:99419175 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0002g0233 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-111-2763_-111-274 others(20): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419175 | |||||||
chr6:99419176 | AAAAAAAA others(8): Show |
A | 6 | a0001c0001t0002g0005 a0001c0001t0002g0161 a0001c0001t0002g0168 others(3): Show |
8 | HG01081.hp2 HG03710.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.-111-2763_-111-274 others(19): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419176 | |||||||
chr6:99419177 | AAAAAAAA others(7): Show |
A | 13 | a0001c0001t0002g0032 a0001c0001t0002g0044 a0001c0001t0002g0146 others(10): Show |
13 | HG01167.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-111-2763_-111-275 others(18): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419177 | |||||||
chr6:99419178 | AAAAAAAA others(6): Show |
A | 16 | a0001c0001t0002g0003 a0001c0001t0002g0020 a0001c0001t0002g0032 others(13): Show |
35 | HG00609.hp1 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.-111-2763_-111-275 others(17): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419178 | |||||||
chr6:99419179 | AAAAAAAA others(5): Show |
A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0128 others(14): Show |
19 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.-111-2763_-111-275 others(16): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419179 | |||||||
chr6:99419180 | AAAAAAAA others(4): Show |
A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(33): Show |
80 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-111-2763_-111-275 others(15): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419180 | |||||||
chr6:99419181 | AAAAAAAA others(3): Show |
A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(51): Show |
93 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.-111-2763_-111-275 others(14): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419181 | |||||||
chr6:99419182 | AAAAAAAA others(2): Show |
A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(15): Show |
26 | HG00544.hp2 HG01099.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-111-2763_-111-275 others(13): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419182 | |||||||
chr6:99419191 | G | A | 68 | a0001c0001t0002g0011 a0001c0001t0002g0021 a0001c0001t0002g0034 others(65): Show |
91 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-111-2763C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419191 | |||||||
chr6:99419258 | C | T | 9 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(6): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-111-2830G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419258 | |||||||
chr6:99419354 | A | C | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0164 |
3 | NA18980.hp2 NA19055.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-111-2926T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419354 | |||||||
chr6:99419455 | C | T | 1 | a0001c0001t0017g0137 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-111-3027G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419455 | |||||||
chr6:99419519 | A | G | 1 | a0001c0001t0013g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-111-3091T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419519 | |||||||
chr6:99419519 | A | T | 1 | a0001c0001t0002g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-111-3091T>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419519 | |||||||
chr6:99419626 | G | A | 1 | a0001c0001t0002g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-111-3198C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419626 | |||||||
chr6:99419783 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(219): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.-111-3355T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419783 | |||||||
chr6:99419873 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-111-3445G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419873 | |||||||
chr6:99419890 | C | CT | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0002g0232 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-111-3463dupA | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419890 | |||||||
chr6:99419890 | C | CTT | 8 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(5): Show |
22 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.-111-3464_-111-346 others(6): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419890 | |||||||
chr6:99419947 | C | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0066 others(4): Show |
12 | HG00323.hp2 HG00733.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-111-3519G>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99419947 | |||||||
chr6:99420108 | C | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(48): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-111-3680G>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420108 | |||||||
chr6:99420196 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0057 |
5 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-3768A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420196 | |||||||
chr6:99420207 | G | A | 9 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(6): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-111-3779C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420207 | |||||||
chr6:99420297 | C | T | 1 | a0001c0001t0013g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-111-3869G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420297 | |||||||
chr6:99420331 | T | G | 108 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(105): Show |
154 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-111-3903A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420331 | |||||||
chr6:99420378 | G | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0066 others(4): Show |
12 | HG00323.hp2 HG00733.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-111-3950C>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420378 | |||||||
chr6:99420500 | T | G | 1 | a0001c0001t0002g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-111-4072A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420500 | |||||||
chr6:99420596 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-111-4168T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420596 | |||||||
chr6:99420675 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-111-4247G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420675 | |||||||
chr6:99420677 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-111-4249A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420677 | |||||||
chr6:99420816 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-111-4388T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420816 | |||||||
chr6:99420912 | A | C | 77 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0021 others(74): Show |
99 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.-112+4303T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99420912 | |||||||
chr6:99421016 | A | G | 5 | a0001c0001t0004g0048 a0001c0001t0004g0058 a0001c0001t0004g0059 others(2): Show |
5 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112+4199T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99421016 | |||||||
chr6:99421410 | T | G | 1 | a0001c0001t0002g0219 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-112+3805A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99421410 | |||||||
chr6:99421419 | A | T | 1 | a0010c0008t0004g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-112+3796T>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99421419 | |||||||
chr6:99421441 | G | A | 1 | a0001c0001t0001g0030 | 2 | NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-112+3774C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99421441 | |||||||
chr6:99421456 | C | T | 4 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0064 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+3759G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99421456 | |||||||
chr6:99421813 | T | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(219): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.-112+3402A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99421813 | |||||||
chr6:99421920 | C | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(3): Show |
11 | HG01099.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-112+3295G>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99421920 | |||||||
chr6:99422291 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG00438.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-112+2924T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422291 | |||||||
chr6:99422400 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-112+2815A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422400 | |||||||
chr6:99422489 | C | T | 18 | a0001c0001t0002g0003 a0001c0001t0002g0020 a0001c0001t0002g0033 others(15): Show |
41 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.-112+2726G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422489 | |||||||
chr6:99422649 | T | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(109): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-112+2566A>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422649 | |||||||
chr6:99422664 | AG | A | 18 | a0001c0001t0002g0003 a0001c0001t0002g0020 a0001c0001t0002g0033 others(15): Show |
41 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.-112+2550delC | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422664 | |||||||
chr6:99422694 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-112+2521G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422694 | |||||||
chr6:99422698 | A | C | 1 | a0001c0001t0003g0054 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-112+2517T>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422698 | |||||||
chr6:99422699 | C | CCACCTCC others(25): Show |
1 | a0001c0001t0003g0054 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-112+2515_-112+251 others(36): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422699 | |||||||
chr6:99422749 | C | T | 4 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0064 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+2466G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422749 | |||||||
chr6:99422799 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(3): Show |
11 | HG01099.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-112+2416C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422799 | |||||||
chr6:99422806 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(229): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-112+2409T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422806 | |||||||
chr6:99422843 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0057 |
5 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112+2372G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422843 | |||||||
chr6:99422876 | C | CA | 11 | a0001c0001t0002g0031 a0001c0001t0002g0138 a0001c0001t0002g0139 others(8): Show |
12 | HG00735.hp2 HG02055.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-112+2338dupT | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422876 | |||||||
chr6:99422876 | C | CAA | 13 | a0001c0001t0002g0032 a0001c0001t0002g0146 a0001c0001t0002g0168 others(10): Show |
14 | HG01884.hp2 HG01993.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-112+2337_-112+233 others(6): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422876 | |||||||
chr6:99422876 | C | CAAA | 59 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0021 others(56): Show |
80 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.-112+2336_-112+233 others(7): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422876 | |||||||
chr6:99422876 | C | CAAAA | 14 | a0001c0001t0002g0043 a0001c0001t0002g0220 a0001c0001t0002g0221 others(11): Show |
15 | HG01261.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-112+2335_-112+233 others(8): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422876 | |||||||
chr6:99422876 | CA | C | 14 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0044 others(11): Show |
35 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.-112+2338delT | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422876 | |||||||
chr6:99422876 | CAAAA | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
10 | HG00099.hp1 HG00140.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-112+2335_-112+233 others(8): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422876 | |||||||
chr6:99422876 | CAAAAA | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(88): Show |
194 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.-112+2334_-112+233 others(9): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422876 | |||||||
chr6:99422876 | CAAAAAAA | C | 9 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(6): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-112+2332_-112+233 others(11): Show |
PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422876 | |||||||
chr6:99422969 | C | T | 9 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(6): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-112+2246G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422969 | |||||||
chr6:99422983 | C | G | 1 | a0001c0001t0002g0149 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-112+2232G>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99422983 | |||||||
chr6:99423009 | C | T | 2 | a0001c0001t0002g0148 a0010c0008t0004g0055 |
2 | NA19043.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-112+2206G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423009 | |||||||
chr6:99423054 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0066 others(4): Show |
12 | HG00323.hp2 HG00733.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-112+2161T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423054 | |||||||
chr6:99423109 | C | T | 9 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0023 others(6): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-112+2106G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423109 | |||||||
chr6:99423134 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(109): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-112+2081G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423134 | |||||||
chr6:99423315 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-112+1900G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423315 | |||||||
chr6:99423466 | A | G | 3 | a0001c0001t0002g0032 a0001c0001t0002g0146 a0001c0001t0002g0147 |
4 | HG02145.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112+1749T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423466 | |||||||
chr6:99423483 | G | T | 1 | a0001c0001t0001g0072 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-112+1732C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423483 | |||||||
chr6:99423663 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-112+1552C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423663 | |||||||
chr6:99423687 | C | A | 1 | a0001c0001t0002g0232 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-112+1528G>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423687 | |||||||
chr6:99423769 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-112+1446G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423769 | |||||||
chr6:99423850 | T | C | 1 | a0001c0001t0002g0233 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-112+1365A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423850 | |||||||
chr6:99423943 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0066 others(4): Show |
12 | HG00323.hp2 HG00733.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-112+1272A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423943 | |||||||
chr6:99423954 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0066 others(4): Show |
12 | HG00323.hp2 HG00733.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-112+1261C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99423954 | |||||||
chr6:99424148 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-112+1067C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99424148 | |||||||
chr6:99424192 | G | A | 110 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(107): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.-112+1023C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99424192 | |||||||
chr6:99424256 | T | C | 1 | a0001c0001t0002g0044 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-112+959A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99424256 | |||||||
chr6:99424368 | C | T | 1 | a0001c0001t0004g0048 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-112+847G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99424368 | |||||||
chr6:99424369 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-112+846C>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99424369 | |||||||
chr6:99424411 | T | TA | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(80): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.-112+803dupT | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99424411 | |||||||
chr6:99424626 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(3): Show |
11 | HG01099.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-112+589G>A | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99424626 | |||||||
chr6:99424665 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-112+550A>G | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99424665 | |||||||
chr6:99424836 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-112+379C>T | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99424836 | |||||||
chr6:99425193 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(109): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-112+22T>C | PNISR | ENSG00000132424.17 | transcript | ENST00000369239.10 | protein_coding | 1/11 | chr6 | 99425193 |