Item | Value |
---|---|
geneid | 64434 |
ensemblid | ENSG00000146909.8 |
hgncid | 13244 |
symbol | NOM1 |
name | nucleolar protein with MIF4G domain 1 |
refseq_nuc | NM_138400.2 |
refseq_prot | NP_612409.1 |
ensembl_nuc | ENST00000275820.4 |
ensembl_prot | ENSP00000275820.3 |
mane_status | MANE Select |
chr | chr7 |
start | 156949712 |
end | 156973176 |
strand | + |
ver | v1.2 |
region | chr7:156949712-156973176 |
region5000 | chr7:156944712-156978176 |
regionname0 | NOM1_chr7_156949712_156973176 |
regionname5000 | NOM1_chr7_156944712_156978176 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 860 | 145 | 38 | 39 | 41 | 11 | 15 | 32 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0002 | 1/0 | 860 | 141 | 22 | 14 | 83 | 2 | 19 | 61 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0003 | 0/0 | 860 | 79 | 6 | 16 | 45 | 5 | 7 | 35 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0004 | 0/0 | 860 | 11 | 0 | 0 | 11 | 0 | 0 | 10 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0005 | 0/0 | 860 | 10 | 0 | 0 | 10 | 0 | 0 | 8 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0006 | 0/0 | 859 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(854): Show |
chr7 | 156944712 | 156978176 |
a0007 | 0/0 | 860 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0008 | 0/0 | 860 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0009 | 0/0 | 860 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0010 | 0/0 | 860 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0011 | 0/0 | 860 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0012 | 0/0 | 860 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0013 | 0/0 | 860 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0014 | 0/0 | 860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0015 | 0/0 | 860 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0016 | 0/0 | 860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0017 | 0/0 | 860 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0018 | 0/0 | 860 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0019 | 0/0 | 860 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0020 | 0/0 | 860 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0021 | 0/0 | 860 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
a0022 | 0/0 | 860 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | MAASR others(855): Show |
chr7 | 156944712 | 156978176 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2580 | 128 | 30 | 35 | 36 | 11 | 15 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0001c0011 | 0/0 | 2580 | 5 | 0 | 0 | 5 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0001c0013 | 0/0 | 2580 | 4 | 3 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0001c0017 | 0/0 | 2580 | 2 | 1 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0001c0018 | 0/0 | 2580 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0001c0021 | 0/0 | 2580 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0001c0030 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0001c0031 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0002c0002 | 1/0 | 2580 | 84 | 16 | 9 | 45 | 1 | 12 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0002c0004 | 0/0 | 2580 | 42 | 0 | 2 | 37 | 1 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0002c0010 | 0/0 | 2580 | 7 | 0 | 3 | 0 | 0 | 4 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0002c0014 | 0/0 | 2580 | 3 | 3 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0002c0019 | 0/0 | 2580 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0002c0026 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0002c0028 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0002c0029 | 0/0 | 2580 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0003c0003 | 0/0 | 2580 | 70 | 0 | 13 | 45 | 5 | 7 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0003c0007 | 0/0 | 2580 | 9 | 6 | 3 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0004c0005 | 0/0 | 2580 | 11 | 0 | 0 | 11 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0005c0006 | 0/0 | 2580 | 10 | 0 | 0 | 10 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0006c0008 | 0/0 | 2577 | 8 | 7 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2572): Show |
chr7 | 156944712 | 156978176 | ||
a0007c0009 | 0/0 | 2580 | 7 | 7 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0008c0012 | 0/0 | 2580 | 5 | 5 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0009c0015 | 0/0 | 2580 | 3 | 3 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0010c0020 | 0/0 | 2580 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0011c0022 | 0/0 | 2580 | 2 | 0 | 0 | 0 | 0 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0012c0023 | 0/0 | 2580 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0013c0016 | 0/0 | 2580 | 2 | 0 | 0 | 0 | 0 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0014c0025 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0015c0037 | 0/0 | 2580 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0016c0032 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0017c0027 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0018c0034 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0019c0024 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0020c0036 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0021c0035 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 | ||
a0022c0033 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | ATGGC others(2575): Show |
chr7 | 156944712 | 156978176 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6084 | 74 | 11 | 24 | 23 | 3 | 12 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0004 | 0/0 | 6084 | 36 | 16 | 6 | 6 | 6 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0012 | 0/0 | 6085 | 3 | 1 | 1 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6080): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0014 | 0/0 | 6073 | 4 | 0 | 3 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6068): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0016 | 0/0 | 6084 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0021 | 0/0 | 6084 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0031 | 0/0 | 6085 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6080): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0032 | 0/0 | 6084 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0033 | 0/0 | 6084 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0034 | 0/0 | 6086 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6081): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0036 | 0/0 | 6085 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6080): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0037 | 0/0 | 6084 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0001t0038 | 0/0 | 6084 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0011t0001 | 0/0 | 6084 | 5 | 0 | 0 | 5 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0013t0001 | 0/0 | 6084 | 4 | 3 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0017t0001 | 0/0 | 6084 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0017t0012 | 0/0 | 6085 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6080): Show |
chr7 | 156944712 | 156978176 |
a0001c0018t0022 | 0/0 | 6083 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6078): Show |
chr7 | 156944712 | 156978176 |
a0001c0021t0001 | 0/0 | 6084 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0030t0004 | 0/0 | 6084 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0001c0031t0001 | 0/0 | 6084 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0002c0002t0003 | 1/0 | 6082 | 66 | 7 | 6 | 40 | 1 | 11 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0002c0002t0005 | 0/0 | 6082 | 3 | 0 | 0 | 3 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0002c0002t0006 | 0/0 | 6082 | 6 | 4 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0002c0002t0007 | 0/0 | 6083 | 5 | 4 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6078): Show |
chr7 | 156944712 | 156978176 |
a0002c0002t0013 | 0/0 | 6082 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0002c0002t0018 | 0/0 | 6082 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0002c0002t0030 | 0/0 | 6082 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0002c0004t0005 | 0/0 | 6082 | 30 | 0 | 0 | 29 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0002c0004t0006 | 0/0 | 6082 | 9 | 0 | 2 | 5 | 1 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0002c0004t0023 | 0/0 | 6083 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6078): Show |
chr7 | 156944712 | 156978176 |
a0002c0004t0024 | 0/0 | 6083 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6078): Show |
chr7 | 156944712 | 156978176 |
a0002c0004t0025 | 0/0 | 6082 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0002c0010t0008 | 0/0 | 6083 | 7 | 0 | 3 | 0 | 0 | 4 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6078): Show |
chr7 | 156944712 | 156978176 |
a0002c0014t0013 | 0/0 | 6082 | 3 | 3 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0002c0019t0007 | 0/0 | 6083 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6078): Show |
chr7 | 156944712 | 156978176 |
a0002c0026t0005 | 0/0 | 6082 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0002c0028t0007 | 0/0 | 6083 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6078): Show |
chr7 | 156944712 | 156978176 |
a0002c0029t0003 | 0/0 | 6082 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0003c0003t0002 | 0/0 | 6082 | 60 | 0 | 13 | 41 | 2 | 4 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0003c0003t0010 | 0/0 | 6083 | 5 | 0 | 0 | 1 | 2 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6078): Show |
chr7 | 156944712 | 156978176 |
a0003c0003t0019 | 0/0 | 6081 | 2 | 0 | 0 | 1 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6076): Show |
chr7 | 156944712 | 156978176 |
a0003c0003t0027 | 0/0 | 6082 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0003c0003t0028 | 0/0 | 6082 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0003c0003t0029 | 0/0 | 6082 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0003c0007t0002 | 0/0 | 6082 | 6 | 4 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0003c0007t0017 | 0/0 | 6082 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0003c0007t0026 | 0/0 | 6082 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0004c0005t0001 | 0/0 | 6084 | 10 | 0 | 0 | 10 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0004c0005t0012 | 0/0 | 6085 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6080): Show |
chr7 | 156944712 | 156978176 |
a0005c0006t0002 | 0/0 | 6082 | 10 | 0 | 0 | 10 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0006c0008t0003 | 0/0 | 6079 | 8 | 7 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6074): Show |
chr7 | 156944712 | 156978176 |
a0007c0009t0009 | 0/0 | 6084 | 6 | 6 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0007c0009t0035 | 0/0 | 6085 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6080): Show |
chr7 | 156944712 | 156978176 |
a0008c0012t0011 | 0/0 | 6082 | 5 | 5 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0009c0015t0015 | 0/0 | 6082 | 3 | 3 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0010c0020t0001 | 0/0 | 6084 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0011c0022t0020 | 0/0 | 6084 | 2 | 0 | 0 | 0 | 0 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0012c0023t0002 | 0/0 | 6082 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0013c0016t0003 | 0/0 | 6082 | 2 | 0 | 0 | 0 | 0 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0014c0025t0006 | 0/0 | 6082 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0015c0037t0002 | 0/0 | 6082 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0016c0032t0001 | 0/0 | 6084 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0017c0027t0001 | 0/0 | 6084 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0018c0034t0002 | 0/0 | 6082 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0019c0024t0016 | 0/0 | 6084 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
a0020c0036t0002 | 0/0 | 6082 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0021c0035t0002 | 0/0 | 6082 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6077): Show |
chr7 | 156944712 | 156978176 |
a0022c0033t0001 | 0/0 | 6084 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | AGTCG others(6079): Show |
chr7 | 156944712 | 156978176 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/1 | 9 | 0 | 4 | 1 | 1 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0003 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0011 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0012g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0012g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0012g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0014g0006 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0016g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0016g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0021g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0021g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0031g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0032g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0033g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0034g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0036g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0037g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0001t0038g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0011t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0011t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0011t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0013t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0013t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0013t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0013t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0017t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0017t0012g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0018t0022g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0021t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0030t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0001c0031t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0013 | 1/0 | 4 | 0 | 0 | 2 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0054 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0056 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0057 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0006g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0007g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0013g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0018g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0002t0030g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0075 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0076 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0006g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0006g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0006g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0023g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0024g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0004t0025g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0010t0008g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0010t0008g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0010t0008g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0010t0008g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0010t0008g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0010t0008g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0010t0008g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0014t0013g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0019t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0019t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0026t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0028t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0002c0029t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0001 | 0/0 | 10 | 0 | 6 | 4 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0059 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0062 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0065 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0068 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0069 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0010g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0010g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0010g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0010g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0010g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0019g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0019g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0027g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0028g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0003t0029g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0007t0002g0070 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0007t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0007t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0007t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0007t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0007t0017g0073 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0003c0007t0026g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0004c0005t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0004c0005t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0004c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0004c0005t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0004c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0004c0005t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0004c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0004c0005t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0004c0005t0012g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0005c0006t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0005c0006t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0005c0006t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0005c0006t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0005c0006t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0005c0006t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0005c0006t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0005c0006t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0005c0006t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0005c0006t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0006c0008t0003g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0006c0008t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0006c0008t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0006c0008t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0006c0008t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0007c0009t0009g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0007c0009t0009g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0007c0009t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0007c0009t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0007c0009t0035g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0008c0012t0011g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0008c0012t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0008c0012t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0008c0012t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0009c0015t0015g0067 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0009c0015t0015g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0010c0020t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0010c0020t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0011c0022t0020g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0012c0023t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0012c0023t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0013c0016t0003g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0014c0025t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0015c0037t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0016c0032t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0017c0027t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0018c0034t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0019c0024t0016g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0020c0036t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0021c0035t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
a0022c0033t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00099 | hp2 | a0003 | c0003 | t0010 | g0005 | EUR | GBR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0179 | EUR | GBR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00140 | hp2 | a0003 | c0003 | t0029 | g0220 | EUR | GBR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00280 | hp2 | a0002 | c0004 | t0006 | g0023 | EUR | FIN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00323 | hp1 | a0002 | c0002 | t0003 | g0181 | EUR | FIN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0136 | EUR | FIN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00408 | hp2 | a0002 | c0002 | t0003 | g0187 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00438 | hp1 | a0002 | c0004 | t0005 | g0271 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00544 | hp1 | a0002 | c0004 | t0005 | g0275 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00544 | hp2 | a0003 | c0003 | t0002 | g0064 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00558 | hp1 | a0005 | c0006 | t0002 | g0066 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00558 | hp2 | a0003 | c0003 | t0002 | g0066 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00597 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00597 | hp2 | a0002 | c0002 | t0003 | g0154 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00609 | hp1 | a0002 | c0002 | t0003 | g0167 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00621 | hp1 | a0002 | c0004 | t0005 | g0278 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00621 | hp2 | a0002 | c0004 | t0005 | g0025 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00639 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00642 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00642 | hp2 | a0002 | c0002 | t0003 | g0200 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00673 | hp1 | a0002 | c0002 | t0006 | g0132 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00673 | hp2 | a0002 | c0002 | t0003 | g0186 | EAS | CHS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00738 | hp1 | a0002 | c0002 | t0003 | g0180 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00738 | hp2 | a0001 | c0001 | t0034 | g0033 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00741 | hp1 | a0002 | c0010 | t0008 | g0085 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01069 | hp2 | a0001 | c0001 | t0014 | g0006 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01070 | hp1 | a0002 | c0002 | t0018 | g0017 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01071 | hp1 | a0002 | c0002 | t0018 | g0017 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01071 | hp2 | a0001 | c0001 | t0014 | g0006 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01074 | hp1 | a0003 | c0003 | t0002 | g0077 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0141 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01106 | hp1 | a0003 | c0003 | t0002 | g0059 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01109 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01167 | hp1 | a0003 | c0007 | t0002 | g0070 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01167 | hp2 | a0002 | c0010 | t0008 | g0084 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01168 | hp2 | a0002 | c0004 | t0006 | g0004 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01169 | hp1 | a0002 | c0004 | t0006 | g0004 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01169 | hp2 | a0003 | c0007 | t0002 | g0070 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01175 | hp1 | a0001 | c0001 | t0012 | g0033 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01175 | hp2 | a0003 | c0003 | t0002 | g0217 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01192 | hp1 | a0001 | c0001 | t0014 | g0006 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01192 | hp2 | a0002 | c0002 | t0030 | g0150 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01243 | hp1 | a0002 | c0002 | t0003 | g0052 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01243 | hp2 | a0001 | c0017 | t0001 | g0009 | AMR | PUR | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01255 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01256 | hp1 | a0001 | c0021 | t0001 | g0002 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01257 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01258 | hp2 | a0001 | c0021 | t0001 | g0002 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01346 | hp2 | a0003 | c0003 | t0002 | g0237 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01361 | hp1 | a0010 | c0020 | t0001 | g0113 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01361 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01496 | hp1 | a0001 | c0013 | t0001 | g0121 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01515 | hp1 | a0003 | c0003 | t0002 | g0213 | EUR | IBS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0140 | EUR | IBS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | IBS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01516 | hp2 | a0001 | c0001 | t0033 | g0131 | EUR | IBS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0112 | EUR | IBS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01517 | hp2 | a0003 | c0003 | t0002 | g0059 | EUR | IBS | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01884 | hp1 | a0002 | c0014 | t0013 | g0021 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01891 | hp1 | a0002 | c0002 | t0006 | g0129 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01891 | hp2 | a0001 | c0013 | t0001 | g0122 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01928 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01934 | hp1 | a0003 | c0007 | t0026 | g0231 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01934 | hp2 | a0002 | c0010 | t0008 | g0079 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01952 | hp1 | a0006 | c0008 | t0003 | g0012 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01952 | hp2 | a0002 | c0002 | t0003 | g0054 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01975 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01978 | hp1 | a0002 | c0002 | t0003 | g0057 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02027 | hp2 | a0002 | c0002 | t0003 | g0192 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02055 | hp1 | a0002 | c0002 | t0007 | g0092 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02055 | hp2 | a0006 | c0008 | t0003 | g0156 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02056 | hp1 | a0002 | c0004 | t0006 | g0267 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02056 | hp2 | a0002 | c0004 | t0005 | g0279 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02071 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02074 | hp1 | a0002 | c0002 | t0003 | g0185 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02074 | hp2 | a0005 | c0006 | t0002 | g0242 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02080 | hp2 | a0003 | c0003 | t0002 | g0233 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02083 | hp1 | a0002 | c0002 | t0003 | g0174 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02083 | hp2 | a0002 | c0002 | t0003 | g0054 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0183 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02129 | hp2 | a0002 | c0002 | t0003 | g0013 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02132 | hp1 | a0002 | c0002 | t0006 | g0135 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02132 | hp2 | a0003 | c0003 | t0002 | g0238 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02135 | hp1 | a0004 | c0005 | t0001 | g0206 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02145 | hp1 | a0008 | c0012 | t0011 | g0048 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02145 | hp2 | a0001 | c0001 | t0012 | g0003 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CDX | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02155 | hp2 | a0003 | c0003 | t0002 | g0244 | EAS | CDX | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02165 | hp1 | a0002 | c0002 | t0003 | g0172 | EAS | CDX | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0178 | EAS | CDX | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02257 | hp1 | a0002 | c0014 | t0013 | g0021 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02257 | hp2 | a0007 | c0009 | t0009 | g0049 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02258 | hp2 | a0006 | c0008 | t0003 | g0169 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02273 | hp2 | a0003 | c0003 | t0002 | g0019 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02280 | hp1 | a0002 | c0019 | t0007 | g0203 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02280 | hp2 | a0014 | c0025 | t0006 | g0283 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02293 | hp2 | a0003 | c0003 | t0002 | g0219 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02300 | hp2 | a0010 | c0020 | t0001 | g0114 | AMR | PEL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02451 | hp1 | a0006 | c0008 | t0003 | g0012 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02451 | hp2 | a0002 | c0019 | t0007 | g0202 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02523 | hp1 | a0002 | c0004 | t0005 | g0276 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02523 | hp2 | a0002 | c0002 | t0003 | g0013 | EAS | KHV | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02572 | hp2 | a0002 | c0002 | t0006 | g0044 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02602 | hp2 | a0003 | c0003 | t0010 | g0001 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02615 | hp2 | a0009 | c0015 | t0015 | g0067 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02622 | hp1 | a0008 | c0012 | t0011 | g0257 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02622 | hp2 | a0006 | c0008 | t0003 | g0012 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02630 | hp1 | a0008 | c0012 | t0011 | g0048 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02647 | hp2 | a0002 | c0002 | t0006 | g0128 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02683 | hp1 | a0011 | c0022 | t0020 | g0035 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02683 | hp2 | a0002 | c0010 | t0008 | g0081 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02698 | hp1 | a0003 | c0003 | t0002 | g0214 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02698 | hp2 | a0002 | c0010 | t0008 | g0082 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02717 | hp1 | a0007 | c0009 | t0009 | g0093 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02717 | hp2 | a0003 | c0007 | t0002 | g0240 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02738 | hp1 | a0003 | c0003 | t0002 | g0062 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02809 | hp1 | a0002 | c0002 | t0007 | g0090 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02809 | hp2 | a0006 | c0008 | t0003 | g0012 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02818 | hp2 | a0003 | c0007 | t0002 | g0230 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02886 | hp1 | a0002 | c0002 | t0003 | g0170 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02886 | hp2 | a0002 | c0002 | t0003 | g0191 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02895 | hp2 | a0002 | c0002 | t0007 | g0089 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02896 | hp2 | a0003 | c0007 | t0002 | g0232 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02922 | hp2 | a0002 | c0002 | t0003 | g0051 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02970 | hp1 | a0009 | c0015 | t0015 | g0226 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02976 | hp1 | a0007 | c0009 | t0009 | g0103 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03017 | hp2 | a0011 | c0022 | t0020 | g0035 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03041 | hp1 | a0001 | c0001 | t0032 | g0008 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03041 | hp2 | a0007 | c0009 | t0009 | g0014 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03098 | hp1 | a0002 | c0002 | t0013 | g0258 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03098 | hp2 | a0001 | c0030 | t0004 | g0008 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03130 | hp1 | a0002 | c0002 | t0003 | g0051 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03130 | hp2 | a0001 | c0013 | t0001 | g0120 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03139 | hp1 | a0002 | c0002 | t0007 | g0091 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03225 | hp1 | a0007 | c0009 | t0009 | g0014 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03225 | hp2 | a0002 | c0014 | t0013 | g0021 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03453 | hp1 | a0002 | c0028 | t0007 | g0088 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03486 | hp1 | a0007 | c0009 | t0035 | g0014 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03486 | hp2 | a0001 | c0013 | t0001 | g0146 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03490 | hp1 | a0013 | c0016 | t0003 | g0050 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03490 | hp2 | a0015 | c0037 | t0002 | g0250 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03492 | hp1 | a0013 | c0016 | t0003 | g0050 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03516 | hp2 | a0006 | c0008 | t0003 | g0165 | AFR | ESN | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03540 | hp1 | a0007 | c0009 | t0009 | g0049 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03579 | hp1 | a0002 | c0002 | t0006 | g0044 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03579 | hp2 | a0008 | c0012 | t0011 | g0284 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03654 | hp1 | a0002 | c0002 | t0003 | g0176 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03654 | hp2 | a0002 | c0002 | t0003 | g0057 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03669 | hp1 | a0003 | c0003 | t0002 | g0065 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0017 | SAS | STU | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03688 | hp2 | a0001 | c0001 | t0037 | g0027 | SAS | STU | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03704 | hp1 | a0002 | c0004 | t0006 | g0261 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03831 | hp1 | a0002 | c0002 | t0003 | g0013 | SAS | BEB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03831 | hp2 | a0003 | c0003 | t0002 | g0221 | SAS | BEB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03834 | hp1 | a0003 | c0003 | t0019 | g0005 | SAS | BEB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03834 | hp2 | a0002 | c0010 | t0008 | g0080 | SAS | BEB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03927 | hp1 | a0002 | c0002 | t0003 | g0056 | SAS | BEB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03927 | hp2 | a0003 | c0003 | t0010 | g0215 | SAS | BEB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03942 | hp1 | a0002 | c0002 | t0003 | g0155 | SAS | BEB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03942 | hp2 | a0002 | c0002 | t0003 | g0157 | SAS | BEB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG04115 | hp1 | a0002 | c0004 | t0005 | g0075 | SAS | STU | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG04115 | hp2 | a0002 | c0002 | t0003 | g0177 | SAS | STU | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG04184 | hp1 | a0002 | c0002 | t0007 | g0204 | SAS | BEB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0147 | SAS | BEB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG04199 | hp1 | a0002 | c0002 | t0003 | g0164 | SAS | STU | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG04199 | hp2 | a0002 | c0002 | t0003 | g0198 | SAS | STU | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG04204 | hp2 | a0002 | c0010 | t0008 | g0083 | SAS | STU | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG04228 | hp1 | a0002 | c0002 | t0003 | g0166 | SAS | STU | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18522 | hp1 | a0012 | c0023 | t0002 | g0235 | AFR | YRI | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18522 | hp2 | a0016 | c0032 | t0001 | g0255 | AFR | YRI | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18612 | hp1 | a0003 | c0003 | t0002 | g0058 | EAS | CHB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18612 | hp2 | a0003 | c0003 | t0002 | g0058 | EAS | CHB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18747 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | CHB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18939 | hp1 | a0001 | c0011 | t0001 | g0074 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18939 | hp2 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18941 | hp1 | a0003 | c0003 | t0002 | g0224 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18941 | hp2 | a0002 | c0002 | t0003 | g0149 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18942 | hp1 | a0001 | c0001 | t0021 | g0010 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18942 | hp2 | a0002 | c0002 | t0003 | g0188 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18943 | hp1 | a0002 | c0004 | t0005 | g0273 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18943 | hp2 | a0001 | c0001 | t0038 | g0201 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18944 | hp1 | a0002 | c0002 | t0003 | g0161 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18944 | hp2 | a0003 | c0003 | t0002 | g0068 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18945 | hp1 | a0002 | c0002 | t0003 | g0163 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18945 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18946 | hp1 | a0003 | c0003 | t0002 | g0218 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18946 | hp2 | a0001 | c0011 | t0001 | g0262 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18947 | hp1 | a0002 | c0004 | t0005 | g0270 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18947 | hp2 | a0002 | c0002 | t0005 | g0134 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18949 | hp1 | a0002 | c0002 | t0003 | g0153 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18949 | hp2 | a0005 | c0006 | t0002 | g0229 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18950 | hp1 | a0003 | c0003 | t0010 | g0060 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18950 | hp2 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18951 | hp1 | a0002 | c0002 | t0003 | g0196 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18952 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18953 | hp1 | a0002 | c0004 | t0005 | g0004 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18953 | hp2 | a0001 | c0011 | t0001 | g0022 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18954 | hp2 | a0002 | c0002 | t0003 | g0182 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18956 | hp1 | a0004 | c0005 | t0001 | g0211 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18956 | hp2 | a0002 | c0004 | t0005 | g0004 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18957 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18957 | hp2 | a0002 | c0002 | t0003 | g0197 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18959 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18960 | hp2 | a0003 | c0003 | t0028 | g0078 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18961 | hp1 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18961 | hp2 | a0001 | c0001 | t0016 | g0030 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18962 | hp2 | a0002 | c0004 | t0005 | g0025 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18963 | hp2 | a0002 | c0002 | t0003 | g0159 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18965 | hp2 | a0003 | c0003 | t0002 | g0062 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18967 | hp2 | a0002 | c0004 | t0005 | g0272 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18968 | hp1 | a0003 | c0003 | t0002 | g0020 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18968 | hp2 | a0005 | c0006 | t0002 | g0236 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18970 | hp1 | a0003 | c0003 | t0002 | g0060 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18970 | hp2 | a0004 | c0005 | t0001 | g0018 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18971 | hp1 | a0003 | c0003 | t0002 | g0227 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18971 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18973 | hp1 | a0001 | c0011 | t0001 | g0022 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18973 | hp2 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18974 | hp1 | a0002 | c0004 | t0024 | g0263 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18974 | hp2 | a0002 | c0002 | t0003 | g0158 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18978 | hp1 | a0002 | c0026 | t0005 | g0024 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18978 | hp2 | a0017 | c0027 | t0001 | g0074 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18979 | hp1 | a0004 | c0005 | t0001 | g0225 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18979 | hp2 | a0002 | c0004 | t0005 | g0024 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18980 | hp2 | a0002 | c0002 | t0005 | g0190 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18981 | hp1 | a0002 | c0002 | t0003 | g0056 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18981 | hp2 | a0002 | c0004 | t0005 | g0004 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18982 | hp1 | a0003 | c0003 | t0002 | g0247 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18982 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18983 | hp1 | a0002 | c0004 | t0005 | g0004 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18983 | hp2 | a0003 | c0003 | t0002 | g0212 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18986 | hp1 | a0002 | c0004 | t0005 | g0025 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18986 | hp2 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18988 | hp2 | a0002 | c0002 | t0003 | g0148 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18991 | hp1 | a0002 | c0004 | t0005 | g0205 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18991 | hp2 | a0003 | c0003 | t0002 | g0243 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18992 | hp1 | a0002 | c0004 | t0005 | g0268 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18992 | hp2 | a0003 | c0003 | t0002 | g0072 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18993 | hp1 | a0002 | c0004 | t0006 | g0264 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18993 | hp2 | a0004 | c0005 | t0001 | g0208 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18994 | hp1 | a0001 | c0001 | t0031 | g0133 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18994 | hp2 | a0004 | c0005 | t0001 | g0061 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18995 | hp1 | a0002 | c0002 | t0003 | g0184 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18995 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18997 | hp1 | a0003 | c0003 | t0002 | g0241 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18997 | hp2 | a0002 | c0004 | t0005 | g0023 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18998 | hp1 | a0002 | c0004 | t0005 | g0075 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA18998 | hp2 | a0001 | c0001 | t0021 | g0047 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19000 | hp1 | a0001 | c0001 | t0012 | g0139 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19000 | hp2 | a0004 | c0005 | t0012 | g0061 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19001 | hp1 | a0002 | c0002 | t0003 | g0175 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19001 | hp2 | a0002 | c0004 | t0005 | g0076 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19002 | hp1 | a0002 | c0002 | t0003 | g0152 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19003 | hp2 | a0002 | c0004 | t0005 | g0281 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19005 | hp1 | a0002 | c0002 | t0005 | g0189 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19005 | hp2 | a0001 | c0011 | t0001 | g0022 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19007 | hp1 | a0004 | c0005 | t0001 | g0018 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19007 | hp2 | a0003 | c0003 | t0002 | g0020 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19009 | hp1 | a0002 | c0002 | t0003 | g0195 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19009 | hp2 | a0003 | c0003 | t0002 | g0210 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19010 | hp1 | a0002 | c0004 | t0005 | g0274 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19010 | hp2 | a0003 | c0003 | t0002 | g0069 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19011 | hp1 | a0005 | c0006 | t0002 | g0253 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19012 | hp1 | a0002 | c0002 | t0003 | g0193 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19012 | hp2 | a0002 | c0004 | t0005 | g0269 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19030 | hp1 | a0003 | c0007 | t0017 | g0073 | AFR | LWK | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | LWK | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19043 | hp1 | a0001 | c0001 | t0036 | g0110 | AFR | LWK | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19054 | hp1 | a0002 | c0004 | t0006 | g0265 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19054 | hp2 | a0002 | c0004 | t0005 | g0280 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19055 | hp1 | a0018 | c0034 | t0002 | g0254 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19055 | hp2 | a0002 | c0004 | t0006 | g0266 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19056 | hp1 | a0003 | c0003 | t0002 | g0228 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19057 | hp1 | a0005 | c0006 | t0002 | g0246 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19057 | hp2 | a0019 | c0024 | t0016 | g0106 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19058 | hp2 | a0003 | c0003 | t0019 | g0020 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19060 | hp1 | a0020 | c0036 | t0002 | g0071 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19060 | hp2 | a0002 | c0002 | t0003 | g0162 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19064 | hp1 | a0002 | c0004 | t0025 | g0259 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19064 | hp2 | a0003 | c0003 | t0002 | g0216 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19065 | hp1 | a0002 | c0004 | t0005 | g0004 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19065 | hp2 | a0021 | c0035 | t0002 | g0222 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19066 | hp1 | a0004 | c0005 | t0001 | g0207 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19066 | hp2 | a0002 | c0004 | t0023 | g0023 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19067 | hp2 | a0003 | c0003 | t0002 | g0068 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19068 | hp2 | a0003 | c0003 | t0002 | g0069 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19070 | hp1 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19070 | hp2 | a0005 | c0006 | t0002 | g0072 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19077 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19077 | hp2 | a0005 | c0006 | t0002 | g0234 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19080 | hp1 | a0003 | c0003 | t0002 | g0209 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19081 | hp1 | a0005 | c0006 | t0002 | g0252 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19081 | hp2 | a0002 | c0002 | t0003 | g0173 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19082 | hp1 | a0003 | c0003 | t0002 | g0223 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19082 | hp2 | a0002 | c0002 | t0003 | g0282 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19083 | hp1 | a0002 | c0004 | t0005 | g0076 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19083 | hp2 | a0005 | c0006 | t0002 | g0248 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19084 | hp1 | a0003 | c0003 | t0002 | g0251 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19084 | hp2 | a0022 | c0033 | t0001 | g0063 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19085 | hp1 | a0004 | c0005 | t0001 | g0018 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19085 | hp2 | a0002 | c0004 | t0005 | g0277 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19087 | hp1 | a0002 | c0002 | t0003 | g0160 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19089 | hp1 | a0003 | c0003 | t0027 | g0001 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19089 | hp2 | a0001 | c0001 | t0016 | g0040 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19090 | hp1 | a0004 | c0005 | t0001 | g0063 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19090 | hp2 | a0002 | c0004 | t0006 | g0260 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19091 | hp1 | a0003 | c0003 | t0002 | g0065 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19091 | hp2 | a0002 | c0004 | t0005 | g0024 | EAS | JPT | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19240 | hp1 | a0001 | c0018 | t0022 | g0055 | AFR | YRI | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA19240 | hp2 | a0001 | c0017 | t0012 | g0009 | AFR | YRI | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA20129 | hp1 | a0002 | c0002 | t0003 | g0168 | AFR | ASW | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA20129 | hp2 | a0003 | c0007 | t0002 | g0239 | AFR | ASW | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA20752 | hp1 | a0003 | c0003 | t0010 | g0249 | EUR | TSI | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0137 | EUR | TSI | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA20805 | hp2 | a0001 | c0001 | t0014 | g0006 | EUR | TSI | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA20905 | hp1 | a0002 | c0029 | t0003 | g0171 | SAS | GIH | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | GIH | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02109 | hp1 | a0006 | c0008 | t0003 | g0194 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02109 | hp2 | a0002 | c0002 | t0003 | g0151 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02486 | hp1 | a0001 | c0031 | t0001 | g0142 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02486 | hp2 | a0001 | c0018 | t0022 | g0055 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG02559 | hp2 | a0003 | c0007 | t0017 | g0073 | AFR | ACB | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG03471 | hp2 | a0012 | c0023 | t0002 | g0245 | AFR | MSL | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | USA | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
HG06807 | hp2 | a0008 | c0012 | t0011 | g0145 | AFR | USA | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA20300 | hp1 | a0002 | c0002 | t0003 | g0052 | AFR | USA | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA20300 | hp2 | a0009 | c0015 | t0015 | g0067 | AFR | USA | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0094 | AFR | LWK | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0002 | REF | REF | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
homoSapiens | grch38p0 | a0002 | c0002 | t0003 | g0013 | REF | REF | NOM1_chr7_156944712_156978176 | NOM1 | chr7 | 156944712 | 156978176 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156949807 | C | G | 10 | a0003 a0004 a0005 others(7): Show |
110 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(107): Show |
missense_variant | MODERATE | c.70C>G | p.Arg24Gly | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 96/6082 | 70/2583 | 24/860 | chr7 | 156949807 | |||
chr7:156949817 | G | A | 1 | a0019 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.80G>A | p.Gly27Glu | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 106/6082 | 80/2583 | 27/860 | chr7 | 156949817 | |||
chr7:156949858 | G | A | 1 | a0022 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.121G>A | p.Ala41Thr | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 147/6082 | 121/2583 | 41/860 | chr7 | 156949858 | |||
chr7:156949921 | C | T | 2 | a0011 a0016 |
3 | HG02683.hp1 HG03017.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.184C>T | p.Pro62Ser | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 210/6082 | 184/2583 | 62/860 | chr7 | 156949921 | |||
chr7:156949942 | G | A | 1 | a0013 | 2 | HG03490.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.205G>A | p.Gly69Ser | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 231/6082 | 205/2583 | 69/860 | chr7 | 156949942 | |||
chr7:156950048 | C | T | 1 | a0016 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.311C>T | p.Pro104Leu | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 337/6082 | 311/2583 | 104/860 | chr7 | 156950048 | |||
chr7:156950052 | A | C | 1 | a0016 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.315A>C | p.Glu105Asp | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 341/6082 | 315/2583 | 105/860 | chr7 | 156950052 | |||
chr7:156950102 | A | C | 9 | a0003 a0004 a0009 others(6): Show |
100 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(97): Show |
missense_variant | MODERATE | c.365A>C | p.His122Pro | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 391/6082 | 365/2583 | 122/860 | chr7 | 156950102 | |||
chr7:156950334 | AAAG | A | 1 | a0006 | 8 | HG01952.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
conservative_inframe_deletion | MODERATE | c.601_603delAAG | p.Lys201del | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 627/6082 | 601/2583 | 201/860 | INFO_REALIGN_3_PRIME | chr7 | 156950334 | ||
chr7:156950519 | A | T | 1 | a0017 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.782A>T | p.Glu261Val | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 808/6082 | 782/2583 | 261/860 | chr7 | 156950519 | |||
chr7:156950570 | C | A | 11 | a0003 a0004 a0005 others(8): Show |
111 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(108): Show |
missense_variant | MODERATE | c.833C>A | p.Ala278Glu | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 859/6082 | 833/2583 | 278/860 | chr7 | 156950570 | |||
chr7:156954295 | C | G | 1 | a0014 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.1305C>G | p.Ile435Met | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/11 | 1331/6082 | 1305/2583 | 435/860 | chr7 | 156954295 | |||
chr7:156963087 | G | A | 1 | a0010 | 2 | HG01361.hp1 HG02300.hp2 |
missense_variant | MODERATE | c.1823G>A | p.Arg608His | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/11 | 1849/6082 | 1823/2583 | 608/860 | chr7 | 156963087 | |||
chr7:156963110 | T | C | 1 | a0018 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.1846T>C | p.Trp616Arg | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/11 | 1872/6082 | 1846/2583 | 616/860 | chr7 | 156963110 | |||
chr7:156963130 | C | G | 1 | a0016 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1866C>G | p.Ile622Met | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/11 | 1892/6082 | 1866/2583 | 622/860 | chr7 | 156963130 | |||
chr7:156963168 | T | C | 1 | a0008 | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
missense_variant | MODERATE | c.1904T>C | p.Val635Ala | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/11 | 1930/6082 | 1904/2583 | 635/860 | chr7 | 156963168 | |||
chr7:156963929 | G | T | 1 | a0015 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.1936G>T | p.Ala646Ser | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/11 | 1962/6082 | 1936/2583 | 646/860 | chr7 | 156963929 | |||
chr7:156966378 | C | A | 1 | a0021 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.2142C>A | p.Phe714Leu | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 8/11 | 2168/6082 | 2142/2583 | 714/860 | chr7 | 156966378 | |||
chr7:156969123 | C | T | 1 | a0009 | 3 | HG02615.hp2 HG02970.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.2335C>T | p.Arg779Cys | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 10/11 | 2361/6082 | 2335/2583 | 779/860 | chr7 | 156969123 | |||
chr7:156969124 | G | A | 9 | a0001 a0004 a0008 others(6): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
missense_variant | MODERATE | c.2336G>A | p.Arg779His | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 10/11 | 2362/6082 | 2336/2583 | 779/860 | chr7 | 156969124 | |||
chr7:156969133 | G | A | 1 | a0020 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.2345G>A | p.Arg782Gln | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 10/11 | 2371/6082 | 2345/2583 | 782/860 | chr7 | 156969133 | |||
chr7:156969530 | G | C | 9 | a0001 a0004 a0007 others(6): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
missense_variant&splice_region_variant | MODERATE | c.2410G>C | p.Val804Leu | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2436/6082 | 2410/2583 | 804/860 | chr7 | 156969530 | |||
chr7:156969554 | G | A | 11 | a0001 a0004 a0007 others(8): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
missense_variant | MODERATE | c.2434G>A | p.Val812Met | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2460/6082 | 2434/2583 | 812/860 | chr7 | 156969554 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156949911 | A | G | 1 | a0016c0032 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.174A>G | p.Glu58Glu | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 200/6082 | 174/2583 | 58/860 | chr7 | 156949911 | |||
chr7:156950031 | G | A | 1 | a0014c0025 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.294G>A | p.Leu98Leu | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 320/6082 | 294/2583 | 98/860 | chr7 | 156950031 | |||
chr7:156950055 | G | A | 11 | a0003c0003 a0003c0007 a0004c0005 others(8): Show |
110 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(107): Show |
synonymous_variant | LOW | c.318G>A | p.Gln106Gln | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 344/6082 | 318/2583 | 106/860 | chr7 | 156950055 | |||
chr7:156950085 | C | A | 4 | a0001c0011 a0002c0004 a0002c0026 others(1): Show |
49 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
synonymous_variant | LOW | c.348C>A | p.Ala116Ala | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 374/6082 | 348/2583 | 116/860 | chr7 | 156950085 | |||
chr7:156950148 | C | T | 1 | a0001c0021 | 2 | HG01256.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.411C>T | p.Asp137Asp | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 437/6082 | 411/2583 | 137/860 | chr7 | 156950148 | |||
chr7:156950271 | G | C | 14 | a0002c0014 a0002c0026 a0003c0003 others(11): Show |
115 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(112): Show |
synonymous_variant | LOW | c.534G>C | p.Ala178Ala | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 560/6082 | 534/2583 | 178/860 | chr7 | 156950271 | |||
chr7:156950316 | C | A | 1 | a0001c0017 | 2 | HG01243.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.579C>A | p.Leu193Leu | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 605/6082 | 579/2583 | 193/860 | chr7 | 156950316 | |||
chr7:156950379 | C | T | 1 | a0014c0025 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.642C>T | p.Asp214Asp | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 668/6082 | 642/2583 | 214/860 | chr7 | 156950379 | |||
chr7:156950463 | C | G | 2 | a0001c0013 a0010c0020 |
6 | HG01361.hp1 HG01496.hp1 HG01891.hp2 others(3): Show |
synonymous_variant | LOW | c.726C>G | p.Ala242Ala | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/11 | 752/6082 | 726/2583 | 242/860 | chr7 | 156950463 | |||
chr7:156952530 | G | A | 3 | a0003c0007 a0009c0015 a0012c0023 |
14 | HG01167.hp1 HG01169.hp2 HG01934.hp1 others(11): Show |
synonymous_variant | LOW | c.1044G>A | p.Glu348Glu | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/11 | 1070/6082 | 1044/2583 | 348/860 | chr7 | 156952530 | |||
chr7:156952593 | T | G | 1 | a0002c0028 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1107T>G | p.Leu369Leu | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/11 | 1133/6082 | 1107/2583 | 369/860 | chr7 | 156952593 | |||
chr7:156954196 | C | T | 1 | a0002c0010 | 7 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(4): Show |
synonymous_variant | LOW | c.1206C>T | p.Ser402Ser | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/11 | 1232/6082 | 1206/2583 | 402/860 | chr7 | 156954196 | |||
chr7:156963046 | C | T | 1 | a0001c0031 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1782C>T | p.Arg594Arg | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/11 | 1808/6082 | 1782/2583 | 594/860 | chr7 | 156963046 | |||
chr7:156963082 | G | A | 1 | a0002c0029 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1818G>A | p.Thr606Thr | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/11 | 1844/6082 | 1818/2583 | 606/860 | chr7 | 156963082 | |||
chr7:156963952 | A | G | 4 | a0001c0018 a0002c0019 a0007c0009 others(1): Show |
16 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(13): Show |
synonymous_variant | LOW | c.1959A>G | p.Thr653Thr | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/11 | 1985/6082 | 1959/2583 | 653/860 | chr7 | 156963952 | |||
chr7:156969628 | C | T | 1 | a0001c0030 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.2508C>T | p.Asp836Asp | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2534/6082 | 2508/2583 | 836/860 | chr7 | 156969628 | |||
chr7:156969646 | A | G | 1 | a0008c0012 | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
synonymous_variant | LOW | c.2526A>G | p.Arg842Arg | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2552/6082 | 2526/2583 | 842/860 | chr7 | 156969646 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156969752 | G | T | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*49G>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 49 | chr7 | 156969752 | ||||||
chr7:156970005 | T | C | 4 | a0002c0002t0005 a0002c0004t0005 a0002c0004t0023 others(1): Show |
35 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*302T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 302 | chr7 | 156970005 | ||||||
chr7:156970010 | G | A | 1 | a0008c0012t0011 | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*307G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 307 | chr7 | 156970010 | ||||||
chr7:156970125 | T | C | 5 | a0001c0001t0004 a0001c0001t0031 a0001c0001t0032 others(2): Show |
40 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*422T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 422 | chr7 | 156970125 | ||||||
chr7:156970271 | CT | C | 43 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(40): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*572delT | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 572 | INFO_REALIGN_3_PRIME | chr7 | 156970271 | |||||
chr7:156970290 | C | CA | 31 | a0001c0001t0012 a0001c0001t0031 a0001c0001t0036 others(28): Show |
159 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*603dupA | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 604 | INFO_REALIGN_3_PRIME | chr7 | 156970290 | |||||
chr7:156970290 | C | CAA | 4 | a0001c0001t0034 a0002c0004t0023 a0002c0004t0024 others(1): Show |
8 | HG00099.hp2 HG00738.hp2 HG02602.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*602_*603dupAA | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 604 | INFO_REALIGN_3_PRIME | chr7 | 156970290 | |||||
chr7:156970290 | CA | C | 2 | a0001c0018t0022 a0008c0012t0011 |
7 | HG02145.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*603delA | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 603 | INFO_REALIGN_3_PRIME | chr7 | 156970290 | |||||
chr7:156970394 | A | G | 1 | a0001c0001t0021 | 2 | NA18942.hp1 NA18998.hp2 |
3_prime_UTR_variant | MODIFIER | c.*691A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 691 | chr7 | 156970394 | ||||||
chr7:156970402 | C | T | 1 | a0001c0018t0022 | 2 | HG02486.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*699C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 699 | chr7 | 156970402 | ||||||
chr7:156970494 | T | C | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*791T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 791 | chr7 | 156970494 | ||||||
chr7:156970538 | TGGGACTA others(4): Show |
T | 1 | a0001c0001t0014 | 4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*836_*846delGGGACT others(5): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 836 | chr7 | 156970538 | ||||||
chr7:156970554 | C | T | 28 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(25): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*851C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 851 | chr7 | 156970554 | ||||||
chr7:156970604 | A | G | 1 | a0001c0001t0038 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 901 | chr7 | 156970604 | ||||||
chr7:156970645 | A | C | 63 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(60): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
3_prime_UTR_variant | MODIFIER | c.*942A>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 942 | chr7 | 156970645 | ||||||
chr7:156970652 | T | C | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*949T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 949 | chr7 | 156970652 | ||||||
chr7:156970671 | T | C | 1 | a0001c0001t0032 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*968T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 968 | chr7 | 156970671 | ||||||
chr7:156970696 | G | A | 1 | a0003c0007t0026 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*993G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 993 | chr7 | 156970696 | ||||||
chr7:156970856 | A | G | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1153A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1153 | chr7 | 156970856 | ||||||
chr7:156970875 | T | G | 1 | a0011c0022t0020 | 2 | HG02683.hp1 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1172T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1172 | chr7 | 156970875 | ||||||
chr7:156970894 | C | T | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1191C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1191 | chr7 | 156970894 | ||||||
chr7:156970895 | A | T | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1192A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1192 | chr7 | 156970895 | ||||||
chr7:156970908 | C | CT | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1206dupT | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1207 | INFO_REALIGN_3_PRIME | chr7 | 156970908 | |||||
chr7:156970952 | C | T | 15 | a0003c0003t0002 a0003c0003t0010 a0003c0003t0019 others(12): Show |
95 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1249C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1249 | chr7 | 156970952 | ||||||
chr7:156971026 | A | T | 11 | a0002c0002t0005 a0002c0002t0006 a0002c0002t0013 others(8): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1323A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1323 | chr7 | 156971026 | ||||||
chr7:156971032 | A | G | 1 | a0008c0012t0011 | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1329A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1329 | chr7 | 156971032 | ||||||
chr7:156971153 | A | G | 11 | a0002c0002t0005 a0002c0002t0006 a0002c0002t0013 others(8): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1450A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1450 | chr7 | 156971153 | ||||||
chr7:156971230 | T | G | 1 | a0003c0003t0027 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1527T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1527 | chr7 | 156971230 | ||||||
chr7:156971237 | A | C | 2 | a0001c0001t0016 a0019c0024t0016 |
3 | NA18961.hp2 NA19057.hp2 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1534A>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1534 | chr7 | 156971237 | ||||||
chr7:156971290 | C | T | 1 | a0003c0003t0029 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1587C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1587 | chr7 | 156971290 | ||||||
chr7:156971345 | T | C | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1642T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1642 | chr7 | 156971345 | ||||||
chr7:156971378 | T | C | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1675T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1675 | chr7 | 156971378 | ||||||
chr7:156971460 | T | TA | 1 | a0002c0010t0008 | 7 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1758dupA | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1759 | INFO_REALIGN_3_PRIME | chr7 | 156971460 | |||||
chr7:156971551 | T | C | 11 | a0002c0002t0005 a0002c0002t0006 a0002c0002t0013 others(8): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1848T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1848 | chr7 | 156971551 | ||||||
chr7:156971575 | T | TG | 31 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(28): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1873dupG | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1874 | INFO_REALIGN_3_PRIME | chr7 | 156971575 | |||||
chr7:156971585 | A | G | 31 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(28): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1882A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1882 | chr7 | 156971585 | ||||||
chr7:156971656 | G | C | 4 | a0002c0002t0007 a0002c0010t0008 a0002c0019t0007 others(1): Show |
15 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1953G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1953 | chr7 | 156971656 | ||||||
chr7:156971672 | G | A | 1 | a0001c0001t0037 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1969G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 1969 | chr7 | 156971672 | ||||||
chr7:156971737 | T | G | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*2034T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2034 | chr7 | 156971737 | ||||||
chr7:156971745 | A | G | 1 | a0008c0012t0011 | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2042A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2042 | chr7 | 156971745 | ||||||
chr7:156971810 | C | G | 1 | a0002c0002t0030 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2107C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2107 | chr7 | 156971810 | ||||||
chr7:156971920 | T | C | 4 | a0002c0002t0007 a0002c0010t0008 a0002c0019t0007 others(1): Show |
15 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2217T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2217 | chr7 | 156971920 | ||||||
chr7:156971990 | C | G | 1 | a0002c0004t0025 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2287C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2287 | chr7 | 156971990 | ||||||
chr7:156972033 | G | A | 1 | a0003c0007t0017 | 2 | HG02559.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2330G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2330 | chr7 | 156972033 | ||||||
chr7:156972072 | A | C | 28 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(25): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*2369A>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2369 | chr7 | 156972072 | ||||||
chr7:156972156 | G | A | 1 | a0001c0018t0022 | 2 | HG02486.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2453G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2453 | chr7 | 156972156 | ||||||
chr7:156972193 | G | A | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*2490G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2490 | chr7 | 156972193 | ||||||
chr7:156972271 | T | C | 1 | a0001c0001t0033 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2568T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2568 | chr7 | 156972271 | ||||||
chr7:156972277 | C | T | 15 | a0003c0003t0002 a0003c0003t0010 a0003c0003t0019 others(12): Show |
95 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2574C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2574 | chr7 | 156972277 | ||||||
chr7:156972278 | G | A | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*2575G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2575 | chr7 | 156972278 | ||||||
chr7:156972302 | C | T | 2 | a0002c0002t0013 a0002c0014t0013 |
4 | HG01884.hp1 HG02257.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2599C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2599 | chr7 | 156972302 | ||||||
chr7:156972349 | C | A | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*2646C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2646 | chr7 | 156972349 | ||||||
chr7:156972410 | TC | T | 15 | a0003c0003t0002 a0003c0003t0010 a0003c0003t0019 others(12): Show |
95 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2710delC | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2710 | INFO_REALIGN_3_PRIME | chr7 | 156972410 | |||||
chr7:156972413 | C | G | 15 | a0003c0003t0002 a0003c0003t0010 a0003c0003t0019 others(12): Show |
95 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2710C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2710 | chr7 | 156972413 | ||||||
chr7:156972419 | T | C | 1 | a0008c0012t0011 | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2716T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2716 | chr7 | 156972419 | ||||||
chr7:156972462 | GT | G | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*2761delT | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2761 | INFO_REALIGN_3_PRIME | chr7 | 156972462 | |||||
chr7:156972549 | A | G | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*2846A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2846 | chr7 | 156972549 | ||||||
chr7:156972674 | A | G | 1 | a0002c0002t0018 | 2 | HG01070.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2971A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 2971 | chr7 | 156972674 | ||||||
chr7:156972761 | C | T | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*3058C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 3058 | chr7 | 156972761 | ||||||
chr7:156972784 | C | T | 1 | a0001c0001t0036 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3081C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 3081 | chr7 | 156972784 | ||||||
chr7:156973103 | A | ATC | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(29): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*3401_*3402dupTC | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 3403 | INFO_REALIGN_3_PRIME | chr7 | 156973103 | |||||
chr7:156973112 | A | G | 1 | a0003c0003t0028 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3409A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 11/11 | 3409 | chr7 | 156973112 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156950761 | C | T | 1 | a0008c0012t0011g0284 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.987+37C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156950761 | |||||||
chr7:156950816 | G | C | 1 | a0003c0003t0002g0077 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.987+92G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156950816 | |||||||
chr7:156950954 | A | C | 1 | a0014c0025t0006g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.987+230A>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156950954 | |||||||
chr7:156950961 | A | G | 1 | a0002c0002t0003g0282 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.987+237A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156950961 | |||||||
chr7:156950975 | G | A | 1 | a0003c0003t0028g0078 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.987+251G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156950975 | |||||||
chr7:156950998 | G | T | 36 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(33): Show |
48 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.987+274G>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156950998 | |||||||
chr7:156951123 | C | T | 3 | a0002c0002t0013g0258 a0002c0014t0013g0021 a0008c0012t0011g0257 |
5 | HG01884.hp1 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+399C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951123 | |||||||
chr7:156951247 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.987+523A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951247 | |||||||
chr7:156951253 | C | A | 7 | a0002c0010t0008g0079 a0002c0010t0008g0080 a0002c0010t0008g0081 others(4): Show |
7 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.987+529C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951253 | |||||||
chr7:156951295 | A | G | 85 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(82): Show |
112 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.987+571A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951295 | |||||||
chr7:156951329 | C | G | 85 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(82): Show |
112 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.987+605C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951329 | |||||||
chr7:156951348 | C | A | 84 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(81): Show |
111 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.987+624C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951348 | |||||||
chr7:156951349 | T | G | 84 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(81): Show |
111 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.987+625T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951349 | |||||||
chr7:156951374 | C | G | 132 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(129): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.987+650C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951374 | |||||||
chr7:156951433 | T | C | 85 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(82): Show |
112 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.987+709T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951433 | |||||||
chr7:156951436 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG00609.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.987+712T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951436 | |||||||
chr7:156951613 | A | T | 84 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(81): Show |
111 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.988-861A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951613 | |||||||
chr7:156951748 | T | C | 137 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(134): Show |
176 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.988-726T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951748 | |||||||
chr7:156951762 | G | T | 1 | a0001c0001t0038g0201 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.988-712G>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156951762 | |||||||
chr7:156952001 | C | T | 2 | a0002c0002t0003g0057 a0002c0002t0003g0200 |
3 | HG00642.hp2 HG01978.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.988-473C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156952001 | |||||||
chr7:156952058 | A | C | 1 | a0016c0032t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.988-416A>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156952058 | |||||||
chr7:156952078 | C | T | 3 | a0005c0006t0002g0252 a0005c0006t0002g0253 a0018c0034t0002g0254 |
3 | NA19011.hp1 NA19055.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.988-396C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156952078 | |||||||
chr7:156952132 | A | G | 25 | a0002c0004t0005g0004 a0002c0004t0005g0023 a0002c0004t0005g0024 others(22): Show |
35 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.988-342A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156952132 | |||||||
chr7:156952156 | G | A | 1 | a0016c0032t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.988-318G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156952156 | |||||||
chr7:156952163 | A | T | 1 | a0003c0003t0002g0251 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.988-311A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 1/10 | chr7 | 156952163 | |||||||
chr7:156952776 | C | T | 83 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(80): Show |
110 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1112+178C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156952776 | |||||||
chr7:156952951 | C | G | 1 | a0016c0032t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1112+353C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156952951 | |||||||
chr7:156953029 | C | T | 1 | a0001c0001t0004g0199 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1112+431C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953029 | |||||||
chr7:156953059 | G | T | 1 | a0014c0025t0006g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1112+461G>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953059 | |||||||
chr7:156953115 | TTTTTG | T | 85 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(82): Show |
112 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1112+538_1112+542d others(7): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 156953115 | ||||||
chr7:156953180 | A | G | 1 | a0001c0011t0001g0022 | 3 | NA18953.hp2 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1112+582A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953180 | |||||||
chr7:156953193 | G | A | 84 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(81): Show |
111 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1112+595G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953193 | |||||||
chr7:156953375 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1113-728G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953375 | |||||||
chr7:156953380 | A | G | 84 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(81): Show |
111 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1113-723A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953380 | |||||||
chr7:156953387 | G | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(247): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.1113-716G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953387 | |||||||
chr7:156953418 | G | A | 6 | a0001c0001t0004g0008 a0001c0001t0004g0026 a0001c0001t0004g0094 others(3): Show |
8 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113-685G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953418 | |||||||
chr7:156953423 | G | T | 1 | a0001c0001t0004g0147 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1113-680G>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953423 | |||||||
chr7:156953456 | C | T | 1 | a0014c0025t0006g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1113-647C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953456 | |||||||
chr7:156953468 | G | A | 129 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(126): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1113-635G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953468 | |||||||
chr7:156953602 | G | A | 45 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(42): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1113-501G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953602 | |||||||
chr7:156953625 | A | G | 1 | a0001c0013t0001g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1113-478A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953625 | |||||||
chr7:156953870 | A | G | 1 | a0002c0002t0003g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1113-233A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953870 | |||||||
chr7:156953884 | A | G | 84 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(81): Show |
111 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1113-219A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156953884 | |||||||
chr7:156954007 | T | C | 84 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(81): Show |
111 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1113-96T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156954007 | |||||||
chr7:156954033 | T | C | 84 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(81): Show |
111 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1113-70T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 2/10 | chr7 | 156954033 | |||||||
chr7:156954441 | A | G | 2 | a0007c0009t0009g0049 a0007c0009t0009g0093 |
3 | HG02257.hp2 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1308+143A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954441 | |||||||
chr7:156954447 | T | C | 2 | a0002c0002t0003g0148 a0002c0002t0007g0204 |
2 | HG04184.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1308+149T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954447 | |||||||
chr7:156954466 | C | G | 1 | a0015c0037t0002g0250 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1308+168C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954466 | |||||||
chr7:156954488 | TTTTGCTT others(3): Show |
T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(111): Show |
166 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1308+198_1308+207d others(12): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954488 | ||||||
chr7:156954510 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1308+212G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954510 | |||||||
chr7:156954522 | C | CT | 44 | a0001c0001t0004g0143 a0001c0001t0004g0144 a0001c0011t0001g0022 others(41): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1308+244dupT | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | C | CTT | 10 | a0002c0002t0007g0089 a0002c0002t0007g0090 a0002c0002t0007g0091 others(7): Show |
11 | HG02056.hp1 HG02809.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1308+243_1308+244d others(4): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | C | CTTT | 6 | a0002c0002t0007g0092 a0003c0003t0002g0058 a0008c0012t0011g0048 others(3): Show |
8 | HG02055.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1308+242_1308+244d others(5): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | C | CTTTTTTT others(9): Show |
12 | a0003c0003t0002g0019 a0003c0003t0002g0059 a0003c0003t0002g0060 others(9): Show |
17 | HG01106.hp1 HG01515.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.1308+229_1308+244d others(18): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | C | CTTTTTTT others(10): Show |
18 | a0003c0003t0002g0001 a0003c0003t0002g0020 a0003c0003t0002g0062 others(15): Show |
30 | HG00140.hp2 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1308+228_1308+244d others(19): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | C | CTTTTTTT others(11): Show |
19 | a0003c0003t0002g0005 a0003c0003t0002g0065 a0003c0003t0002g0066 others(16): Show |
25 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.1308+227_1308+244d others(20): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | C | CTTTTTTT others(12): Show |
13 | a0003c0003t0002g0069 a0003c0003t0002g0071 a0003c0003t0002g0233 others(10): Show |
15 | HG01167.hp1 HG01169.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1308+226_1308+244d others(21): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | C | CTTTTTTT others(13): Show |
8 | a0003c0003t0002g0072 a0003c0003t0002g0238 a0003c0003t0002g0241 others(5): Show |
8 | HG02074.hp2 HG02132.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1308+225_1308+244d others(22): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | C | CTTTTTTT others(14): Show |
3 | a0003c0003t0002g0244 a0005c0006t0002g0246 a0012c0023t0002g0245 |
3 | HG02155.hp2 HG03471.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1308+244_1308+245i others(23): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | C | CTTTTTTT others(15): Show |
2 | a0003c0003t0002g0247 a0005c0006t0002g0248 |
2 | NA18982.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1308+244_1308+245i others(24): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | C | CTTTTTTT others(17): Show |
2 | a0003c0007t0017g0073 a0018c0034t0002g0254 |
3 | HG02559.hp2 NA19030.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1308+244_1308+245i others(26): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | C | CTTTTTTT others(18): Show |
1 | a0003c0003t0010g0249 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1308+244_1308+245i others(27): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | CT | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(43): Show |
71 | HG00408.hp1 HG01069.hp2 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.1308+244delT | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954522 | CTT | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0027 others(34): Show |
55 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1308+243_1308+244d others(4): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954522 | ||||||
chr7:156954548 | AG | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(157): Show |
224 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1308+253delG | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156954548 | ||||||
chr7:156954555 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(157): Show |
224 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1308+257C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954555 | |||||||
chr7:156954592 | A | G | 5 | a0002c0004t0005g0076 a0002c0004t0005g0278 a0002c0004t0005g0279 others(2): Show |
6 | HG00621.hp1 HG02056.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+294A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954592 | |||||||
chr7:156954634 | G | C | 1 | a0002c0002t0030g0150 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1308+336G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954634 | |||||||
chr7:156954756 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1308+458T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954756 | |||||||
chr7:156954787 | G | T | 1 | a0001c0031t0001g0142 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1308+489G>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954787 | |||||||
chr7:156954856 | G | A | 3 | a0002c0002t0006g0044 a0002c0002t0006g0128 a0002c0002t0006g0129 |
4 | HG01891.hp1 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308+558G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954856 | |||||||
chr7:156954861 | A | G | 2 | a0001c0001t0004g0140 a0001c0001t0004g0141 |
2 | HG01099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1308+563A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954861 | |||||||
chr7:156954903 | A | G | 17 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(14): Show |
33 | HG00408.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1308+605A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156954903 | |||||||
chr7:156955002 | A | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(241): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.1308+704A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955002 | |||||||
chr7:156955141 | C | T | 36 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(33): Show |
48 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1308+843C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955141 | |||||||
chr7:156955163 | T | C | 2 | a0002c0002t0003g0051 a0002c0002t0003g0151 |
3 | HG02109.hp2 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1308+865T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955163 | |||||||
chr7:156955201 | C | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1308+903C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955201 | |||||||
chr7:156955225 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1308+927T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955225 | |||||||
chr7:156955347 | T | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1308+1049T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955347 | |||||||
chr7:156955372 | GT | G | 5 | a0002c0002t0007g0089 a0002c0002t0007g0090 a0002c0002t0007g0091 others(2): Show |
5 | HG02055.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1308+1076delT | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156955372 | ||||||
chr7:156955387 | A | G | 1 | a0001c0001t0004g0147 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1308+1089A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955387 | |||||||
chr7:156955482 | T | TAC | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(241): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.1308+1185_1308+118 others(6): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156955482 | ||||||
chr7:156955503 | C | G | 1 | a0016c0032t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1308+1205C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955503 | |||||||
chr7:156955543 | T | C | 1 | a0001c0001t0004g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1308+1245T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955543 | |||||||
chr7:156955580 | A | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1308+1282A>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955580 | |||||||
chr7:156955609 | C | T | 3 | a0002c0002t0013g0258 a0002c0014t0013g0021 a0008c0012t0011g0257 |
5 | HG01884.hp1 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1308+1311C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955609 | |||||||
chr7:156955668 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1308+1370T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955668 | |||||||
chr7:156955702 | C | T | 7 | a0003c0003t0002g0020 a0003c0003t0002g0068 a0003c0003t0002g0216 others(4): Show |
9 | NA18944.hp2 NA18960.hp2 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.1308+1404C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955702 | |||||||
chr7:156955727 | G | A | 3 | a0002c0002t0006g0044 a0002c0002t0006g0128 a0002c0002t0006g0129 |
4 | HG01891.hp1 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308+1429G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955727 | |||||||
chr7:156955816 | A | T | 1 | a0003c0003t0002g0237 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1308+1518A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955816 | |||||||
chr7:156955821 | A | G | 2 | a0002c0004t0006g0265 a0002c0004t0006g0267 |
2 | HG02056.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1308+1523A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955821 | |||||||
chr7:156955851 | T | C | 3 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0284 |
4 | HG02145.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308+1553T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955851 | |||||||
chr7:156955865 | A | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(241): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.1308+1567A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955865 | |||||||
chr7:156955918 | C | T | 5 | a0002c0019t0007g0202 a0002c0019t0007g0203 a0008c0012t0011g0048 others(2): Show |
6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+1620C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955918 | |||||||
chr7:156955929 | T | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1308+1631T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156955929 | |||||||
chr7:156956061 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1308+1763C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956061 | |||||||
chr7:156956142 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0256 a0001c0017t0001g0009 others(1): Show |
5 | HG01243.hp2 HG01884.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1308+1844G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956142 | |||||||
chr7:156956147 | C | T | 1 | a0005c0006t0002g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1308+1849C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956147 | |||||||
chr7:156956192 | C | CA | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(116): Show |
171 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1308+1908dupA | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156956192 | ||||||
chr7:156956216 | A | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1308+1918A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956216 | |||||||
chr7:156956314 | A | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1308+2016A>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956314 | |||||||
chr7:156956315 | C | G | 5 | a0002c0019t0007g0202 a0002c0019t0007g0203 a0008c0012t0011g0048 others(2): Show |
6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+2017C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956315 | |||||||
chr7:156956316 | G | A | 128 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(125): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1308+2018G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956316 | |||||||
chr7:156956342 | A | G | 128 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(125): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1308+2044A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956342 | |||||||
chr7:156956535 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1308+2237G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956535 | |||||||
chr7:156956570 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1308+2272G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956570 | |||||||
chr7:156956582 | T | C | 5 | a0002c0019t0007g0202 a0002c0019t0007g0203 a0008c0012t0011g0048 others(2): Show |
6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+2284T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956582 | |||||||
chr7:156956589 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1308+2291G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956589 | |||||||
chr7:156956739 | T | G | 1 | a0002c0028t0007g0088 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1308+2441T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956739 | |||||||
chr7:156956897 | T | G | 2 | a0003c0003t0002g0238 a0003c0003t0002g0244 |
2 | HG02132.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1308+2599T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956897 | |||||||
chr7:156956905 | T | C | 1 | a0016c0032t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1308+2607T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956905 | |||||||
chr7:156956919 | A | G | 3 | a0002c0004t0005g0025 a0002c0004t0005g0205 a0002c0004t0005g0277 |
5 | HG00621.hp2 NA18962.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1308+2621A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156956919 | |||||||
chr7:156957021 | AT | A | 128 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(125): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1308+2726delT | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156957021 | ||||||
chr7:156957047 | A | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1308+2749A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957047 | |||||||
chr7:156957391 | C | A | 3 | a0002c0002t0013g0258 a0002c0014t0013g0021 a0008c0012t0011g0257 |
5 | HG01884.hp1 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309-2460C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957391 | |||||||
chr7:156957461 | A | T | 1 | a0003c0003t0010g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1309-2390A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957461 | |||||||
chr7:156957469 | G | A | 83 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0019 others(80): Show |
110 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1309-2382G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957469 | |||||||
chr7:156957542 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1309-2309G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957542 | |||||||
chr7:156957647 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1309-2204T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957647 | |||||||
chr7:156957716 | A | G | 1 | a0014c0025t0006g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1309-2135A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957716 | |||||||
chr7:156957723 | C | T | 1 | a0014c0025t0006g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1309-2128C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957723 | |||||||
chr7:156957733 | CCACTG | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1309-2113_1309-210 others(9): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156957733 | ||||||
chr7:156957753 | C | T | 128 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(125): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1309-2098C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957753 | |||||||
chr7:156957761 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0021g0010 others(1): Show |
6 | NA18942.hp1 NA18954.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1309-2090C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957761 | |||||||
chr7:156957774 | C | CA | 70 | a0002c0002t0003g0052 a0002c0002t0003g0057 a0002c0002t0003g0148 others(67): Show |
93 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1309-2051dupA | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156957774 | ||||||
chr7:156957774 | C | CAA | 23 | a0002c0002t0007g0089 a0002c0002t0007g0090 a0002c0028t0007g0088 others(20): Show |
28 | HG01106.hp1 HG01175.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.1309-2052_1309-205 others(6): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156957774 | ||||||
chr7:156957774 | CA | C | 33 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(30): Show |
46 | HG00544.hp1 HG00621.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1309-2051delA | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156957774 | ||||||
chr7:156957774 | CAA | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0028 others(93): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1309-2052_1309-205 others(6): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156957774 | ||||||
chr7:156957774 | CAAAAAAA others(6): Show |
C | 1 | a0003c0003t0002g0251 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1309-2063_1309-205 others(17): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156957774 | ||||||
chr7:156957774 | CAAAAAAA others(7): Show |
C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(18): Show |
38 | HG00408.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1309-2064_1309-205 others(18): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156957774 | ||||||
chr7:156957774 | CAAAAAAA others(8): Show |
C | 1 | a0003c0003t0002g0241 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1309-2065_1309-205 others(19): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156957774 | ||||||
chr7:156957789 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0028 others(79): Show |
113 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1309-2062A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957789 | |||||||
chr7:156957795 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0027 others(91): Show |
129 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1309-2056A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957795 | |||||||
chr7:156957823 | A | G | 1 | a0002c0002t0003g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1309-2028A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156957823 | |||||||
chr7:156958001 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(102): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1309-1850G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958001 | |||||||
chr7:156958146 | T | G | 1 | a0014c0025t0006g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1309-1705T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958146 | |||||||
chr7:156958149 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1309-1702G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958149 | |||||||
chr7:156958170 | C | T | 4 | a0002c0002t0003g0051 a0002c0002t0003g0151 a0002c0002t0003g0191 others(1): Show |
5 | HG02109.hp2 HG02280.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1309-1681C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958170 | |||||||
chr7:156958251 | C | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1309-1600C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958251 | |||||||
chr7:156958264 | A | G | 1 | a0001c0001t0004g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1309-1587A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958264 | |||||||
chr7:156958274 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1309-1577T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958274 | |||||||
chr7:156958322 | C | T | 3 | a0002c0002t0013g0258 a0002c0014t0013g0021 a0008c0012t0011g0257 |
5 | HG01884.hp1 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309-1529C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958322 | |||||||
chr7:156958379 | C | T | 45 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(42): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1309-1472C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958379 | |||||||
chr7:156958403 | G | A | 7 | a0002c0010t0008g0079 a0002c0010t0008g0080 a0002c0010t0008g0081 others(4): Show |
7 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1309-1448G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958403 | |||||||
chr7:156958470 | T | G | 1 | a0003c0003t0002g0209 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1309-1381T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958470 | |||||||
chr7:156958536 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1309-1315G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958536 | |||||||
chr7:156958602 | A | G | 1 | a0006c0008t0003g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1309-1249A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958602 | |||||||
chr7:156958618 | G | A | 1 | a0001c0001t0004g0147 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1309-1233G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958618 | |||||||
chr7:156958671 | T | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1309-1180T>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958671 | |||||||
chr7:156958683 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(102): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1309-1168T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958683 | |||||||
chr7:156958757 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0047 others(2): Show |
8 | NA18942.hp1 NA18954.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.1309-1094C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958757 | |||||||
chr7:156958821 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
5 | HG00438.hp2 HG02027.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309-1030A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156958821 | |||||||
chr7:156959106 | CT | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(197): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.1309-730delT | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156959106 | ||||||
chr7:156959117 | T | C | 1 | a0003c0007t0002g0230 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1309-734T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959117 | |||||||
chr7:156959145 | C | T | 1 | a0001c0001t0004g0137 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1309-706C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959145 | |||||||
chr7:156959167 | A | G | 1 | a0016c0032t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1309-684A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959167 | |||||||
chr7:156959263 | C | T | 128 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(125): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1309-588C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959263 | |||||||
chr7:156959303 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(102): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1309-548C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959303 | |||||||
chr7:156959324 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1309-527G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959324 | |||||||
chr7:156959337 | T | TGACTATA others(157): Show |
7 | a0002c0010t0008g0079 a0002c0010t0008g0080 a0002c0010t0008g0081 others(4): Show |
7 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1309-513_1309-512i others(166): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156959337 | ||||||
chr7:156959347 | C | G | 1 | a0014c0025t0006g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1309-504C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959347 | |||||||
chr7:156959349 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1309-502A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959349 | |||||||
chr7:156959383 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1309-468G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959383 | |||||||
chr7:156959404 | A | AT | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(106): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1309-438dupT | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156959404 | ||||||
chr7:156959404 | A | ATT | 5 | a0001c0001t0001g0036 a0001c0001t0001g0097 a0007c0009t0009g0014 others(2): Show |
7 | HG01496.hp2 HG02602.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1309-439_1309-438d others(4): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 156959404 | ||||||
chr7:156959442 | G | T | 3 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0284 |
4 | HG02145.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1309-409G>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959442 | |||||||
chr7:156959537 | T | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(113): Show |
168 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.1309-314T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959537 | |||||||
chr7:156959637 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1309-214G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959637 | |||||||
chr7:156959681 | G | A | 127 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(124): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1309-170G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959681 | |||||||
chr7:156959720 | C | T | 7 | a0002c0010t0008g0079 a0002c0010t0008g0080 a0002c0010t0008g0081 others(4): Show |
7 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1309-131C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959720 | |||||||
chr7:156959775 | T | C | 1 | a0002c0004t0005g0277 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1309-76T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 3/10 | chr7 | 156959775 | |||||||
chr7:156960382 | T | C | 5 | a0002c0002t0007g0089 a0002c0002t0007g0090 a0002c0002t0007g0091 others(2): Show |
5 | HG02055.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632+208T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960382 | |||||||
chr7:156960398 | T | TA | 6 | a0003c0007t0002g0070 a0003c0007t0002g0230 a0003c0007t0002g0232 others(3): Show |
7 | HG01167.hp1 HG01169.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.1632+230dupA | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 156960398 | ||||||
chr7:156960424 | A | G | 1 | a0016c0032t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1632+250A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960424 | |||||||
chr7:156960482 | A | G | 1 | a0002c0010t0008g0083 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1632+308A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960482 | |||||||
chr7:156960549 | C | T | 5 | a0002c0019t0007g0202 a0002c0019t0007g0203 a0008c0012t0011g0048 others(2): Show |
6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1632+375C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960549 | |||||||
chr7:156960566 | A | T | 1 | a0003c0007t0017g0073 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1632+392A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960566 | |||||||
chr7:156960652 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(239): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1632+478A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960652 | |||||||
chr7:156960660 | A | G | 1 | a0001c0013t0001g0121 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1632+486A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960660 | |||||||
chr7:156960687 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1632+513T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960687 | |||||||
chr7:156960749 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1632+575C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960749 | |||||||
chr7:156960862 | G | A | 5 | a0002c0002t0007g0089 a0002c0002t0007g0090 a0002c0002t0007g0091 others(2): Show |
5 | HG02055.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632+688G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960862 | |||||||
chr7:156960894 | T | A | 1 | a0002c0002t0006g0132 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1632+720T>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960894 | |||||||
chr7:156960905 | G | A | 3 | a0002c0002t0006g0044 a0002c0002t0006g0128 a0002c0002t0006g0129 |
4 | HG01891.hp1 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632+731G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960905 | |||||||
chr7:156960953 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG03704.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1632+779C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960953 | |||||||
chr7:156960960 | T | C | 1 | a0002c0002t0003g0153 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1632+786T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156960960 | |||||||
chr7:156961217 | A | T | 3 | a0002c0002t0013g0258 a0002c0014t0013g0021 a0008c0012t0011g0257 |
5 | HG01884.hp1 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1633-934A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961217 | |||||||
chr7:156961229 | C | T | 1 | a0003c0003t0002g0243 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1633-922C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961229 | |||||||
chr7:156961269 | C | T | 9 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(6): Show |
11 | NA18939.hp1 NA18946.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.1633-882C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961269 | |||||||
chr7:156961335 | C | T | 2 | a0002c0019t0007g0202 a0002c0019t0007g0203 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1633-816C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961335 | |||||||
chr7:156961385 | G | C | 127 | a0001c0011t0001g0022 a0001c0011t0001g0074 a0001c0011t0001g0262 others(124): Show |
165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1633-766G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961385 | |||||||
chr7:156961390 | G | C | 8 | a0002c0002t0013g0258 a0002c0014t0013g0021 a0002c0019t0007g0202 others(5): Show |
11 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1633-761G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961390 | |||||||
chr7:156961448 | C | G | 1 | a0011c0022t0020g0035 | 2 | HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1633-703C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961448 | |||||||
chr7:156961655 | G | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(242): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.1633-496G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961655 | |||||||
chr7:156961756 | A | T | 1 | a0012c0023t0002g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1633-395A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961756 | |||||||
chr7:156961778 | A | G | 2 | a0001c0013t0001g0120 a0001c0013t0001g0146 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1633-373A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961778 | |||||||
chr7:156961822 | A | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(199): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1633-329A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961822 | |||||||
chr7:156961849 | G | A | 1 | a0001c0001t0038g0201 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1633-302G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961849 | |||||||
chr7:156961852 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1633-299G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961852 | |||||||
chr7:156961883 | C | T | 5 | a0002c0002t0007g0204 a0002c0010t0008g0080 a0002c0010t0008g0081 others(2): Show |
5 | HG00741.hp1 HG02683.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1633-268C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961883 | |||||||
chr7:156961887 | T | C | 2 | a0001c0001t0036g0110 a0001c0013t0001g0146 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1633-264T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961887 | |||||||
chr7:156961905 | A | AGT | 10 | a0002c0002t0007g0204 a0002c0010t0008g0079 a0002c0010t0008g0080 others(7): Show |
12 | HG00741.hp1 HG01167.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1633-245_1633-244i others(4): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 156961905 | ||||||
chr7:156961940 | T | C | 85 | a0001c0001t0001g0037 a0001c0001t0001g0104 a0001c0001t0001g0115 others(82): Show |
112 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1633-211T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961940 | |||||||
chr7:156961955 | C | A | 1 | a0001c0031t0001g0142 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1633-196C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961955 | |||||||
chr7:156961961 | T | G | 1 | a0003c0007t0002g0230 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1633-190T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961961 | |||||||
chr7:156961977 | C | T | 16 | a0001c0013t0001g0120 a0001c0013t0001g0121 a0001c0013t0001g0122 others(13): Show |
18 | HG01361.hp1 HG01496.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1633-174C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961977 | |||||||
chr7:156961979 | T | C | 104 | a0001c0001t0001g0099 a0001c0001t0004g0046 a0001c0001t0004g0111 others(101): Show |
136 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1633-172T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156961979 | |||||||
chr7:156962002 | T | C | 6 | a0001c0018t0022g0055 a0008c0012t0011g0048 a0008c0012t0011g0145 others(3): Show |
9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1633-149T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156962002 | |||||||
chr7:156962051 | C | T | 35 | a0002c0002t0005g0189 a0002c0002t0005g0190 a0002c0002t0006g0128 others(32): Show |
45 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1633-100C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156962051 | |||||||
chr7:156962076 | A | G | 1 | a0002c0002t0003g0177 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1633-75A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 4/10 | chr7 | 156962076 | |||||||
chr7:156962277 | T | G | 1 | a0002c0002t0003g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1743+16T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962277 | |||||||
chr7:156962281 | A | G | 14 | a0001c0018t0022g0055 a0002c0002t0007g0089 a0002c0002t0007g0090 others(11): Show |
15 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1743+20A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962281 | |||||||
chr7:156962287 | T | C | 96 | a0001c0018t0022g0055 a0002c0002t0003g0192 a0002c0002t0007g0089 others(93): Show |
124 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1743+26T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962287 | |||||||
chr7:156962304 | G | C | 1 | a0002c0002t0005g0134 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1743+43G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962304 | |||||||
chr7:156962316 | G | A | 1 | a0010c0020t0001g0113 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1743+55G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962316 | |||||||
chr7:156962353 | G | A | 1 | a0002c0002t0006g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1743+92G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962353 | |||||||
chr7:156962358 | G | A | 14 | a0001c0018t0022g0055 a0002c0002t0007g0089 a0002c0002t0007g0090 others(11): Show |
15 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1743+97G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962358 | |||||||
chr7:156962477 | T | C | 1 | a0002c0029t0003g0171 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1743+216T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962477 | |||||||
chr7:156962573 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1743+312C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962573 | |||||||
chr7:156962616 | T | C | 6 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(3): Show |
8 | HG02145.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1743+355T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962616 | |||||||
chr7:156962632 | T | G | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1743+371T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962632 | |||||||
chr7:156962656 | T | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(250): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1744-352T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962656 | |||||||
chr7:156962694 | A | G | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1744-314A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962694 | |||||||
chr7:156962722 | A | G | 1 | a0002c0002t0003g0188 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1744-286A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962722 | |||||||
chr7:156962759 | T | C | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1744-249T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962759 | |||||||
chr7:156962910 | C | T | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1744-98C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962910 | |||||||
chr7:156962943 | C | T | 1 | a0002c0004t0005g0280 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1744-65C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 5/10 | chr7 | 156962943 | |||||||
chr7:156963436 | G | A | 1 | a0001c0018t0022g0055 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1911+261G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/10 | chr7 | 156963436 | |||||||
chr7:156963443 | G | A | 1 | a0001c0001t0036g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1911+268G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/10 | chr7 | 156963443 | |||||||
chr7:156963477 | C | T | 5 | a0002c0002t0007g0089 a0002c0002t0007g0090 a0002c0002t0007g0091 others(2): Show |
5 | HG02055.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1911+302C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/10 | chr7 | 156963477 | |||||||
chr7:156963482 | C | CT | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1911+307_1911+308i others(3): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/10 | chr7 | 156963482 | |||||||
chr7:156963491 | C | A | 2 | a0001c0001t0004g0015 a0001c0001t0004g0108 |
4 | HG02258.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1911+316C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/10 | chr7 | 156963491 | |||||||
chr7:156963632 | G | A | 1 | a0003c0003t0002g0210 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1912-273G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/10 | chr7 | 156963632 | |||||||
chr7:156963738 | T | C | 1 | a0003c0003t0002g0219 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1912-167T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/10 | chr7 | 156963738 | |||||||
chr7:156963759 | G | T | 1 | a0003c0003t0028g0078 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1912-146G>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 6/10 | chr7 | 156963759 | |||||||
chr7:156964088 | T | A | 1 | a0008c0012t0011g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2033+62T>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964088 | |||||||
chr7:156964272 | G | GT | 7 | a0001c0018t0022g0055 a0002c0002t0003g0153 a0007c0009t0009g0014 others(4): Show |
10 | HG02257.hp2 HG02486.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2033+257dupT | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 156964272 | ||||||
chr7:156964272 | G | T | 13 | a0002c0002t0007g0089 a0002c0002t0007g0090 a0002c0002t0007g0091 others(10): Show |
13 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.2033+246G>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964272 | |||||||
chr7:156964301 | T | G | 5 | a0002c0002t0007g0089 a0002c0002t0007g0090 a0002c0002t0007g0091 others(2): Show |
5 | HG02055.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2033+275T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964301 | |||||||
chr7:156964319 | CTG | C | 2 | a0002c0002t0013g0258 a0002c0014t0013g0021 |
4 | HG01884.hp1 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2033+294_2033+295d others(4): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964319 | |||||||
chr7:156964346 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0034 |
4 | HG01070.hp2 HG01109.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2033+320A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964346 | |||||||
chr7:156964451 | G | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(164): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.2033+425G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964451 | |||||||
chr7:156964587 | GA | G | 12 | a0001c0018t0022g0055 a0002c0019t0007g0202 a0002c0019t0007g0203 others(9): Show |
16 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2033+571delA | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 156964587 | ||||||
chr7:156964599 | C | T | 85 | a0001c0018t0022g0055 a0002c0019t0007g0202 a0002c0019t0007g0203 others(82): Show |
114 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.2033+573C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964599 | |||||||
chr7:156964737 | T | C | 1 | a0002c0002t0007g0204 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2033+711T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964737 | |||||||
chr7:156964759 | T | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(250): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.2033+733T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964759 | |||||||
chr7:156964805 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG00735.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2033+779G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964805 | |||||||
chr7:156964819 | C | A | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(237): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2033+793C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964819 | |||||||
chr7:156964925 | T | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(238): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.2033+899T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156964925 | |||||||
chr7:156965089 | T | G | 1 | a0008c0012t0011g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2033+1063T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965089 | |||||||
chr7:156965146 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2033+1120T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965146 | |||||||
chr7:156965167 | G | A | 1 | a0016c0032t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2034-1103G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965167 | |||||||
chr7:156965192 | T | C | 1 | a0001c0001t0004g0117 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2034-1078T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965192 | |||||||
chr7:156965281 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2034-989A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965281 | |||||||
chr7:156965353 | C | G | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2034-917C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965353 | |||||||
chr7:156965414 | G | A | 11 | a0002c0019t0007g0202 a0002c0019t0007g0203 a0007c0009t0009g0014 others(8): Show |
14 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2034-856G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965414 | |||||||
chr7:156965420 | C | T | 12 | a0001c0018t0022g0055 a0002c0019t0007g0202 a0002c0019t0007g0203 others(9): Show |
16 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2034-850C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965420 | |||||||
chr7:156965431 | T | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(237): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2034-839T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965431 | |||||||
chr7:156965502 | C | T | 5 | a0002c0002t0007g0089 a0002c0002t0007g0090 a0002c0002t0007g0091 others(2): Show |
5 | HG02055.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2034-768C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965502 | |||||||
chr7:156965796 | T | TC | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(223): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2034-472dupC | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 156965796 | ||||||
chr7:156965916 | AAAAAAG | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(223): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2034-353_2034-348d others(8): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965916 | |||||||
chr7:156965942 | C | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(233): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.2034-328C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965942 | |||||||
chr7:156965976 | G | A | 12 | a0001c0018t0022g0055 a0002c0019t0007g0202 a0002c0019t0007g0203 others(9): Show |
16 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2034-294G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965976 | |||||||
chr7:156965999 | C | T | 9 | a0002c0002t0003g0170 a0006c0008t0003g0012 a0006c0008t0003g0156 others(6): Show |
13 | HG01952.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2034-271C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156965999 | |||||||
chr7:156966033 | A | AC | 5 | a0007c0009t0009g0014 a0007c0009t0009g0049 a0007c0009t0009g0093 others(2): Show |
7 | HG02257.hp2 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2034-232dupC | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 156966033 | ||||||
chr7:156966040 | A | G | 2 | a0012c0023t0002g0235 a0012c0023t0002g0245 |
2 | HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2034-230A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156966040 | |||||||
chr7:156966100 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2034-170G>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156966100 | |||||||
chr7:156966155 | C | T | 1 | a0002c0004t0005g0276 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2034-115C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156966155 | |||||||
chr7:156966163 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0127 |
2 | HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2034-107G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 7/10 | chr7 | 156966163 | |||||||
chr7:156966532 | G | A | 1 | a0002c0002t0003g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2166+130G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 8/10 | chr7 | 156966532 | |||||||
chr7:156966720 | T | C | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2167-241T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 8/10 | chr7 | 156966720 | |||||||
chr7:156966749 | TG | T | 8 | a0001c0018t0022g0055 a0002c0019t0007g0202 a0002c0019t0007g0203 others(5): Show |
11 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2167-206delG | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 156966749 | ||||||
chr7:156966863 | T | A | 23 | a0001c0001t0004g0011 a0001c0001t0004g0015 a0001c0001t0004g0026 others(20): Show |
32 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.2167-98T>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 8/10 | chr7 | 156966863 | |||||||
chr7:156966881 | C | A | 4 | a0003c0007t0002g0070 a0003c0007t0002g0230 a0003c0007t0002g0239 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.2167-80C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 8/10 | chr7 | 156966881 | |||||||
chr7:156966903 | ATATAT | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(114): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2167-53_2167-49del others(5): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 156966903 | ||||||
chr7:156967147 | T | C | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298+55T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156967147 | |||||||
chr7:156967515 | A | G | 5 | a0003c0007t0002g0070 a0003c0007t0002g0230 a0003c0007t0002g0239 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2298+423A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156967515 | |||||||
chr7:156967542 | T | TC | 74 | a0001c0001t0001g0104 a0001c0001t0001g0126 a0001c0001t0004g0138 others(71): Show |
99 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.2298+458dupC | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156967542 | ||||||
chr7:156967546 | C | T | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298+454C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156967546 | |||||||
chr7:156967548 | C | G | 7 | a0002c0010t0008g0079 a0002c0010t0008g0080 a0002c0010t0008g0081 others(4): Show |
7 | HG00741.hp1 HG01167.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.2298+456C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156967548 | |||||||
chr7:156967628 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2298+536G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156967628 | |||||||
chr7:156967654 | G | A | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(245): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.2298+562G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156967654 | |||||||
chr7:156967706 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(116): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2298+614A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156967706 | |||||||
chr7:156967791 | A | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(119): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.2298+699A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156967791 | |||||||
chr7:156967880 | G | C | 5 | a0002c0002t0007g0089 a0002c0002t0007g0090 a0002c0002t0007g0091 others(2): Show |
5 | HG02055.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2298+788G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156967880 | |||||||
chr7:156967909 | CA | C | 151 | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0013t0001g0120 others(148): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2298+828delA | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156967909 | ||||||
chr7:156967930 | C | G | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298+838C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156967930 | |||||||
chr7:156968005 | C | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(151): Show |
217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.2298+913C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968005 | |||||||
chr7:156968007 | G | A | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298+915G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968007 | |||||||
chr7:156968080 | G | A | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298+988G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968080 | |||||||
chr7:156968142 | C | A | 1 | a0001c0018t0022g0055 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-945C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968142 | |||||||
chr7:156968192 | C | A | 1 | a0001c0018t0022g0055 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-895C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968192 | |||||||
chr7:156968195 | C | A | 3 | a0002c0002t0003g0181 a0003c0007t0002g0232 a0003c0007t0002g0240 |
3 | HG00323.hp1 HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2299-892C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968195 | |||||||
chr7:156968223 | C | T | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2299-864C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968223 | |||||||
chr7:156968239 | T | G | 2 | a0002c0002t0006g0132 a0002c0002t0006g0135 |
2 | HG00673.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2299-848T>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968239 | |||||||
chr7:156968256 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(127): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.2299-831A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968256 | |||||||
chr7:156968275 | C | T | 2 | a0009c0015t0015g0067 a0009c0015t0015g0226 |
3 | HG02615.hp2 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2299-812C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968275 | |||||||
chr7:156968330 | C | T | 2 | a0002c0002t0003g0178 a0002c0002t0007g0204 |
2 | HG02165.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2299-757C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968330 | |||||||
chr7:156968344 | G | A | 2 | a0012c0023t0002g0235 a0012c0023t0002g0245 |
2 | HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2299-743G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968344 | |||||||
chr7:156968377 | G | A | 44 | a0002c0002t0005g0134 a0002c0002t0005g0189 a0002c0002t0005g0190 others(41): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.2299-710G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968377 | |||||||
chr7:156968397 | G | A | 1 | a0002c0002t0006g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2299-690G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968397 | |||||||
chr7:156968402 | G | C | 5 | a0002c0002t0003g0160 a0002c0002t0003g0173 a0002c0002t0003g0174 others(2): Show |
5 | HG02083.hp1 HG02129.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.2299-685G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968402 | |||||||
chr7:156968408 | G | A | 3 | a0002c0002t0003g0017 a0002c0002t0003g0157 a0002c0002t0018g0017 |
4 | HG01070.hp1 HG01071.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2299-679G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968408 | |||||||
chr7:156968419 | C | T | 44 | a0002c0002t0005g0134 a0002c0002t0005g0189 a0002c0002t0005g0190 others(41): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.2299-668C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968419 | |||||||
chr7:156968437 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2299-650G>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968437 | |||||||
chr7:156968443 | C | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(119): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.2299-644C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968443 | |||||||
chr7:156968451 | T | C | 19 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0040 others(16): Show |
22 | HG00438.hp2 HG02027.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.2299-636T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968451 | |||||||
chr7:156968466 | C | T | 1 | a0002c0002t0003g0187 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2299-621C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968466 | |||||||
chr7:156968501 | T | C | 2 | a0002c0002t0003g0154 a0002c0002t0003g0167 |
2 | HG00597.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.2299-586T>C | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968501 | |||||||
chr7:156968516 | A | T | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2299-571A>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968516 | |||||||
chr7:156968521 | A | G | 74 | a0001c0001t0001g0126 a0003c0003t0002g0001 a0003c0003t0002g0005 others(71): Show |
99 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.2299-566A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968521 | |||||||
chr7:156968538 | G | A | 5 | a0002c0002t0007g0089 a0002c0002t0007g0090 a0002c0002t0007g0091 others(2): Show |
5 | HG02055.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2299-549G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968538 | |||||||
chr7:156968599 | C | A | 2 | a0001c0001t0004g0046 a0001c0001t0004g0143 |
3 | NA18960.hp1 NA18988.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2299-488C>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968599 | |||||||
chr7:156968687 | T | TTA | 15 | a0002c0002t0003g0148 a0002c0002t0003g0159 a0002c0002t0003g0163 others(12): Show |
16 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.2299-355_2299-354d others(4): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | T | TTATA | 4 | a0002c0002t0003g0164 a0002c0002t0003g0186 a0002c0002t0007g0090 others(1): Show |
4 | HG00673.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2299-357_2299-354d others(6): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | T | TTATATAT others(3): Show |
1 | a0002c0002t0003g0174 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2299-363_2299-354d others(12): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTA | T | 19 | a0002c0002t0003g0007 a0002c0002t0003g0017 a0002c0002t0003g0057 others(16): Show |
28 | HG00323.hp1 HG00642.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.2299-355_2299-354d others(4): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTATA | T | 18 | a0002c0002t0003g0053 a0002c0002t0003g0054 a0002c0002t0003g0149 others(15): Show |
21 | HG00408.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.2299-357_2299-354d others(6): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTATATA | T | 11 | a0002c0002t0003g0051 a0002c0002t0003g0052 a0002c0002t0003g0155 others(8): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2299-359_2299-354d others(8): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTATATAT others(1): Show |
T | 4 | a0002c0002t0003g0168 a0002c0002t0003g0172 a0002c0004t0005g0273 others(1): Show |
4 | HG02165.hp1 NA18943.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.2299-361_2299-354d others(10): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTATATAT others(3): Show |
T | 12 | a0002c0002t0003g0151 a0002c0002t0005g0134 a0002c0002t0006g0132 others(9): Show |
13 | HG00673.hp1 HG02056.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2299-363_2299-354d others(12): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTATATAT others(5): Show |
T | 19 | a0002c0002t0005g0189 a0002c0002t0005g0190 a0002c0002t0006g0044 others(16): Show |
28 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.2299-365_2299-354d others(14): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTATATAT others(7): Show |
T | 12 | a0002c0002t0006g0135 a0002c0004t0006g0260 a0002c0004t0006g0261 others(9): Show |
13 | HG01934.hp1 HG02132.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2299-367_2299-354d others(16): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTATATAT others(9): Show |
T | 11 | a0002c0014t0013g0021 a0003c0003t0002g0059 a0003c0003t0002g0066 others(8): Show |
15 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.2299-369_2299-354d others(18): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTATATAT others(11): Show |
T | 58 | a0001c0001t0001g0126 a0002c0002t0007g0204 a0002c0002t0013g0258 others(55): Show |
80 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.2299-371_2299-354d others(20): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTATATAT others(13): Show |
T | 2 | a0012c0023t0002g0235 a0012c0023t0002g0245 |
2 | HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2299-373_2299-354d others(22): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTATATAT others(21): Show |
T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0014g0006 |
8 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2299-381_2299-354d others(30): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968687 | TTATATAT others(23): Show |
T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(112): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.2299-383_2299-354d others(32): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156968687 | ||||||
chr7:156968733 | A | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(37): Show |
56 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2299-354A>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968733 | |||||||
chr7:156968873 | C | T | 1 | a0002c0002t0003g0200 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2299-214C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968873 | |||||||
chr7:156968969 | C | T | 1 | a0013c0016t0003g0050 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2299-118C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156968969 | |||||||
chr7:156969003 | TACTCTAA others(3): Show |
T | 1 | a0001c0001t0004g0094 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2299-80_2299-71del others(10): Show |
NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 156969003 | ||||||
chr7:156969057 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(113): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2299-30C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 9/10 | chr7 | 156969057 | |||||||
chr7:156969215 | C | G | 4 | a0008c0012t0011g0048 a0008c0012t0011g0145 a0008c0012t0011g0257 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2408+19C>G | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 10/10 | chr7 | 156969215 | |||||||
chr7:156969219 | C | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(111): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.2408+23C>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 10/10 | chr7 | 156969219 | |||||||
chr7:156969222 | G | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0118 |
3 | HG01123.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2408+26G>T | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 10/10 | chr7 | 156969222 | |||||||
chr7:156969290 | G | A | 2 | a0002c0010t0008g0081 a0002c0010t0008g0082 |
2 | HG02683.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2408+94G>A | NOM1 | ENSG00000146909.8 | transcript | ENST00000275820.4 | protein_coding | 10/10 | chr7 | 156969290 |