Item | Value |
---|---|
geneid | 4843 |
ensemblid | ENSG00000007171.19 |
hgncid | 7873 |
symbol | NOS2 |
name | nitric oxide synthase 2 |
refseq_nuc | NM_000625.4 |
refseq_prot | NP_000616.3 |
ensembl_nuc | ENST00000313735.11 |
ensembl_prot | ENSP00000327251.6 |
mane_status | MANE Select |
chr | chr17 |
start | 27756766 |
end | 27800529 |
strand | - |
ver | v1.2 |
region | chr17:27756766-27800529 |
region5000 | chr17:27751766-27805529 |
regionname0 | NOS2_chr17_27756766_27800529 |
regionname5000 | NOS2_chr17_27751766_27805529 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1153 | 321 | 65 | 54 | 156 | 15 | 30 | 122 | NOS2_chr17_27751766_27805529 | NOS2 | MACPW others(1148): Show |
chr17 | 27751766 | 27805529 |
a0002 | 0/1 | 1153 | 58 | 12 | 16 | 18 | 3 | 8 | 12 | NOS2_chr17_27751766_27805529 | NOS2 | MACPW others(1148): Show |
chr17 | 27751766 | 27805529 |
a0003 | 0/0 | 1153 | 14 | 9 | 2 | 1 | 0 | 2 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | MACPW others(1148): Show |
chr17 | 27751766 | 27805529 |
a0004 | 0/0 | 1153 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | MACPW others(1148): Show |
chr17 | 27751766 | 27805529 |
a0005 | 0/0 | 1153 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | MACPW others(1148): Show |
chr17 | 27751766 | 27805529 |
a0006 | 0/0 | 1153 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | MACPW others(1148): Show |
chr17 | 27751766 | 27805529 |
a0007 | 0/0 | 1153 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | MACPW others(1148): Show |
chr17 | 27751766 | 27805529 |
a0008 | 0/0 | 1153 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | MACPW others(1148): Show |
chr17 | 27751766 | 27805529 |
a0009 | 0/0 | 1153 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | MACPW others(1148): Show |
chr17 | 27751766 | 27805529 |
a0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | MQ | chr17 | 27751766 | 27805529 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3459 | 190 | 32 | 30 | 101 | 6 | 21 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0002 | 1/0 | 3459 | 87 | 17 | 18 | 38 | 8 | 5 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0005 | 0/0 | 3459 | 12 | 6 | 3 | 2 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0007 | 0/0 | 3459 | 8 | 1 | 1 | 5 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0009 | 0/0 | 3459 | 7 | 0 | 0 | 7 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0010 | 0/0 | 3459 | 4 | 4 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0012 | 0/0 | 3459 | 2 | 1 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0013 | 0/0 | 3459 | 2 | 0 | 0 | 0 | 0 | 2 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0016 | 0/0 | 3459 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0018 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0019 | 0/0 | 3459 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0020 | 0/0 | 3459 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0022 | 0/0 | 3459 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0025 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0027 | 0/0 | 3459 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0028 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0001c0029 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0002c0003 | 0/1 | 3459 | 40 | 11 | 5 | 13 | 2 | 8 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0002c0006 | 0/0 | 3459 | 9 | 0 | 7 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0002c0008 | 0/0 | 3459 | 7 | 0 | 4 | 2 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0002c0015 | 0/0 | 3459 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0002c0026 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0003c0004 | 0/0 | 3459 | 14 | 9 | 2 | 1 | 0 | 2 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0004c0011 | 0/0 | 3459 | 3 | 0 | 0 | 3 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0005c0021 | 0/0 | 3459 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0006c0014 | 0/0 | 3459 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0007c0023 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0008c0017 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0009c0024 | 0/0 | 3459 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATGGC others(3454): Show |
chr17 | 27751766 | 27805529 | ||
a0010c0030 | 0/0 | 3458 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | TGGCC others(3453): Show |
chr17 | 27751766 | 27805529 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4206 | 131 | 28 | 24 | 63 | 5 | 11 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0001t0002 | 0/0 | 4206 | 49 | 4 | 5 | 34 | 0 | 6 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0001t0003 | 0/0 | 4206 | 3 | 0 | 0 | 1 | 0 | 2 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0001t0004 | 0/0 | 4206 | 3 | 0 | 1 | 0 | 1 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0001t0006 | 0/0 | 4206 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0001t0013 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0001t0015 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0002t0001 | 0/0 | 4206 | 24 | 4 | 8 | 6 | 4 | 2 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0002t0002 | 1/0 | 4206 | 60 | 13 | 10 | 31 | 2 | 3 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0002t0007 | 0/0 | 4206 | 2 | 0 | 0 | 0 | 2 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0002t0014 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0005t0001 | 0/0 | 4206 | 10 | 5 | 3 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0005t0002 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0005t0009 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0007t0001 | 0/0 | 4206 | 6 | 0 | 1 | 4 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0007t0002 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0007t0008 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0009t0002 | 0/0 | 4206 | 7 | 0 | 0 | 7 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0010t0001 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0010t0002 | 0/0 | 4206 | 3 | 3 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0012t0001 | 0/0 | 4206 | 2 | 1 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0013t0001 | 0/0 | 4206 | 2 | 0 | 0 | 0 | 0 | 2 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0016t0001 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0018t0002 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0019t0001 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0020t0002 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0022t0002 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0025t0002 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0027t0002 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0028t0001 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0001c0029t0001 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0002c0003t0001 | 0/1 | 4206 | 27 | 2 | 4 | 13 | 1 | 6 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0002c0003t0002 | 0/0 | 4206 | 10 | 9 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0002c0003t0005 | 0/0 | 4206 | 2 | 0 | 0 | 0 | 1 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0002c0003t0012 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0002c0006t0001 | 0/0 | 4206 | 9 | 0 | 7 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0002c0008t0001 | 0/0 | 4206 | 3 | 0 | 1 | 1 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0002c0008t0002 | 0/0 | 4206 | 4 | 0 | 3 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0002c0015t0001 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0002c0026t0002 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0003c0004t0001 | 0/0 | 4206 | 12 | 7 | 2 | 1 | 0 | 2 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0003c0004t0002 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0003c0004t0010 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0004c0011t0002 | 0/0 | 4206 | 3 | 0 | 0 | 3 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0005c0021t0002 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0006c0014t0001 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0007c0023t0001 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0008c0017t0001 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0009c0024t0002 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4201): Show |
chr17 | 27751766 | 27805529 |
a0010c0030t0011 | 0/0 | 4187 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | ATAAC others(4182): Show |
chr17 | 27751766 | 27805529 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 2 | 4 | 4 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0004g0006 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0006g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0013g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0001t0015g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0007g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0002t0014g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0005t0009g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0007t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0007t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0007t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0007t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0007t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0007t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0007t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0009t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0009t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0009t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0009t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0010t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0010t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0010t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0010t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0012t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0012t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0013t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0013t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0016t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0018t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0019t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0020t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0022t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0025t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0027t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0028t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0001c0029t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0005g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0003t0012g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0006t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0006t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0006t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0006t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0006t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0006t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0006t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0008t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0008t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0008t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0008t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0008t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0008t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0008t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0015t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0002c0026t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0003c0004t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0004c0011t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0004c0011t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0005c0021t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0006c0014t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0007c0023t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0008c0017t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0009c0024t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
a0010c0030t0011g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0258 | EUR | GBR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00099 | hp2 | a0002 | c0003 | t0001 | g0216 | EUR | GBR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00140 | hp1 | a0001 | c0007 | t0001 | g0199 | EUR | GBR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0035 | EUR | FIN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | FIN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0154 | EUR | FIN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | FIN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00408 | hp2 | a0002 | c0008 | t0001 | g0221 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0312 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00558 | hp1 | a0004 | c0011 | t0002 | g0266 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0310 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00639 | hp2 | a0001 | c0005 | t0001 | g0217 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00642 | hp1 | a0002 | c0006 | t0001 | g0194 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00673 | hp1 | a0001 | c0009 | t0002 | g0009 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00673 | hp2 | a0001 | c0007 | t0001 | g0202 | EAS | CHS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00733 | hp2 | a0001 | c0005 | t0001 | g0218 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00738 | hp2 | a0002 | c0003 | t0001 | g0238 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG00741 | hp2 | a0002 | c0006 | t0001 | g0203 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01070 | hp2 | a0003 | c0004 | t0001 | g0063 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01081 | hp2 | a0002 | c0003 | t0001 | g0239 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0327 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01099 | hp2 | a0002 | c0008 | t0001 | g0149 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01106 | hp1 | a0002 | c0006 | t0001 | g0190 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01109 | hp2 | a0001 | c0012 | t0001 | g0111 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01167 | hp2 | a0002 | c0006 | t0001 | g0191 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01168 | hp2 | a0002 | c0003 | t0001 | g0201 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01169 | hp1 | a0002 | c0006 | t0001 | g0019 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01169 | hp2 | a0002 | c0003 | t0012 | g0240 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01175 | hp2 | a0005 | c0021 | t0002 | g0285 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01192 | hp1 | a0002 | c0008 | t0002 | g0273 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01192 | hp2 | a0002 | c0006 | t0001 | g0019 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01261 | hp1 | a0001 | c0016 | t0001 | g0147 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01361 | hp2 | a0002 | c0008 | t0002 | g0317 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01433 | hp1 | a0001 | c0007 | t0001 | g0211 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0280 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01496 | hp1 | a0002 | c0003 | t0001 | g0204 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01496 | hp2 | a0003 | c0004 | t0001 | g0058 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01515 | hp2 | a0002 | c0008 | t0001 | g0205 | EUR | IBS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01516 | hp2 | a0001 | c0002 | t0007 | g0024 | EUR | IBS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01517 | hp1 | a0001 | c0002 | t0007 | g0024 | EUR | IBS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01891 | hp1 | a0002 | c0003 | t0002 | g0025 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01928 | hp2 | a0002 | c0006 | t0001 | g0198 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01934 | hp1 | a0001 | c0005 | t0001 | g0234 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01943 | hp2 | a0006 | c0014 | t0001 | g0121 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0291 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01993 | hp1 | a0002 | c0008 | t0002 | g0256 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0303 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0247 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02040 | hp2 | a0002 | c0003 | t0001 | g0078 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02055 | hp2 | a0001 | c0005 | t0001 | g0212 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02071 | hp1 | a0002 | c0003 | t0001 | g0189 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02074 | hp1 | a0001 | c0009 | t0002 | g0009 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0075 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0338 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02135 | hp2 | a0001 | c0007 | t0001 | g0153 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02145 | hp2 | a0001 | c0005 | t0001 | g0215 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0284 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | CDX | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02165 | hp2 | a0002 | c0003 | t0001 | g0195 | EAS | CDX | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02258 | hp2 | a0002 | c0003 | t0001 | g0173 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02280 | hp2 | a0001 | c0010 | t0002 | g0295 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0309 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02451 | hp1 | a0001 | c0005 | t0001 | g0232 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02523 | hp1 | a0004 | c0011 | t0002 | g0029 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0248 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02615 | hp1 | a0007 | c0023 | t0001 | g0054 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0264 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02630 | hp1 | a0002 | c0003 | t0002 | g0260 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02647 | hp1 | a0003 | c0004 | t0002 | g0251 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0306 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02698 | hp2 | a0002 | c0003 | t0001 | g0018 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02717 | hp2 | a0001 | c0018 | t0002 | g0296 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02723 | hp1 | a0003 | c0004 | t0001 | g0067 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02735 | hp2 | a0001 | c0020 | t0002 | g0318 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02738 | hp1 | a0002 | c0003 | t0001 | g0213 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02809 | hp1 | a0001 | c0005 | t0001 | g0210 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02809 | hp2 | a0002 | c0003 | t0001 | g0207 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02818 | hp2 | a0002 | c0003 | t0002 | g0036 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0246 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02895 | hp1 | a0003 | c0004 | t0001 | g0085 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02895 | hp2 | a0002 | c0003 | t0002 | g0302 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02922 | hp2 | a0003 | c0004 | t0010 | g0087 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02976 | hp1 | a0001 | c0010 | t0002 | g0292 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03041 | hp2 | a0001 | c0005 | t0002 | g0253 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03098 | hp1 | a0003 | c0004 | t0001 | g0086 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03098 | hp2 | a0002 | c0003 | t0002 | g0298 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03130 | hp1 | a0001 | c0007 | t0008 | g0040 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03139 | hp2 | a0001 | c0028 | t0001 | g0052 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03195 | hp1 | a0001 | c0025 | t0002 | g0299 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03209 | hp1 | a0002 | c0003 | t0002 | g0301 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03209 | hp2 | a0001 | c0029 | t0001 | g0070 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03225 | hp1 | a0003 | c0004 | t0001 | g0079 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03239 | hp1 | a0003 | c0004 | t0001 | g0066 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0188 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03486 | hp1 | a0001 | c0010 | t0001 | g0180 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03486 | hp2 | a0001 | c0012 | t0001 | g0105 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03491 | hp2 | a0002 | c0003 | t0001 | g0206 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03516 | hp1 | a0001 | c0010 | t0002 | g0294 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03516 | hp2 | a0002 | c0003 | t0002 | g0036 | AFR | ESN | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0243 | AFR | GWD | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03579 | hp1 | a0003 | c0004 | t0001 | g0064 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03654 | hp2 | a0001 | c0005 | t0009 | g0193 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03669 | hp1 | a0002 | c0003 | t0001 | g0018 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03669 | hp2 | a0001 | c0013 | t0001 | g0165 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | STU | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0278 | SAS | PJL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03831 | hp1 | a0002 | c0003 | t0005 | g0208 | SAS | BEB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0139 | SAS | BEB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | BEB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03927 | hp2 | a0001 | c0001 | t0015 | g0344 | SAS | BEB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0335 | SAS | BEB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0311 | SAS | BEB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG04199 | hp1 | a0001 | c0013 | t0001 | g0164 | SAS | STU | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0281 | SAS | STU | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG04204 | hp1 | a0003 | c0004 | t0001 | g0061 | SAS | STU | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG04204 | hp2 | a0002 | c0003 | t0002 | g0328 | SAS | STU | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | STU | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0134 | SAS | STU | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | CHB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18612 | hp2 | a0002 | c0006 | t0001 | g0021 | EAS | CHB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0329 | EAS | CHB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18906 | hp1 | a0003 | c0004 | t0001 | g0065 | AFR | YRI | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0319 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18943 | hp1 | a0002 | c0003 | t0001 | g0196 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18944 | hp2 | a0001 | c0007 | t0001 | g0020 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18950 | hp2 | a0002 | c0006 | t0001 | g0021 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18952 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18963 | hp2 | a0001 | c0009 | t0002 | g0034 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18966 | hp2 | a0001 | c0009 | t0002 | g0275 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0322 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18968 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18969 | hp2 | a0009 | c0024 | t0002 | g0340 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0334 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18977 | hp2 | a0001 | c0005 | t0001 | g0073 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18979 | hp2 | a0002 | c0003 | t0001 | g0072 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18980 | hp1 | a0002 | c0008 | t0002 | g0320 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18986 | hp1 | a0002 | c0015 | t0001 | g0192 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18987 | hp1 | a0010 | c0030 | t0011 | g0220 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18988 | hp1 | a0001 | c0009 | t0002 | g0034 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0325 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18989 | hp2 | a0002 | c0003 | t0001 | g0074 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18990 | hp1 | a0001 | c0009 | t0002 | g0009 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18994 | hp1 | a0001 | c0007 | t0001 | g0020 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0333 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19001 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19006 | hp1 | a0001 | c0022 | t0002 | g0289 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19006 | hp2 | a0001 | c0005 | t0001 | g0076 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19009 | hp2 | a0001 | c0027 | t0002 | g0332 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19043 | hp2 | a0002 | c0026 | t0002 | g0259 | AFR | LWK | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19055 | hp1 | a0002 | c0003 | t0001 | g0236 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19057 | hp2 | a0001 | c0007 | t0002 | g0339 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19060 | hp1 | a0001 | c0001 | t0013 | g0342 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19060 | hp2 | a0004 | c0011 | t0002 | g0029 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19064 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19065 | hp1 | a0002 | c0003 | t0001 | g0237 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19068 | hp1 | a0001 | c0009 | t0002 | g0288 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19068 | hp2 | a0003 | c0004 | t0001 | g0062 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0308 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19080 | hp2 | a0002 | c0003 | t0001 | g0071 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19081 | hp1 | a0001 | c0002 | t0014 | g0337 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19090 | hp1 | a0001 | c0019 | t0001 | g0113 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | YRI | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA19240 | hp2 | a0003 | c0004 | t0001 | g0053 | AFR | YRI | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | ASW | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0080 | EUR | TSI | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0183 | EUR | TSI | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0148 | EUR | TSI | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA20805 | hp2 | a0002 | c0003 | t0005 | g0209 | EUR | TSI | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA20905 | hp1 | a0002 | c0003 | t0001 | g0200 | SAS | GIH | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0323 | SAS | GIH | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0297 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02109 | hp2 | a0001 | c0005 | t0001 | g0233 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02486 | hp1 | a0002 | c0003 | t0002 | g0300 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0244 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02559 | hp1 | a0002 | c0003 | t0002 | g0025 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03471 | hp1 | a0008 | c0017 | t0001 | g0056 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | MSL | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | USA | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | USA | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
homoSapiens | chm13v2 | a0002 | c0003 | t0001 | g0214 | REF | REF | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0262 | REF | REF | NOS2_chr17_27751766_27805529 | NOS2 | chr17 | 27751766 | 27805529 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:27758979 | G | A | 1 | a0008 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.3256C>T | p.Arg1086Cys | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/27 | 3520/4206 | 3256/3462 | 1086/1153 | chr17 | 27758979 | |||
chr17:27766517 | T | C | 1 | a0004 | 3 | HG00558.hp1 HG02523.hp1 NA19060.hp2 |
missense_variant | MODERATE | c.2239A>G | p.Thr747Ala | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 19/27 | 2503/4206 | 2239/3462 | 747/1153 | chr17 | 27766517 | |||
chr17:27767734 | T | G | 1 | a0005 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.2138A>C | p.Gln713Pro | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/27 | 2402/4206 | 2138/3462 | 713/1153 | chr17 | 27767734 | |||
chr17:27769571 | G | A | 2 | a0002 a0010 |
58 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(55): Show |
missense_variant | MODERATE | c.1823C>T | p.Ser608Leu | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 16/27 | 2087/4206 | 1823/3462 | 608/1153 | chr17 | 27769571 | |||
chr17:27772337 | C | A | 1 | a0007 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.1675G>T | p.Ala559Ser | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 14/27 | 1939/4206 | 1675/3462 | 559/1153 | chr17 | 27772337 | |||
chr17:27772424 | G | A | 1 | a0009 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.1588C>T | p.Arg530Cys | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 14/27 | 1852/4206 | 1588/3462 | 530/1153 | chr17 | 27772424 | |||
chr17:27774283 | C | T | 1 | a0006 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.1450G>A | p.Val484Ile | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/27 | 1714/4206 | 1450/3462 | 484/1153 | chr17 | 27774283 | |||
chr17:27782076 | G | A | 1 | a0003 | 14 | HG01070.hp2 HG01496.hp2 HG02647.hp1 others(11): Show |
missense_variant | MODERATE | c.661C>T | p.Arg221Trp | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 7/27 | 925/4206 | 661/3462 | 221/1153 | chr17 | 27782076 | |||
chr17:27798808 | ATCTCTAT others(12): Show |
A | 1 | a0010 | 1 | NA18987.hp1 | frameshift_variant&start_lost | HIGH | c.-18_1delCTTTGTAAAG others(9): Show |
p.Met1fs | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/27 | 265/4206 | 1/3462 | 1/1153 | chr17 | 27798808 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:27757252 | C | T | 1 | a0001c0020 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.3456G>A | p.Ala1152Ala | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 27/27 | 3720/4206 | 3456/3462 | 1152/1153 | chr17 | 27757252 | |||
chr17:27758905 | G | A | 2 | a0001c0010 a0002c0026 |
5 | HG02280.hp2 HG02976.hp1 HG03486.hp1 others(2): Show |
synonymous_variant | LOW | c.3330C>T | p.Val1110Val | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/27 | 3594/4206 | 3330/3462 | 1110/1153 | chr17 | 27758905 | |||
chr17:27760741 | G | C | 1 | a0001c0018 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.2892C>G | p.Ala964Ala | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 24/27 | 3156/4206 | 2892/3462 | 964/1153 | chr17 | 27760741 | |||
chr17:27760741 | G | T | 1 | a0001c0016 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.2892C>A | p.Ala964Ala | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 24/27 | 3156/4206 | 2892/3462 | 964/1153 | chr17 | 27760741 | |||
chr17:27762814 | G | A | 1 | a0001c0019 | 1 | NA19090.hp1 | synonymous_variant | LOW | c.2784C>T | p.Val928Val | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/27 | 3048/4206 | 2784/3462 | 928/1153 | chr17 | 27762814 | |||
chr17:27762841 | T | C | 24 | a0001c0001 a0001c0005 a0001c0009 others(21): Show |
302 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(299): Show |
synonymous_variant | LOW | c.2757A>G | p.Thr919Thr | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/27 | 3021/4206 | 2757/3462 | 919/1153 | chr17 | 27762841 | |||
chr17:27765605 | A | G | 23 | a0001c0001 a0001c0005 a0001c0009 others(20): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(298): Show |
synonymous_variant | LOW | c.2358T>C | p.Gly786Gly | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/27 | 2622/4206 | 2358/3462 | 786/1153 | chr17 | 27765605 | |||
chr17:27769010 | G | A | 1 | a0001c0022 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.2001C>T | p.Asp667Asp | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/27 | 2265/4206 | 2001/3462 | 667/1153 | chr17 | 27769010 | |||
chr17:27770967 | C | T | 3 | a0002c0006 a0002c0015 a0010c0030 |
11 | HG00642.hp1 HG00741.hp2 HG01106.hp1 others(8): Show |
synonymous_variant | LOW | c.1755G>A | p.Leu585Leu | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/27 | 2019/4206 | 1755/3462 | 585/1153 | chr17 | 27770967 | |||
chr17:27778906 | G | A | 7 | a0001c0005 a0001c0007 a0001c0025 others(4): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(68): Show |
synonymous_variant | LOW | c.1155C>T | p.Asp385Asp | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 10/27 | 1419/4206 | 1155/3462 | 385/1153 | chr17 | 27778906 | |||
chr17:27780814 | G | A | 1 | a0001c0012 | 2 | HG01109.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.957C>T | p.Phe319Phe | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/27 | 1221/4206 | 957/3462 | 319/1153 | chr17 | 27780814 | |||
chr17:27781051 | G | A | 1 | a0001c0027 | 1 | NA19009.hp2 | synonymous_variant | LOW | c.849C>T | p.Asn283Asn | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 8/27 | 1113/4206 | 849/3462 | 283/1153 | chr17 | 27781051 | |||
chr17:27788830 | T | A | 1 | a0001c0009 | 7 | HG00673.hp1 HG02074.hp1 NA18963.hp2 others(4): Show |
synonymous_variant | LOW | c.297A>T | p.Thr99Thr | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/27 | 561/4206 | 297/3462 | 99/1153 | chr17 | 27788830 | |||
chr17:27788923 | T | C | 3 | a0001c0028 a0001c0029 a0003c0004 |
16 | HG01070.hp2 HG01496.hp2 HG02647.hp1 others(13): Show |
synonymous_variant | LOW | c.204A>G | p.Pro68Pro | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/27 | 468/4206 | 204/3462 | 68/1153 | chr17 | 27788923 | |||
chr17:27798717 | G | A | 1 | a0001c0013 | 2 | HG03669.hp2 HG04199.hp1 |
synonymous_variant | LOW | c.93C>T | p.Ala31Ala | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/27 | 357/4206 | 93/3462 | 31/1153 | chr17 | 27798717 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:27756893 | A | G | 1 | a0001c0001t0004 | 3 | HG00323.hp2 HG00639.hp1 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*353T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 27/27 | 353 | chr17 | 27756893 | ||||||
chr17:27756919 | C | T | 1 | a0002c0003t0005 | 2 | HG03831.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*327G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 27/27 | 327 | chr17 | 27756919 | ||||||
chr17:27756920 | G | A | 1 | a0003c0004t0010 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*326C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 27/27 | 326 | chr17 | 27756920 | ||||||
chr17:27756922 | T | C | 1 | a0002c0003t0005 | 2 | HG03831.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*324A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 27/27 | 324 | chr17 | 27756922 | ||||||
chr17:27756944 | G | C | 1 | a0001c0001t0006 | 2 | NA18952.hp2 NA18968.hp1 |
3_prime_UTR_variant | MODIFIER | c.*302C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 27/27 | 302 | chr17 | 27756944 | ||||||
chr17:27756970 | C | T | 2 | a0001c0001t0003 a0001c0001t0013 |
4 | HG03834.hp1 HG04228.hp2 NA18941.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*276G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 27/27 | 276 | chr17 | 27756970 | ||||||
chr17:27757055 | G | A | 1 | a0001c0002t0014 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*191C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 27/27 | 191 | chr17 | 27757055 | ||||||
chr17:27757201 | A | G | 1 | a0001c0005t0009 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*45T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 27/27 | 45 | chr17 | 27757201 | ||||||
chr17:27757203 | C | G | 1 | a0001c0005t0009 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*43G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 27/27 | 43 | chr17 | 27757203 | ||||||
chr17:27757204 | C | G | 1 | a0001c0005t0009 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 27/27 | 42 | chr17 | 27757204 | ||||||
chr17:27798852 | G | T | 1 | a0001c0002t0007 | 2 | HG01516.hp2 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-43C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/27 | 43 | chr17 | 27798852 | ||||||
chr17:27800356 | T | G | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-91A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1547 | chr17 | 27800356 | ||||||
chr17:27800357 | G | C | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-92C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1548 | chr17 | 27800357 | ||||||
chr17:27800360 | T | C | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1551 | chr17 | 27800360 | ||||||
chr17:27800368 | G | C | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-103C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1559 | chr17 | 27800368 | ||||||
chr17:27800376 | A | C | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-111T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1567 | chr17 | 27800376 | ||||||
chr17:27800377 | G | C | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-112C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1568 | chr17 | 27800377 | ||||||
chr17:27800380 | A | T | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-115T>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1571 | chr17 | 27800380 | ||||||
chr17:27800382 | A | C | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-117T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1573 | chr17 | 27800382 | ||||||
chr17:27800388 | A | C | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-123T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | chr17 | 27800388 | |||||||
chr17:27800390 | G | T | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-125C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1581 | chr17 | 27800390 | ||||||
chr17:27800392 | G | T | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-127C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1583 | chr17 | 27800392 | ||||||
chr17:27800400 | C | A | 1 | a0002c0003t0012 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-135G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1591 | chr17 | 27800400 | ||||||
chr17:27800481 | T | G | 1 | a0001c0001t0015 | 1 | HG03927.hp2 | 5_prime_UTR_variant | MODIFIER | c.-216A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1672 | chr17 | 27800481 | ||||||
chr17:27800492 | C | G | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(25): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
5_prime_UTR_variant | MODIFIER | c.-227G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1683 | chr17 | 27800492 | ||||||
chr17:27800511 | C | T | 1 | a0001c0007t0008 | 1 | HG03130.hp1 | 5_prime_UTR_variant | MODIFIER | c.-246G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/27 | 1702 | chr17 | 27800511 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:27757506 | C | G | 57 | a0001c0001t0001g0005 a0001c0001t0001g0060 a0001c0001t0001g0077 others(54): Show |
71 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.3355-153G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27757506 | |||||||
chr17:27757530 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0104 |
4 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3355-177C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27757530 | |||||||
chr17:27757774 | C | T | 2 | a0001c0028t0001g0052 a0008c0017t0001g0056 |
2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3355-421G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27757774 | |||||||
chr17:27757856 | C | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0219 |
2 | NA18947.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.3355-503G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27757856 | |||||||
chr17:27757866 | G | A | 2 | a0001c0001t0001g0115 a0008c0017t0001g0056 |
2 | HG03471.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.3355-513C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27757866 | |||||||
chr17:27757887 | G | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0081 others(31): Show |
37 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.3355-534C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27757887 | |||||||
chr17:27757903 | C | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0219 |
2 | NA18947.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.3355-550G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27757903 | |||||||
chr17:27757960 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(117): Show |
140 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.3355-607G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27757960 | |||||||
chr17:27758034 | C | T | 1 | a0001c0010t0002g0294 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3355-681G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758034 | |||||||
chr17:27758082 | C | G | 39 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0096 others(36): Show |
53 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.3355-729G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758082 | |||||||
chr17:27758088 | T | C | 1 | a0002c0008t0001g0221 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3355-735A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758088 | |||||||
chr17:27758118 | T | C | 1 | a0003c0004t0001g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3354+763A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758118 | |||||||
chr17:27758251 | G | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | NA18983.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3354+630C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758251 | |||||||
chr17:27758267 | A | G | 1 | a0008c0017t0001g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3354+614T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758267 | |||||||
chr17:27758277 | C | T | 2 | a0001c0001t0002g0268 a0001c0001t0002g0283 |
2 | NA19000.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3354+604G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758277 | |||||||
chr17:27758345 | G | T | 2 | a0001c0002t0001g0177 a0007c0023t0001g0054 |
2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3354+536C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758345 | |||||||
chr17:27758357 | A | G | 1 | a0002c0008t0002g0273 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3354+524T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758357 | |||||||
chr17:27758533 | G | A | 4 | a0001c0002t0001g0177 a0001c0010t0002g0292 a0002c0026t0002g0259 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3354+348C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758533 | |||||||
chr17:27758534 | G | A | 4 | a0001c0002t0001g0177 a0001c0010t0002g0292 a0002c0026t0002g0259 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3354+347C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758534 | |||||||
chr17:27758600 | G | A | 1 | a0008c0017t0001g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3354+281C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758600 | |||||||
chr17:27758697 | C | T | 1 | a0008c0017t0001g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3354+184G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758697 | |||||||
chr17:27758711 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(220): Show |
265 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.3354+170T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758711 | |||||||
chr17:27758769 | T | C | 3 | a0002c0003t0001g0189 a0002c0003t0001g0195 a0002c0003t0001g0196 |
3 | HG02071.hp1 HG02165.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.3354+112A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758769 | |||||||
chr17:27758867 | A | T | 2 | a0001c0002t0001g0059 a0001c0002t0001g0129 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3354+14T>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 26/26 | chr17 | 27758867 | |||||||
chr17:27759201 | C | T | 1 | a0003c0004t0001g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3160-126G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 25/26 | chr17 | 27759201 | |||||||
chr17:27759240 | T | C | 39 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0096 others(36): Show |
53 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.3160-165A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 25/26 | chr17 | 27759240 | |||||||
chr17:27759382 | C | T | 1 | a0002c0003t0001g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3160-307G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 25/26 | chr17 | 27759382 | |||||||
chr17:27759453 | G | A | 6 | a0001c0001t0001g0235 a0003c0004t0001g0058 a0003c0004t0001g0061 others(3): Show |
6 | HG01070.hp2 HG01496.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.3160-378C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 25/26 | chr17 | 27759453 | |||||||
chr17:27759603 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0096 others(35): Show |
52 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.3159+427G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 25/26 | chr17 | 27759603 | |||||||
chr17:27759641 | G | A | 1 | a0008c0017t0001g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3159+389C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 25/26 | chr17 | 27759641 | |||||||
chr17:27759675 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3159+355G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 25/26 | chr17 | 27759675 | |||||||
chr17:27759787 | C | G | 1 | a0001c0020t0002g0318 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3159+243G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 25/26 | chr17 | 27759787 | |||||||
chr17:27759995 | G | A | 1 | a0001c0001t0004g0006 | 3 | HG00323.hp2 HG00639.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.3159+35C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 25/26 | chr17 | 27759995 | |||||||
chr17:27760196 | T | C | 1 | a0001c0005t0001g0215 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3011-18A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 24/26 | chr17 | 27760196 | |||||||
chr17:27760199 | T | A | 1 | a0002c0003t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3011-21A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 24/26 | chr17 | 27760199 | |||||||
chr17:27760290 | C | T | 57 | a0001c0001t0001g0013 a0001c0001t0001g0094 a0001c0001t0001g0095 others(54): Show |
65 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3011-112G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 24/26 | chr17 | 27760290 | |||||||
chr17:27760419 | T | C | 57 | a0001c0001t0001g0013 a0001c0001t0001g0094 a0001c0001t0001g0095 others(54): Show |
65 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3010+204A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 24/26 | chr17 | 27760419 | |||||||
chr17:27760941 | T | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(204): Show |
249 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.2889-197A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 23/26 | chr17 | 27760941 | |||||||
chr17:27760952 | A | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(98): Show |
121 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.2888+192T>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 23/26 | chr17 | 27760952 | |||||||
chr17:27761020 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2888+124G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 23/26 | chr17 | 27761020 | |||||||
chr17:27761021 | C | T | 20 | a0001c0001t0001g0060 a0001c0001t0001g0179 a0001c0001t0001g0235 others(17): Show |
20 | HG01070.hp2 HG01496.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.2888+123G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 23/26 | chr17 | 27761021 | |||||||
chr17:27761298 | C | T | 1 | a0001c0002t0001g0022 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2801-67G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27761298 | |||||||
chr17:27761406 | C | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0096 others(38): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.2801-175G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27761406 | |||||||
chr17:27761491 | C | T | 2 | a0001c0009t0002g0034 a0001c0009t0002g0288 |
3 | NA18963.hp2 NA18988.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2801-260G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27761491 | |||||||
chr17:27761709 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(224): Show |
269 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.2801-478A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27761709 | |||||||
chr17:27761829 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
244 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.2801-598C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27761829 | |||||||
chr17:27761873 | G | A | 1 | a0002c0008t0002g0273 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2801-642C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27761873 | |||||||
chr17:27762035 | A | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(215): Show |
260 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.2800+763T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762035 | |||||||
chr17:27762078 | C | A | 5 | a0001c0010t0001g0180 a0001c0010t0002g0292 a0001c0010t0002g0294 others(2): Show |
5 | HG02280.hp2 HG02976.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2800+720G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762078 | |||||||
chr17:27762125 | G | A | 1 | a0001c0018t0002g0296 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2800+673C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762125 | |||||||
chr17:27762138 | G | A | 44 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0096 others(41): Show |
58 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.2800+660C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762138 | |||||||
chr17:27762141 | A | ACCCCG | 4 | a0001c0002t0001g0059 a0001c0002t0001g0129 a0001c0002t0002g0297 others(1): Show |
4 | HG02109.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2800+656_2800+657i others(7): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762141 | |||||||
chr17:27762148 | G | GCCACCCC others(6): Show |
4 | a0001c0002t0001g0059 a0001c0002t0001g0129 a0001c0002t0002g0297 others(1): Show |
4 | HG02109.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2800+649_2800+650i others(15): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762148 | |||||||
chr17:27762151 | C | T | 4 | a0001c0002t0001g0059 a0001c0002t0001g0129 a0001c0002t0002g0297 others(1): Show |
4 | HG02109.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2800+647G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762151 | |||||||
chr17:27762201 | A | G | 155 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(152): Show |
180 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2800+597T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762201 | |||||||
chr17:27762205 | C | A | 97 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0055 others(94): Show |
114 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.2800+593G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762205 | |||||||
chr17:27762226 | A | C | 4 | a0001c0010t0001g0180 a0001c0010t0002g0292 a0001c0010t0002g0294 others(1): Show |
4 | HG02280.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2800+572T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762226 | |||||||
chr17:27762239 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(195): Show |
235 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.2800+559G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762239 | |||||||
chr17:27762240 | G | A | 1 | a0001c0002t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2800+558C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762240 | |||||||
chr17:27762244 | C | T | 1 | a0001c0007t0008g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2800+554G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762244 | |||||||
chr17:27762288 | T | C | 58 | a0001c0001t0001g0013 a0001c0001t0001g0094 a0001c0001t0001g0095 others(55): Show |
66 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.2800+510A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762288 | |||||||
chr17:27762347 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2800+451G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762347 | |||||||
chr17:27762348 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(153): Show |
179 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.2800+450T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762348 | |||||||
chr17:27762377 | T | G | 1 | a0001c0001t0001g0224 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2800+421A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762377 | |||||||
chr17:27762384 | G | C | 58 | a0001c0001t0001g0013 a0001c0001t0001g0094 a0001c0001t0001g0095 others(55): Show |
66 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.2800+414C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762384 | |||||||
chr17:27762576 | T | G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0096 others(40): Show |
57 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.2800+222A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762576 | |||||||
chr17:27762767 | G | C | 1 | a0001c0002t0002g0334 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2800+31C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 22/26 | chr17 | 27762767 | |||||||
chr17:27763078 | T | C | 1 | a0008c0017t0001g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2593-73A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 21/26 | chr17 | 27763078 | |||||||
chr17:27763200 | A | G | 46 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(43): Show |
51 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2593-195T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 21/26 | chr17 | 27763200 | |||||||
chr17:27763375 | A | G | 1 | a0008c0017t0001g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2593-370T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 21/26 | chr17 | 27763375 | |||||||
chr17:27763461 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2593-456C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 21/26 | chr17 | 27763461 | |||||||
chr17:27763537 | C | A | 1 | a0002c0008t0001g0205 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2592+444G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 21/26 | chr17 | 27763537 | |||||||
chr17:27763598 | C | G | 4 | a0001c0010t0001g0180 a0001c0010t0002g0292 a0001c0010t0002g0294 others(1): Show |
4 | HG02280.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2592+383G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 21/26 | chr17 | 27763598 | |||||||
chr17:27763646 | T | C | 4 | a0001c0010t0001g0180 a0001c0010t0002g0292 a0001c0010t0002g0294 others(1): Show |
4 | HG02280.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2592+335A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 21/26 | chr17 | 27763646 | |||||||
chr17:27763707 | C | T | 1 | a0001c0002t0002g0324 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2592+274G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 21/26 | chr17 | 27763707 | |||||||
chr17:27763728 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(254): Show |
302 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.2592+253A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 21/26 | chr17 | 27763728 | |||||||
chr17:27764201 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.2429-57G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27764201 | |||||||
chr17:27764526 | C | T | 2 | a0001c0028t0001g0052 a0003c0004t0001g0053 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2429-382G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27764526 | |||||||
chr17:27764635 | C | T | 2 | a0001c0018t0002g0296 a0002c0003t0002g0302 |
2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2429-491G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27764635 | |||||||
chr17:27764751 | T | C | 1 | a0001c0007t0001g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2429-607A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27764751 | |||||||
chr17:27764787 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2429-643A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27764787 | |||||||
chr17:27764949 | G | A | 4 | a0001c0010t0001g0180 a0001c0010t0002g0292 a0001c0010t0002g0294 others(1): Show |
4 | HG02280.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2428+586C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27764949 | |||||||
chr17:27765011 | C | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(254): Show |
302 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.2428+524G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765011 | |||||||
chr17:27765113 | G | A | 1 | a0001c0002t0002g0324 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2428+422C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765113 | |||||||
chr17:27765177 | G | A | 1 | a0001c0002t0007g0024 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2428+358C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765177 | |||||||
chr17:27765192 | T | C | 2 | a0001c0001t0001g0060 a0003c0004t0001g0067 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2428+343A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765192 | |||||||
chr17:27765235 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(258): Show |
306 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.2428+300T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765235 | |||||||
chr17:27765303 | C | T | 4 | a0001c0010t0001g0180 a0001c0010t0002g0292 a0001c0010t0002g0294 others(1): Show |
4 | HG02280.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2428+232G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765303 | |||||||
chr17:27765417 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2428+118C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765417 | |||||||
chr17:27765512 | T | C | 1 | a0002c0015t0001g0192 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2428+23A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765512 | |||||||
chr17:27765518 | T | G | 1 | a0002c0015t0001g0192 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2428+17A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765518 | |||||||
chr17:27765525 | C | G | 1 | a0002c0015t0001g0192 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2428+10G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765525 | |||||||
chr17:27765529 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(254): Show |
302 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(299): Show |
splice_region_variant&intron_variant | LOW | c.2428+6C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765529 | |||||||
chr17:27765533 | A | AGGGGGGG others(23): Show |
1 | a0002c0015t0001g0192 | 1 | NA18986.hp1 | splice_donor_variant&intron_variant | HIGH | c.2428+1_2428+2insCC others(28): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 20/26 | chr17 | 27765533 | |||||||
chr17:27765748 | T | C | 1 | a0001c0018t0002g0296 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2247-32A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 19/26 | chr17 | 27765748 | |||||||
chr17:27765760 | C | T | 2 | a0001c0002t0002g0319 a0001c0002t0002g0324 |
2 | NA18939.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.2247-44G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 19/26 | chr17 | 27765760 | |||||||
chr17:27765958 | C | T | 58 | a0001c0001t0001g0013 a0001c0001t0001g0094 a0001c0001t0001g0095 others(55): Show |
66 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.2247-242G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 19/26 | chr17 | 27765958 | |||||||
chr17:27765963 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2247-247C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 19/26 | chr17 | 27765963 | |||||||
chr17:27765979 | C | A | 1 | a0001c0001t0002g0270 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2247-263G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 19/26 | chr17 | 27765979 | |||||||
chr17:27766096 | C | T | 1 | a0001c0001t0002g0335 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2247-380G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 19/26 | chr17 | 27766096 | |||||||
chr17:27766289 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
233 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.2246+221A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 19/26 | chr17 | 27766289 | |||||||
chr17:27766307 | A | C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(43): Show |
51 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2246+203T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 19/26 | chr17 | 27766307 | |||||||
chr17:27766487 | C | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG00558.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.2246+23G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 19/26 | chr17 | 27766487 | |||||||
chr17:27766750 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2168-162T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27766750 | |||||||
chr17:27766766 | G | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(255): Show |
303 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.2168-178C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27766766 | |||||||
chr17:27766838 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(255): Show |
303 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.2168-250T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27766838 | |||||||
chr17:27766845 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2168-257C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27766845 | |||||||
chr17:27767000 | C | CA | 72 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0057 others(69): Show |
81 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.2168-413dupT | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27767000 | |||||||
chr17:27767000 | C | CAA | 10 | a0001c0001t0001g0157 a0001c0001t0001g0219 a0002c0003t0001g0072 others(7): Show |
10 | HG00140.hp2 HG01515.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.2168-414_2168-413d others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27767000 | |||||||
chr17:27767000 | CA | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0158 others(7): Show |
10 | HG02132.hp1 HG02145.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.2168-413delT | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27767000 | |||||||
chr17:27767024 | A | G | 1 | a0001c0001t0002g0336 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2168-436T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27767024 | |||||||
chr17:27767025 | G | A | 1 | a0001c0002t0002g0284 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2168-437C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27767025 | |||||||
chr17:27767253 | C | A | 58 | a0001c0001t0001g0013 a0001c0001t0001g0094 a0001c0001t0001g0095 others(55): Show |
66 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.2167+452G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27767253 | |||||||
chr17:27767278 | C | T | 1 | a0001c0001t0002g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2167+427G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27767278 | |||||||
chr17:27767561 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2167+144G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27767561 | |||||||
chr17:27767570 | C | T | 3 | a0001c0002t0001g0154 a0001c0002t0001g0156 a0001c0002t0001g0162 |
3 | HG00323.hp1 HG01358.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2167+135G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 18/26 | chr17 | 27767570 | |||||||
chr17:27767993 | G | A | 2 | a0002c0003t0001g0236 a0002c0003t0001g0237 |
2 | NA19055.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2035-156C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27767993 | |||||||
chr17:27768169 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(234): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.2035-332A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768169 | |||||||
chr17:27768171 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(234): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.2035-334G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768171 | |||||||
chr17:27768173 | G | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(234): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.2035-336C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768173 | |||||||
chr17:27768174 | TAC | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(234): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.2035-339_2035-338d others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768174 | |||||||
chr17:27768177 | C | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(234): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.2035-340G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768177 | |||||||
chr17:27768178 | T | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(234): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.2035-341A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768178 | |||||||
chr17:27768349 | C | A | 1 | a0001c0001t0001g0167 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2035-512G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768349 | |||||||
chr17:27768352 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(232): Show |
280 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.2035-515G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768352 | |||||||
chr17:27768535 | C | T | 1 | a0001c0001t0002g0343 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2034+442G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768535 | |||||||
chr17:27768536 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(231): Show |
279 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.2034+441C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768536 | |||||||
chr17:27768671 | G | A | 1 | a0001c0002t0001g0183 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2034+306C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768671 | |||||||
chr17:27768704 | A | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
212 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2034+273T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768704 | |||||||
chr17:27768794 | G | A | 1 | a0001c0002t0002g0243 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2034+183C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768794 | |||||||
chr17:27768820 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2034+157A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 17/26 | chr17 | 27768820 | |||||||
chr17:27769294 | C | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG00558.hp2 NA18940.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.1860-143G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 16/26 | chr17 | 27769294 | |||||||
chr17:27769330 | C | T | 1 | a0002c0003t0001g0200 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1860-179G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 16/26 | chr17 | 27769330 | |||||||
chr17:27769376 | T | C | 2 | a0001c0001t0002g0261 a0001c0001t0002g0271 |
2 | NA19010.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1859+159A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 16/26 | chr17 | 27769376 | |||||||
chr17:27769447 | C | A | 99 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(96): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1859+88G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 16/26 | chr17 | 27769447 | |||||||
chr17:27769698 | C | T | 4 | a0001c0010t0001g0180 a0001c0010t0002g0292 a0001c0010t0002g0294 others(1): Show |
4 | HG02280.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1810-114G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27769698 | |||||||
chr17:27769777 | A | G | 2 | a0001c0002t0002g0242 a0001c0007t0001g0211 |
2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1810-193T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27769777 | |||||||
chr17:27769867 | C | G | 1 | a0001c0002t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1810-283G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27769867 | |||||||
chr17:27769930 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1810-346C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27769930 | |||||||
chr17:27770105 | T | C | 58 | a0001c0001t0001g0013 a0001c0001t0001g0094 a0001c0001t0001g0095 others(55): Show |
66 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.1810-521A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27770105 | |||||||
chr17:27770355 | G | A | 1 | a0001c0002t0002g0291 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1809+558C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27770355 | |||||||
chr17:27770454 | C | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(244): Show |
292 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.1809+459G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27770454 | |||||||
chr17:27770488 | GTAAA | G | 20 | a0001c0002t0001g0123 a0001c0002t0002g0010 a0001c0002t0002g0037 others(17): Show |
25 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1809+421_1809+424d others(6): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27770488 | |||||||
chr17:27770515 | A | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(248): Show |
296 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.1809+398T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27770515 | |||||||
chr17:27770632 | T | C | 20 | a0001c0001t0001g0060 a0001c0001t0001g0179 a0001c0001t0001g0235 others(17): Show |
20 | HG01070.hp2 HG01496.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.1809+281A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27770632 | |||||||
chr17:27770838 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0187 |
3 | NA18942.hp1 NA18959.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1809+75C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27770838 | |||||||
chr17:27770883 | C | A | 1 | a0001c0005t0002g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1809+30G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 15/26 | chr17 | 27770883 | |||||||
chr17:27771086 | CCTGGGCT others(37): Show |
C | 1 | a0001c0002t0002g0241 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1705-113_1705-70de others(45): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 14/26 | chr17 | 27771086 | |||||||
chr17:27771161 | G | A | 1 | a0003c0004t0001g0063 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1705-144C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 14/26 | chr17 | 27771161 | |||||||
chr17:27771191 | G | C | 2 | a0001c0005t0001g0215 a0001c0018t0002g0296 |
2 | HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1705-174C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 14/26 | chr17 | 27771191 | |||||||
chr17:27771612 | G | A | 27 | a0001c0001t0001g0077 a0001c0001t0002g0002 a0001c0001t0002g0028 others(24): Show |
39 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1705-595C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 14/26 | chr17 | 27771612 | |||||||
chr17:27771755 | G | A | 50 | a0002c0003t0001g0004 a0002c0003t0001g0018 a0002c0003t0001g0071 others(47): Show |
57 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.1704+553C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 14/26 | chr17 | 27771755 | |||||||
chr17:27771879 | A | G | 6 | a0001c0005t0001g0215 a0001c0010t0001g0180 a0001c0010t0002g0292 others(3): Show |
6 | HG02145.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1704+429T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 14/26 | chr17 | 27771879 | |||||||
chr17:27772145 | T | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(254): Show |
302 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.1704+163A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 14/26 | chr17 | 27772145 | |||||||
chr17:27772298 | G | A | 4 | a0001c0010t0001g0180 a0001c0010t0002g0292 a0001c0010t0002g0294 others(1): Show |
4 | HG02280.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1704+10C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 14/26 | chr17 | 27772298 | |||||||
chr17:27772482 | G | C | 1 | a0001c0002t0002g0321 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1560-30C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 13/26 | chr17 | 27772482 | |||||||
chr17:27772541 | G | A | 1 | a0003c0004t0010g0087 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1560-89C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 13/26 | chr17 | 27772541 | |||||||
chr17:27772594 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1560-142C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 13/26 | chr17 | 27772594 | |||||||
chr17:27772735 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0138 a0001c0001t0001g0140 others(1): Show |
4 | NA18980.hp2 NA19007.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1560-283C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 13/26 | chr17 | 27772735 | |||||||
chr17:27772898 | G | T | 2 | a0001c0002t0002g0008 a0001c0002t0002g0243 |
4 | HG02615.hp2 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1559+263C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 13/26 | chr17 | 27772898 | |||||||
chr17:27772990 | G | C | 1 | a0007c0023t0001g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1559+171C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 13/26 | chr17 | 27772990 | |||||||
chr17:27773065 | T | C | 6 | a0001c0005t0001g0215 a0001c0010t0001g0180 a0001c0010t0002g0292 others(3): Show |
6 | HG02145.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1559+96A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 13/26 | chr17 | 27773065 | |||||||
chr17:27773090 | G | GAGGCAGA others(7): Show |
1 | a0003c0004t0001g0062 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1559+57_1559+70dup others(14): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 13/26 | chr17 | 27773090 | |||||||
chr17:27773118 | T | G | 6 | a0001c0005t0001g0215 a0001c0010t0001g0180 a0001c0010t0002g0292 others(3): Show |
6 | HG02145.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1559+43A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 13/26 | chr17 | 27773118 | |||||||
chr17:27773295 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.1477-52T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/26 | chr17 | 27773295 | |||||||
chr17:27773300 | G | A | 1 | a0001c0002t0002g0265 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1477-57C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/26 | chr17 | 27773300 | |||||||
chr17:27773465 | G | C | 1 | a0001c0025t0002g0299 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1477-222C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/26 | chr17 | 27773465 | |||||||
chr17:27773806 | A | C | 4 | a0001c0010t0001g0180 a0001c0010t0002g0292 a0001c0010t0002g0294 others(1): Show |
4 | HG02280.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1476+451T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/26 | chr17 | 27773806 | |||||||
chr17:27773860 | G | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0096 others(38): Show |
56 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1476+397C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/26 | chr17 | 27773860 | |||||||
chr17:27773949 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1476+308C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/26 | chr17 | 27773949 | |||||||
chr17:27774048 | G | A | 1 | a0002c0003t0001g0188 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1476+209C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/26 | chr17 | 27774048 | |||||||
chr17:27774162 | G | A | 4 | a0001c0002t0001g0059 a0001c0002t0001g0129 a0001c0002t0002g0280 others(1): Show |
4 | HG01433.hp2 HG02109.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476+95C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/26 | chr17 | 27774162 | |||||||
chr17:27774188 | G | GCA | 55 | a0001c0001t0001g0110 a0001c0001t0001g0161 a0001c0001t0002g0033 others(52): Show |
62 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1476+67_1476+68dup others(2): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/26 | chr17 | 27774188 | |||||||
chr17:27774211 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(84): Show |
107 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1476+46C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/26 | chr17 | 27774211 | |||||||
chr17:27774250 | C | A | 1 | a0001c0002t0002g0323 | 1 | NA20905.hp2 | splice_region_variant&intron_variant | LOW | c.1476+7G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 12/26 | chr17 | 27774250 | |||||||
chr17:27774560 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0002g0269 a0001c0022t0002g0289 |
3 | HG02083.hp2 HG02129.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1282-109A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27774560 | |||||||
chr17:27774843 | G | A | 1 | a0001c0002t0002g0323 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1282-392C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27774843 | |||||||
chr17:27775290 | T | A | 1 | a0001c0001t0002g0315 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1282-839A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27775290 | |||||||
chr17:27775326 | C | G | 4 | a0001c0001t0002g0257 a0001c0002t0001g0022 a0001c0002t0002g0258 others(1): Show |
6 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282-875G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27775326 | |||||||
chr17:27775363 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0109 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1282-912G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27775363 | |||||||
chr17:27775388 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0104 |
3 | HG02622.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1282-937C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27775388 | |||||||
chr17:27775571 | C | G | 4 | a0002c0003t0001g0213 a0002c0003t0001g0238 a0002c0003t0002g0328 others(1): Show |
4 | HG00738.hp2 HG01361.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282-1120G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27775571 | |||||||
chr17:27775572 | A | G | 4 | a0002c0003t0001g0213 a0002c0003t0001g0238 a0002c0003t0002g0328 others(1): Show |
4 | HG00738.hp2 HG01361.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282-1121T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27775572 | |||||||
chr17:27775631 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1282-1180T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27775631 | |||||||
chr17:27775797 | CT | C | 3 | a0001c0002t0001g0059 a0001c0002t0001g0129 a0001c0002t0002g0297 |
3 | HG02109.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1282-1347delA | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27775797 | |||||||
chr17:27775915 | C | T | 1 | a0001c0002t0001g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1282-1464G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27775915 | |||||||
chr17:27776008 | C | T | 59 | a0001c0005t0009g0193 a0001c0007t0001g0153 a0001c0007t0001g0199 others(56): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1282-1557G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776008 | |||||||
chr17:27776061 | A | G | 59 | a0001c0005t0009g0193 a0001c0007t0001g0153 a0001c0007t0001g0199 others(56): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1282-1610T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776061 | |||||||
chr17:27776303 | T | G | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1852A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776303 | |||||||
chr17:27776304 | T | C | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1853A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776304 | |||||||
chr17:27776305 | G | T | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1854C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776305 | |||||||
chr17:27776306 | T | C | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1855A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776306 | |||||||
chr17:27776307 | G | T | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1856C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776307 | |||||||
chr17:27776308 | G | C | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1857C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776308 | |||||||
chr17:27776311 | G | C | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1860C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776311 | |||||||
chr17:27776313 | G | A | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1862C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776313 | |||||||
chr17:27776314 | G | T | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1863C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776314 | |||||||
chr17:27776315 | G | C | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1864C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776315 | |||||||
chr17:27776319 | T | C | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1868A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776319 | |||||||
chr17:27776322 | T | A | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1871A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776322 | |||||||
chr17:27776328 | T | G | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1877A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776328 | |||||||
chr17:27776349 | CTCCTGGG others(7): Show |
C | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1912_1282-189 others(18): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776349 | |||||||
chr17:27776397 | G | GTGCAGTG others(12): Show |
1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1947_1282-194 others(23): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776397 | |||||||
chr17:27776409 | A | C | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1958T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776409 | |||||||
chr17:27776436 | GCAGAGAC others(4): Show |
G | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1282-1996_1282-198 others(15): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776436 | |||||||
chr17:27776502 | A | C | 1 | a0002c0006t0001g0198 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1282-2051T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776502 | |||||||
chr17:27776655 | G | C | 1 | a0001c0010t0002g0294 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1281+2035C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776655 | |||||||
chr17:27776677 | G | GA | 26 | a0001c0001t0001g0081 a0001c0001t0001g0116 a0001c0001t0001g0122 others(23): Show |
27 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.1281+2012dupT | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776677 | |||||||
chr17:27776677 | GAAA | G | 54 | a0001c0005t0009g0193 a0001c0007t0001g0199 a0001c0007t0001g0202 others(51): Show |
61 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1281+2010_1281+201 others(7): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776677 | |||||||
chr17:27776964 | C | T | 55 | a0001c0005t0009g0193 a0001c0007t0001g0153 a0001c0007t0001g0199 others(52): Show |
62 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1281+1726G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776964 | |||||||
chr17:27776998 | G | A | 3 | a0001c0002t0001g0059 a0001c0002t0001g0129 a0001c0002t0002g0297 |
3 | HG02109.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1281+1692C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27776998 | |||||||
chr17:27777084 | C | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(300): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1281+1606G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777084 | |||||||
chr17:27777126 | G | A | 4 | a0001c0010t0001g0180 a0001c0010t0002g0292 a0001c0010t0002g0294 others(1): Show |
4 | HG02280.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281+1564C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777126 | |||||||
chr17:27777136 | G | C | 1 | a0001c0007t0008g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1281+1554C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777136 | |||||||
chr17:27777250 | G | T | 1 | a0001c0007t0008g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1281+1440C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777250 | |||||||
chr17:27777260 | C | T | 59 | a0001c0005t0009g0193 a0001c0007t0001g0153 a0001c0007t0001g0199 others(56): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1281+1430G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777260 | |||||||
chr17:27777285 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1281+1405T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777285 | |||||||
chr17:27777328 | C | T | 1 | a0001c0010t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1281+1362G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777328 | |||||||
chr17:27777405 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1281+1285T>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777405 | |||||||
chr17:27777485 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(214): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.1281+1205A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777485 | |||||||
chr17:27777521 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1281+1169G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777521 | |||||||
chr17:27777569 | T | C | 5 | a0002c0003t0001g0173 a0002c0003t0002g0036 a0002c0003t0002g0298 others(2): Show |
6 | HG02258.hp2 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281+1121A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777569 | |||||||
chr17:27777596 | T | A | 59 | a0001c0005t0009g0193 a0001c0007t0001g0153 a0001c0007t0001g0199 others(56): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1281+1094A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777596 | |||||||
chr17:27777597 | C | T | 1 | a0001c0013t0001g0164 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1281+1093G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777597 | |||||||
chr17:27777598 | G | A | 2 | a0002c0003t0002g0025 a0002c0003t0002g0260 |
3 | HG01891.hp1 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1281+1092C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777598 | |||||||
chr17:27777706 | G | T | 55 | a0001c0005t0009g0193 a0001c0007t0001g0153 a0001c0007t0001g0199 others(52): Show |
62 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1281+984C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777706 | |||||||
chr17:27777738 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(86): Show |
109 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1281+952C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777738 | |||||||
chr17:27777797 | C | T | 54 | a0001c0005t0009g0193 a0001c0007t0001g0153 a0001c0007t0001g0199 others(51): Show |
61 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1281+893G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777797 | |||||||
chr17:27777803 | G | A | 26 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0094 others(23): Show |
27 | HG00741.hp1 HG01070.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.1281+887C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777803 | |||||||
chr17:27777820 | G | A | 1 | a0010c0030t0011g0220 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1281+870C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777820 | |||||||
chr17:27777837 | G | C | 3 | a0002c0003t0001g0189 a0002c0003t0001g0195 a0002c0003t0001g0196 |
3 | HG02071.hp1 HG02165.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1281+853C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777837 | |||||||
chr17:27777909 | G | A | 2 | a0001c0005t0001g0215 a0001c0007t0008g0040 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1281+781C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27777909 | |||||||
chr17:27778034 | C | CA | 36 | a0001c0001t0001g0077 a0001c0001t0002g0002 a0001c0001t0002g0028 others(33): Show |
49 | HG00408.hp1 HG00673.hp1 HG01433.hp1 others(46): Show |
intron_variant | MODIFIER | c.1281+655dupT | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27778034 | |||||||
chr17:27778156 | G | T | 1 | a0001c0001t0002g0335 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1281+534C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27778156 | |||||||
chr17:27778223 | T | A | 1 | a0001c0002t0002g0323 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1281+467A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27778223 | |||||||
chr17:27778289 | T | C | 1 | a0001c0001t0002g0272 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1281+401A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27778289 | |||||||
chr17:27778402 | G | C | 1 | a0002c0003t0005g0209 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1281+288C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27778402 | |||||||
chr17:27778549 | C | G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | NA18945.hp1 NA19011.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1281+141G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 11/26 | chr17 | 27778549 | |||||||
chr17:27779066 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1005-10T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27779066 | |||||||
chr17:27779288 | C | CTTA | 5 | a0001c0001t0001g0095 a0001c0001t0006g0016 a0001c0002t0002g0023 others(2): Show |
7 | HG00741.hp1 HG02572.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005-235_1005-233d others(5): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27779288 | |||||||
chr17:27779288 | CTTA | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0069 others(27): Show |
33 | HG01070.hp2 HG01123.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.1005-235_1005-233d others(5): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27779288 | |||||||
chr17:27779288 | CTTATTA | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(190): Show |
234 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1005-238_1005-233d others(8): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27779288 | |||||||
chr17:27779288 | CTTATTAT others(2): Show |
C | 35 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0060 others(32): Show |
37 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1005-241_1005-233d others(11): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27779288 | |||||||
chr17:27779288 | CTTATTAT others(5): Show |
C | 69 | a0001c0001t0001g0104 a0001c0001t0002g0249 a0001c0002t0002g0297 others(66): Show |
77 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1005-244_1005-233d others(14): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27779288 | |||||||
chr17:27779448 | G | A | 3 | a0001c0001t0001g0060 a0001c0002t0001g0059 a0001c0002t0001g0129 |
3 | HG02647.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1005-392C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27779448 | |||||||
chr17:27779649 | A | G | 99 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0112 others(96): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.1005-593T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27779649 | |||||||
chr17:27779730 | G | GA | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(223): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.1005-675dupT | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27779730 | |||||||
chr17:27779764 | G | T | 1 | a0002c0006t0001g0194 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1005-708C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27779764 | |||||||
chr17:27779982 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1004+785G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27779982 | |||||||
chr17:27780107 | G | T | 1 | a0002c0006t0001g0194 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1004+660C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27780107 | |||||||
chr17:27780229 | T | C | 12 | a0001c0001t0001g0055 a0001c0001t0001g0097 a0001c0001t0001g0098 others(9): Show |
12 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1004+538A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27780229 | |||||||
chr17:27780267 | G | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0104 |
3 | HG02622.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1004+500C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27780267 | |||||||
chr17:27780372 | C | T | 66 | a0001c0002t0002g0297 a0001c0005t0001g0073 a0001c0005t0001g0076 others(63): Show |
74 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1004+395G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27780372 | |||||||
chr17:27780452 | G | A | 31 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0112 others(28): Show |
33 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1004+315C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 9/26 | chr17 | 27780452 | |||||||
chr17:27780920 | C | T | 1 | a0001c0005t0002g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.865-14G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 8/26 | chr17 | 27780920 | |||||||
chr17:27780950 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0110 |
2 | HG00735.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.865-44G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 8/26 | chr17 | 27780950 | |||||||
chr17:27781014 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(229): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.864+22A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 8/26 | chr17 | 27781014 | |||||||
chr17:27781305 | G | A | 1 | a0001c0002t0002g0316 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.723-128C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 7/26 | chr17 | 27781305 | |||||||
chr17:27781388 | G | C | 1 | a0001c0002t0002g0258 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.723-211C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 7/26 | chr17 | 27781388 | |||||||
chr17:27781469 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.723-292G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 7/26 | chr17 | 27781469 | |||||||
chr17:27781704 | C | T | 1 | a0001c0005t0009g0193 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.722+311G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 7/26 | chr17 | 27781704 | |||||||
chr17:27781816 | T | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0187 |
3 | NA18942.hp1 NA18959.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.722+199A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 7/26 | chr17 | 27781816 | |||||||
chr17:27781902 | CCTGGTTT others(9): Show |
C | 70 | a0001c0001t0001g0197 a0001c0001t0001g0219 a0001c0002t0001g0022 others(67): Show |
79 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.722+97_722+112delC others(15): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 7/26 | chr17 | 27781902 | |||||||
chr17:27782004 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(226): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.722+11A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 7/26 | chr17 | 27782004 | |||||||
chr17:27782369 | C | T | 4 | a0001c0001t0001g0060 a0001c0002t0001g0059 a0001c0002t0001g0129 others(1): Show |
4 | HG02647.hp2 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-263G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 6/26 | chr17 | 27782369 | |||||||
chr17:27782391 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(90): Show |
112 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.631-285G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 6/26 | chr17 | 27782391 | |||||||
chr17:27782545 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.630+399G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 6/26 | chr17 | 27782545 | |||||||
chr17:27783156 | T | C | 10 | a0001c0001t0002g0245 a0001c0002t0002g0008 a0001c0002t0002g0023 others(7): Show |
13 | HG01192.hp1 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.468-50A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783156 | |||||||
chr17:27783240 | C | A | 1 | a0001c0002t0002g0264 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.468-134G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783240 | |||||||
chr17:27783297 | T | G | 1 | a0001c0001t0003g0139 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.468-191A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783297 | |||||||
chr17:27783443 | T | G | 1 | a0002c0003t0001g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.468-337A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783443 | |||||||
chr17:27783617 | C | T | 1 | a0001c0018t0002g0296 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.468-511G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783617 | |||||||
chr17:27783722 | G | A | 31 | a0001c0001t0001g0007 a0001c0001t0001g0112 a0001c0001t0001g0131 others(28): Show |
33 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.468-616C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783722 | |||||||
chr17:27783731 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(178): Show |
209 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.468-625G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783731 | |||||||
chr17:27783788 | C | T | 43 | a0001c0002t0001g0022 a0001c0002t0002g0297 a0001c0005t0001g0073 others(40): Show |
48 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.468-682G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783788 | |||||||
chr17:27783797 | G | A | 1 | a0003c0004t0001g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.468-691C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783797 | |||||||
chr17:27783810 | T | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0112 others(31): Show |
36 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.468-704A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783810 | |||||||
chr17:27783850 | C | T | 1 | a0001c0002t0002g0264 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.468-744G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783850 | |||||||
chr17:27783851 | G | A | 3 | a0003c0004t0001g0085 a0003c0004t0001g0086 a0003c0004t0010g0087 |
3 | HG02895.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.468-745C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27783851 | |||||||
chr17:27784131 | G | GACACACA others(7): Show |
1 | a0001c0001t0001g0222 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.468-1026_468-1025i others(16): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784131 | |||||||
chr17:27784133 | A | AAC | 48 | a0001c0001t0001g0060 a0001c0002t0001g0022 a0001c0002t0001g0059 others(45): Show |
53 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.468-1029_468-1028d others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784133 | |||||||
chr17:27784133 | A | AACAC | 29 | a0001c0001t0001g0007 a0001c0001t0001g0112 a0001c0001t0001g0131 others(26): Show |
31 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.468-1031_468-1028d others(6): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784133 | |||||||
chr17:27784133 | A | AACACACA others(3): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0181 |
2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.468-1037_468-1028d others(12): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784133 | |||||||
chr17:27784133 | A | AACACACA others(5): Show |
14 | a0001c0001t0001g0012 a0001c0001t0001g0117 a0001c0001t0001g0166 others(11): Show |
15 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-1039_468-1028d others(14): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784133 | |||||||
chr17:27784133 | A | AACACACA others(7): Show |
17 | a0001c0001t0001g0017 a0001c0001t0001g0103 a0001c0001t0001g0110 others(14): Show |
20 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.468-1041_468-1028d others(16): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784133 | |||||||
chr17:27784133 | A | AACACACA others(9): Show |
54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(51): Show |
69 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.468-1043_468-1028d others(18): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784133 | |||||||
chr17:27784133 | A | AACACACA others(11): Show |
17 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0041 others(14): Show |
20 | HG01168.hp1 HG01358.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.468-1045_468-1028d others(20): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784133 | |||||||
chr17:27784133 | A | AACACACA others(15): Show |
1 | a0001c0001t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.468-1049_468-1028d others(24): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784133 | |||||||
chr17:27784133 | A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0097 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.468-1028_468-1027i others(19): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784133 | |||||||
chr17:27784133 | A | C | 1 | a0001c0001t0001g0222 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.468-1027T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784133 | |||||||
chr17:27784133 | AACAC | A | 3 | a0001c0001t0002g0249 a0001c0010t0002g0294 a0001c0010t0002g0295 |
3 | HG02280.hp2 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.468-1031_468-1028d others(6): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784133 | |||||||
chr17:27784162 | TACC | T | 7 | a0001c0002t0002g0297 a0001c0025t0002g0299 a0002c0003t0001g0173 others(4): Show |
8 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.468-1059_468-1057d others(5): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784162 | |||||||
chr17:27784170 | C | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
129 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.468-1064G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784170 | |||||||
chr17:27784172 | A | G | 5 | a0003c0004t0001g0058 a0003c0004t0001g0061 a0003c0004t0001g0062 others(2): Show |
5 | HG01070.hp2 HG01496.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.468-1066T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784172 | |||||||
chr17:27784173 | C | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
172 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.468-1067G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784173 | |||||||
chr17:27784176 | A | C | 6 | a0001c0001t0001g0060 a0001c0002t0001g0059 a0001c0002t0001g0129 others(3): Show |
6 | HG01192.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.468-1070T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784176 | |||||||
chr17:27784200 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
129 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.468-1094C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784200 | |||||||
chr17:27784305 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.468-1199C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784305 | |||||||
chr17:27784335 | G | A | 1 | a0001c0002t0002g0281 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.468-1229C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784335 | |||||||
chr17:27784402 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
116 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.468-1296C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784402 | |||||||
chr17:27784597 | C | G | 1 | a0001c0001t0001g0175 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468-1491G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784597 | |||||||
chr17:27784860 | T | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(201): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.468-1754A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27784860 | |||||||
chr17:27785474 | CAT | C | 3 | a0001c0001t0002g0330 a0001c0001t0002g0331 a0001c0002t0001g0088 |
3 | HG00423.hp1 NA18612.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.467+2202_467+2203d others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27785474 | |||||||
chr17:27785520 | C | T | 2 | a0001c0001t0002g0330 a0001c0002t0001g0088 |
2 | HG00423.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.467+2158G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27785520 | |||||||
chr17:27785738 | G | C | 1 | a0001c0001t0002g0272 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.467+1940C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27785738 | |||||||
chr17:27785951 | G | A | 2 | a0002c0003t0005g0208 a0002c0003t0005g0209 |
2 | HG03831.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.467+1727C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27785951 | |||||||
chr17:27785957 | C | CA | 40 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0047 others(37): Show |
44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.467+1720dupT | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27785957 | |||||||
chr17:27785957 | CA | C | 38 | a0001c0001t0001g0042 a0001c0001t0001g0068 a0001c0001t0001g0090 others(35): Show |
41 | HG00140.hp1 HG01069.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.467+1720delT | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27785957 | |||||||
chr17:27785957 | CAA | C | 26 | a0001c0005t0001g0073 a0001c0005t0001g0076 a0001c0005t0001g0217 others(23): Show |
29 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.467+1719_467+1720d others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27785957 | |||||||
chr17:27785984 | G | T | 1 | a0001c0001t0002g0304 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.467+1694C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27785984 | |||||||
chr17:27786264 | TA | T | 45 | a0001c0001t0002g0249 a0001c0002t0001g0022 a0001c0002t0002g0297 others(42): Show |
51 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.467+1413delT | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27786264 | |||||||
chr17:27786340 | C | T | 3 | a0003c0004t0001g0064 a0003c0004t0001g0079 a0003c0004t0002g0251 |
3 | HG02647.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.467+1338G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27786340 | |||||||
chr17:27786574 | C | T | 1 | a0001c0012t0001g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.467+1104G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27786574 | |||||||
chr17:27786615 | G | A | 1 | a0001c0001t0002g0341 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.467+1063C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27786615 | |||||||
chr17:27786721 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0108 |
3 | HG02055.hp1 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.467+957A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27786721 | |||||||
chr17:27786753 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.467+925A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27786753 | |||||||
chr17:27787163 | A | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
7 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.467+515T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27787163 | |||||||
chr17:27787362 | T | G | 46 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(43): Show |
50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.467+316A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27787362 | |||||||
chr17:27787381 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.467+297A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27787381 | |||||||
chr17:27787422 | A | G | 1 | a0001c0002t0002g0241 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.467+256T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27787422 | |||||||
chr17:27787427 | G | A | 1 | a0003c0004t0001g0061 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.467+251C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27787427 | |||||||
chr17:27787616 | G | T | 3 | a0001c0001t0002g0002 a0001c0002t0002g0265 a0001c0027t0002g0332 |
7 | NA18951.hp1 NA18984.hp2 NA19005.hp2 others(4): Show |
intron_variant | MODIFIER | c.467+62C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 5/26 | chr17 | 27787616 | |||||||
chr17:27787837 | A | T | 1 | a0001c0002t0002g0316 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.319-11T>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27787837 | |||||||
chr17:27787976 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.319-150A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27787976 | |||||||
chr17:27788011 | T | G | 1 | a0003c0004t0001g0061 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.319-185A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788011 | |||||||
chr17:27788192 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.319-366C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788192 | |||||||
chr17:27788196 | G | GCA | 7 | a0001c0001t0002g0261 a0001c0001t0002g0263 a0001c0002t0002g0264 others(4): Show |
7 | HG00438.hp2 HG02622.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-372_319-371dup others(2): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788196 | |||||||
chr17:27788196 | G | GCACA | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(149): Show |
186 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.319-374_319-371dup others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788196 | |||||||
chr17:27788196 | G | GCACACA | 76 | a0001c0001t0001g0014 a0001c0001t0001g0055 a0001c0001t0001g0089 others(73): Show |
88 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.319-376_319-371dup others(6): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788196 | |||||||
chr17:27788196 | G | GCACACAC others(1): Show |
10 | a0001c0001t0002g0249 a0001c0002t0002g0327 a0001c0005t0001g0217 others(7): Show |
11 | HG00639.hp2 HG00733.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.319-378_319-371dup others(8): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788196 | |||||||
chr17:27788196 | G | GCACACAC others(3): Show |
46 | a0001c0001t0001g0197 a0001c0001t0001g0219 a0001c0002t0001g0022 others(43): Show |
51 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.319-380_319-371dup others(10): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788196 | |||||||
chr17:27788196 | G | GCACACAC others(5): Show |
9 | a0001c0002t0002g0297 a0002c0003t0001g0201 a0002c0003t0002g0025 others(6): Show |
11 | HG00741.hp2 HG01168.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.319-382_319-371dup others(12): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788196 | |||||||
chr17:27788196 | G | GCACACAC others(7): Show |
2 | a0002c0003t0001g0018 a0002c0003t0001g0188 |
3 | HG02698.hp2 HG03239.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.319-384_319-371dup others(14): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788196 | |||||||
chr17:27788196 | G | GCGCACAC others(3): Show |
2 | a0002c0003t0001g0213 a0002c0003t0001g0238 |
2 | HG00738.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.319-371_319-370ins others(10): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788196 | |||||||
chr17:27788196 | G | GCGCACAC others(5): Show |
1 | a0002c0003t0002g0328 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.319-371_319-370ins others(12): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788196 | |||||||
chr17:27788223 | C | CACACACA others(3): Show |
1 | a0001c0007t0001g0202 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.319-398_319-397ins others(10): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788223 | |||||||
chr17:27788276 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.319-450A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788276 | |||||||
chr17:27788549 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0170 |
3 | NA18960.hp2 NA18963.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.318+260C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 4/26 | chr17 | 27788549 | |||||||
chr17:27788998 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.196-67C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 3/26 | chr17 | 27788998 | |||||||
chr17:27789035 | G | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0096 |
4 | HG02965.hp2 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-104C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 3/26 | chr17 | 27789035 | |||||||
chr17:27789437 | T | C | 1 | a0001c0002t0002g0329 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.195+167A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 3/26 | chr17 | 27789437 | |||||||
chr17:27789486 | A | T | 1 | a0001c0001t0002g0341 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.195+118T>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 3/26 | chr17 | 27789486 | |||||||
chr17:27789756 | T | C | 1 | a0001c0001t0002g0276 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.111-68A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27789756 | |||||||
chr17:27789822 | C | T | 57 | a0001c0001t0002g0255 a0001c0001t0002g0257 a0001c0001t0002g0277 others(54): Show |
63 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.111-134G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27789822 | |||||||
chr17:27789870 | C | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(62): Show |
83 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.111-182G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27789870 | |||||||
chr17:27789881 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.111-193G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27789881 | |||||||
chr17:27789891 | A | G | 1 | a0001c0002t0002g0247 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.111-203T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27789891 | |||||||
chr17:27790381 | A | G | 130 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.111-693T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27790381 | |||||||
chr17:27790386 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.111-698C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27790386 | |||||||
chr17:27790436 | G | A | 1 | a0003c0004t0001g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.111-748C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27790436 | |||||||
chr17:27790576 | G | A | 1 | a0001c0001t0002g0249 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.111-888C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27790576 | |||||||
chr17:27790579 | C | T | 78 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(75): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.111-891G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27790579 | |||||||
chr17:27790917 | C | T | 1 | a0001c0002t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111-1229G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27790917 | |||||||
chr17:27790920 | G | A | 1 | a0001c0001t0002g0341 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.111-1232C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27790920 | |||||||
chr17:27791044 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.111-1356C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791044 | |||||||
chr17:27791070 | G | A | 3 | a0001c0001t0002g0330 a0001c0001t0002g0331 a0001c0002t0001g0088 |
3 | HG00423.hp1 NA18612.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.111-1382C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791070 | |||||||
chr17:27791381 | C | T | 1 | a0001c0002t0001g0162 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.111-1693G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791381 | |||||||
chr17:27791495 | G | A | 19 | a0001c0001t0002g0255 a0001c0001t0002g0257 a0001c0001t0002g0277 others(16): Show |
21 | HG00099.hp1 HG00280.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.111-1807C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791495 | |||||||
chr17:27791575 | C | G | 1 | a0003c0004t0001g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.111-1887G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791575 | |||||||
chr17:27791769 | G | GAAAAAAA others(4): Show |
1 | a0002c0003t0001g0206 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.111-2082_111-2081i others(13): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791769 | |||||||
chr17:27791769 | G | GAAAAAAA others(5): Show |
20 | a0001c0001t0001g0159 a0001c0002t0001g0022 a0001c0005t0001g0073 others(17): Show |
23 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.111-2082_111-2081i others(14): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791769 | |||||||
chr17:27791769 | G | GAAAAAAA others(6): Show |
16 | a0001c0001t0001g0077 a0001c0001t0001g0145 a0001c0001t0001g0160 others(13): Show |
16 | HG00280.hp2 HG00408.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.111-2082_111-2081i others(15): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791769 | |||||||
chr17:27791769 | G | GAAAAAAA others(7): Show |
2 | a0002c0003t0002g0036 a0002c0003t0002g0300 |
3 | HG02486.hp1 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.111-2082_111-2081i others(16): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791769 | |||||||
chr17:27791769 | G | GAAAAAAA others(8): Show |
3 | a0001c0005t0001g0212 a0001c0025t0002g0299 a0002c0003t0002g0298 |
3 | HG02055.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.111-2082_111-2081i others(17): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791769 | |||||||
chr17:27791769 | G | GAAAAAAA others(10): Show |
1 | a0002c0003t0002g0302 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.111-2082_111-2081i others(19): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791769 | |||||||
chr17:27791772 | AAAAAC | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
7 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-2089_111-2085d others(7): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791772 | |||||||
chr17:27791775 | AAC | A | 9 | a0001c0001t0001g0060 a0001c0002t0001g0059 a0001c0002t0001g0129 others(6): Show |
9 | HG01070.hp2 HG01496.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-2089_111-2088d others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791775 | |||||||
chr17:27791776 | AC | A | 12 | a0001c0001t0001g0068 a0001c0010t0002g0294 a0001c0010t0002g0295 others(9): Show |
12 | HG02280.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.111-2089delG | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791776 | |||||||
chr17:27791777 | C | A | 70 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0131 others(67): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.111-2089G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791777 | |||||||
chr17:27791779 | A | AAAAAAAA others(8): Show |
2 | a0001c0001t0001g0140 a0001c0001t0013g0342 |
2 | NA18980.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.111-2092_111-2091i others(17): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791779 | |||||||
chr17:27791779 | A | AAAAAAAA others(7): Show |
10 | a0001c0001t0001g0135 a0001c0001t0001g0138 a0001c0001t0001g0141 others(7): Show |
10 | HG01358.hp1 HG03669.hp2 HG03834.hp1 others(7): Show |
intron_variant | MODIFIER | c.111-2092_111-2091i others(16): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791779 | |||||||
chr17:27791779 | A | AAAAAAAA others(6): Show |
12 | a0001c0001t0001g0007 a0001c0001t0001g0131 a0001c0001t0001g0155 others(9): Show |
14 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-2092_111-2091i others(15): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791779 | |||||||
chr17:27791779 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0002g0249 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.111-2092_111-2091i others(14): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791779 | |||||||
chr17:27791779 | A | AAAAACAA others(7): Show |
1 | a0001c0002t0001g0130 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.111-2092_111-2091i others(16): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791779 | |||||||
chr17:27791782 | C | A | 80 | a0001c0001t0001g0007 a0001c0001t0001g0068 a0001c0001t0001g0077 others(77): Show |
86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.111-2094G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791782 | |||||||
chr17:27791787 | C | A | 9 | a0001c0002t0002g0297 a0001c0025t0002g0299 a0002c0003t0001g0173 others(6): Show |
10 | HG00738.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.111-2099G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791787 | |||||||
chr17:27791806 | A | AAT | 3 | a0001c0002t0002g0303 a0002c0003t0001g0236 a0002c0003t0001g0237 |
3 | HG02004.hp1 NA19055.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.111-2120_111-2119d others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791806 | |||||||
chr17:27791808 | T | A | 4 | a0001c0007t0001g0199 a0002c0003t0001g0200 a0002c0003t0001g0201 others(1): Show |
4 | HG00140.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-2120A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27791808 | |||||||
chr17:27792167 | C | T | 27 | a0001c0001t0001g0007 a0001c0001t0001g0131 a0001c0001t0001g0135 others(24): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.111-2479G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27792167 | |||||||
chr17:27792268 | C | CTG | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0002c0008t0001g0221 |
3 | HG00408.hp2 NA18983.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.111-2582_111-2581d others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27792268 | |||||||
chr17:27792268 | C | CTGTG | 19 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0002t0001g0059 others(16): Show |
19 | HG01070.hp2 HG01496.hp2 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.111-2584_111-2581d others(6): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27792268 | |||||||
chr17:27792528 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.111-2840A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27792528 | |||||||
chr17:27792610 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.111-2922G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27792610 | |||||||
chr17:27792707 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.111-3019C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27792707 | |||||||
chr17:27792815 | C | CA | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(184): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.111-3128dupT | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27792815 | |||||||
chr17:27792815 | C | CAA | 35 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0060 others(32): Show |
36 | HG00438.hp1 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.111-3129_111-3128d others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27792815 | |||||||
chr17:27792815 | C | CAAA | 14 | a0001c0001t0001g0068 a0001c0001t0001g0126 a0001c0010t0002g0295 others(11): Show |
14 | HG02056.hp2 HG02280.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-3130_111-3128d others(5): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27792815 | |||||||
chr17:27792994 | T | C | 3 | a0002c0003t0002g0025 a0002c0003t0002g0260 a0002c0026t0002g0259 |
4 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-3306A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27792994 | |||||||
chr17:27792998 | G | A | 1 | a0002c0003t0001g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.111-3310C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27792998 | |||||||
chr17:27793068 | G | A | 1 | a0001c0001t0002g0336 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.111-3380C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27793068 | |||||||
chr17:27793106 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.111-3418C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27793106 | |||||||
chr17:27793195 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.111-3507C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27793195 | |||||||
chr17:27793212 | C | G | 1 | a0002c0003t0001g0189 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.111-3524G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27793212 | |||||||
chr17:27793355 | T | C | 1 | a0001c0002t0014g0337 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.111-3667A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27793355 | |||||||
chr17:27793392 | T | G | 31 | a0001c0001t0001g0007 a0001c0001t0001g0112 a0001c0001t0001g0131 others(28): Show |
33 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.111-3704A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27793392 | |||||||
chr17:27793404 | G | T | 1 | a0002c0008t0001g0221 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.111-3716C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27793404 | |||||||
chr17:27793511 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.111-3823G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27793511 | |||||||
chr17:27793832 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.111-4144G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27793832 | |||||||
chr17:27793840 | G | A | 2 | a0001c0005t0001g0217 a0001c0005t0001g0218 |
2 | HG00639.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.111-4152C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27793840 | |||||||
chr17:27793946 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(59): Show |
79 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.111-4258C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27793946 | |||||||
chr17:27794063 | T | A | 1 | a0001c0001t0001g0127 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.111-4375A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794063 | |||||||
chr17:27794086 | C | G | 1 | a0003c0004t0001g0061 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.111-4398G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794086 | |||||||
chr17:27794595 | A | T | 1 | a0001c0001t0002g0249 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.110+4105T>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794595 | |||||||
chr17:27794627 | C | T | 2 | a0001c0010t0002g0294 a0001c0010t0002g0295 |
2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.110+4073G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794627 | |||||||
chr17:27794702 | A | G | 1 | a0001c0002t0001g0150 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.110+3998T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794702 | |||||||
chr17:27794703 | C | T | 1 | a0001c0002t0001g0150 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.110+3997G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794703 | |||||||
chr17:27794714 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.110+3986C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794714 | |||||||
chr17:27794714 | G | GCA | 68 | a0001c0001t0001g0012 a0001c0001t0001g0069 a0001c0001t0001g0077 others(65): Show |
76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.110+3984_110+3985d others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794714 | |||||||
chr17:27794714 | G | GCACA | 6 | a0001c0002t0002g0290 a0001c0002t0002g0291 a0002c0003t0001g0078 others(3): Show |
6 | HG01981.hp2 HG02040.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+3982_110+3985d others(6): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794714 | |||||||
chr17:27794714 | G | GCACACA | 8 | a0001c0010t0002g0294 a0001c0010t0002g0295 a0003c0004t0001g0062 others(5): Show |
8 | HG01070.hp2 HG02280.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.110+3980_110+3985d others(8): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794714 | |||||||
chr17:27794714 | G | GCACACAC others(1): Show |
4 | a0003c0004t0001g0065 a0003c0004t0001g0066 a0003c0004t0001g0067 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+3978_110+3985d others(10): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794714 | |||||||
chr17:27794714 | G | GCACACAC others(3): Show |
1 | a0003c0004t0002g0251 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.110+3976_110+3985d others(12): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794714 | |||||||
chr17:27794714 | G | GCACACAC others(7): Show |
2 | a0001c0001t0001g0068 a0003c0004t0001g0053 |
2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.110+3972_110+3985d others(16): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794714 | |||||||
chr17:27794714 | G | GCGCACA | 4 | a0001c0001t0001g0060 a0001c0002t0001g0059 a0001c0002t0001g0129 others(1): Show |
4 | HG02647.hp2 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+3985_110+3986i others(8): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794714 | |||||||
chr17:27794714 | GCA | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0131 a0001c0001t0001g0135 others(35): Show |
41 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.110+3984_110+3985d others(4): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794714 | |||||||
chr17:27794714 | GCACA | G | 7 | a0001c0001t0001g0166 a0001c0001t0002g0257 a0001c0002t0002g0258 others(4): Show |
8 | HG00099.hp1 HG01261.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.110+3982_110+3985d others(6): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794714 | |||||||
chr17:27794716 | A | G | 5 | a0001c0001t0002g0252 a0001c0002t0002g0307 a0002c0003t0002g0025 others(2): Show |
6 | HG00609.hp2 HG01891.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+3984T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794716 | |||||||
chr17:27794895 | C | T | 66 | a0001c0001t0001g0077 a0001c0001t0001g0197 a0001c0001t0001g0219 others(63): Show |
74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.110+3805G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794895 | |||||||
chr17:27794949 | T | C | 2 | a0001c0010t0002g0294 a0001c0010t0002g0295 |
2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.110+3751A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27794949 | |||||||
chr17:27795088 | A | G | 1 | a0001c0001t0002g0255 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.110+3612T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27795088 | |||||||
chr17:27795129 | G | A | 1 | a0001c0007t0008g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.110+3571C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27795129 | |||||||
chr17:27795159 | G | A | 69 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0131 others(66): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.110+3541C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27795159 | |||||||
chr17:27795161 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | NA18944.hp1 NA18947.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.110+3539C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27795161 | |||||||
chr17:27795412 | A | G | 1 | a0001c0028t0001g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.110+3288T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27795412 | |||||||
chr17:27795591 | T | G | 1 | a0001c0001t0001g0219 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.110+3109A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27795591 | |||||||
chr17:27795711 | A | G | 67 | a0001c0001t0001g0077 a0001c0001t0001g0197 a0001c0001t0001g0219 others(64): Show |
75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.110+2989T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27795711 | |||||||
chr17:27795735 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.110+2965C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27795735 | |||||||
chr17:27795790 | A | G | 1 | a0007c0023t0001g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110+2910T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27795790 | |||||||
chr17:27795851 | C | T | 1 | a0003c0004t0001g0085 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.110+2849G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27795851 | |||||||
chr17:27796182 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.110+2518C>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27796182 | |||||||
chr17:27796468 | T | A | 1 | a0001c0001t0002g0249 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.110+2232A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27796468 | |||||||
chr17:27796609 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.110+2091C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27796609 | |||||||
chr17:27796615 | G | A | 1 | a0001c0007t0002g0339 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.110+2085C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27796615 | |||||||
chr17:27796687 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+2013C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27796687 | |||||||
chr17:27796767 | C | T | 1 | a0001c0002t0002g0305 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.110+1933G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27796767 | |||||||
chr17:27796836 | G | A | 2 | a0002c0003t0001g0173 a0002c0003t0002g0301 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.110+1864C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27796836 | |||||||
chr17:27796935 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.110+1765T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27796935 | |||||||
chr17:27797570 | G | A | 1 | a0001c0010t0002g0292 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.110+1130C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27797570 | |||||||
chr17:27797579 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(230): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.110+1121A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27797579 | |||||||
chr17:27797632 | G | T | 1 | a0003c0004t0001g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.110+1068C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27797632 | |||||||
chr17:27797673 | T | C | 66 | a0001c0001t0001g0077 a0001c0001t0001g0197 a0001c0001t0001g0219 others(63): Show |
74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.110+1027A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27797673 | |||||||
chr17:27797701 | G | A | 1 | a0002c0003t0002g0302 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.110+999C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27797701 | |||||||
chr17:27797791 | T | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0235 |
3 | HG02027.hp1 NA18945.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.110+909A>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27797791 | |||||||
chr17:27797793 | C | T | 6 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(3): Show |
6 | HG00408.hp2 NA18957.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+907G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27797793 | |||||||
chr17:27797882 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0081 a0001c0001t0001g0145 others(24): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.110+818C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27797882 | |||||||
chr17:27797896 | G | A | 3 | a0003c0004t0001g0085 a0003c0004t0001g0086 a0003c0004t0010g0087 |
3 | HG02895.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.110+804C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27797896 | |||||||
chr17:27797957 | G | T | 2 | a0001c0001t0002g0304 a0001c0002t0002g0303 |
2 | HG01993.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.110+743C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 2/26 | chr17 | 27797957 | |||||||
chr17:27798892 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(122): Show |
147 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.-73-10C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27798892 | |||||||
chr17:27798911 | G | T | 1 | a0001c0028t0001g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-73-29C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27798911 | |||||||
chr17:27799060 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0166 a0001c0001t0001g0167 others(5): Show |
9 | HG00544.hp1 HG00597.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.-73-178A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799060 | |||||||
chr17:27799104 | AC | A | 49 | a0001c0001t0002g0002 a0001c0001t0002g0304 a0001c0001t0002g0311 others(46): Show |
58 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-73-223delG | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799104 | |||||||
chr17:27799131 | A | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0043 others(9): Show |
13 | HG02083.hp2 NA18944.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.-73-249T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799131 | |||||||
chr17:27799183 | C | CAGACCCA others(17): Show |
1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-73-325_-73-302dup others(24): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799183 | |||||||
chr17:27799319 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(229): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.-73-437T>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799319 | |||||||
chr17:27799522 | A | C | 1 | a0001c0001t0001g0041 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-73-640T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799522 | |||||||
chr17:27799537 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-73-655C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799537 | |||||||
chr17:27799610 | G | A | 9 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-728C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799610 | |||||||
chr17:27799790 | C | CA | 63 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(60): Show |
68 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.-74+548dupT | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799790 | |||||||
chr17:27799932 | AGTTATGT others(3): Show |
A | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+397_-74+406del others(10): Show |
NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799932 | |||||||
chr17:27799956 | T | A | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+383A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799956 | |||||||
chr17:27799967 | C | G | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+372G>C | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799967 | |||||||
chr17:27799969 | C | T | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+370G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799969 | |||||||
chr17:27799975 | T | C | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+364A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799975 | |||||||
chr17:27799979 | T | A | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+360A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799979 | |||||||
chr17:27799984 | A | T | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+355T>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799984 | |||||||
chr17:27799987 | A | T | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+352T>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799987 | |||||||
chr17:27799988 | T | A | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+351A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799988 | |||||||
chr17:27799991 | G | T | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+348C>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799991 | |||||||
chr17:27799997 | T | A | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+342A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27799997 | |||||||
chr17:27800000 | A | T | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+339T>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27800000 | |||||||
chr17:27800001 | T | A | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+338A>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27800001 | |||||||
chr17:27800002 | C | T | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+337G>A | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27800002 | |||||||
chr17:27800013 | G | A | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+326C>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27800013 | |||||||
chr17:27800033 | T | C | 1 | a0002c0003t0001g0238 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-74+306A>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27800033 | |||||||
chr17:27800291 | C | A | 1 | a0002c0003t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-74+48G>T | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27800291 | |||||||
chr17:27800327 | A | C | 1 | a0002c0003t0012g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+12T>G | NOS2 | ENSG00000007171.19 | transcript | ENST00000313735.11 | protein_coding | 1/26 | chr17 | 27800327 |