Item | Value |
---|---|
geneid | 9324 |
ensemblid | ENSG00000118418.16 |
hgncid | 12312 |
symbol | HMGN3 |
name | high mobility group nucleosomal binding domain 3 |
refseq_nuc | NM_001201363.2 |
refseq_prot | NP_001188292.1 |
ensembl_nuc | ENST00000620514.2 |
ensembl_prot | ENSP00000482613.1 |
mane_status | MANE Select |
chr | chr6 |
start | 79201245 |
end | 79234682 |
strand | - |
ver | v1.2 |
region | chr6:79201245-79234682 |
region5000 | chr6:79196245-79239682 |
regionname0 | HMGN3_chr6_79201245_79234682 |
regionname5000 | HMGN3_chr6_79196245_79239682 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 390 | 322 | 94 | 64 | 112 | 12 | 38 | HMGN3_chr6_79196245_79239682 | HMGN3 | ATGCC others(385): Show |
chr6 | 79196245 | 79239682 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 958 | 276 | 60 | 61 | 111 | 12 | 31 | HMGN3_chr6_79196245_79239682 | HMGN3 | GAAGA others(953): Show |
chr6 | 79196245 | 79239682 |
a0001c0001t0002 | 1/0 | 958 | 19 | 18 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | GAAGA others(953): Show |
chr6 | 79196245 | 79239682 |
a0001c0001t0003 | 0/0 | 958 | 15 | 8 | 3 | 0 | 0 | 4 | HMGN3_chr6_79196245_79239682 | HMGN3 | GAAGA others(953): Show |
chr6 | 79196245 | 79239682 |
a0001c0001t0004 | 0/0 | 958 | 4 | 4 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | GAAGA others(953): Show |
chr6 | 79196245 | 79239682 |
a0001c0001t0005 | 0/0 | 958 | 3 | 1 | 0 | 0 | 0 | 2 | HMGN3_chr6_79196245_79239682 | HMGN3 | GAAGA others(953): Show |
chr6 | 79196245 | 79239682 |
a0001c0001t0006 | 0/0 | 958 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | GAAGA others(953): Show |
chr6 | 79196245 | 79239682 |
a0001c0001t0007 | 0/0 | 958 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | GAAGA others(953): Show |
chr6 | 79196245 | 79239682 |
a0001c0001t0008 | 0/0 | 958 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | GAAGA others(953): Show |
chr6 | 79196245 | 79239682 |
a0001c0001t0009 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | GAAGA others(953): Show |
chr6 | 79196245 | 79239682 |
a0001c0001t0010 | 0/0 | 958 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | GAAGA others(953): Show |
chr6 | 79196245 | 79239682 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 32 | 1 | 6 | 21 | 1 | 3 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0003 | 0/0 | 8 | 2 | 0 | 4 | 0 | 2 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0007 | 0/0 | 6 | 2 | 2 | 0 | 1 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0009 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0002g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0002g0013 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0003g0018 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0003g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0003g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0009g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
a0001c0001t0010g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0048 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0090 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0061 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03688 | hp1 | a0001 | c0001 | t0010 | g0099 | SAS | STU | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | BEB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0050 | SAS | BEB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | STU | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | STU | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | YRI | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0055 | AFR | YRI | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | LWK | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | LWK | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19060 | hp1 | a0001 | c0001 | t0009 | g0148 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ASW | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ACB | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | USA | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | USA | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | USA | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0078 | REF | REF | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0013 | REF | REF | HMGN3_chr6_79196245_79239682 | HMGN3 | chr6 | 79196245 | 79239682 |
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 |
---|
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 |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:79201304 | T | G | 1 | a0001c0001t0009 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*384A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 7/7 | 384 | chr6 | 79201304 | ||||||
chr6:79201473 | G | A | 2 | a0001c0001t0003 a0001c0001t0005 |
18 | HG01109.hp2 HG01256.hp2 HG01346.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*215C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 7/7 | 215 | chr6 | 79201473 | ||||||
chr6:79201544 | C | T | 1 | a0001c0001t0007 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 7/7 | 144 | chr6 | 79201544 | ||||||
chr6:79201560 | C | T | 1 | a0001c0001t0008 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*128G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 7/7 | 128 | chr6 | 79201560 | ||||||
chr6:79201573 | G | A | 3 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 |
22 | HG01109.hp2 HG01256.hp2 HG01346.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*115C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 7/7 | 115 | chr6 | 79201573 | ||||||
chr6:79201576 | T | C | 1 | a0001c0001t0010 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 7/7 | 112 | chr6 | 79201576 | ||||||
chr6:79234601 | G | T | 1 | a0001c0001t0006 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-41C>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/7 | 41 | chr6 | 79234601 | ||||||
chr6:79234638 | T | G | 6 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(3): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
5_prime_UTR_variant | MODIFIER | c.-78A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/7 | 78 | chr6 | 79234638 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:79201742 | GA | G | 15 | a0001c0001t0001g0097 a0001c0001t0001g0170 a0001c0001t0003g0018 others(12): Show |
20 | HG01109.hp2 HG01256.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.355-17delT | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 6/6 | chr6 | 79201742 | |||||||
chr6:79201764 | A | G | 1 | a0001c0001t0004g0088 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.355-38T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 6/6 | chr6 | 79201764 | |||||||
chr6:79201852 | C | A | 1 | a0001c0001t0005g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.355-126G>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 6/6 | chr6 | 79201852 | |||||||
chr6:79202208 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0112 a0001c0001t0001g0114 |
3 | HG02809.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.262-53C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 5/6 | chr6 | 79202208 | |||||||
chr6:79202218 | T | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0092 a0001c0001t0001g0093 |
4 | HG00639.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+58A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 5/6 | chr6 | 79202218 | |||||||
chr6:79202250 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.261+26G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 5/6 | chr6 | 79202250 | |||||||
chr6:79202472 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(37): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.148-83T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79202472 | |||||||
chr6:79202568 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0065 |
4 | HG03041.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-179A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79202568 | |||||||
chr6:79202601 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.148-212G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79202601 | |||||||
chr6:79202643 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.148-254T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79202643 | |||||||
chr6:79202804 | C | G | 2 | a0001c0001t0002g0051 a0001c0001t0008g0061 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.148-415G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79202804 | |||||||
chr6:79202856 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.148-467C>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79202856 | |||||||
chr6:79202967 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0159 |
2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.148-578T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79202967 | |||||||
chr6:79203094 | G | A | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.147+486C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79203094 | |||||||
chr6:79203152 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.147+428G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79203152 | |||||||
chr6:79203288 | C | A | 1 | a0001c0001t0003g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.147+292G>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79203288 | |||||||
chr6:79203381 | C | T | 1 | a0001c0001t0005g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.147+199G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79203381 | |||||||
chr6:79203390 | C | G | 6 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(3): Show |
8 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.147+190G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 4/6 | chr6 | 79203390 | |||||||
chr6:79203662 | GA | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.97-33delT | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79203662 | |||||||
chr6:79203698 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.97-68G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79203698 | |||||||
chr6:79203839 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.97-209A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79203839 | |||||||
chr6:79203893 | G | A | 1 | a0001c0001t0003g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97-263C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79203893 | |||||||
chr6:79204239 | T | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.97-609A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79204239 | |||||||
chr6:79204257 | T | C | 3 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 |
3 | HG02559.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.97-627A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79204257 | |||||||
chr6:79204331 | T | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0170 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.97-701A>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79204331 | |||||||
chr6:79204442 | A | G | 3 | a0001c0001t0003g0026 a0001c0001t0003g0044 a0001c0001t0003g0130 |
6 | HG01109.hp2 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-812T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79204442 | |||||||
chr6:79204535 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.97-905G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79204535 | |||||||
chr6:79204935 | T | C | 2 | a0001c0001t0002g0051 a0001c0001t0008g0061 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.97-1305A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79204935 | |||||||
chr6:79205016 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.97-1386C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79205016 | |||||||
chr6:79205072 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.97-1442C>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79205072 | |||||||
chr6:79205170 | G | T | 1 | a0001c0001t0001g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.97-1540C>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79205170 | |||||||
chr6:79205228 | C | T | 6 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(3): Show |
8 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-1598G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79205228 | |||||||
chr6:79205518 | T | C | 1 | a0001c0001t0007g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-1888A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79205518 | |||||||
chr6:79205588 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0094 others(3): Show |
13 | HG01123.hp1 HG01496.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.97-1958T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79205588 | |||||||
chr6:79205617 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.97-1987T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79205617 | |||||||
chr6:79205803 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.97-2173T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79205803 | |||||||
chr6:79205957 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.97-2327C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79205957 | |||||||
chr6:79205967 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.97-2337T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79205967 | |||||||
chr6:79206402 | C | T | 6 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(3): Show |
8 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+2145G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206402 | |||||||
chr6:79206500 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0139 a0001c0001t0001g0146 |
4 | HG01192.hp2 HG01516.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+2047G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206500 | |||||||
chr6:79206613 | G | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0120 a0001c0001t0001g0125 others(5): Show |
10 | HG01081.hp1 HG01257.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+1934C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206613 | |||||||
chr6:79206632 | A | C | 6 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(3): Show |
8 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+1915T>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206632 | |||||||
chr6:79206692 | T | G | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.96+1855A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206692 | |||||||
chr6:79206730 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.96+1817G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206730 | |||||||
chr6:79206740 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.96+1807A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206740 | |||||||
chr6:79206763 | G | A | 1 | a0001c0001t0003g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.96+1784C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206763 | |||||||
chr6:79206848 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.96+1699C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206848 | |||||||
chr6:79206851 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.96+1696C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206851 | |||||||
chr6:79206857 | C | T | 3 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 |
3 | HG02559.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.96+1690G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206857 | |||||||
chr6:79206889 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.96+1658C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79206889 | |||||||
chr6:79207091 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.96+1456T>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79207091 | |||||||
chr6:79207156 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.96+1391T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79207156 | |||||||
chr6:79207312 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.96+1235C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79207312 | |||||||
chr6:79207377 | G | A | 3 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 |
3 | HG02559.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.96+1170C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79207377 | |||||||
chr6:79207411 | T | C | 3 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 |
3 | HG02559.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.96+1136A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79207411 | |||||||
chr6:79207478 | G | A | 2 | a0001c0001t0004g0089 a0001c0001t0004g0090 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.96+1069C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79207478 | |||||||
chr6:79208370 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.96+177G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79208370 | |||||||
chr6:79208434 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0168 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.96+113T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79208434 | |||||||
chr6:79208450 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.96+97A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 3/6 | chr6 | 79208450 | |||||||
chr6:79208592 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.67-16C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79208592 | |||||||
chr6:79208712 | A | G | 1 | a0001c0001t0003g0111 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.67-136T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79208712 | |||||||
chr6:79208812 | C | A | 1 | a0001c0001t0001g0022 | 3 | HG02622.hp2 HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.67-236G>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79208812 | |||||||
chr6:79209433 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.67-857T>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79209433 | |||||||
chr6:79209859 | C | A | 1 | a0001c0001t0001g0034 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67-1283G>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79209859 | |||||||
chr6:79210120 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.67-1544T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79210120 | |||||||
chr6:79210175 | G | A | 1 | a0001c0001t0001g0021 | 3 | HG02572.hp1 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.67-1599C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79210175 | |||||||
chr6:79210309 | G | C | 1 | a0001c0001t0005g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.67-1733C>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79210309 | |||||||
chr6:79210344 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.67-1768A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79210344 | |||||||
chr6:79210351 | C | T | 2 | a0001c0001t0002g0051 a0001c0001t0008g0061 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.67-1775G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79210351 | |||||||
chr6:79210594 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0006g0045 |
7 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-2018C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79210594 | |||||||
chr6:79210605 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.67-2029C>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79210605 | |||||||
chr6:79210713 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.67-2137T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79210713 | |||||||
chr6:79210749 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.67-2173A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79210749 | |||||||
chr6:79210765 | T | A | 1 | a0001c0001t0001g0149 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.67-2189A>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79210765 | |||||||
chr6:79211000 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.67-2424C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211000 | |||||||
chr6:79211011 | C | CA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0153 others(2): Show |
10 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-2436dupT | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211011 | |||||||
chr6:79211011 | C | CAA | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(53): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.67-2437_67-2436dup others(2): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211011 | |||||||
chr6:79211011 | C | CAAA | 23 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0029 others(20): Show |
33 | HG00621.hp2 HG01069.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.67-2438_67-2436dup others(3): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211011 | |||||||
chr6:79211011 | CA | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(50): Show |
91 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.67-2436delT | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211011 | |||||||
chr6:79211011 | CAA | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0077 a0001c0001t0001g0113 others(3): Show |
8 | HG01517.hp1 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-2437_67-2436del others(2): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211011 | |||||||
chr6:79211011 | CAAA | C | 3 | a0001c0001t0001g0112 a0001c0001t0002g0006 a0001c0001t0006g0045 |
8 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-2438_67-2436del others(3): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211011 | |||||||
chr6:79211032 | AAT | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(1): Show |
6 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-2458_67-2457del others(2): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211032 | |||||||
chr6:79211044 | G | C | 4 | a0001c0001t0001g0170 a0001c0001t0004g0088 a0001c0001t0004g0089 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-2468C>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211044 | |||||||
chr6:79211052 | C | G | 3 | a0001c0001t0002g0006 a0001c0001t0006g0045 a0001c0001t0007g0055 |
8 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-2476G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211052 | |||||||
chr6:79211088 | A | T | 1 | a0001c0001t0004g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.67-2512T>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211088 | |||||||
chr6:79211091 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.67-2515T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211091 | |||||||
chr6:79211465 | GT | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.67-2890delA | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211465 | |||||||
chr6:79211465 | GTT | G | 10 | a0001c0001t0001g0092 a0001c0001t0001g0143 a0001c0001t0002g0006 others(7): Show |
17 | HG00639.hp2 HG01256.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.67-2891_67-2890del others(2): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211465 | |||||||
chr6:79211467 | T | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-2891A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211467 | |||||||
chr6:79211550 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.67-2974A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79211550 | |||||||
chr6:79212043 | T | TA | 10 | a0001c0001t0001g0058 a0001c0001t0001g0082 a0001c0001t0001g0132 others(7): Show |
10 | HG01169.hp1 HG01169.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+2928dupT | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79212043 | |||||||
chr6:79212043 | T | TAA | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.66+2927_66+2928dup others(2): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79212043 | |||||||
chr6:79212043 | T | TAAA | 5 | a0001c0001t0001g0011 a0001c0001t0001g0075 a0001c0001t0001g0087 others(2): Show |
9 | HG01891.hp2 HG02056.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.66+2926_66+2928dup others(3): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79212043 | |||||||
chr6:79212215 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.66+2757T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79212215 | |||||||
chr6:79212228 | A | G | 5 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(2): Show |
7 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+2744T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79212228 | |||||||
chr6:79212263 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.66+2709G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79212263 | |||||||
chr6:79212290 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
7 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+2682C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79212290 | |||||||
chr6:79212294 | T | C | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+2678A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79212294 | |||||||
chr6:79212539 | C | T | 5 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(2): Show |
7 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+2433G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79212539 | |||||||
chr6:79212561 | C | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(60): Show |
116 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.66+2411G>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79212561 | |||||||
chr6:79212762 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
9 | HG00621.hp1 HG02129.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+2210A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79212762 | |||||||
chr6:79213105 | C | G | 5 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(2): Show |
7 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+1867G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79213105 | |||||||
chr6:79213141 | GAGATGGG others(9): Show |
G | 3 | a0001c0001t0002g0006 a0001c0001t0006g0045 a0001c0001t0007g0055 |
8 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+1815_66+1830del others(16): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79213141 | |||||||
chr6:79213158 | T | G | 3 | a0001c0001t0002g0006 a0001c0001t0006g0045 a0001c0001t0007g0055 |
8 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+1814A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79213158 | |||||||
chr6:79213350 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.66+1622A>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79213350 | |||||||
chr6:79213492 | AT | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.66+1479delA | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79213492 | |||||||
chr6:79213771 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.66+1201A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79213771 | |||||||
chr6:79213947 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.66+1025G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79213947 | |||||||
chr6:79214151 | A | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0020 others(24): Show |
47 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.66+821T>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214151 | |||||||
chr6:79214171 | T | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0035 others(9): Show |
24 | HG00408.hp1 HG00621.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.66+801A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214171 | |||||||
chr6:79214209 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.66+763A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214209 | |||||||
chr6:79214242 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.66+730G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214242 | |||||||
chr6:79214283 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.66+689G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214283 | |||||||
chr6:79214351 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.66+621T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214351 | |||||||
chr6:79214375 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.66+597T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214375 | |||||||
chr6:79214391 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0091 |
3 | HG01106.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.66+581A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214391 | |||||||
chr6:79214424 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0094 others(3): Show |
13 | HG01123.hp1 HG01496.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.66+548T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214424 | |||||||
chr6:79214436 | C | T | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+536G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214436 | |||||||
chr6:79214444 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0060 others(4): Show |
13 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.66+528C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214444 | |||||||
chr6:79214457 | A | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0154 a0001c0001t0001g0159 |
3 | HG02145.hp1 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.66+515T>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214457 | |||||||
chr6:79214621 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.66+351G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 2/6 | chr6 | 79214621 | |||||||
chr6:79215274 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0074 a0001c0001t0001g0075 |
4 | HG00741.hp2 HG01433.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-252T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79215274 | |||||||
chr6:79215441 | G | A | 1 | a0001c0001t0001g0011 | 5 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-419C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79215441 | |||||||
chr6:79215787 | C | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.16-765G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79215787 | |||||||
chr6:79215910 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.16-888C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79215910 | |||||||
chr6:79216273 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.16-1251C>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79216273 | |||||||
chr6:79216671 | C | G | 3 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 |
3 | HG02559.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.16-1649G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79216671 | |||||||
chr6:79217268 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.16-2246T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79217268 | |||||||
chr6:79217272 | T | G | 5 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(2): Show |
7 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-2250A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79217272 | |||||||
chr6:79217364 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.16-2342G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79217364 | |||||||
chr6:79217421 | G | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0069 |
5 | HG02083.hp2 NA18747.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-2399C>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79217421 | |||||||
chr6:79217451 | T | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0146 |
3 | HG01192.hp2 HG01516.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.16-2429A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79217451 | |||||||
chr6:79217532 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.16-2510G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79217532 | |||||||
chr6:79217550 | T | C | 3 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 |
3 | HG02559.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.16-2528A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79217550 | |||||||
chr6:79217573 | A | G | 5 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(2): Show |
7 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-2551T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79217573 | |||||||
chr6:79217811 | G | A | 5 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(2): Show |
7 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-2789C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79217811 | |||||||
chr6:79218058 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.16-3036G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79218058 | |||||||
chr6:79218219 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.16-3197C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79218219 | |||||||
chr6:79218534 | G | A | 1 | a0001c0001t0004g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.16-3512C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79218534 | |||||||
chr6:79218737 | G | A | 5 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(2): Show |
7 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-3715C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79218737 | |||||||
chr6:79218779 | A | G | 5 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(2): Show |
7 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-3757T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79218779 | |||||||
chr6:79218791 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0152 a0001c0001t0001g0162 |
5 | HG00639.hp1 HG00642.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-3769C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79218791 | |||||||
chr6:79218904 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.16-3882A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79218904 | |||||||
chr6:79219013 | C | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.16-3991G>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79219013 | |||||||
chr6:79219086 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.16-4064A>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79219086 | |||||||
chr6:79219451 | G | A | 1 | a0001c0001t0003g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.16-4429C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79219451 | |||||||
chr6:79219538 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.16-4516T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79219538 | |||||||
chr6:79219572 | T | C | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.16-4550A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79219572 | |||||||
chr6:79219831 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.16-4809A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79219831 | |||||||
chr6:79219929 | A | G | 5 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(2): Show |
7 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-4907T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79219929 | |||||||
chr6:79220071 | A | G | 3 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0090 |
3 | HG02559.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.16-5049T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220071 | |||||||
chr6:79220463 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.16-5441A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220463 | |||||||
chr6:79220469 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.16-5447G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220469 | |||||||
chr6:79220508 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(33): Show |
64 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.16-5486C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220508 | |||||||
chr6:79220535 | C | G | 5 | a0001c0001t0003g0018 a0001c0001t0003g0057 a0001c0001t0003g0062 others(2): Show |
7 | HG01256.hp2 HG01346.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-5513G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220535 | |||||||
chr6:79220577 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.16-5555C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220577 | |||||||
chr6:79220692 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.16-5670G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220692 | |||||||
chr6:79220722 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.16-5700G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220722 | |||||||
chr6:79220738 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.16-5716G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220738 | |||||||
chr6:79220739 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG02056.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.16-5717C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220739 | |||||||
chr6:79220839 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.16-5817G>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220839 | |||||||
chr6:79220851 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.16-5829C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79220851 | |||||||
chr6:79221009 | A | G | 1 | a0001c0001t0003g0044 | 2 | HG01109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.16-5987T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79221009 | |||||||
chr6:79221140 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.16-6118G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79221140 | |||||||
chr6:79221216 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.16-6194T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79221216 | |||||||
chr6:79221314 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.16-6292C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79221314 | |||||||
chr6:79221373 | C | T | 1 | a0001c0001t0007g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.16-6351G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79221373 | |||||||
chr6:79221767 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.16-6745T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79221767 | |||||||
chr6:79221835 | GCA | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0150 |
5 | HG01884.hp1 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-6815_16-6814del others(2): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79221835 | |||||||
chr6:79221876 | C | CTTCATTG others(16): Show |
82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
154 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.16-6877_16-6855dup others(23): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79221876 | |||||||
chr6:79221876 | C | CTTCATTG others(39): Show |
15 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0035 others(12): Show |
27 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.16-6855_16-6854ins others(46): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79221876 | |||||||
chr6:79221947 | T | C | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.16-6925A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79221947 | |||||||
chr6:79222023 | C | T | 1 | a0001c0001t0001g0021 | 3 | HG02572.hp1 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.16-7001G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222023 | |||||||
chr6:79222032 | C | T | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.16-7010G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222032 | |||||||
chr6:79222084 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.16-7062C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222084 | |||||||
chr6:79222126 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.16-7104A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222126 | |||||||
chr6:79222232 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0159 |
2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.16-7210C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222232 | |||||||
chr6:79222426 | CA | C | 2 | a0001c0001t0002g0006 a0001c0001t0006g0045 |
7 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-7405delT | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222426 | |||||||
chr6:79222604 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.16-7582C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222604 | |||||||
chr6:79222617 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.16-7595A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222617 | |||||||
chr6:79222733 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7711G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222733 | |||||||
chr6:79222820 | TCACTGCA others(5): Show |
T | 1 | a0001c0001t0001g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.16-7810_16-7799del others(12): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222820 | |||||||
chr6:79222920 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG02809.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.16-7898A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222920 | |||||||
chr6:79222960 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.16-7938T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79222960 | |||||||
chr6:79223173 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.16-8151C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223173 | |||||||
chr6:79223177 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.16-8155C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223177 | |||||||
chr6:79223231 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18977.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.16-8209C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223231 | |||||||
chr6:79223240 | A | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(8): Show |
16 | HG01256.hp2 HG01346.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.16-8218T>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223240 | |||||||
chr6:79223278 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-8256C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223278 | |||||||
chr6:79223305 | A | T | 1 | a0001c0001t0001g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.16-8283T>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223305 | |||||||
chr6:79223327 | C | T | 2 | a0001c0001t0003g0057 a0001c0001t0003g0062 |
2 | HG01346.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.16-8305G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223327 | |||||||
chr6:79223386 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.16-8364G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223386 | |||||||
chr6:79223501 | A | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0175 a0001c0001t0001g0176 |
12 | HG02129.hp1 NA18955.hp2 NA18963.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-8479T>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223501 | |||||||
chr6:79223539 | A | C | 3 | a0001c0001t0002g0006 a0001c0001t0006g0045 a0001c0001t0007g0055 |
8 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-8517T>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223539 | |||||||
chr6:79223721 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.16-8699G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223721 | |||||||
chr6:79223739 | C | CT | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(39): Show |
79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.16-8718dupA | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223739 | |||||||
chr6:79223739 | C | CTTTT | 10 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(7): Show |
15 | HG01256.hp2 HG01346.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.16-8721_16-8718dup others(4): Show |
HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223739 | |||||||
chr6:79223739 | CT | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
145 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.16-8718delA | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223739 | |||||||
chr6:79223769 | T | C | 1 | a0001c0001t0007g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.16-8747A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79223769 | |||||||
chr6:79224063 | G | T | 1 | a0001c0001t0001g0069 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.16-9041C>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224063 | |||||||
chr6:79224165 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.16-9143G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224165 | |||||||
chr6:79224332 | G | A | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.16-9310C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224332 | |||||||
chr6:79224398 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.16-9376A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224398 | |||||||
chr6:79224429 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0082 |
4 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-9407A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224429 | |||||||
chr6:79224653 | A | G | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.16-9631T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224653 | |||||||
chr6:79224714 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.16-9692T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224714 | |||||||
chr6:79224742 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.16-9720C>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224742 | |||||||
chr6:79224809 | G | T | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.15+9737C>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224809 | |||||||
chr6:79224852 | G | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(10): Show |
18 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.15+9694C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224852 | |||||||
chr6:79224929 | T | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0115 |
3 | HG02809.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.15+9617A>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224929 | |||||||
chr6:79224939 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.15+9607A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224939 | |||||||
chr6:79224958 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0115 |
3 | HG02809.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.15+9588C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79224958 | |||||||
chr6:79225153 | T | C | 2 | a0001c0001t0003g0057 a0001c0001t0003g0062 |
2 | HG01346.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.15+9393A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79225153 | |||||||
chr6:79225163 | A | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(8): Show |
16 | HG01256.hp2 HG01346.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+9383T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79225163 | |||||||
chr6:79225269 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.15+9277G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79225269 | |||||||
chr6:79225768 | C | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(8): Show |
16 | HG01256.hp2 HG01346.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+8778G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79225768 | |||||||
chr6:79225912 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.15+8634T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79225912 | |||||||
chr6:79226070 | A | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(50): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.15+8476T>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79226070 | |||||||
chr6:79226282 | C | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
145 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.15+8264G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79226282 | |||||||
chr6:79226374 | C | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(8): Show |
16 | HG01256.hp2 HG01346.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+8172G>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79226374 | |||||||
chr6:79226605 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.15+7941C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79226605 | |||||||
chr6:79226653 | G | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(8): Show |
16 | HG01256.hp2 HG01346.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+7893C>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79226653 | |||||||
chr6:79226712 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.15+7834A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79226712 | |||||||
chr6:79226798 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.15+7748A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79226798 | |||||||
chr6:79226890 | T | C | 11 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(8): Show |
16 | HG01256.hp2 HG01346.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+7656A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79226890 | |||||||
chr6:79226917 | T | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(8): Show |
16 | HG01256.hp2 HG01346.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+7629A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79226917 | |||||||
chr6:79227082 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.15+7464G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79227082 | |||||||
chr6:79227270 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.15+7276G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79227270 | |||||||
chr6:79227271 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.15+7275T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79227271 | |||||||
chr6:79227424 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.15+7122G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79227424 | |||||||
chr6:79227602 | T | C | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.15+6944A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79227602 | |||||||
chr6:79227839 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0034 others(14): Show |
30 | HG00408.hp1 HG00621.hp1 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.15+6707G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79227839 | |||||||
chr6:79228010 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.15+6536G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79228010 | |||||||
chr6:79228088 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.15+6458C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79228088 | |||||||
chr6:79228247 | G | T | 1 | a0001c0001t0003g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.15+6299C>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79228247 | |||||||
chr6:79228346 | T | G | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.15+6200A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79228346 | |||||||
chr6:79228514 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.15+6032G>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79228514 | |||||||
chr6:79228750 | A | G | 3 | a0001c0001t0002g0006 a0001c0001t0006g0045 a0001c0001t0007g0055 |
8 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5796T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79228750 | |||||||
chr6:79228798 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
6 | HG02280.hp1 HG03041.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+5748G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79228798 | |||||||
chr6:79228895 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0006g0045 |
7 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.15+5651G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79228895 | |||||||
chr6:79229314 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.15+5232G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79229314 | |||||||
chr6:79229693 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0092 a0001c0001t0001g0093 |
4 | HG00639.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+4853G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79229693 | |||||||
chr6:79229705 | G | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(8): Show |
16 | HG01256.hp2 HG01346.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+4841C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79229705 | |||||||
chr6:79229844 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0006g0045 |
7 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.15+4702G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79229844 | |||||||
chr6:79230130 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.15+4416C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79230130 | |||||||
chr6:79230152 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.15+4394T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79230152 | |||||||
chr6:79230363 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0034 others(15): Show |
31 | HG00408.hp1 HG00621.hp1 HG02056.hp2 others(28): Show |
intron_variant | MODIFIER | c.15+4183G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79230363 | |||||||
chr6:79230817 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.15+3729T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79230817 | |||||||
chr6:79230859 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+3687C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79230859 | |||||||
chr6:79230876 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.15+3670T>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79230876 | |||||||
chr6:79231061 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.15+3485T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79231061 | |||||||
chr6:79231151 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.15+3395T>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79231151 | |||||||
chr6:79231204 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
7 | HG01069.hp2 HG01099.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+3342C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79231204 | |||||||
chr6:79231247 | G | A | 1 | a0001c0001t0008g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.15+3299C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79231247 | |||||||
chr6:79231275 | A | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG01099.hp2 HG03654.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.15+3271T>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79231275 | |||||||
chr6:79231400 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(35): Show |
73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.15+3146G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79231400 | |||||||
chr6:79231666 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.15+2880C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79231666 | |||||||
chr6:79231857 | T | C | 3 | a0001c0001t0002g0006 a0001c0001t0006g0045 a0001c0001t0007g0055 |
8 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+2689A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79231857 | |||||||
chr6:79231945 | G | A | 1 | a0001c0001t0003g0026 | 3 | HG02559.hp1 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15+2601C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79231945 | |||||||
chr6:79232009 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.15+2537G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232009 | |||||||
chr6:79232116 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(70): Show |
141 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.15+2430A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232116 | |||||||
chr6:79232150 | G | C | 11 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(8): Show |
16 | HG01256.hp2 HG01346.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+2396C>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232150 | |||||||
chr6:79232234 | T | C | 1 | a0001c0001t0007g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.15+2312A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232234 | |||||||
chr6:79232285 | G | T | 1 | a0001c0001t0002g0046 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.15+2261C>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232285 | |||||||
chr6:79232392 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.15+2154C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232392 | |||||||
chr6:79232601 | GT | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(8): Show |
16 | HG01256.hp2 HG01346.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+1944delA | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232601 | |||||||
chr6:79232644 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0063 others(6): Show |
14 | HG01256.hp2 HG02280.hp1 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.15+1902C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232644 | |||||||
chr6:79232757 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+1789A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232757 | |||||||
chr6:79232767 | G | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.15+1779C>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232767 | |||||||
chr6:79232792 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.15+1754A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232792 | |||||||
chr6:79232820 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.15+1726G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232820 | |||||||
chr6:79232845 | T | A | 3 | a0001c0001t0001g0168 a0001c0001t0003g0026 a0001c0001t0003g0044 |
6 | HG01109.hp2 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+1701A>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79232845 | |||||||
chr6:79233159 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.15+1387T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79233159 | |||||||
chr6:79233212 | T | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.15+1334A>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79233212 | |||||||
chr6:79233244 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.15+1302A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79233244 | |||||||
chr6:79233517 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.15+1029A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79233517 | |||||||
chr6:79233536 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.15+1010C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79233536 | |||||||
chr6:79233590 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.15+956A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79233590 | |||||||
chr6:79233687 | C | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0092 a0001c0001t0001g0093 |
4 | HG00639.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+859G>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79233687 | |||||||
chr6:79233720 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.15+826C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79233720 | |||||||
chr6:79233995 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.15+551G>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79233995 | |||||||
chr6:79234069 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
202 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.15+477C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79234069 | |||||||
chr6:79234111 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.15+435T>C | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79234111 | |||||||
chr6:79234145 | C | T | 1 | a0001c0001t0003g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.15+401G>A | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79234145 | |||||||
chr6:79234273 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0174 |
7 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+273C>T | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79234273 | |||||||
chr6:79234379 | C | CAG | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.15+165_15+166dupCT | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79234379 | |||||||
chr6:79234529 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0175 others(4): Show |
18 | HG02015.hp2 HG02129.hp1 NA18955.hp2 others(15): Show |
intron_variant | MODIFIER | c.15+17A>G | HMGN3 | ENSG00000118418.16 | transcript | ENST00000620514.2 | protein_coding | 1/6 | chr6 | 79234529 |