Item | Value |
---|---|
geneid | 4846 |
ensemblid | ENSG00000164867.11 |
hgncid | 7876 |
symbol | NOS3 |
name | nitric oxide synthase 3 |
refseq_nuc | NM_000603.5 |
refseq_prot | NP_000594.2 |
ensembl_nuc | ENST00000297494.8 |
ensembl_prot | ENSP00000297494.3 |
mane_status | MANE Select |
chr | chr7 |
start | 150991017 |
end | 151014588 |
strand | + |
ver | v1.2 |
region | chr7:150991017-151014588 |
region5000 | chr7:150986017-151019588 |
regionname0 | NOS3_chr7_150991017_151014588 |
regionname5000 | NOS3_chr7_150986017_151019588 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1203 | 308 | 77 | 50 | 139 | 8 | 33 | 102 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0002 | 1/0 | 1203 | 47 | 3 | 18 | 17 | 3 | 5 | 9 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0003 | 0/0 | 1203 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0004 | 0/0 | 1203 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0005 | 0/0 | 1203 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0006 | 0/0 | 1203 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0007 | 0/0 | 1203 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0008 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0009 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0010 | 0/0 | 1203 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0011 | 0/0 | 241 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(236): Show |
chr7 | 150986017 | 151019588 |
a0012 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0013 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0014 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0015 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0016 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
a0017 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | MGNLK others(1198): Show |
chr7 | 150986017 | 151019588 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3609 | 144 | 35 | 22 | 61 | 7 | 18 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0002 | 0/0 | 3609 | 138 | 29 | 25 | 68 | 1 | 15 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0004 | 0/0 | 3609 | 8 | 0 | 0 | 8 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0005 | 0/0 | 3609 | 6 | 6 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0010 | 0/0 | 3609 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0011 | 0/0 | 3609 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0021 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0022 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0023 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0024 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0027 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0029 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0032 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0001c0033 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0002c0003 | 1/0 | 3609 | 41 | 3 | 17 | 14 | 3 | 3 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0002c0008 | 0/0 | 3609 | 3 | 0 | 0 | 2 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0002c0018 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0002c0030 | 0/0 | 3609 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0002c0034 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0003c0006 | 0/0 | 3609 | 5 | 4 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0003c0014 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0003c0037 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0004c0007 | 0/0 | 3609 | 3 | 1 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0005c0013 | 0/0 | 3609 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0005c0031 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0006c0012 | 0/0 | 3609 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0007c0009 | 0/0 | 3609 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0008c0017 | 0/0 | 3609 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0009c0028 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0010c0025 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0011c0035 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0012c0015 | 0/0 | 3609 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0013c0020 | 0/0 | 3609 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0014c0026 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0015c0016 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0016c0036 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 | ||
a0017c0019 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | ATGGG others(3604): Show |
chr7 | 150986017 | 151019588 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4366 | 140 | 35 | 19 | 61 | 7 | 17 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0001t0002 | 0/0 | 4366 | 3 | 0 | 2 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTT others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0001t0006 | 0/0 | 4366 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0002t0001 | 0/0 | 4366 | 134 | 26 | 25 | 67 | 1 | 15 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0002t0003 | 0/0 | 4366 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0002t0004 | 0/0 | 4390 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4385): Show |
chr7 | 150986017 | 151019588 |
a0001c0002t0007 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0004t0001 | 0/0 | 4366 | 8 | 0 | 0 | 8 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0005t0001 | 0/0 | 4366 | 6 | 6 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0010t0001 | 0/0 | 4366 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0011t0001 | 0/0 | 4366 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0021t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0022t0001 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0023t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0024t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0027t0001 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0029t0001 | 0/0 | 4366 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0032t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0001c0033t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0002c0003t0001 | 1/0 | 4366 | 41 | 3 | 17 | 14 | 3 | 3 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0002c0008t0001 | 0/0 | 4366 | 3 | 0 | 0 | 2 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0002c0018t0001 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0002c0030t0001 | 0/0 | 4366 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0002c0034t0001 | 0/0 | 4366 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0003c0006t0001 | 0/0 | 4366 | 5 | 4 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0003c0014t0005 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0003c0037t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0004c0007t0001 | 0/0 | 4366 | 3 | 1 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0005c0013t0001 | 0/0 | 4366 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0005c0031t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0006c0012t0001 | 0/0 | 4366 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0007c0009t0001 | 0/0 | 4366 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0008c0017t0001 | 0/0 | 4366 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0009c0028t0001 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0010c0025t0001 | 0/0 | 4366 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0011c0035t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0012c0015t0001 | 0/0 | 4366 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0013c0020t0001 | 0/0 | 4366 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0014c0026t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0015c0016t0001 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0016c0036t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
a0017c0019t0001 | 0/0 | 4366 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | AGTTC others(4361): Show |
chr7 | 150986017 | 151019588 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 5 | 1 | 2 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0011 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0001t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0001 | 0/0 | 24 | 1 | 10 | 13 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0002 | 0/0 | 11 | 0 | 3 | 7 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0015 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0002t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0004t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0004t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0005t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0010t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0010t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0011t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0021t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0022t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0023t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0024t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0027t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0029t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0032t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0001c0033t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0006 | 0/0 | 7 | 0 | 4 | 0 | 2 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0008t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0008t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0008t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0018t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0030t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0002c0034t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0006t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0006t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0006t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0006t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0014t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0003c0037t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0004c0007t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0004c0007t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0004c0007t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0005c0013t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0005c0031t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0006c0012t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0007c0009t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0007c0009t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0008c0017t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0009c0028t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0010c0025t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0011c0035t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0012c0015t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0013c0020t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0014c0026t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0015c0016t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0016c0036t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
a0017c0019t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0001 | g0006 | EUR | GBR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | GBR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | GBR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00280 | hp1 | a0008 | c0017 | t0001 | g0003 | EUR | FIN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0176 | EUR | FIN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00423 | hp2 | a0002 | c0003 | t0001 | g0107 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00597 | hp1 | a0001 | c0004 | t0001 | g0135 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00621 | hp1 | a0002 | c0003 | t0001 | g0103 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00639 | hp2 | a0002 | c0003 | t0001 | g0038 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00642 | hp1 | a0002 | c0034 | t0001 | g0111 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00673 | hp1 | a0009 | c0028 | t0001 | g0001 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00733 | hp1 | a0002 | c0003 | t0001 | g0006 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00741 | hp1 | a0002 | c0003 | t0001 | g0066 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01070 | hp1 | a0002 | c0003 | t0001 | g0039 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0039 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01074 | hp1 | a0002 | c0003 | t0001 | g0051 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01081 | hp2 | a0001 | c0011 | t0001 | g0001 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01106 | hp1 | a0002 | c0003 | t0001 | g0016 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01106 | hp2 | a0002 | c0003 | t0001 | g0038 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01109 | hp1 | a0004 | c0007 | t0001 | g0087 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01109 | hp2 | a0001 | c0011 | t0001 | g0001 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01167 | hp1 | a0002 | c0003 | t0001 | g0114 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01167 | hp2 | a0003 | c0006 | t0001 | g0252 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01169 | hp2 | a0002 | c0003 | t0001 | g0113 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01175 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01192 | hp1 | a0002 | c0003 | t0001 | g0006 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01243 | hp1 | a0002 | c0003 | t0001 | g0067 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01256 | hp2 | a0002 | c0003 | t0001 | g0040 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01258 | hp1 | a0002 | c0003 | t0001 | g0040 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01346 | hp1 | a0002 | c0003 | t0001 | g0235 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01361 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01517 | hp1 | a0002 | c0003 | t0001 | g0006 | EUR | IBS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0062 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01891 | hp1 | a0001 | c0005 | t0001 | g0050 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01952 | hp1 | a0004 | c0007 | t0001 | g0088 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01993 | hp1 | a0001 | c0029 | t0001 | g0001 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01993 | hp2 | a0010 | c0025 | t0001 | g0143 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02015 | hp1 | a0002 | c0008 | t0001 | g0106 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02071 | hp1 | a0002 | c0003 | t0001 | g0025 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02074 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0120 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02080 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02129 | hp1 | a0002 | c0003 | t0001 | g0025 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02129 | hp2 | a0006 | c0012 | t0001 | g0021 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02155 | hp1 | a0006 | c0012 | t0001 | g0021 | EAS | CDX | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | CDX | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02165 | hp1 | a0002 | c0003 | t0001 | g0104 | EAS | CDX | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02280 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02572 | hp2 | a0001 | c0032 | t0001 | g0049 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02630 | hp1 | a0003 | c0006 | t0001 | g0251 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02683 | hp2 | a0012 | c0015 | t0001 | g0112 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02698 | hp1 | a0002 | c0030 | t0001 | g0016 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02723 | hp2 | a0001 | c0033 | t0001 | g0083 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0098 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02809 | hp1 | a0001 | c0021 | t0001 | g0182 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02818 | hp1 | a0003 | c0006 | t0001 | g0250 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02886 | hp2 | a0001 | c0005 | t0001 | g0009 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02896 | hp2 | a0001 | c0005 | t0001 | g0009 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02970 | hp2 | a0001 | c0005 | t0001 | g0009 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02976 | hp2 | a0001 | c0010 | t0001 | g0242 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0181 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03041 | hp2 | a0001 | c0010 | t0001 | g0084 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03098 | hp1 | a0002 | c0003 | t0001 | g0195 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03130 | hp2 | a0005 | c0013 | t0001 | g0024 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03139 | hp1 | a0003 | c0006 | t0001 | g0253 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0105 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03453 | hp1 | a0003 | c0037 | t0001 | g0248 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03490 | hp2 | a0002 | c0003 | t0001 | g0117 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03516 | hp2 | a0003 | c0006 | t0001 | g0093 | AFR | ESN | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0241 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03540 | hp2 | a0001 | c0005 | t0001 | g0009 | AFR | GWD | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03579 | hp1 | a0001 | c0023 | t0001 | g0086 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03579 | hp2 | a0004 | c0007 | t0001 | g0054 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0097 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0168 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03831 | hp1 | a0002 | c0008 | t0001 | g0115 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0172 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0006 | SAS | BEB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04204 | hp1 | a0013 | c0020 | t0001 | g0007 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | STU | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18612 | hp1 | a0002 | c0003 | t0001 | g0016 | EAS | CHB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | CHB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18906 | hp1 | a0001 | c0002 | t0007 | g0243 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18943 | hp2 | a0002 | c0008 | t0001 | g0210 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18960 | hp2 | a0002 | c0003 | t0001 | g0100 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18964 | hp2 | a0001 | c0027 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18970 | hp1 | a0001 | c0022 | t0001 | g0220 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18970 | hp2 | a0007 | c0009 | t0001 | g0075 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18973 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18980 | hp2 | a0002 | c0003 | t0001 | g0102 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18984 | hp2 | a0001 | c0002 | t0004 | g0229 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19000 | hp1 | a0002 | c0018 | t0001 | g0073 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19003 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19007 | hp2 | a0002 | c0003 | t0001 | g0108 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19009 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0022 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19043 | hp2 | a0014 | c0026 | t0001 | g0213 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19055 | hp1 | a0002 | c0003 | t0001 | g0095 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19062 | hp2 | a0002 | c0003 | t0001 | g0222 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19064 | hp1 | a0002 | c0003 | t0001 | g0221 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19065 | hp1 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19070 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19084 | hp2 | a0015 | c0016 | t0001 | g0225 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19085 | hp1 | a0007 | c0009 | t0001 | g0003 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19088 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA19240 | hp2 | a0005 | c0013 | t0001 | g0024 | AFR | YRI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20129 | hp1 | a0016 | c0036 | t0001 | g0179 | AFR | ASW | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20129 | hp2 | a0001 | c0002 | t0003 | g0022 | AFR | ASW | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20752 | hp1 | a0002 | c0003 | t0001 | g0237 | EUR | TSI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | GIH | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02109 | hp1 | a0005 | c0031 | t0001 | g0055 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02486 | hp1 | a0002 | c0003 | t0001 | g0056 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02559 | hp1 | a0011 | c0035 | t0001 | g0070 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG03471 | hp2 | a0003 | c0014 | t0005 | g0249 | AFR | MSL | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG06807 | hp1 | a0002 | c0003 | t0001 | g0110 | AFR | USA | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | USA | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | USA | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | USA | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA21309 | hp1 | a0017 | c0019 | t0001 | g0012 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
NA21309 | hp2 | a0001 | c0024 | t0001 | g0085 | AFR | LWK | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0094 | REF | REF | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
homoSapiens | grch38p0 | a0002 | c0003 | t0001 | g0236 | REF | REF | NOS3_chr7_150986017_151019588 | NOS3 | chr7 | 150986017 | 151019588 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:150996468 | G | A | 1 | a0003 | 7 | HG01167.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
missense_variant | MODERATE | c.335G>A | p.Arg112Gln | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/27 | 670/4366 | 335/3612 | 112/1203 | chr7 | 150996468 | |||
chr7:150996479 | G | A | 1 | a0007 | 2 | NA18970.hp2 NA19085.hp1 |
missense_variant | MODERATE | c.346G>A | p.Gly116Ser | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/27 | 681/4366 | 346/3612 | 116/1203 | chr7 | 150996479 | |||
chr7:150996497 | C | G | 1 | a0016 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.364C>G | p.Gln122Glu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/27 | 699/4366 | 364/3612 | 122/1203 | chr7 | 150996497 | |||
chr7:150996809 | G | A | 1 | a0012 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.466G>A | p.Glu156Lys | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/27 | 801/4366 | 466/3612 | 156/1203 | chr7 | 150996809 | |||
chr7:150998588 | C | T | 1 | a0011 | 1 | HG02559.hp1 | stop_gained | HIGH | c.724C>T | p.Arg242* | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/27 | 1059/4366 | 724/3612 | 242/1203 | chr7 | 150998588 | |||
chr7:150998676 | C | A | 1 | a0015 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.812C>A | p.Thr271Asn | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/27 | 1147/4366 | 812/3612 | 271/1203 | chr7 | 150998676 | |||
chr7:150998988 | G | A | 1 | a0008 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.859G>A | p.Asp287Asn | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 8/27 | 1194/4366 | 859/3612 | 287/1203 | chr7 | 150998988 | |||
chr7:150999023 | T | G | 14 | a0001 a0003 a0004 others(11): Show |
332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
missense_variant | MODERATE | c.894T>G | p.Asp298Glu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 8/27 | 1229/4366 | 894/3612 | 298/1203 | chr7 | 150999023 | |||
chr7:151001261 | G | A | 1 | a0017 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1264G>A | p.Ala422Thr | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 11/27 | 1599/4366 | 1264/3612 | 422/1203 | chr7 | 151001261 | |||
chr7:151001264 | G | A | 1 | a0013 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1267G>A | p.Ala423Thr | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 11/27 | 1602/4366 | 1267/3612 | 423/1203 | chr7 | 151001264 | |||
chr7:151001835 | C | T | 1 | a0009 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.1517C>T | p.Ser506Phe | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 13/27 | 1852/4366 | 1517/3612 | 506/1203 | chr7 | 151001835 | |||
chr7:151007158 | G | A | 1 | a0005 | 3 | HG02109.hp1 HG03130.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.1994G>A | p.Arg665His | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/27 | 2329/4366 | 1994/3612 | 665/1203 | chr7 | 151007158 | |||
chr7:151009457 | C | T | 1 | a0006 | 2 | HG02129.hp2 HG02155.hp1 |
missense_variant | MODERATE | c.2384C>T | p.Pro795Leu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/27 | 2719/4366 | 2384/3612 | 795/1203 | chr7 | 151009457 | |||
chr7:151010256 | G | T | 1 | a0004 | 3 | HG01109.hp1 HG01952.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.2654G>T | p.Arg885Met | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 21/27 | 2989/4366 | 2654/3612 | 885/1203 | chr7 | 151010256 | |||
chr7:151013799 | A | G | 1 | a0014 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.3331A>G | p.Met1111Val | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 26/27 | 3666/4366 | 3331/3612 | 1111/1203 | chr7 | 151013799 | |||
chr7:151014140 | C | T | 1 | a0010 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.3583C>T | p.Pro1195Ser | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 27/27 | 3918/4366 | 3583/3612 | 1195/1203 | chr7 | 151014140 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:150993938 | A | G | 1 | a0003c0037 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.135A>G | p.Leu45Leu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/27 | 470/4366 | 135/3612 | 45/1203 | chr7 | 150993938 | |||
chr7:150998638 | T | C | 31 | a0001c0001 a0001c0002 a0001c0005 others(28): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
synonymous_variant | LOW | c.774T>C | p.Asp258Asp | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/27 | 1109/4366 | 774/3612 | 258/1203 | chr7 | 150998638 | |||
chr7:150998978 | C | T | 4 | a0001c0005 a0001c0032 a0005c0013 others(1): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
synonymous_variant | LOW | c.849C>T | p.Asn283Asn | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 8/27 | 1184/4366 | 849/3612 | 283/1203 | chr7 | 150998978 | |||
chr7:150998990 | C | T | 2 | a0003c0006 a0003c0037 |
6 | HG01167.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
synonymous_variant | LOW | c.861C>T | p.Asp287Asp | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 8/27 | 1196/4366 | 861/3612 | 287/1203 | chr7 | 150998990 | |||
chr7:150999023 | T | C | 1 | a0002c0018 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.894T>C | p.Asp298Asp | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 8/27 | 1229/4366 | 894/3612 | 298/1203 | chr7 | 150999023 | |||
chr7:150999286 | C | T | 1 | a0001c0029 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.1053C>T | p.Ala351Ala | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/27 | 1388/4366 | 1053/3612 | 351/1203 | chr7 | 150999286 | |||
chr7:151002235 | C | T | 1 | a0001c0027 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.1683C>T | p.Leu561Leu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/27 | 2018/4366 | 1683/3612 | 561/1203 | chr7 | 151002235 | |||
chr7:151007162 | C | G | 22 | a0001c0002 a0001c0005 a0001c0010 others(19): Show |
174 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
synonymous_variant | LOW | c.1998C>G | p.Ala666Ala | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/27 | 2333/4366 | 1998/3612 | 666/1203 | chr7 | 151007162 | |||
chr7:151009425 | C | T | 1 | a0002c0030 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.2352C>T | p.Asp784Asp | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/27 | 2687/4366 | 2352/3612 | 784/1203 | chr7 | 151009425 | |||
chr7:151009533 | G | A | 1 | a0001c0023 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.2460G>A | p.Pro820Pro | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/27 | 2795/4366 | 2460/3612 | 820/1203 | chr7 | 151009533 | |||
chr7:151010224 | G | A | 1 | a0001c0024 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.2622G>A | p.Leu874Leu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 21/27 | 2957/4366 | 2622/3612 | 874/1203 | chr7 | 151010224 | |||
chr7:151012396 | C | T | 1 | a0001c0022 | 1 | NA18970.hp1 | synonymous_variant | LOW | c.3030C>T | p.Ile1010Ile | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/27 | 3365/4366 | 3030/3612 | 1010/1203 | chr7 | 151012396 | |||
chr7:151013819 | T | C | 5 | a0001c0005 a0001c0010 a0001c0021 others(2): Show |
14 | HG01109.hp1 HG01891.hp1 HG01952.hp1 others(11): Show |
synonymous_variant | LOW | c.3351T>C | p.Val1117Val | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 26/27 | 3686/4366 | 3351/3612 | 1117/1203 | chr7 | 151013819 | |||
chr7:151013882 | G | A | 1 | a0001c0011 | 2 | HG01081.hp2 HG01109.hp2 |
synonymous_variant | LOW | c.3414G>A | p.Glu1138Glu | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 26/27 | 3749/4366 | 3414/3612 | 1138/1203 | chr7 | 151013882 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:150991021 | C | T | 1 | a0001c0001t0002 | 3 | HG01069.hp2 HG01071.hp1 HG04204.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-331C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/27 | chr7 | 150991021 | |||||||
chr7:150991038 | G | A | 1 | a0001c0002t0003 | 2 | NA19030.hp1 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-314G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/27 | 2766 | chr7 | 150991038 | ||||||
chr7:150991088 | A | C | 1 | a0001c0002t0007 | 1 | NA18906.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-264A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/27 | chr7 | 150991088 | |||||||
chr7:150991148 | G | GAGAGGAT others(17): Show |
1 | a0001c0002t0004 | 1 | NA18984.hp2 | 5_prime_UTR_variant | MODIFIER | c.-203_-180dupAGAGGA others(18): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/27 | 2631 | INFO_REALIGN_3_PRIME | chr7 | 150991148 | |||||
chr7:151014198 | G | A | 1 | a0003c0014t0005 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*29G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 27/27 | 29 | chr7 | 151014198 | ||||||
chr7:151014417 | C | G | 1 | a0001c0001t0006 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*248C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 27/27 | 248 | chr7 | 151014417 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:150991391 | G | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+91G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991391 | |||||||
chr7:150991428 | C | T | 6 | a0003c0006t0001g0250 a0003c0006t0001g0251 a0003c0006t0001g0252 others(3): Show |
6 | HG01167.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+128C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991428 | |||||||
chr7:150991587 | G | A | 2 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+287G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991587 | |||||||
chr7:150991679 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-52+379C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991679 | |||||||
chr7:150991857 | G | A | 3 | a0001c0005t0001g0009 a0001c0005t0001g0050 a0001c0032t0001g0049 |
7 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+557G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991857 | |||||||
chr7:150991928 | G | A | 1 | a0002c0003t0001g0051 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-52+628G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150991928 | |||||||
chr7:150991996 | C | CA | 13 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0068 others(10): Show |
14 | HG00741.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52+711dupA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr7 | 150991996 | ||||||
chr7:150991996 | CA | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
9 | HG00323.hp2 HG01243.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+711delA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr7 | 150991996 | ||||||
chr7:150992012 | T | A | 7 | a0001c0001t0001g0057 a0001c0002t0001g0052 a0001c0002t0001g0053 others(4): Show |
7 | HG02109.hp1 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+712T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992012 | |||||||
chr7:150992038 | G | T | 3 | a0001c0002t0001g0241 a0001c0002t0007g0243 a0001c0010t0001g0242 |
3 | HG02976.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-52+738G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992038 | |||||||
chr7:150992147 | T | A | 1 | a0001c0002t0001g0023 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-52+847T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992147 | |||||||
chr7:150992147 | T | TA | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.-52+861dupA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr7 | 150992147 | ||||||
chr7:150992147 | T | TAA | 15 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0072 others(12): Show |
16 | HG00735.hp1 HG01517.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.-52+860_-52+861dup others(2): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr7 | 150992147 | ||||||
chr7:150992309 | A | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.-52+1009A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992309 | |||||||
chr7:150992338 | A | T | 2 | a0001c0002t0001g0244 a0003c0006t0001g0093 |
2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-52+1038A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992338 | |||||||
chr7:150992405 | T | G | 1 | a0002c0003t0001g0095 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-52+1105T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992405 | |||||||
chr7:150992612 | C | T | 1 | a0001c0002t0001g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-51-1141C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992612 | |||||||
chr7:150992682 | C | T | 3 | a0001c0005t0001g0009 a0001c0005t0001g0050 a0001c0032t0001g0049 |
7 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51-1071C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992682 | |||||||
chr7:150992694 | T | C | 3 | a0001c0005t0001g0009 a0001c0005t0001g0050 a0001c0032t0001g0049 |
7 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51-1059T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992694 | |||||||
chr7:150992772 | G | C | 1 | a0001c0002t0001g0224 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-51-981G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992772 | |||||||
chr7:150992802 | G | A | 1 | a0002c0003t0001g0051 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-51-951G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992802 | |||||||
chr7:150992844 | C | G | 2 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-909C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992844 | |||||||
chr7:150992855 | G | A | 224 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.-51-898G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992855 | |||||||
chr7:150992882 | C | T | 7 | a0001c0001t0001g0057 a0001c0002t0001g0052 a0001c0002t0001g0053 others(4): Show |
7 | HG02109.hp1 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51-871C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992882 | |||||||
chr7:150992991 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.-51-762C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150992991 | |||||||
chr7:150993037 | C | T | 2 | a0002c0003t0001g0221 a0002c0003t0001g0222 |
2 | NA19062.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-51-716C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993037 | |||||||
chr7:150993045 | G | A | 4 | a0001c0002t0001g0065 a0001c0002t0001g0071 a0001c0002t0001g0097 others(1): Show |
4 | HG02683.hp1 HG02735.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-708G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993045 | |||||||
chr7:150993088 | C | T | 4 | a0002c0003t0001g0040 a0002c0003t0001g0051 a0002c0003t0001g0237 others(1): Show |
5 | HG01074.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-665C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993088 | |||||||
chr7:150993135 | GGGTTCCA others(23): Show |
G | 1 | a0015c0016t0001g0225 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-51-615_-51-586del others(30): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr7 | 150993135 | ||||||
chr7:150993141 | C | T | 1 | a0003c0006t0001g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-51-612C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993141 | |||||||
chr7:150993198 | A | G | 3 | a0001c0023t0001g0086 a0004c0007t0001g0087 a0004c0007t0001g0088 |
3 | HG01109.hp1 HG01952.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-51-555A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993198 | |||||||
chr7:150993204 | T | A | 3 | a0001c0023t0001g0086 a0004c0007t0001g0087 a0004c0007t0001g0088 |
3 | HG01109.hp1 HG01952.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-51-549T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993204 | |||||||
chr7:150993431 | G | A | 1 | a0001c0002t0003g0022 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-51-322G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993431 | |||||||
chr7:150993562 | A | C | 8 | a0001c0002t0001g0014 a0001c0002t0001g0214 a0001c0002t0001g0215 others(5): Show |
11 | HG02080.hp2 HG02155.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51-191A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993562 | |||||||
chr7:150993597 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-51-156A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993597 | |||||||
chr7:150993666 | G | A | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-51-87G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993666 | |||||||
chr7:150993751 | A | G | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.-51-2A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993751 | |||||||
chr7:150993752 | G | T | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.-51-1G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 1/26 | chr7 | 150993752 | |||||||
chr7:150994085 | C | T | 9 | a0001c0001t0001g0057 a0001c0002t0001g0052 a0001c0002t0001g0053 others(6): Show |
9 | HG02109.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.158+124C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994085 | |||||||
chr7:150994330 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.158+369G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994330 | |||||||
chr7:150994344 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.158+383C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994344 | |||||||
chr7:150994386 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.158+425G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994386 | |||||||
chr7:150994547 | A | G | 1 | a0001c0002t0001g0211 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.158+586A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994547 | |||||||
chr7:150994571 | G | C | 4 | a0001c0002t0001g0065 a0001c0002t0001g0071 a0001c0002t0001g0097 others(1): Show |
4 | HG02683.hp1 HG02735.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+610G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994571 | |||||||
chr7:150994810 | C | T | 1 | a0002c0008t0001g0210 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.159-393C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150994810 | |||||||
chr7:150995049 | C | T | 3 | a0001c0023t0001g0086 a0004c0007t0001g0087 a0004c0007t0001g0088 |
3 | HG01109.hp1 HG01952.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.159-154C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150995049 | |||||||
chr7:150995098 | G | T | 4 | a0001c0005t0001g0009 a0001c0005t0001g0050 a0001c0032t0001g0049 others(1): Show |
8 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.159-105G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150995098 | |||||||
chr7:150995135 | G | A | 1 | a0002c0003t0001g0237 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.159-68G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 2/26 | chr7 | 150995135 | |||||||
chr7:150995356 | G | A | 20 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(17): Show |
37 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.270+42G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995356 | |||||||
chr7:150995451 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.270+137A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995451 | |||||||
chr7:150995535 | C | T | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.270+221C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995535 | |||||||
chr7:150995583 | T | C | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+269T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995583 | |||||||
chr7:150995584 | C | T | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+270C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995584 | |||||||
chr7:150995593 | C | CCCCATCC others(190): Show |
1 | a0002c0003t0001g0095 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.270+282_270+283ins others(197): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(330): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0072 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(305): Show |
1 | a0002c0003t0001g0100 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(312): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(304): Show |
19 | a0001c0001t0001g0109 a0002c0003t0001g0016 a0002c0003t0001g0025 others(16): Show |
21 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(311): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(597): Show |
1 | a0002c0003t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(604): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(565): Show |
1 | a0002c0003t0001g0113 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(572): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(362): Show |
1 | a0002c0008t0001g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(369): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
3 | a0001c0001t0001g0118 a0001c0002t0001g0116 a0002c0003t0001g0117 |
3 | HG03490.hp2 NA18959.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
1 | a0001c0001t0001g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
14 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(11): Show |
14 | HG01243.hp2 HG02055.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
5 | a0003c0006t0001g0093 a0003c0006t0001g0250 a0003c0006t0001g0251 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(393): Show |
1 | a0001c0002t0001g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(400): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
15 | a0001c0001t0001g0004 a0001c0001t0001g0121 a0001c0002t0001g0062 others(12): Show |
26 | HG01109.hp1 HG01167.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
2 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
3 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 |
3 | HG02451.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
1 | a0001c0002t0001g0244 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
9 | a0001c0001t0001g0057 a0001c0002t0001g0052 a0001c0002t0001g0058 others(6): Show |
9 | HG02109.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(879): Show |
1 | a0001c0024t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(886): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(230): Show |
1 | a0001c0002t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(237): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(164): Show |
1 | a0014c0026t0001g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(171): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(389): Show |
1 | a0001c0001t0001g0060 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(396): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(462): Show |
1 | a0001c0001t0001g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(469): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(332): Show |
1 | a0001c0002t0001g0124 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(339): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(331): Show |
1 | a0001c0002t0001g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(338): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(331): Show |
1 | a0001c0001t0001g0125 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(338): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(457): Show |
1 | a0002c0018t0001g0073 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(464): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
1 | a0001c0002t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(305): Show |
2 | a0001c0002t0001g0127 a0001c0002t0001g0128 |
2 | HG03669.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.270+283_270+284ins others(312): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(355): Show |
1 | a0002c0003t0001g0038 | 2 | HG00639.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.270+283_270+284ins others(362): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(305): Show |
1 | a0001c0001t0001g0074 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(312): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(305): Show |
4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG00544.hp2 HG02717.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(312): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(305): Show |
1 | a0001c0002t0001g0215 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(312): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(362): Show |
2 | a0001c0001t0001g0245 a0001c0002t0001g0017 |
4 | HG01978.hp1 HG03195.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(369): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(330): Show |
92 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(89): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(821): Show |
1 | a0001c0002t0001g0133 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(828): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(263): Show |
1 | a0001c0001t0001g0178 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(270): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(331): Show |
1 | a0016c0036t0001g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(338): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(331): Show |
2 | a0001c0001t0001g0180 a0001c0001t0001g0239 |
2 | HG02300.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.270+283_270+284ins others(338): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(542): Show |
1 | a0001c0002t0001g0181 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(549): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(354): Show |
3 | a0002c0003t0001g0040 a0002c0003t0001g0237 a0011c0035t0001g0070 |
4 | HG01256.hp2 HG01258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(361): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(330): Show |
4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(328): Show |
1 | a0001c0002t0001g0219 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(335): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
1 | a0001c0002t0001g0186 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(429): Show |
3 | a0001c0001t0001g0188 a0001c0002t0001g0187 a0001c0002t0001g0189 |
3 | NA18945.hp2 NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.270+283_270+284ins others(436): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(330): Show |
1 | a0001c0001t0001g0190 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(394): Show |
1 | a0001c0001t0001g0191 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(401): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(362): Show |
1 | a0001c0001t0001g0192 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(369): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(428): Show |
1 | a0001c0002t0001g0193 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(435): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(297): Show |
1 | a0001c0001t0001g0205 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(304): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(330): Show |
17 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0032 others(14): Show |
28 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(355): Show |
1 | a0001c0022t0001g0220 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(362): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(329): Show |
1 | a0001c0001t0001g0240 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCATC others(330): Show |
2 | a0001c0001t0001g0035 a0001c0001t0001g0080 |
3 | HG01257.hp1 HG01258.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.270+283_270+284ins others(337): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCCAT others(598): Show |
1 | a0001c0001t0001g0206 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.270+284_270+285ins others(605): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCCAT others(331): Show |
2 | a0001c0001t0001g0081 a0001c0001t0001g0096 |
2 | HG00738.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.270+284_270+285ins others(338): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | CCCCCCAT others(298): Show |
1 | a0001c0001t0001g0207 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.270+284_270+285ins others(305): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995593 | C | T | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+279C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995593 | |||||||
chr7:150995593 | CCCCCCGT others(26): Show |
C | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+284_270+316del others(33): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995593 | ||||||
chr7:150995594 | C | CCCCATCC others(564): Show |
1 | a0002c0003t0001g0114 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.270+283_270+284ins others(571): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995594 | ||||||
chr7:150995594 | C | CCCCATCC others(329): Show |
1 | a0001c0001t0001g0177 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.270+283_270+284ins others(336): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995594 | ||||||
chr7:150995594 | CCCCCGTC others(25): Show |
C | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+285_270+316del others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995594 | ||||||
chr7:150995599 | G | C | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+285G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995599 | |||||||
chr7:150995600 | T | A | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+286T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995600 | |||||||
chr7:150995607 | C | CCCCCCCT others(12): Show |
1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+294_270+295ins others(19): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995607 | ||||||
chr7:150995610 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+296G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995610 | |||||||
chr7:150995611 | C | A | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+297C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995611 | |||||||
chr7:150995613 | T | C | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+299T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995613 | |||||||
chr7:150995614 | T | C | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+300T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995614 | |||||||
chr7:150995630 | C | T | 1 | a0001c0002t0001g0189 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.270+316C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995630 | |||||||
chr7:150995631 | A | G | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+317A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995631 | |||||||
chr7:150995634 | T | C | 21 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(18): Show |
38 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+320T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995634 | |||||||
chr7:150995642 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+328G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995642 | |||||||
chr7:150995643 | C | A | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+329C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995643 | |||||||
chr7:150995647 | CCT | C | 42 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(39): Show |
44 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.270+336_270+337del others(2): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995647 | ||||||
chr7:150995649 | T | A | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+335T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995649 | |||||||
chr7:150995649 | TCTTC | T | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+337_270+340del others(4): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995649 | ||||||
chr7:150995651 | T | C | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+337T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995651 | |||||||
chr7:150995656 | T | C | 20 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(17): Show |
37 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.270+342T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995656 | |||||||
chr7:150995657 | C | A | 20 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(17): Show |
37 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.270+343C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995657 | |||||||
chr7:150995657 | C | G | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+343C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995657 | |||||||
chr7:150995658 | T | TCCCACCC others(122): Show |
1 | a0002c0034t0001g0111 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.270+375_270+503dup others(129): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995658 | ||||||
chr7:150995665 | C | T | 21 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(18): Show |
38 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+351C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995665 | |||||||
chr7:150995668 | G | A | 21 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(18): Show |
38 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+354G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995668 | |||||||
chr7:150995669 | C | A | 21 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(18): Show |
38 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+355C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995669 | |||||||
chr7:150995673 | C | T | 1 | a0003c0006t0001g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.270+359C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995673 | |||||||
chr7:150995683 | C | G | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+369C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995683 | |||||||
chr7:150995684 | T | TC | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+374dupC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995684 | ||||||
chr7:150995688 | CGTCCCAC others(22): Show |
C | 1 | a0001c0002t0001g0036 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+375_270+403del others(29): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995688 | |||||||
chr7:150995689 | G | C | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+375G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995689 | |||||||
chr7:150995692 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+378C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995692 | |||||||
chr7:150995693 | C | A | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+379C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995693 | |||||||
chr7:150995695 | C | A | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+381C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995695 | |||||||
chr7:150995698 | T | C | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+384T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995698 | |||||||
chr7:150995699 | G | T | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+385G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995699 | |||||||
chr7:150995700 | C | A | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+386C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995700 | |||||||
chr7:150995701 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.270+387A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995701 | |||||||
chr7:150995702 | C | A | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+388C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995702 | |||||||
chr7:150995703 | T | C | 20 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(17): Show |
36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+389T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995703 | |||||||
chr7:150995704 | C | A | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+390C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995704 | |||||||
chr7:150995707 | G | A | 18 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(15): Show |
34 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+393G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995707 | |||||||
chr7:150995707 | G | C | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+393G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995707 | |||||||
chr7:150995707 | G | T | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+393G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995707 | |||||||
chr7:150995708 | C | A | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+394C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995708 | |||||||
chr7:150995708 | CCCT | C | 17 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(14): Show |
33 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.270+396_270+398del others(3): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995708 | ||||||
chr7:150995709 | C | T | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+395C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995709 | |||||||
chr7:150995711 | T | C | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+397T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995711 | |||||||
chr7:150995713 | T | C | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.270+399T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995713 | |||||||
chr7:150995715 | CA | C | 18 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(15): Show |
34 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+402delA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995715 | |||||||
chr7:150995717 | G | C | 18 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(15): Show |
34 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+403G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995717 | |||||||
chr7:150995718 | C | T | 18 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(15): Show |
34 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+404C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995718 | |||||||
chr7:150995719 | G | A | 18 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(15): Show |
19 | HG01243.hp2 HG02055.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.270+405G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995719 | |||||||
chr7:150995723 | CA | C | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+410delA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995723 | |||||||
chr7:150995727 | C | T | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
35 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+413C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995727 | |||||||
chr7:150995730 | A | G | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+416A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995730 | |||||||
chr7:150995731 | C | A | 20 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(17): Show |
37 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.270+417C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995731 | |||||||
chr7:150995732 | A | ACCCCTCC others(27): Show |
1 | a0001c0002t0001g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.270+438_270+471dup others(34): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995732 | ||||||
chr7:150995736 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+422C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995736 | |||||||
chr7:150995737 | T | A | 1 | a0001c0002t0001g0036 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+423T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995737 | |||||||
chr7:150995745 | C | G | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+431C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995745 | |||||||
chr7:150995747 | G | C | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+433G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995747 | |||||||
chr7:150995749 | C | T | 11 | a0001c0001t0001g0057 a0001c0002t0001g0047 a0001c0002t0001g0048 others(8): Show |
12 | HG02109.hp1 HG02486.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.270+435C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995749 | |||||||
chr7:150995751 | CAT | C | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+438_270+439del others(2): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995751 | |||||||
chr7:150995752 | A | G | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+438A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995752 | |||||||
chr7:150995753 | T | G | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+439T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995753 | |||||||
chr7:150995754 | T | C | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+440T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995754 | |||||||
chr7:150995756 | C | T | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+442C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995756 | |||||||
chr7:150995757 | A | C | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+443A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995757 | |||||||
chr7:150995757 | ACCCCTGC | A | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+444_270+450del others(7): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995757 | |||||||
chr7:150995759 | C | G | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+445C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995759 | |||||||
chr7:150995760 | C | T | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+446C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995760 | |||||||
chr7:150995763 | G | A | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+449G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995763 | |||||||
chr7:150995764 | C | A | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+450C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995764 | |||||||
chr7:150995764 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+450C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995764 | |||||||
chr7:150995766 | C | A | 19 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(16): Show |
36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+452C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995766 | |||||||
chr7:150995766 | CCCCCTCC others(26): Show |
C | 1 | a0001c0001t0001g0007 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.270+467_270+499del others(33): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995766 | ||||||
chr7:150995768 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+454C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995768 | |||||||
chr7:150995770 | C | T | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+456C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995770 | |||||||
chr7:150995771 | T | C | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+457T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995771 | |||||||
chr7:150995779 | C | G | 1 | a0001c0002t0001g0036 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+465C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995779 | |||||||
chr7:150995780 | TG | T | 18 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(15): Show |
34 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+467delG | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995780 | |||||||
chr7:150995781 | G | C | 3 | a0001c0001t0001g0031 a0001c0002t0001g0208 a0001c0002t0001g0227 |
4 | HG02015.hp2 HG03834.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+467G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995781 | |||||||
chr7:150995786 | G | A | 21 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(18): Show |
37 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.270+472G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995786 | |||||||
chr7:150995787 | A | ACCCACCC others(794): Show |
3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | HG02258.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.270+534_270+535ins others(801): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995787 | ||||||
chr7:150995787 | A | ACCCACCC others(126): Show |
7 | a0001c0002t0001g0034 a0001c0002t0001g0122 a0001c0002t0001g0202 others(4): Show |
8 | HG02615.hp2 HG02622.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.270+485_270+486ins others(133): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995787 | ||||||
chr7:150995787 | A | ACCCACCC others(125): Show |
7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG01243.hp2 HG02683.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+485_270+486ins others(132): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995787 | ||||||
chr7:150995787 | A | T | 23 | a0001c0001t0001g0031 a0001c0001t0001g0226 a0001c0001t0001g0233 others(20): Show |
41 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.270+473A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995787 | |||||||
chr7:150995787 | ACCCACCC others(26): Show |
A | 2 | a0001c0001t0001g0201 a0001c0002t0001g0203 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.270+486_270+518del others(33): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995787 | ||||||
chr7:150995789 | C | A | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+475C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995789 | |||||||
chr7:150995791 | A | C | 1 | a0001c0002t0001g0036 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+477A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995791 | |||||||
chr7:150995794 | C | T | 1 | a0001c0002t0001g0036 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+480C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995794 | |||||||
chr7:150995797 | G | A | 2 | a0001c0002t0001g0030 a0001c0002t0001g0036 |
4 | HG00639.hp1 HG01099.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+483G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995797 | |||||||
chr7:150995798 | C | A | 1 | a0001c0002t0001g0036 | 2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.270+484C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995798 | |||||||
chr7:150995800 | C | T | 3 | a0001c0001t0001g0044 a0001c0002t0001g0045 a0001c0002t0001g0046 |
3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.270+486C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995800 | |||||||
chr7:150995814 | C | G | 3 | a0001c0001t0001g0044 a0001c0002t0001g0045 a0001c0002t0001g0046 |
3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.270+500C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995814 | |||||||
chr7:150995818 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270+504C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995818 | |||||||
chr7:150995819 | G | A | 3 | a0001c0002t0001g0030 a0001c0002t0001g0036 a0001c0002t0001g0208 |
5 | HG00639.hp1 HG01099.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+505G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995819 | |||||||
chr7:150995819 | G | GTCCCACC others(92): Show |
3 | a0001c0001t0001g0044 a0001c0002t0001g0045 a0001c0002t0001g0046 |
3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.270+515_270+516ins others(99): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995819 | ||||||
chr7:150995822 | C | T | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+508C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995822 | |||||||
chr7:150995825 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+511C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995825 | |||||||
chr7:150995833 | T | C | 5 | a0001c0001t0001g0044 a0001c0002t0001g0036 a0001c0002t0001g0045 others(2): Show |
6 | HG00639.hp1 HG01099.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.270+519T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995833 | |||||||
chr7:150995847 | G | C | 4 | a0001c0001t0001g0044 a0001c0002t0001g0036 a0001c0002t0001g0045 others(1): Show |
5 | HG00639.hp1 HG01099.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+533G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995847 | |||||||
chr7:150995852 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.270+538G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995852 | |||||||
chr7:150995863 | A | ACACCCCT others(472): Show |
1 | a0003c0037t0001g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-488_271-487ins others(479): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995863 | ||||||
chr7:150995863 | A | ACACCCCT others(25): Show |
4 | a0003c0006t0001g0093 a0003c0006t0001g0250 a0003c0006t0001g0251 others(1): Show |
4 | HG02630.hp1 HG02818.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-521_271-520ins others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995863 | ||||||
chr7:150995863 | A | G | 4 | a0001c0001t0001g0044 a0001c0002t0001g0036 a0001c0002t0001g0045 others(1): Show |
5 | HG00639.hp1 HG01099.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-541A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995863 | |||||||
chr7:150995866 | C | T | 4 | a0001c0001t0001g0044 a0001c0002t0001g0036 a0001c0002t0001g0045 others(1): Show |
5 | HG00639.hp1 HG01099.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-538C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995866 | |||||||
chr7:150995880 | C | G | 3 | a0001c0001t0001g0044 a0001c0002t0001g0045 a0001c0002t0001g0046 |
3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.271-524C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995880 | |||||||
chr7:150995885 | A | G | 3 | a0001c0001t0001g0044 a0001c0002t0001g0045 a0001c0002t0001g0046 |
3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.271-519A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995885 | |||||||
chr7:150995891 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.271-513C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995891 | |||||||
chr7:150995896 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.271-508A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995896 | |||||||
chr7:150995897 | A | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0226 a0001c0002t0001g0045 others(1): Show |
4 | HG02055.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-507A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995897 | |||||||
chr7:150995903 | T | C | 1 | a0015c0016t0001g0225 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.271-501T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995903 | |||||||
chr7:150995904 | C | T | 1 | a0015c0016t0001g0225 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.271-500C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995904 | |||||||
chr7:150995913 | C | CCCCGTCC others(89): Show |
4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-488_271-487ins others(96): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995913 | ||||||
chr7:150995916 | CT | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG01243.hp2 HG02683.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-487delT | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995916 | |||||||
chr7:150995917 | T | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0226 a0001c0002t0001g0045 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-487T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995917 | |||||||
chr7:150995917 | T | TGTCCCAT others(25): Show |
1 | a0001c0001t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.271-437_271-406dup others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995917 | ||||||
chr7:150995917 | TGTCCCAT others(25): Show |
T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0209 |
2 | HG00140.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.271-437_271-406del others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995917 | ||||||
chr7:150995918 | G | A | 3 | a0001c0001t0001g0044 a0001c0002t0001g0045 a0001c0002t0001g0046 |
3 | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.271-486G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995918 | |||||||
chr7:150995919 | T | A | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-485T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995919 | |||||||
chr7:150995924 | T | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0226 a0001c0002t0001g0045 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-480T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995924 | |||||||
chr7:150995929 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0226 a0001c0002t0001g0045 others(1): Show |
4 | HG02055.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-475G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995929 | |||||||
chr7:150995930 | C | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0226 a0001c0002t0001g0045 others(1): Show |
4 | HG02055.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-474C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995930 | |||||||
chr7:150995930 | C | CACCCCTC others(126): Show |
7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG01243.hp2 HG02683.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-470_271-469ins others(133): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995930 | ||||||
chr7:150995930 | C | T | 1 | a0001c0002t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.271-474C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995930 | |||||||
chr7:150995935 | T | C | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
15 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-469T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995935 | |||||||
chr7:150995956 | T | C | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-448T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995956 | |||||||
chr7:150995964 | C | T | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-440C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995964 | |||||||
chr7:150995965 | C | T | 63 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
86 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.271-439C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995965 | |||||||
chr7:150995967 | T | C | 67 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(64): Show |
90 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.271-437T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995967 | |||||||
chr7:150995969 | C | A | 63 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
86 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.271-435C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995969 | |||||||
chr7:150995972 | C | A | 22 | a0001c0001t0001g0233 a0001c0002t0001g0002 a0001c0002t0001g0015 others(19): Show |
43 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-432C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995972 | |||||||
chr7:150995977 | T | TC | 64 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(61): Show |
87 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.271-423dupC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995977 | ||||||
chr7:150995977 | T | TG | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-427_271-426ins others(1): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995977 | |||||||
chr7:150995978 | CCCCGTCC others(92): Show |
C | 1 | a0001c0002t0001g0228 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.271-422_271-324del others(99): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995978 | ||||||
chr7:150995981 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.271-423C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995981 | |||||||
chr7:150995982 | G | C | 1 | a0001c0001t0001g0177 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.271-422G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995982 | |||||||
chr7:150995988 | T | C | 5 | a0001c0001t0001g0177 a0001c0002t0001g0089 a0001c0002t0001g0090 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-416T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995988 | |||||||
chr7:150995988 | T | TCCCTGCA others(27): Show |
1 | a0002c0034t0001g0111 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.271-392_271-359dup others(34): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150995988 | ||||||
chr7:150995993 | G | A | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-411G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995993 | |||||||
chr7:150995997 | C | T | 4 | a0001c0001t0001g0226 a0001c0002t0001g0061 a0001c0002t0001g0062 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-407C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150995997 | |||||||
chr7:150996001 | C | A | 4 | a0001c0001t0001g0226 a0001c0002t0001g0061 a0001c0002t0001g0062 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-403C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996001 | |||||||
chr7:150996004 | C | A | 4 | a0001c0001t0001g0226 a0001c0002t0001g0061 a0001c0002t0001g0062 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-400C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996004 | |||||||
chr7:150996009 | TG | T | 4 | a0001c0001t0001g0226 a0001c0002t0001g0061 a0001c0002t0001g0062 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-394delG | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996009 | |||||||
chr7:150996009 | TGC | T | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-394_271-393del others(2): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996009 | |||||||
chr7:150996012 | T | C | 8 | a0001c0001t0001g0226 a0001c0002t0001g0061 a0001c0002t0001g0062 others(5): Show |
8 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-392T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996012 | |||||||
chr7:150996012 | TCCCATCC others(59): Show |
T | 23 | a0001c0001t0001g0031 a0001c0001t0001g0233 a0001c0002t0001g0002 others(20): Show |
44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.271-346_271-281del others(66): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996012 | ||||||
chr7:150996016 | A | G | 4 | a0001c0001t0001g0226 a0001c0002t0001g0061 a0001c0002t0001g0062 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-388A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996016 | |||||||
chr7:150996022 | C | T | 4 | a0001c0001t0001g0226 a0001c0002t0001g0061 a0001c0002t0001g0062 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-382C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996022 | |||||||
chr7:150996033 | C | T | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-371C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996033 | |||||||
chr7:150996045 | CCCCTACC others(25): Show |
C | 4 | a0001c0001t0001g0226 a0001c0002t0001g0061 a0001c0002t0001g0062 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-355_271-324del others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996045 | ||||||
chr7:150996049 | T | C | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-355T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996049 | |||||||
chr7:150996050 | A | G | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-354A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996050 | |||||||
chr7:150996051 | C | T | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-353C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996051 | |||||||
chr7:150996056 | C | CGCCTGTA others(91): Show |
4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-348_271-347ins others(98): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996056 | |||||||
chr7:150996058 | T | C | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-346T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996058 | |||||||
chr7:150996074 | T | C | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-330T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996074 | |||||||
chr7:150996077 | T | TGC | 4 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-327_271-326ins others(2): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996077 | |||||||
chr7:150996078 | C | T | 8 | a0001c0001t0001g0226 a0001c0002t0001g0061 a0001c0002t0001g0062 others(5): Show |
8 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-326C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996078 | |||||||
chr7:150996082 | A | G | 1 | a0001c0002t0001g0228 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.271-322A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996082 | |||||||
chr7:150996088 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.271-316C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996088 | |||||||
chr7:150996124 | C | CCTGCACC others(188): Show |
1 | a0002c0003t0001g0095 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.271-265_271-264ins others(195): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996124 | ||||||
chr7:150996124 | C | CCTGCACC others(191): Show |
4 | a0002c0003t0001g0101 a0002c0003t0001g0102 a0002c0003t0001g0103 others(1): Show |
4 | HG00621.hp1 HG02074.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-265_271-264ins others(198): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996124 | ||||||
chr7:150996195 | C | T | 1 | a0002c0003t0001g0110 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.271-209C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996195 | |||||||
chr7:150996197 | C | T | 1 | a0001c0002t0001g0234 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.271-207C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996197 | |||||||
chr7:150996242 | ACCCATCC others(26): Show |
A | 1 | a0001c0004t0001g0135 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.271-150_271-118del others(33): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996242 | ||||||
chr7:150996248 | C | G | 1 | a0002c0003t0001g0040 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.271-156C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996248 | |||||||
chr7:150996267 | TC | T | 3 | a0001c0002t0001g0134 a0002c0003t0001g0095 a0015c0016t0001g0225 |
3 | HG03669.hp1 NA19055.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.271-134delC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | 150996267 | ||||||
chr7:150996342 | C | G | 12 | a0001c0001t0001g0057 a0001c0002t0001g0052 a0001c0002t0001g0053 others(9): Show |
12 | HG02486.hp1 HG02647.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-62C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | chr7 | 150996342 | |||||||
chr7:150996595 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.419+43G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/26 | chr7 | 150996595 | |||||||
chr7:150996597 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.419+45C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/26 | chr7 | 150996597 | |||||||
chr7:150996614 | C | T | 1 | a0001c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.419+62C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/26 | chr7 | 150996614 | |||||||
chr7:150996746 | A | G | 3 | a0001c0002t0001g0241 a0001c0002t0007g0243 a0001c0010t0001g0242 |
3 | HG02976.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.420-17A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 4/26 | chr7 | 150996746 | |||||||
chr7:150997141 | T | G | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.582+216T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997141 | |||||||
chr7:150997169 | A | AGAAGTCT others(20): Show |
5 | a0001c0002t0001g0034 a0001c0002t0001g0122 a0001c0002t0001g0202 others(2): Show |
6 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.582+317_582+343dup others(27): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr7 | 150997169 | ||||||
chr7:150997169 | AGAAGTCT others(20): Show |
A | 49 | a0001c0001t0001g0057 a0001c0001t0001g0226 a0001c0001t0001g0233 others(46): Show |
67 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.582+317_582+343del others(27): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr7 | 150997169 | ||||||
chr7:150997242 | A | G | 2 | a0001c0001t0001g0200 a0015c0016t0001g0225 |
2 | HG00408.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.582+317A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997242 | |||||||
chr7:150997269 | GGGGGTGA others(19): Show |
G | 1 | a0015c0016t0001g0225 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.582+349_582+374del others(26): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr7 | 150997269 | ||||||
chr7:150997334 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18952.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.582+409G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997334 | |||||||
chr7:150997351 | C | G | 1 | a0001c0002t0001g0176 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.582+426C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997351 | |||||||
chr7:150997450 | A | AC | 15 | a0001c0001t0001g0078 a0001c0001t0001g0096 a0001c0001t0001g0119 others(12): Show |
15 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.582+529dupC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr7 | 150997450 | ||||||
chr7:150997474 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.582+549G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997474 | |||||||
chr7:150997502 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.582+577A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997502 | |||||||
chr7:150997518 | A | G | 74 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(71): Show |
98 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.582+593A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997518 | |||||||
chr7:150997583 | C | G | 1 | a0001c0002t0001g0181 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.582+658C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997583 | |||||||
chr7:150997807 | C | T | 2 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.583-550C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997807 | |||||||
chr7:150997820 | G | A | 1 | a0001c0002t0004g0229 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.583-537G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997820 | |||||||
chr7:150997975 | A | T | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.583-382A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997975 | |||||||
chr7:150997976 | T | A | 1 | a0001c0002t0001g0227 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.583-381T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997976 | |||||||
chr7:150997992 | G | A | 1 | a0003c0006t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.583-365G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150997992 | |||||||
chr7:150998096 | T | C | 3 | a0001c0002t0001g0241 a0001c0002t0007g0243 a0001c0010t0001g0242 |
3 | HG02976.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.583-261T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150998096 | |||||||
chr7:150998107 | G | A | 27 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0002t0001g0002 others(24): Show |
44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.583-250G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150998107 | |||||||
chr7:150998126 | A | G | 74 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(71): Show |
98 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.583-231A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 5/26 | chr7 | 150998126 | |||||||
chr7:150998504 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02602.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.675-35G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 6/26 | chr7 | 150998504 | |||||||
chr7:150998714 | C | A | 1 | a0015c0016t0001g0225 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.816+34C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/26 | chr7 | 150998714 | |||||||
chr7:150998717 | G | A | 1 | a0001c0002t0001g0141 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.816+37G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/26 | chr7 | 150998717 | |||||||
chr7:150998811 | A | C | 1 | a0002c0003t0001g0110 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.816+131A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/26 | chr7 | 150998811 | |||||||
chr7:150998871 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.817-75A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/26 | chr7 | 150998871 | |||||||
chr7:150998920 | A | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.817-26A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 7/26 | chr7 | 150998920 | |||||||
chr7:150999385 | C | G | 2 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1131+21C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999385 | |||||||
chr7:150999542 | AGGGGTGT others(5): Show |
A | 1 | a0001c0023t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1131+187_1131+198d others(14): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr7 | 150999542 | ||||||
chr7:150999839 | G | T | 2 | a0007c0009t0001g0003 a0007c0009t0001g0075 |
2 | NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1131+475G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999839 | |||||||
chr7:150999896 | GTGA | G | 18 | a0001c0001t0001g0154 a0002c0003t0001g0016 a0002c0003t0001g0025 others(15): Show |
20 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1131+533_1131+535d others(5): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999896 | |||||||
chr7:150999899 | A | G | 1 | a0002c0003t0001g0095 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1131+535A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999899 | |||||||
chr7:150999909 | A | G | 19 | a0001c0001t0001g0154 a0002c0003t0001g0016 a0002c0003t0001g0025 others(16): Show |
21 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1131+545A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999909 | |||||||
chr7:150999911 | T | C | 19 | a0001c0001t0001g0154 a0002c0003t0001g0016 a0002c0003t0001g0025 others(16): Show |
21 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1131+547T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999911 | |||||||
chr7:150999925 | T | C | 19 | a0001c0001t0001g0154 a0002c0003t0001g0016 a0002c0003t0001g0025 others(16): Show |
21 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1131+561T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999925 | |||||||
chr7:150999956 | G | C | 1 | a0004c0007t0001g0087 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1132-542G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 150999956 | |||||||
chr7:151000007 | G | A | 16 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(13): Show |
17 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1132-491G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000007 | |||||||
chr7:151000008 | C | T | 1 | a0001c0002t0007g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1132-490C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000008 | |||||||
chr7:151000058 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1132-440G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000058 | |||||||
chr7:151000099 | A | T | 1 | a0015c0016t0001g0225 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1132-399A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000099 | |||||||
chr7:151000101 | T | A | 1 | a0015c0016t0001g0225 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1132-397T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000101 | |||||||
chr7:151000118 | G | A | 5 | a0001c0002t0001g0061 a0001c0002t0001g0062 a0001c0002t0001g0063 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132-380G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000118 | |||||||
chr7:151000120 | G | T | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1132-378G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000120 | |||||||
chr7:151000206 | A | G | 29 | a0001c0002t0001g0002 a0001c0002t0001g0015 a0001c0002t0001g0021 others(26): Show |
46 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1132-292A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000206 | |||||||
chr7:151000245 | C | A | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(202): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1132-253C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000245 | |||||||
chr7:151000293 | A | G | 1 | a0001c0002t0001g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1132-205A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000293 | |||||||
chr7:151000299 | G | A | 5 | a0001c0005t0001g0009 a0001c0005t0001g0050 a0001c0032t0001g0049 others(2): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1132-199G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000299 | |||||||
chr7:151000451 | C | G | 1 | a0001c0002t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1132-47C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 9/26 | chr7 | 151000451 | |||||||
chr7:151000712 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1233+113A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000712 | |||||||
chr7:151000723 | C | T | 1 | a0001c0002t0001g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1233+124C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000723 | |||||||
chr7:151000743 | G | A | 1 | a0001c0002t0001g0211 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1233+144G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000743 | |||||||
chr7:151000872 | G | A | 1 | a0001c0002t0001g0234 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1233+273G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000872 | |||||||
chr7:151000986 | T | G | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1234-245T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000986 | |||||||
chr7:151000988 | G | T | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1234-243G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000988 | |||||||
chr7:151000991 | T | G | 1 | a0001c0002t0001g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1234-240T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000991 | |||||||
chr7:151000992 | G | T | 1 | a0002c0003t0001g0095 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1234-239G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151000992 | |||||||
chr7:151001008 | G | A | 2 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1234-223G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151001008 | |||||||
chr7:151001181 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0081 |
2 | HG00735.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1234-50C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 10/26 | chr7 | 151001181 | |||||||
chr7:151001690 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1502+73A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 12/26 | chr7 | 151001690 | |||||||
chr7:151001740 | G | A | 1 | a0001c0002t0001g0241 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1503-81G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 12/26 | chr7 | 151001740 | |||||||
chr7:151001791 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1503-30A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 12/26 | chr7 | 151001791 | |||||||
chr7:151002157 | C | A | 1 | a0001c0002t0001g0230 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1648-43C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 13/26 | chr7 | 151002157 | |||||||
chr7:151002162 | G | T | 32 | a0001c0002t0001g0002 a0001c0002t0001g0021 a0001c0002t0001g0023 others(29): Show |
44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1648-38G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 13/26 | chr7 | 151002162 | |||||||
chr7:151002383 | A | AAC | 21 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(18): Show |
26 | HG00140.hp1 HG01074.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1752+148_1752+149d others(4): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | A | AACAC | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(19): Show |
24 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.1752+146_1752+149d others(6): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | A | AACACAC | 21 | a0001c0001t0001g0041 a0001c0001t0001g0154 a0001c0001t0001g0177 others(18): Show |
24 | HG00423.hp2 HG00639.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1752+144_1752+149d others(8): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | A | AACACACA others(1): Show |
15 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0059 others(12): Show |
17 | HG00621.hp2 HG01099.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1752+142_1752+149d others(10): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | A | AACACACA others(3): Show |
5 | a0001c0002t0001g0001 a0001c0002t0001g0045 a0001c0002t0001g0148 others(2): Show |
5 | HG00621.hp1 HG01192.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.1752+140_1752+149d others(12): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | A | AACACACA others(5): Show |
2 | a0001c0002t0001g0001 a0001c0002t0001g0002 |
2 | HG01070.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1752+138_1752+149d others(14): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | A | AACACACA others(9): Show |
1 | a0001c0002t0001g0199 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1752+134_1752+149d others(18): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | A | AACACACA others(11): Show |
1 | a0001c0002t0001g0001 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1752+132_1752+149d others(20): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AAC | A | 27 | a0001c0001t0001g0044 a0001c0001t0001g0077 a0001c0001t0001g0123 others(24): Show |
30 | HG00408.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1752+148_1752+149d others(4): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACAC | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0057 a0001c0001t0001g0125 others(27): Show |
30 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1752+146_1752+149d others(6): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACAC | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0043 others(17): Show |
21 | HG00733.hp1 HG01243.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.1752+144_1752+149d others(8): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(1): Show |
A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0031 others(19): Show |
26 | HG00544.hp1 HG00609.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1752+142_1752+149d others(10): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(3): Show |
A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(22): Show |
28 | HG00438.hp1 HG00558.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1752+140_1752+149d others(12): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(5): Show |
A | 17 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0035 others(14): Show |
17 | HG00323.hp1 HG00597.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1752+138_1752+149d others(14): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(7): Show |
A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0012 others(7): Show |
14 | HG01069.hp2 HG02602.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.1752+136_1752+149d others(16): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(9): Show |
A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(13): Show |
19 | HG00423.hp1 HG00597.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1752+134_1752+149d others(18): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(11): Show |
A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
18 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1752+132_1752+149d others(20): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(13): Show |
A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(9): Show |
13 | HG00323.hp2 HG00438.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1752+130_1752+149d others(22): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(15): Show |
A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0019 others(7): Show |
12 | HG01978.hp2 HG02027.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1752+128_1752+149d others(24): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(17): Show |
A | 2 | a0001c0001t0001g0156 a0001c0002t0001g0062 |
2 | HG01884.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1752+126_1752+149d others(26): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(19): Show |
A | 4 | a0001c0002t0001g0001 a0001c0002t0001g0061 a0001c0002t0001g0126 others(1): Show |
4 | HG02258.hp2 HG02886.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752+124_1752+149d others(28): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(23): Show |
A | 2 | a0001c0002t0001g0058 a0001c0002t0001g0223 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1752+120_1752+149d others(32): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(25): Show |
A | 2 | a0001c0002t0001g0052 a0001c0002t0001g0053 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1752+118_1752+149d others(34): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(29): Show |
A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18963.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1752+114_1752+149d others(38): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002383 | AACACACA others(33): Show |
A | 1 | a0001c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1752+110_1752+149d others(42): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002383 | ||||||
chr7:151002384 | A | C | 1 | a0010c0025t0001g0143 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1752+80A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002384 | |||||||
chr7:151002385 | C | A | 1 | a0010c0025t0001g0143 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1752+81C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002385 | |||||||
chr7:151002444 | ACACACAC others(3): Show |
A | 1 | a0002c0003t0001g0110 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1752+142_1752+151d others(12): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002444 | ||||||
chr7:151002523 | C | G | 35 | a0001c0002t0001g0002 a0001c0002t0001g0021 a0001c0002t0001g0023 others(32): Show |
47 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1752+219C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002523 | |||||||
chr7:151002568 | C | T | 2 | a0002c0003t0001g0113 a0002c0003t0001g0114 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1752+264C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002568 | |||||||
chr7:151002696 | T | C | 1 | a0002c0003t0001g0095 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1752+392T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002696 | |||||||
chr7:151002710 | A | G | 6 | a0001c0002t0001g0034 a0001c0002t0001g0122 a0001c0002t0001g0202 others(3): Show |
8 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1752+406A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002710 | |||||||
chr7:151002789 | G | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
292 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1752+485G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002789 | |||||||
chr7:151002804 | C | CATTTT | 16 | a0001c0002t0001g0034 a0001c0002t0001g0047 a0001c0002t0001g0048 others(13): Show |
18 | HG01109.hp1 HG01952.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1752+510_1752+514d others(7): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002804 | ||||||
chr7:151002806 | TTTTATTT others(2): Show |
T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1752+506_1752+514d others(11): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002806 | ||||||
chr7:151002846 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1752+542C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002846 | |||||||
chr7:151002847 | G | A | 1 | a0001c0002t0007g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1752+543G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002847 | |||||||
chr7:151002864 | T | TG | 4 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0089 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752+561dupG | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151002864 | ||||||
chr7:151002869 | T | C | 1 | a0001c0023t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1752+565T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002869 | |||||||
chr7:151002893 | C | T | 15 | a0001c0002t0001g0034 a0001c0002t0001g0047 a0001c0002t0001g0048 others(12): Show |
17 | HG01109.hp1 HG01952.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1752+589C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151002893 | |||||||
chr7:151003203 | G | A | 30 | a0001c0002t0001g0002 a0001c0002t0001g0021 a0001c0002t0001g0023 others(27): Show |
42 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1752+899G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151003203 | |||||||
chr7:151003395 | C | G | 4 | a0001c0002t0001g0090 a0001c0002t0001g0241 a0001c0010t0001g0242 others(1): Show |
4 | HG02622.hp1 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752+1091C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151003395 | |||||||
chr7:151003427 | T | G | 64 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(61): Show |
103 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1752+1123T>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151003427 | |||||||
chr7:151003549 | A | G | 30 | a0001c0002t0001g0002 a0001c0002t0001g0021 a0001c0002t0001g0023 others(27): Show |
42 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1752+1245A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151003549 | |||||||
chr7:151003858 | C | A | 18 | a0001c0001t0001g0154 a0002c0003t0001g0016 a0002c0003t0001g0025 others(15): Show |
20 | HG00621.hp1 HG00741.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1752+1554C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151003858 | |||||||
chr7:151004004 | T | C | 1 | a0002c0003t0001g0221 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1752+1700T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004004 | |||||||
chr7:151004153 | A | G | 5 | a0001c0005t0001g0009 a0001c0005t0001g0050 a0001c0032t0001g0049 others(2): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1752+1849A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004153 | |||||||
chr7:151004210 | G | A | 4 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0058 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752+1906G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004210 | |||||||
chr7:151004636 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1753-1791T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004636 | |||||||
chr7:151004667 | G | A | 4 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0089 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-1760G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004667 | |||||||
chr7:151004695 | G | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1753-1732G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004695 | |||||||
chr7:151004748 | G | C | 4 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0089 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-1679G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004748 | |||||||
chr7:151004838 | A | ATGTT | 4 | a0001c0002t0001g0090 a0001c0002t0007g0243 a0002c0003t0001g0025 others(1): Show |
5 | HG02071.hp1 HG02129.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1753-1563_1753-156 others(8): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151004838 | ||||||
chr7:151004838 | ATGTT | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1753-1563_1753-156 others(8): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151004838 | ||||||
chr7:151004838 | ATGTTTGT others(5): Show |
A | 4 | a0001c0002t0001g0061 a0001c0002t0001g0062 a0001c0002t0001g0063 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1753-1571_1753-156 others(16): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151004838 | ||||||
chr7:151004951 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1753-1476C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004951 | |||||||
chr7:151004983 | G | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1753-1444G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151004983 | |||||||
chr7:151005131 | C | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1753-1296C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005131 | |||||||
chr7:151005243 | G | A | 4 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0089 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-1184G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005243 | |||||||
chr7:151005344 | A | T | 37 | a0001c0002t0001g0002 a0001c0002t0001g0021 a0001c0002t0001g0023 others(34): Show |
51 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1753-1083A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005344 | |||||||
chr7:151005503 | A | G | 4 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0089 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-924A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005503 | |||||||
chr7:151005536 | T | C | 1 | a0005c0031t0001g0055 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1753-891T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005536 | |||||||
chr7:151005693 | C | A | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1753-734C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005693 | |||||||
chr7:151005693 | C | T | 1 | a0003c0006t0001g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1753-734C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005693 | |||||||
chr7:151005769 | GACTGAGG others(4): Show |
G | 1 | a0001c0001t0001g0166 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1753-657_1753-647d others(13): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005769 | |||||||
chr7:151005933 | A | C | 1 | a0001c0002t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1753-494A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005933 | |||||||
chr7:151005953 | C | T | 98 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0014 others(95): Show |
151 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.1753-474C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151005953 | |||||||
chr7:151006000 | C | T | 1 | a0001c0023t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1753-427C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151006000 | |||||||
chr7:151006042 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1753-385C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151006042 | |||||||
chr7:151006043 | G | A | 2 | a0001c0002t0001g0089 a0001c0002t0001g0091 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1753-384G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151006043 | |||||||
chr7:151006130 | T | TA | 7 | a0001c0001t0001g0155 a0001c0001t0001g0170 a0001c0002t0007g0243 others(4): Show |
7 | HG01109.hp1 HG01952.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753-288dupA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr7 | 151006130 | ||||||
chr7:151006154 | A | G | 58 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0015 others(55): Show |
97 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1753-273A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 14/26 | chr7 | 151006154 | |||||||
chr7:151006604 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0079 others(4): Show |
14 | HG00408.hp1 HG01069.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.1820+110C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 15/26 | chr7 | 151006604 | |||||||
chr7:151006654 | C | CT | 31 | a0001c0002t0001g0002 a0001c0002t0001g0021 a0001c0002t0001g0023 others(28): Show |
43 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1820+160_1820+161i others(3): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 15/26 | chr7 | 151006654 | |||||||
chr7:151006799 | A | T | 1 | a0001c0002t0001g0151 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1821-90A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 15/26 | chr7 | 151006799 | |||||||
chr7:151006827 | G | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
221 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1821-62G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 15/26 | chr7 | 151006827 | |||||||
chr7:151007054 | C | G | 1 | a0001c0002t0001g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1938-48C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 16/26 | chr7 | 151007054 | |||||||
chr7:151007285 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2112+9A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007285 | |||||||
chr7:151007312 | C | A | 39 | a0001c0002t0001g0002 a0001c0002t0001g0021 a0001c0002t0001g0023 others(36): Show |
58 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.2112+36C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007312 | |||||||
chr7:151007391 | A | G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0164 a0001c0001t0001g0183 others(2): Show |
5 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2112+115A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007391 | |||||||
chr7:151007563 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2112+287C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007563 | |||||||
chr7:151007599 | C | A | 1 | a0001c0002t0001g0145 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2112+323C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007599 | |||||||
chr7:151007750 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2112+474G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007750 | |||||||
chr7:151007755 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(143): Show |
223 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.2112+479G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007755 | |||||||
chr7:151007888 | C | T | 2 | a0001c0002t0001g0021 a0006c0012t0001g0021 |
3 | HG02129.hp2 HG02155.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2112+612C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007888 | |||||||
chr7:151007890 | GTTC | G | 5 | a0001c0005t0001g0009 a0001c0005t0001g0050 a0001c0032t0001g0049 others(2): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2112+615_2112+617d others(5): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151007890 | |||||||
chr7:151008111 | TC | T | 4 | a0001c0002t0001g0034 a0001c0002t0001g0202 a0001c0002t0001g0204 others(1): Show |
5 | HG02615.hp2 HG02622.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2113-818delC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008111 | |||||||
chr7:151008136 | T | C | 1 | a0001c0010t0001g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2113-794T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008136 | |||||||
chr7:151008237 | C | T | 2 | a0005c0013t0001g0024 a0005c0031t0001g0055 |
3 | HG02109.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2113-693C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008237 | |||||||
chr7:151008522 | T | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(22): Show |
40 | HG00735.hp1 HG02027.hp1 HG02027.hp2 others(37): Show |
intron_variant | MODIFIER | c.2113-408T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008522 | |||||||
chr7:151008680 | G | A | 1 | a0001c0002t0001g0231 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2113-250G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008680 | |||||||
chr7:151008754 | G | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0032 others(27): Show |
38 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.2113-176G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008754 | |||||||
chr7:151008880 | G | T | 1 | a0001c0002t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2113-50G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | chr7 | 151008880 | |||||||
chr7:151008894 | C | CG | 4 | a0001c0001t0001g0164 a0001c0001t0001g0183 a0001c0001t0001g0185 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2113-33dupG | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr7 | 151008894 | ||||||
chr7:151009089 | G | A | 3 | a0001c0002t0001g0023 a0001c0002t0001g0045 a0001c0002t0001g0046 |
4 | HG01433.hp1 HG01496.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245+27G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 18/26 | chr7 | 151009089 | |||||||
chr7:151009102 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2245+40G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 18/26 | chr7 | 151009102 | |||||||
chr7:151009289 | C | A | 3 | a0001c0005t0001g0009 a0001c0005t0001g0050 a0001c0010t0001g0242 |
7 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2324+22C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 19/26 | chr7 | 151009289 | |||||||
chr7:151009295 | C | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.2324+28C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 19/26 | chr7 | 151009295 | |||||||
chr7:151009348 | G | GC | 117 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0035 others(114): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2325-45dupC | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr7 | 151009348 | ||||||
chr7:151009648 | C | T | 1 | a0001c0023t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2512+63C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151009648 | |||||||
chr7:151009653 | C | A | 2 | a0001c0001t0001g0157 a0003c0006t0001g0253 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2512+68C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151009653 | |||||||
chr7:151009827 | G | A | 197 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(194): Show |
283 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.2512+242G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151009827 | |||||||
chr7:151009994 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2513-121G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151009994 | |||||||
chr7:151010029 | T | C | 20 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0074 others(17): Show |
23 | HG01884.hp2 HG01978.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2513-86T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151010029 | |||||||
chr7:151010093 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2513-22G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151010093 | |||||||
chr7:151010104 | A | G | 1 | a0002c0003t0001g0104 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2513-11A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 20/26 | chr7 | 151010104 | |||||||
chr7:151010400 | C | T | 217 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.2685+113C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 21/26 | chr7 | 151010400 | |||||||
chr7:151010427 | G | A | 1 | a0001c0024t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2685+140G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 21/26 | chr7 | 151010427 | |||||||
chr7:151010437 | G | T | 2 | a0001c0001t0001g0157 a0003c0006t0001g0253 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2685+150G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 21/26 | chr7 | 151010437 | |||||||
chr7:151010855 | G | A | 13 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0074 others(10): Show |
16 | HG01884.hp2 HG01978.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2897-44G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 22/26 | chr7 | 151010855 | |||||||
chr7:151010860 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2897-39C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 22/26 | chr7 | 151010860 | |||||||
chr7:151011001 | A | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
354 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.2984+15A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011001 | |||||||
chr7:151011114 | G | A | 4 | a0001c0001t0001g0060 a0002c0003t0001g0056 a0002c0003t0001g0110 others(1): Show |
4 | HG02486.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2984+128G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011114 | |||||||
chr7:151011127 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0188 |
2 | NA18946.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2984+141T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011127 | |||||||
chr7:151011210 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2984+224C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011210 | |||||||
chr7:151011214 | G | T | 217 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.2984+228G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011214 | |||||||
chr7:151011369 | C | CT | 186 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(183): Show |
271 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.2984+385dupT | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr7 | 151011369 | ||||||
chr7:151011553 | A | G | 3 | a0004c0007t0001g0054 a0004c0007t0001g0087 a0004c0007t0001g0088 |
3 | HG01109.hp1 HG01952.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2984+567A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011553 | |||||||
chr7:151011580 | C | G | 1 | a0001c0010t0001g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2984+594C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011580 | |||||||
chr7:151011611 | CA | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(182): Show |
264 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2984+642delA | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr7 | 151011611 | ||||||
chr7:151011611 | CAA | C | 8 | a0001c0001t0001g0144 a0001c0001t0001g0157 a0001c0002t0001g0018 others(5): Show |
11 | HG00323.hp1 HG00558.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.2984+641_2984+642d others(4): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr7 | 151011611 | ||||||
chr7:151011628 | A | G | 4 | a0001c0001t0001g0157 a0001c0002t0001g0089 a0001c0002t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2984+642A>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011628 | |||||||
chr7:151011762 | G | A | 212 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(209): Show |
296 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.2985-589G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011762 | |||||||
chr7:151011984 | C | T | 1 | a0005c0031t0001g0055 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2985-367C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151011984 | |||||||
chr7:151012008 | A | T | 1 | a0002c0003t0001g0108 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2985-343A>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151012008 | |||||||
chr7:151012059 | G | A | 1 | a0001c0024t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2985-292G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151012059 | |||||||
chr7:151012235 | T | A | 1 | a0001c0010t0001g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2985-116T>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151012235 | |||||||
chr7:151012247 | G | T | 1 | a0001c0002t0001g0124 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2985-104G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 23/26 | chr7 | 151012247 | |||||||
chr7:151012483 | G | T | 97 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0042 others(94): Show |
152 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.3106+11G>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151012483 | |||||||
chr7:151012596 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0076 a0001c0001t0001g0121 others(2): Show |
6 | HG01884.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3106+124C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151012596 | |||||||
chr7:151012763 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3106+291G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151012763 | |||||||
chr7:151012816 | T | C | 1 | a0003c0014t0005g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3106+344T>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151012816 | |||||||
chr7:151012892 | G | C | 4 | a0001c0005t0001g0009 a0001c0005t0001g0050 a0001c0021t0001g0182 others(1): Show |
9 | HG01891.hp1 HG02280.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3107-339G>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151012892 | |||||||
chr7:151013116 | G | A | 4 | a0001c0010t0001g0084 a0004c0007t0001g0054 a0004c0007t0001g0087 others(1): Show |
4 | HG01109.hp1 HG01952.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3107-115G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 24/26 | chr7 | 151013116 | |||||||
chr7:151013540 | A | C | 20 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0074 others(17): Show |
23 | HG01884.hp2 HG01978.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3255+161A>C | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013540 | |||||||
chr7:151013596 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0139 |
2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3256-128G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013596 | |||||||
chr7:151013597 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0139 |
2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3256-127C>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013597 | |||||||
chr7:151013652 | C | T | 1 | a0001c0010t0001g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3256-72C>T | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013652 | |||||||
chr7:151013676 | C | G | 1 | a0002c0003t0001g0235 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3256-48C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013676 | |||||||
chr7:151013712 | G | A | 18 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0074 others(15): Show |
21 | HG01884.hp2 HG01978.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.3256-12G>A | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 25/26 | chr7 | 151013712 | |||||||
chr7:151013945 | C | G | 1 | a0001c0002t0001g0150 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3450+27C>G | NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 26/26 | chr7 | 151013945 |